syndromic X-linked intellectual disability - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

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RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:	syndromic X-linked intellectual disability	go back to main search page
Accession:	DOID:0060309	browse the term
Definition:	A syndromic intellectual disability characterized by an X-linked inheritance pattern. (DO)
Synonyms:	exact_synonym:	syndromic X-linked mental retardation
	xref:	OMIM:PS309510

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Genes (575)

syndromic X-linked intellectual disability

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

aristaless related homeobox

NCBI chrNW_004936836:295,090...306,756
Ensembl chrNW_004936836:295,664...306,756

G

calcium/calmodulin dependent serine protein kinase

ClinVar Annotator: match by term: X-linked syndromic intellectual disability

PMID:22452838 PMID:25741868

NCBI chrNW_004936502:7,933,312...8,281,492
Ensembl chrNW_004936502:7,937,146...8,281,492

G

RAB39B, member RAS oncogene family

NCBI chrNW_004936927:492,114...498,030
Ensembl chrNW_004936927:492,099...498,294

Armfield syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

family with sequence similarity 50 member A

ClinVar Annotator: match by term: Armfield syndrome | ClinVar Annotator: match by term: FAM50A-related condition

PMID:10398235 PMID:25741868 PMID:32703943

NCBI chrNW_004936809:1,195,479...1,202,126

Arts syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

paired like homeodomain 2

DNA, protein:missense mutations, decreased activity:exon:p.Q133P (c.398A>C), p.L152P (c.455T>C) (human)

NCBI chrNW_004936563:1,713,294...1,732,431

G

phosphoribosyl pyrophosphate synthetase 1

ClinVar Annotator: match by term: Arts syndrome | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE | ClinVar Annotator: match by term: X-linked fatal ataxia with deafness and loss of vision

PMID:1664177 PMID:6243137 PMID:7593598 PMID:8253776 PMID:8498830 More...

NCBI chrNW_004936499:7,114,838...7,136,468
Ensembl chrNW_004936499:7,115,780...7,136,449

Basilicata-Akhtar syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

MSL complex subunit 3

ClinVar Annotator: match by term: Basilicata-Akhtar syndrome

PMID:25741868 PMID:30224647 PMID:33173220

NCBI chrNW_004936470:1,572,037...1,587,002
Ensembl chrNW_004936470:1,572,014...1,587,011

Borjeson-Forssman-Lehmann syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

PHD finger protein 6

ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome | ClinVar Annotator: match by term: MENTAL RETARDATION, EPILEPSY, AND ENDOCRINE DISORDERS | ClinVar Annotator: match by term: Mental deficiency, epilepsy and endocrine disorders

PMID:12415272 PMID:13871358 PMID:15241480 PMID:15466013 PMID:15994862 More...

NCBI chrNW_004936691:716,723...767,960
Ensembl chrNW_004936691:716,697...768,016

Christianson syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

adhesion G protein-coupled receptor G4

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,837,036...10,934,833
Ensembl chrNW_004936513:10,845,610...10,947,288

G

Rac/Cdc42 guanine nucleotide exchange factor 6

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,488,525...10,598,366
Ensembl chrNW_004936513:10,488,532...10,598,493

G

bombesin receptor subtype 3

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,784,181...10,788,679
Ensembl chrNW_004936513:10,784,181...10,788,680

G

CD40 ligand

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,607,617...10,620,403
Ensembl chrNW_004936513:10,607,617...10,620,403

G

cyclin dependent kinase like 5

ClinVar Annotator: match by term: Angelman syndrome-like

PMID:15499549 PMID:16015284 PMID:16813600 PMID:18414213 PMID:19241098 More...

NCBI chrNW_004936844:101,815...271,254
Ensembl chrNW_004936844:160,833...271,901

G

four and a half LIM domains 1

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:11,025,753...11,064,312
Ensembl chrNW_004936513:11,025,715...11,064,312

G

G protein-coupled receptor 101

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,282,683...10,284,206
Ensembl chrNW_004936513:10,282,683...10,284,206

G

HIVEP zinc finger 2

ClinVar Annotator: match by term: Angelman syndrome-like

NCBI chrNW_004936625:3,219,260...3,301,361
Ensembl chrNW_004936625:3,267,947...3,301,369

G

HIV-1 Tat specific factor 1

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,762,417...10,779,641
Ensembl chrNW_004936513:10,762,398...10,779,374

G

MAP7 domain containing 3

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,989,123...11,021,086

G

RNA binding motif protein X-linked

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,429,862...10,442,509
Ensembl chrNW_004936513:10,429,824...10,437,108

G

retinoschisin 1

ClinVar Annotator: match by term: Angelman syndrome-like

PMID:15499549 PMID:16813600 PMID:18414213 PMID:19241098 PMID:20479760 More...

NCBI chrNW_004936844:284,938...314,524
Ensembl chrNW_004936844:284,141...314,545

G

solute carrier family 9 member A6

ClinVar Annotator: match by term: Christianson syndrome | ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE | ClinVar Annotator: match by term: X-linked mental retardation, syndromic, Christianson type

PMID:9536098 PMID:15319456 PMID:15358621 PMID:16019685 PMID:16199547 More...

NCBI chrNW_004936513:11,158,609...11,215,477
Ensembl chrNW_004936513:11,158,730...11,215,568

G

vestigial like family member 1

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:10,704,343...10,742,583
Ensembl chrNW_004936513:10,721,500...10,742,670

G

Zic family member 3

ClinVar Annotator: match by term: Christianson syndrome

PMID:15319456 PMID:15358621 PMID:16019685 PMID:18342287 PMID:21465648 More...

NCBI chrNW_004936513:9,780,895...9,792,865
Ensembl chrNW_004936513:9,786,709...9,793,077

corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

immunoglobulin binding protein 1

ClinVar Annotator: match by term: Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome | ClinVar Annotator: match by term: IGBP1-related condition

PMID:25741868 PMID:28492532

NCBI chrNW_004936762:1,292,572...1,319,145

female-restricted syndromic X-linked intellectual disability 99

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ubiquitin specific peptidase 9 X-linked

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED | ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted | ClinVar Annotator: match by term: USP9X-related condition

PMID:25741868 PMID:26833328 PMID:28492532 PMID:31443933 PMID:34008892

NCBI chrNW_004936502:7,649,808...7,732,731
Ensembl chrNW_004936502:7,649,842...7,735,382

INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

NFKB activating protein

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS, 2

PMID:25741868 PMID:26358559 PMID:31587868

NCBI chrNW_004936479:10,024,674...10,041,738
Ensembl chrNW_004936479:10,024,705...10,041,590

MEHMO syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

eukaryotic translation initiation factor 2 subunit gamma

ClinVar Annotator: match by term: MEHMO syndrome

PMID:23063529 PMID:25741868 PMID:25741869 PMID:27333055 PMID:28055140

NCBI chrNW_004936624:516,206...535,749
Ensembl chrNW_004936624:515,864...535,981

Miles-Carpenter syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

zinc finger C4H2-type containing

ClinVar Annotator: match by term: Wieacker-Wolff syndrome | ClinVar Annotator: match by term: Wieacker-Wolff syndrome (spectrum) | ClinVar Annotator: match by term: ZC4H2-related X-linked intellectual disability

PMID:1915520 PMID:2018061 PMID:4039531 PMID:9536098 PMID:17576681 More...

NCBI chrNW_004936635:2,924,632...2,954,003
Ensembl chrNW_004936635:2,924,601...2,953,854

Mullegama-Klein-Martinez syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

SH2 domain containing 1A

ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER, X-LINKED, WITH CRANIOFACIAL ABNORMALITIES

PMID:25741868 PMID:28492532

NCBI chrNW_004936479:6,258,953...6,281,552
Ensembl chrNW_004936479:6,258,953...6,281,552

G

STAG2 cohesin complex component

ClinVar Annotator: match by term: Mullegama-Klein-Martinez syndrome | ClinVar Annotator: match by term: STAG2-related disorder

PMID:25741868 PMID:28296084 PMID:28492532 PMID:29263825 PMID:30158690 More...

NCBI chrNW_004936479:6,508,539...6,635,127
Ensembl chrNW_004936479:6,508,532...6,632,627

Paganini-Miozzo syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

heparan sulfate 6-O-sulfotransferase 2

ClinVar Annotator: match by term: Paganini-Miozzo syndrome

PMID:25741868 PMID:28492532 PMID:30471091

NCBI chrNW_004936691:1,976,449...2,257,303
Ensembl chrNW_004936691:1,976,449...2,255,144

Partington syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

aristaless related homeobox

ClinVar Annotator: match by term: Partington syndrome | ClinVar Annotator: match by term: X-linked spasticity-intellectual disability-epilepsy syndrome

PMID:2080994 PMID:3177452 PMID:5008734 PMID:8826464 PMID:10353782 More...

NCBI chrNW_004936836:295,090...306,756
Ensembl chrNW_004936836:295,664...306,756

Prieto syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

WNK lysine deficient protein kinase 3

ClinVar Annotator: match by term: Prieto syndrome

PMID:3121220 PMID:25741868 PMID:26350204 PMID:35678782

NCBI chrNW_004936751:1,095,578...1,266,772
Ensembl chrNW_004936751:1,100,192...1,266,740

Raynaud-Claes syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

chloride voltage-gated channel 4

ClinVar Annotator: match by term: CLCN4-related X-linked intellectual disability syndrome | ClinVar Annotator: match by term: CLCN4-related disorder | ClinVar Annotator: match by term: MRX49 | ClinVar Annotator: match by term: RAYNAUD-CLAES SYNDROME

PMID:8826458 PMID:9415477 PMID:9536098 PMID:17576681 PMID:23647072 More...

NCBI chrNW_004936470:142,862...214,993
Ensembl chrNW_004936470:142,832...212,154

Renpenning syndrome

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

polyglutamine binding protein 1

ClinVar Annotator: match by term: Renpenning syndrome

PMID:6711604 PMID:9545405 PMID:13981686 PMID:14634649 PMID:15024694 More...

NCBI chrNW_004936721:825,171...830,010
Ensembl chrNW_004936721:825,075...832,755

G

solute carrier family 35 member A2

ClinVar Annotator: match by term: Renpenning syndrome

PMID:25741868 PMID:28492532 PMID:32903913

NCBI chrNW_004936721:830,067...838,783
Ensembl chrNW_004936721:830,042...838,866

Stocco Dos Santos type X-linked intellectual disability

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

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G

A-kinase anchoring protein 4

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,692,623...1,700,256
Ensembl chrNW_004936721:1,692,623...1,702,348

G

bone morphogenetic protein 15

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936873:109,156...115,498

G

cyclin B3

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,729,979...1,782,399

G

chloride voltage-gated channel 5

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,552,312...1,602,360
Ensembl chrNW_004936721:1,445,779...1,596,814

G

diacylglycerol kinase kappa

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,804,746...1,934,854
Ensembl chrNW_004936721:1,804,746...1,934,527

G

G1 to S phase transition 2

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936909:436,004...438,818
Ensembl chrNW_004936909:436,018...438,651

G

uncharacterized LOC110599509

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,347,679...1,350,598

G

MAGE family member D1

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936909:493,998...592,649
Ensembl chrNW_004936909:585,206...592,644

G

shroom family member 4

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

PMID:12673656 PMID:16249884 PMID:18414213 PMID:23757202 PMID:23871722 More...

NCBI chrNW_004936721:2,068,731...2,166,537

G

ubiquitin specific peptidase 27 X-linked

ClinVar Annotator: match by term: X-linked intellectual disability, Stocco dos Santos type

NCBI chrNW_004936721:1,396,103...1,399,718
Ensembl chrNW_004936721:1,396,103...1,399,745

syndromic X-linked intellectual developmental disorder Bain type

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

heterogeneous nuclear ribonucleoprotein H1

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE

NCBI chrNW_004936739:1,135,282...1,144,643
Ensembl chrNW_004936739:1,135,289...1,144,643

G

heterogeneous nuclear ribonucleoprotein H2

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE

PMID:20308327 PMID:24033266 PMID:25741868 PMID:27545675 PMID:28492532 More...

NCBI chrNW_004936813:484,872...489,822
Ensembl chrNW_004936813:484,872...490,615

syndromic X-linked intellectual disability 14

term browser

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Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

A-kinase anchoring protein 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,051,669...10,055,518

G

ATPase Na+/K+ transporting family member beta 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,648,315...9,666,782
Ensembl chrNW_004936479:9,650,598...9,666,782

G

C1GALT1 specific chaperone 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,416,192...9,420,327
Ensembl chrNW_004936479:9,416,284...9,420,177

G

cullin 4B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,490,717...9,535,998
Ensembl chrNW_004936479:9,479,133...9,534,262

G

lysosomal associated membrane protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,584,221...9,622,330
Ensembl chrNW_004936479:9,584,221...9,610,420

G

MCTS1 re-initiation and release factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,432,817...9,491,615

G

NADH:ubiquinone oxidoreductase subunit A1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,074,290...10,078,072
Ensembl chrNW_004936479:10,074,307...10,078,066

G

NFKB activating protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,024,674...10,041,738
Ensembl chrNW_004936479:10,024,705...10,041,590

G

NFKB repressing factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,312,061...10,327,970
Ensembl chrNW_004936479:10,311,996...10,328,393

G

ring finger protein 113A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,078,201...10,079,400
Ensembl chrNW_004936479:10,078,304...10,079,338

G

ribosomal protein L39

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,132,965...10,136,506

G

septin 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,233,035...10,305,327
Ensembl chrNW_004936479:10,233,005...10,305,392

G

sosondowah ankyrin repeat domain family member D

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,162,691...10,164,190

G

transmembrane protein 255A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,721,602...9,781,468
Ensembl chrNW_004936479:9,721,633...9,781,509

G

ubiquitin conjugating enzyme E2 A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:10,330,666...10,340,268
Ensembl chrNW_004936479:10,330,632...10,340,367

G

UPF3B regulator of nonsense mediated mRNA decay

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 14 | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

PMID:9536098 PMID:17576681 PMID:17704778 PMID:18414213 PMID:19238151 More...

NCBI chrNW_004936479:10,093,290...10,111,293
Ensembl chrNW_004936479:10,093,290...10,111,752

G

zinc finger and BTB domain containing 33

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 14

NCBI chrNW_004936479:9,781,923...9,791,000
Ensembl chrNW_004936479:9,781,952...9,790,821

syndromic X-linked intellectual disability 34

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

non-POU domain containing octamer binding

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 34

PMID:25741868 PMID:26571461 PMID:26822237 PMID:27329731 PMID:27550220 More...

NCBI chrNW_004936762:322,413...343,126
Ensembl chrNW_004936762:321,280...341,537

syndromic X-linked intellectual disability 5

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

adaptor related protein complex 1 subunit sigma 2

ClinVar Annotator: match by term: Pettigrew syndrome

PMID:2018058 PMID:5054319 PMID:10398241 PMID:12599187 PMID:17186471 More...

NCBI chrNW_004936470:5,260,984...5,301,552
Ensembl chrNW_004936470:5,257,542...5,289,469

G

cullin 4B

ClinVar Annotator: match by term: Pettigrew syndrome

NCBI chrNW_004936479:9,490,717...9,535,998
Ensembl chrNW_004936479:9,479,133...9,534,262

syndromic X-linked intellectual disability 94

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

glutamate ionotropic receptor AMPA type subunit 3

ClinVar Annotator: match by term: GRIA3-Related Disorder | ClinVar Annotator: match by term: GRIA3-related condition | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability 94

PMID:17989220 PMID:19022251 PMID:20716669 PMID:24721225 PMID:25326635 More...

NCBI chrNW_004936479:7,050,018...7,323,047
Ensembl chrNW_004936479:7,050,016...7,323,196

syndromic X-linked intellectual disability Cabezas type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

A-kinase anchoring protein 14

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,051,669...10,055,518

G

ATPase Na+/K+ transporting family member beta 4

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,648,315...9,666,782
Ensembl chrNW_004936479:9,650,598...9,666,782

G

C1GALT1 specific chaperone 1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,416,192...9,420,327
Ensembl chrNW_004936479:9,416,284...9,420,177

G

cullin 4B

ClinVar Annotator: match by term: CABEZAS SYNDROME | ClinVar Annotator: match by term: CUL4B-Related Disorder | ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED, SYNDROMIC 15 | ClinVar Annotator: match by term: Mental retardation with short stature, hypogonadism and abnormal gait, X-linked

PMID:8135271 PMID:9536098 PMID:10978355 PMID:17236139 PMID:17273978 More...

NCBI chrNW_004936479:9,490,717...9,535,998
Ensembl chrNW_004936479:9,479,133...9,534,262

G

dedicator of cytokinesis 11

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:11,148,877...11,334,381
Ensembl chrNW_004936479:11,148,626...11,334,452

G

interleukin 13 receptor subunit alpha 1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:11,052,077...11,108,915
Ensembl chrNW_004936479:11,050,249...11,108,909

G

KIAA1210 ortholog

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,729,891...10,773,342

G

lysosomal associated membrane protein 2

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,584,221...9,622,330
Ensembl chrNW_004936479:9,584,221...9,610,420

G

LON peptidase N-terminal domain and ring finger 3

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,840,630...10,880,494
Ensembl chrNW_004936479:10,840,448...10,879,906

G

MCTS1 re-initiation and release factor

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,432,817...9,491,615

G

NADH:ubiquinone oxidoreductase subunit A1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,074,290...10,078,072
Ensembl chrNW_004936479:10,074,307...10,078,066

G

NFKB activating protein

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,024,674...10,041,738
Ensembl chrNW_004936479:10,024,705...10,041,590

G

NFKB repressing factor

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,312,061...10,327,970
Ensembl chrNW_004936479:10,311,996...10,328,393

G

progesterone receptor membrane component 1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,625,989...10,634,058
Ensembl chrNW_004936479:10,625,889...10,634,136

G

ring finger protein 113A

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,078,201...10,079,400
Ensembl chrNW_004936479:10,078,304...10,079,338

G

ribosomal protein L39

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,132,965...10,136,506

G

septin 6

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,233,035...10,305,327
Ensembl chrNW_004936479:10,233,005...10,305,392

G

solute carrier family 25 member 43

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,455,632...10,499,224
Ensembl chrNW_004936479:10,453,187...10,499,251

G

solute carrier family 25 member 5

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,432,172...10,435,154

G

sosondowah ankyrin repeat domain family member D

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,162,691...10,164,190

G

STING1 ER exit protein 1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,351,016...10,373,416
Ensembl chrNW_004936479:10,351,059...10,404,657

G

transmembrane protein 255A

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,721,602...9,781,468
Ensembl chrNW_004936479:9,721,633...9,781,509

G

ubiquitin conjugating enzyme E2 A

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,330,666...10,340,268
Ensembl chrNW_004936479:10,330,632...10,340,367

G

UPF3B regulator of nonsense mediated mRNA decay

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:10,093,290...10,111,293
Ensembl chrNW_004936479:10,093,290...10,111,752

G

zinc finger and BTB domain containing 33

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:9,781,923...9,791,000
Ensembl chrNW_004936479:9,781,952...9,790,821

G

zinc finger CCHC-type containing 12

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked syndromic, Cabezas type

PMID:17236139 PMID:25385192 PMID:28492532

NCBI chrNW_004936479:11,021,502...11,024,612

syndromic X-linked intellectual disability Claes-Jensen type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

DEAD-box helicase 3 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Claes-Jensen type

PMID:2563148 PMID:25741868 PMID:26235985

NCBI chrNW_004936502:7,770,896...7,820,555
Ensembl chrNW_004936502:7,804,824...7,820,569

G

lysine demethylase 5C

ClinVar Annotator: match by term: KDM5C-related condition | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Claes-Jensen type

PMID:1605217 PMID:10982473 PMID:15586325 PMID:16538222 PMID:16541399 More...

NCBI chrNW_004936751:159,628...204,136
Ensembl chrNW_004936751:167,920...203,966

syndromic X-linked intellectual disability Hedera type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

aristaless related homeobox

DNA:missense mutation:cds:p.P353L (human)

PMID:12177367 PMID:19605412

RGD:11565831 RGD:11565840

NCBI chrNW_004936836:295,090...306,756
Ensembl chrNW_004936836:295,664...306,756

G

ATPase H+ transporting accessory protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:9536098 PMID:11782983 PMID:15746149 PMID:17576681 PMID:23901204 More...

NCBI chrNW_004936502:7,206,226...7,232,798
Ensembl chrNW_004936502:7,206,172...7,233,912

G

BCL6 corepressor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:6,764,043...6,812,194
Ensembl chrNW_004936502:6,764,907...6,792,916

G

calcium/calmodulin dependent serine protein kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,933,312...8,281,492
Ensembl chrNW_004936502:7,937,146...8,281,492

G

chromosome X CXorf38 homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,260,094...7,278,416
Ensembl chrNW_004936502:7,259,928...7,278,725

G

DEAD-box helicase 3 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,770,896...7,820,555
Ensembl chrNW_004936502:7,804,824...7,820,569

G

G protein-coupled receptor 34

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:8,070,824...8,078,273
Ensembl chrNW_004936502:8,076,590...8,077,714

G

G protein-coupled receptor 82

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:8,100,698...8,102,349
Ensembl chrNW_004936502:8,098,580...8,102,349

G

mediator complex subunit 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,280,606...7,350,750
Ensembl chrNW_004936502:7,280,534...7,350,435

G

mitochondrial pyruvate carrier 1 like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,256,149...7,256,553
Ensembl chrNW_004936502:7,256,149...7,256,553

G

nyctalopin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,890,582...7,909,157
Ensembl chrNW_004936502:7,890,535...7,910,986

G

ubiquitin specific peptidase 9 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Hedera type

PMID:23901204 PMID:26235985 PMID:28492532

NCBI chrNW_004936502:7,649,808...7,732,731
Ensembl chrNW_004936502:7,649,842...7,735,382

syndromic X-linked intellectual disability Lubs type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ATP binding cassette subfamily B member 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,224,703...1,326,761
Ensembl chrNW_004936683:1,222,450...1,326,765

G

ATP binding cassette subfamily D member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:615,133...634,618
Ensembl chrNW_004936809:615,139...635,990

G

angiotensin converting enzyme 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,964,526...5,011,808
Ensembl chrNW_004936470:4,965,332...5,011,702

G

acyl-CoA thioesterase 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:795,272...834,441
Ensembl chrNW_004936624:795,237...836,571

G

acyl-CoA synthetase long chain family member 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:5,456,985...5,540,115
Ensembl chrNW_004936499:5,456,986...5,540,144

G

actin related protein T1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:3,278,795...3,279,928
Ensembl chrNW_004936479:3,278,795...3,279,928

G

adhesion G protein-coupled receptor G2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:552,729...619,429
Ensembl chrNW_004936844:554,171...619,429

G

adhesion G protein-coupled receptor G4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,837,036...10,934,833
Ensembl chrNW_004936513:10,845,610...10,947,288

G

ALF transcription elongation factor 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:414,839...893,670
Ensembl chrNW_004936513:414,574...893,676

G

angiotensin II receptor type 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:13,252,678...13,255,570
Ensembl chrNW_004936479:13,252,678...13,255,570

G

apoptosis inducing factor mitochondria associated 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,441,508...1,477,133
Ensembl chrNW_004936479:1,441,437...1,478,107

G

A-kinase anchoring protein 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,051,669...10,055,518

G

A-kinase anchoring protein 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,692,623...1,700,256
Ensembl chrNW_004936721:1,692,623...1,702,348

G

5'-aminolevulinate synthase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,818,255...1,841,028
Ensembl chrNW_004936751:1,814,446...1,841,531

G

ALG13 UDP-N-acetylglucosaminyltransferase subunit

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:3,558,273...3,629,570
Ensembl chrNW_004936499:3,558,236...3,629,592

G

APC membrane recruitment protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:3,465,473...3,482,311
Ensembl chrNW_004936635:3,478,598...3,482,008

G

AMMECR nuclear protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:4,910,687...5,023,252
Ensembl chrNW_004936499:4,910,686...5,023,293

G

angiomotin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:2,594,190...2,661,307
Ensembl chrNW_004936499:2,594,239...2,661,359

G

adaptor related protein complex 1 subunit sigma 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,260,984...5,301,552
Ensembl chrNW_004936470:5,257,542...5,289,469

G

apurinic/apyrimidinic endodeoxyribonuclease 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,807,867...1,817,780
Ensembl chrNW_004936751:1,807,867...1,819,272

G

apelin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,889,930...1,899,811
Ensembl chrNW_004936479:1,890,229...1,899,730

G

apolipoprotein O

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:667,659...754,944

G

apolipoprotein O like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:5,790,287...5,858,054
Ensembl chrNW_004936547:5,790,283...5,860,198

G

androgen receptor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:485,903...647,820
Ensembl chrNW_004936635:485,903...647,932

G

A-Raf proto-oncogene, serine/threonine kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,323,365...13,335,003
Ensembl chrNW_004936502:13,323,355...13,335,224

G

Rho GTPase activating protein 36

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:569,990...599,778
Ensembl chrNW_004936479:569,990...599,778

G

Rho GTPase activating protein 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:791,275...807,448
Ensembl chrNW_004936809:791,274...807,450

G

Rac/Cdc42 guanine nucleotide exchange factor 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,488,525...10,598,366
Ensembl chrNW_004936513:10,488,532...10,598,493

G

Cdc42 guanine nucleotide exchange factor 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:3,817,034...3,956,928
Ensembl chrNW_004936635:3,816,606...3,960,190

G

ADP ribosylation factor like GTPase 13A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:66,944...80,346

G

armadillo repeat containing X-linked 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:574,939...578,228
Ensembl chrNW_004936813:576,463...577,854

G

armadillo repeat containing X-linked 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:649,463...655,013
Ensembl chrNW_004936813:649,468...653,615

G

armadillo repeat containing X-linked 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:622,501...627,335
Ensembl chrNW_004936813:622,520...625,971

G

armadillo repeat containing X-linked 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:540,574...557,845

G

armadillo repeat containing X-linked 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:1,251,936...1,255,422

G

armadillo repeat containing X-linked 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:614,456...617,354
Ensembl chrNW_004936813:614,521...617,349

G

arrestin 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,194,251...1,207,914
Ensembl chrNW_004936762:1,194,166...1,208,844

G

aristaless related homeobox

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936836:295,090...306,756
Ensembl chrNW_004936836:295,664...306,756

G

ankyrin repeat and SOCS box containing 11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,701,670...4,728,527
Ensembl chrNW_004936470:4,701,681...4,728,555

G

ankyrin repeat and SOCS box containing 12

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:3,447,347...3,453,762
Ensembl chrNW_004936635:3,447,345...3,453,762

G

autophagy related 4A cysteine peptidase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,641,192...6,691,685
Ensembl chrNW_004936499:6,640,957...6,691,995

G

ATPase phospholipid transporting 11C

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:7,701,733...7,889,753
Ensembl chrNW_004936513:7,701,725...7,889,750

G

ATPase Na+/K+ transporting family member beta 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,648,315...9,666,782
Ensembl chrNW_004936479:9,650,598...9,666,782

G

ATPase plasma membrane Ca2+ transporting 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:396,883...466,372
Ensembl chrNW_004936809:396,733...466,524

G

ATPase H+ transporting accessory protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,179,507...1,188,172
Ensembl chrNW_004936809:1,179,464...1,188,283

G

ATPase H+ transporting accessory protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,206,226...7,232,798
Ensembl chrNW_004936502:7,206,172...7,233,912

G

ATPase copper transporting alpha

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,874,022...2,936,214
Ensembl chrNW_004936683:2,874,042...2,935,040

G

ATRX chromatin remodeler

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,496,307...2,718,539
Ensembl chrNW_004936683:2,495,959...2,718,620

G

arginine vasopressin receptor 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:789,337...790,986
Ensembl chrNW_004936809:788,286...790,954

G

acyl-CoA wax alcohol acyltransferase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,238,239...1,244,330
Ensembl chrNW_004936762:1,238,473...1,244,330

G

acyl-CoA wax alcohol acyltransferase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:1,562,900...1,574,018
Ensembl chrNW_004936777:1,563,229...1,573,993

G

B cell receptor associated protein 31

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:582,689...614,800
Ensembl chrNW_004936809:582,649...615,079

G

BCLAF1 and THRAP3 family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:4,177,596...4,238,016
Ensembl chrNW_004936624:4,177,534...4,238,046

G

BCL6 corepressor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:6,764,043...6,812,194
Ensembl chrNW_004936502:6,764,907...6,792,916

G

BCL6 corepressor like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,539,676...1,605,647
Ensembl chrNW_004936479:1,538,051...1,606,344

G

BEN domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:7,379,946...7,441,955

G

brain expressed X-linked 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:7,842,016...7,843,087

G

brain expressed X-linked 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:8,000,064...8,002,029
Ensembl chrNW_004936547:8,000,230...8,001,999

G

brain expressed X-linked 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004937070:148,270...150,535
Ensembl chrNW_004937070:148,400...150,529

G

biglycan

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:375,589...389,718
Ensembl chrNW_004936809:375,543...389,756

G

bone morphogenetic protein 15

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936873:109,156...115,498

G

BMX non-receptor tyrosine kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,914,643...4,962,134
Ensembl chrNW_004936470:4,914,756...4,962,129

G

bombesin receptor subtype 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,784,181...10,788,679
Ensembl chrNW_004936513:10,784,181...10,788,680

G

bromodomain and WD repeat domain containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:2,236,164...2,354,652
Ensembl chrNW_004936547:2,240,314...2,354,796

G

Bruton tyrosine kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:429,400...467,481
Ensembl chrNW_004936813:429,224...463,441

G

C1GALT1 specific chaperone 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,416,192...9,420,327
Ensembl chrNW_004936479:9,416,284...9,420,177

G

carbonic anhydrase 5B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,184,489...5,227,855
Ensembl chrNW_004936470:5,184,483...5,230,214

G

calcium voltage-gated channel subunit alpha1 F

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,078,570...1,106,153
Ensembl chrNW_004936721:1,078,650...1,106,113

G

calpain 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:4,041,837...4,060,895
Ensembl chrNW_004936499:4,035,664...4,060,895

G

calcium/calmodulin dependent serine protein kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,933,312...8,281,492
Ensembl chrNW_004936502:7,937,146...8,281,492

G

coiled-coil domain containing 120

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:954,188...971,507
Ensembl chrNW_004936721:964,603...969,992

G

coiled-coil domain containing 160

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:863,903...875,565

G

coiled-coil domain containing 22

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,107,697...1,118,313
Ensembl chrNW_004936721:1,107,866...1,118,050

G

cyclin B3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,729,979...1,782,399

G

cyclin Q

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:471,619...482,296
Ensembl chrNW_004936809:472,061...482,192

G

CD40 ligand

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,607,617...10,620,403
Ensembl chrNW_004936513:10,607,617...10,620,403

G

CD99 molecule like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,592,214...1,690,811
Ensembl chrNW_004936714:1,592,422...1,688,552

G

cyclin dependent kinase 16

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,987,736...13,000,186
Ensembl chrNW_004936502:12,987,731...13,000,186

G

cyclin dependent kinase like 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:101,815...271,254
Ensembl chrNW_004936844:160,833...271,901

G

cerebellar degeneration related 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:6,965,492...6,967,229

G

caudal type homeobox 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:297,112...305,506
Ensembl chrNW_004936683:297,112...305,506

G

centromere protein I

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:171,187...224,442
Ensembl chrNW_004936813:172,894...244,881

G

centrin 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:274,098...279,177
Ensembl chrNW_004936714:274,036...279,381

G

cilia and flagella associated protein 47

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:3,254,001...3,630,408

G

complement factor properdin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,391,613...13,398,723
Ensembl chrNW_004936502:13,391,535...13,397,440

G

cysteine rich hydrophobic domain 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:397,609...491,491
Ensembl chrNW_004936683:397,568...463,398

G

CHM Rab escort protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:6,368,941...6,533,199
Ensembl chrNW_004936547:6,368,918...6,533,237

G

chordin like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:4,474,899...4,587,563
Ensembl chrNW_004936499:4,474,884...4,587,501

G

carbohydrate sulfotransferase 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,426,821...12,446,127
Ensembl chrNW_004936502:12,426,851...12,445,741

G

Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,387,354...1,392,955
Ensembl chrNW_004936762:1,387,346...1,391,967

G

chloride voltage-gated channel 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,552,312...1,602,360
Ensembl chrNW_004936721:1,445,779...1,596,814

G

claudin 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,818,436...7,828,444
Ensembl chrNW_004936499:7,820,410...7,821,102

G

collectrin, amino acid transport regulator

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,040,831...5,124,611
Ensembl chrNW_004936470:5,040,795...5,124,192

G

cyclic nucleotide gated channel subunit alpha 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,011,736...1,017,722
Ensembl chrNW_004936714:1,011,736...1,017,729

G

connector enhancer of kinase suppressor of Ras 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,727,208...2,989,653
Ensembl chrNW_004936624:2,727,208...2,989,659

G

collagen type IV alpha 5 chain

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,143,736...6,360,565
Ensembl chrNW_004936499:6,144,857...6,360,368

G

collagen type IV alpha 6 chain

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,421,930...6,640,429
Ensembl chrNW_004936499:6,362,295...6,639,047

G

CPX chromosome region candidate 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:12,832,833...12,833,807

G

cleavage stimulation factor subunit 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:6,042,785...6,066,758
Ensembl chrNW_004936584:6,040,336...6,066,703

G

cancer/testis antigen 55

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,473,810...11,496,812

G

cancer/testis antigen 83

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:13,021,400...13,022,724

G

CTP synthase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,889,393...5,988,558
Ensembl chrNW_004936470:5,888,469...5,988,525

G

cullin 4B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,490,717...9,535,998
Ensembl chrNW_004936479:9,479,133...9,534,262

G

C-X-C motif chemokine receptor 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:66,636...69,694
Ensembl chrNW_004936762:66,636...69,373

G

chromosome X CXorf38 homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,260,094...7,278,416
Ensembl chrNW_004936502:7,259,928...7,278,725

G

chromosome X CXorf58 homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:639,842...669,723
Ensembl chrNW_004936624:639,716...665,130

G

chromosome X CXorf65 homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:491,580...493,455
Ensembl chrNW_004936762:491,580...493,455

G

chromosome X CXorf66 homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:7,664,110...7,668,227

G

cylicin 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:4,678,172...4,706,407

G

cysteinyl leukotriene receptor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:479,261...504,757

G

dachshund family transcription factor 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:6,618,236...7,109,458
Ensembl chrNW_004936547:6,618,469...7,109,019

G

doublecortin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:3,905,262...4,004,457
Ensembl chrNW_004936499:3,903,376...4,005,508

G

DEAD-box helicase 3 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,770,896...7,820,555
Ensembl chrNW_004936502:7,804,824...7,820,569

G

DEAD-box helicase 53

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:1,436,134...1,438,389

G

diacylglycerol O-acyltransferase 2 like 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,262,374...1,268,979
Ensembl chrNW_004936762:1,262,870...1,281,432

G

diacylglycerol kinase kappa

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,804,746...1,934,854
Ensembl chrNW_004936721:1,804,746...1,934,527

G

diaphanous related formin 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:2,286,919...3,081,652
Ensembl chrNW_004936584:2,287,288...3,076,788

G

divergent protein kinase domain 2B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:11,243,167...11,284,186
Ensembl chrNW_004936502:11,247,775...11,284,186

G

discs large MAGUK scaffold protein 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:982,331...1,038,486
Ensembl chrNW_004936762:982,258...1,038,492

G

dystrophin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:7,157,526...7,943,703

G

dynein axonemal assembly factor 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,463,225...7,503,322
Ensembl chrNW_004936499:7,462,398...7,494,713

G

deoxyribonuclease 1 like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,151,312...1,159,017
Ensembl chrNW_004936809:1,151,202...1,159,029

G

dedicator of cytokinesis 11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:11,148,877...11,334,381
Ensembl chrNW_004936479:11,148,626...11,334,452

G

dystrophin related protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:292,408...334,079
Ensembl chrNW_004936813:292,396...334,020

G

dual specificity phosphatase 21

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:10,959,019...10,959,588

G

dual specificity phosphatase 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:535,434...538,219
Ensembl chrNW_004936809:535,434...539,319

G

dynein light chain Tctex-type 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,690,810...4,701,615
Ensembl chrNW_004936502:4,690,776...4,701,750

G

EBP cholestenol delta-isomerase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:508,716...515,968
Ensembl chrNW_004936721:509,374...515,918

G

ectodysplasin A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:1,545,293...1,561,109
Ensembl chrNW_004936777:1,238,272...1,557,410

G

ectodysplasin A2 receptor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:1,303,855...1,335,766
Ensembl chrNW_004936635:1,303,858...1,337,868

G

EF-hand domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:10,279,094...10,456,994
Ensembl chrNW_004936502:10,278,816...10,457,086

G

ephrin B1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:434,729...447,778
Ensembl chrNW_004936777:434,692...447,780

G

eukaryotic translation initiation factor 1A X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:4,010,912...4,029,520
Ensembl chrNW_004936624:4,010,753...4,030,374

G

eukaryotic translation initiation factor 2 subunit gamma

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:516,206...535,749
Ensembl chrNW_004936624:515,864...535,981

G

E74 like ETS transcription factor 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,519,663...1,534,510
Ensembl chrNW_004936479:1,519,874...1,530,733

G

ETS transcription factor ELK1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,402,726...13,418,214
Ensembl chrNW_004936502:13,402,728...13,418,214

G

emerin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,127,701...1,130,195
Ensembl chrNW_004936809:1,127,710...1,130,195

G

ecto-NOX disulfide-thiol exchanger 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:750,699...1,048,255
Ensembl chrNW_004936479:871,357...1,049,377

G

endothelium and lymphocyte associated ASCH domain 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:2,447,289...2,453,417

G

ES cell expressed Ras

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:782,343...783,591
Ensembl chrNW_004936721:782,525...783,208

G

ERCC excision repair 6 like, spindle assembly checkpoint helicase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936959:25,084...30,143

G

ESX homeobox 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,151,988...10,156,349

G

coagulation factor IX

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:8,052,998...8,090,245
Ensembl chrNW_004936513:8,053,615...8,090,234

G

fatty acid amide hydrolase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936980:183,629...319,072
Ensembl chrNW_004936980:183,629...260,764

G

family with sequence similarity 133 member A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936649:203,082...274,174

G

family with sequence similarity 199, X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,194,796...10,226,311
Ensembl chrNW_004936499:10,202,109...10,226,406

G

FAM3 metabolism regulating signaling molecule A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,248,865...1,258,894
Ensembl chrNW_004936809:1,249,823...1,258,860

G

family with sequence similarity 50 member A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,195,479...1,202,126

G

fetal and adult testis expressed 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,029,390...1,036,254

G

FYVE, RhoGEF and PH domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,355,606...1,397,282
Ensembl chrNW_004936751:1,351,795...1,397,288

G

fibroblast growth factor 13

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:8,419,588...8,911,010
Ensembl chrNW_004936513:8,714,396...8,911,367

G

fibroblast growth factor 16

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,454,067...2,463,653
Ensembl chrNW_004936683:2,454,067...2,463,635

G

four and a half LIM domains 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,025,753...11,064,312
Ensembl chrNW_004936513:11,025,715...11,064,312

G

filamin A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,097,288...1,123,206
Ensembl chrNW_004936809:1,097,294...1,123,201

G

Fragile X messenger ribonucleoprotein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:1,290,038...1,327,850
Ensembl chrNW_004936513:1,289,558...1,327,856

G

FMR1 neighbor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:1,230,966...1,264,362

G

forkhead box O4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:495,271...501,278
Ensembl chrNW_004936762:493,910...501,531

G

forkhead box P3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,118,376...1,125,282
Ensembl chrNW_004936721:1,118,782...1,132,308

G

forkhead box R2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:1,044,648...1,045,598
Ensembl chrNW_004936819:1,044,654...1,045,598

G

FERM domain containing 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:2,664,968...2,756,300
Ensembl chrNW_004936691:2,701,546...2,755,980

G

FERM and PDZ domain containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,155,413...7,220,876
Ensembl chrNW_004936499:7,155,505...7,220,915

G

FtsJ RNA 2'-O-methyltransferase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:453,789...466,425
Ensembl chrNW_004936721:453,790...466,360

G

FUN14 domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:10,643,172...10,657,118
Ensembl chrNW_004936502:10,643,071...10,657,134

G

glucose-6-phosphate dehydrogenase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,269,900...1,285,853
Ensembl chrNW_004936809:1,269,914...1,285,889

G

gamma-aminobutyric acid type A receptor subunit alpha3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:461,050...675,745
Ensembl chrNW_004936714:548,619...677,411

G

gamma-aminobutyric acid type A receptor subunit epsilon

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:808,287...827,990
Ensembl chrNW_004936714:812,265...827,957

G

gamma-aminobutyric acid type A receptor subunit theta

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:315,585...332,629
Ensembl chrNW_004936714:318,676...332,357

G

GATA binding protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:742,862...750,843
Ensembl chrNW_004936721:742,862...750,768

G

germ cell nuclear acidic peptidase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:71,719...96,816

G

GDP dissociation inhibitor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,188,793...1,194,816
Ensembl chrNW_004936809:1,188,628...1,194,863

G

glycerophosphodiester phosphodiesterase domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,048,597...1,060,085
Ensembl chrNW_004936762:1,048,586...1,060,153

G

gap junction protein beta 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:389,655...398,035
Ensembl chrNW_004936762:389,669...395,898

G

glycerol kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:6,707,148...6,787,245

G

galactosidase alpha

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:474,938...484,753
Ensembl chrNW_004936813:474,949...484,760

G

glyoxalase domain containing 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:719,660...731,800
Ensembl chrNW_004936721:719,651...732,078

G

G protein nucleolar 3 like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,423,822...1,457,257
Ensembl chrNW_004936751:1,423,804...1,459,998

G

glypican 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:1,060,013...1,459,736
Ensembl chrNW_004936691:1,059,994...1,459,740

G

glypican 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:1,564,872...1,676,378
Ensembl chrNW_004936691:1,564,833...1,677,482

G

G-patch domain and KOW motifs

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,013,776...1,031,018
Ensembl chrNW_004936721:1,011,492...1,031,440

G

G protein-coupled receptor 101

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,282,683...10,284,206
Ensembl chrNW_004936513:10,282,683...10,284,206

G

G protein-coupled receptor 119

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,262,399...1,263,596
Ensembl chrNW_004936479:1,262,484...1,263,491

G

G protein-coupled receptor 173

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:61,770...82,769
Ensembl chrNW_004936751:61,936...81,254

G

G protein-coupled receptor 174

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:1,170,718...1,171,958
Ensembl chrNW_004936547:1,170,747...1,171,748

G

G protein-coupled receptor 34

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:8,070,824...8,078,273
Ensembl chrNW_004936502:8,076,590...8,077,714

G

G protein-coupled receptor 50

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,417,044...1,421,782
Ensembl chrNW_004936714:1,417,044...1,421,782

G

G protein-coupled receptor 82

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:8,100,698...8,102,349
Ensembl chrNW_004936502:8,098,580...8,102,349

G

G protein-coupled receptor associated sorting protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:1,208,018...1,213,224
Ensembl chrNW_004936813:1,208,373...1,212,548

G

G protein-coupled receptor associated sorting protein family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:1,099,164...1,137,974

G

glutamate ionotropic receptor AMPA type subunit 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:7,050,018...7,323,047
Ensembl chrNW_004936479:7,050,016...7,323,196

G

GRIP1 associated protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:892,704...916,965
Ensembl chrNW_004936721:891,824...916,984

G

gastrin releasing peptide receptor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,533,256...5,565,827
Ensembl chrNW_004936470:5,533,256...5,565,869

G

G1 to S phase transition 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936909:436,004...438,818
Ensembl chrNW_004936909:436,018...438,651

G

guanylate cyclase 2F, retinal

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:5,653,384...5,752,732

G

HAUS augmin like complex subunit 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:321,906...350,105
Ensembl chrNW_004936809:321,497...350,110

G

host cell factor C1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:827,008...853,689
Ensembl chrNW_004936809:827,031...853,644

G

histone deacetylase 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:757,500...778,416
Ensembl chrNW_004936721:758,181...778,053

G

histone deacetylase 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,425,337...1,652,058
Ensembl chrNW_004936762:1,425,335...1,652,063

G

highly divergent homeobox

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:5,051,555...5,158,383
Ensembl chrNW_004936547:5,049,844...5,158,360

G

hephaestin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:1,954,771...2,022,061
Ensembl chrNW_004936635:1,954,947...2,022,101

G

high mobility group box 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,523,016...1,527,301

G

high mobility group nucleosome binding domain 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:2,607,491...2,614,037

G

heterogeneous nuclear ribonucleoprotein H2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:484,872...489,822
Ensembl chrNW_004936813:484,872...490,615

G

hypoxanthine phosphoribosyltransferase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:650,753...694,362
Ensembl chrNW_004936691:652,769...694,463

G

heparan sulfate 6-O-sulfotransferase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:1,976,449...2,257,303
Ensembl chrNW_004936691:1,976,449...2,255,144

G

hydroxysteroid 17-beta dehydrogenase 10

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:399,743...402,200
Ensembl chrNW_004936751:399,701...402,344

G

HIV-1 Tat specific factor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,762,417...10,779,641
Ensembl chrNW_004936513:10,762,398...10,779,374

G

5-hydroxytryptamine receptor 2C

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:1,002,083...1,109,446
Ensembl chrNW_004936499:1,004,732...1,109,377

G

HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:478,978...622,818
Ensembl chrNW_004936751:478,300...622,820

G

isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit gamma

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:666,231...675,279
Ensembl chrNW_004936809:666,337...675,214

G

iduronate 2-sulfatase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:62,966...88,844
Ensembl chrNW_004936513:62,993...88,774

G

immunoglobulin binding protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,292,572...1,319,145

G

immunoglobulin superfamily member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:402,957...418,400
Ensembl chrNW_004936479:402,957...418,400

G

inhibitor of nuclear factor kappa B kinase regulatory subunit gamma

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,280,254...1,306,964
Ensembl chrNW_004936809:1,257,654...1,301,813

G

interleukin 13 receptor subunit alpha 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:11,052,077...11,108,915
Ensembl chrNW_004936479:11,050,249...11,108,909

G

interleukin 13 receptor subunit alpha 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:860,179...883,884
Ensembl chrNW_004936499:863,599...883,855

G

interleukin 1 receptor accessory protein like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:5,063,042...5,824,427
Ensembl chrNW_004936553:6,055,179...6,099,514

G

interleukin 1 receptor accessory protein like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:8,788,093...9,048,583
Ensembl chrNW_004936499:8,790,139...9,771,800

G

interleukin 2 receptor subunit gamma

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:487,414...491,028
Ensembl chrNW_004936762:487,380...491,044

G

integrator complex subunit 6 like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,322,311...11,388,952
Ensembl chrNW_004936513:11,322,410...11,386,850

G

IQ motif and Sec7 domain ArfGEF 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:210,800...294,358
Ensembl chrNW_004936751:210,761...294,399

G

interleukin 1 receptor associated kinase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:891,407...900,311
Ensembl chrNW_004936809:890,717...900,326

G

insulin receptor substrate 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,111,422...6,127,487
Ensembl chrNW_004936499:6,111,487...6,115,272

G

integrin subunit beta 1 binding protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:318,055...322,358
Ensembl chrNW_004936762:318,055...321,843

G

inter-alpha-trypsin inhibitor heavy chain family member 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,601,650...1,630,115
Ensembl chrNW_004936751:1,601,650...1,630,115

G

integral membrane protein 2A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:1,260,705...1,267,443
Ensembl chrNW_004936547:1,260,696...1,267,618

G

jade family PHD finger 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,727,685...12,863,074
Ensembl chrNW_004936502:12,727,649...12,863,083

G

potassium voltage-gated channel subfamily D member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:881,162...890,939
Ensembl chrNW_004936721:880,774...889,874

G

potassium voltage-gated channel subfamily E regulatory subunit 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:5,557,076...5,558,467
Ensembl chrNW_004936499:5,557,202...5,557,627

G

lysine demethylase 5C

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:159,628...204,136
Ensembl chrNW_004936751:167,920...203,966

G

lysine demethylase 6A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:10,980,303...11,196,711
Ensembl chrNW_004936502:10,980,118...11,196,163

G

KIAA1210 ortholog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,729,891...10,773,342

G

kinesin family member 4A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,062,570...1,194,192
Ensembl chrNW_004936762:1,061,526...1,187,863

G

KLF transcription factor 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:633,562...673,365
Ensembl chrNW_004936819:634,503...673,174

G

kelch like family member 13

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:11,671,773...11,853,531
Ensembl chrNW_004936479:11,744,058...11,853,558

G

kelch like family member 15

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:552,220...593,546
Ensembl chrNW_004936624:552,177...591,578

G

kelch like family member 34

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,721,201...2,727,123

G

kelch like family member 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:11,235,844...11,335,678
Ensembl chrNW_004936499:11,235,788...11,334,958

G

KRAB box domain containing 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,335,159...12,349,544

G

L1 cell adhesion molecule

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:736,385...768,822
Ensembl chrNW_004936809:736,319...761,973

G

L antigen family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,229,933...1,232,448

G

lysosomal associated membrane protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,584,221...9,622,330
Ensembl chrNW_004936479:9,584,221...9,610,420

G

LanC like family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,419,279...4,522,025
Ensembl chrNW_004936502:4,419,474...4,520,795

G

LAS1 like ribosome biogenesis factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:2,560,586...2,580,309
Ensembl chrNW_004936635:2,560,471...2,581,785

G

LDOC1 regulator of NFKB signaling

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:6,481,758...6,486,018
Ensembl chrNW_004936513:6,485,442...6,485,882

G

LHFPL tetraspan subfamily member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:2,745,825...2,795,691
Ensembl chrNW_004936499:2,745,825...2,795,721

G

zinc finger protein 182

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:288,584...342,402
Ensembl chrNW_004936721:289,508...323,119

G

ferritin heavy chain

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:7,117,118...7,117,669

G

olfactory receptor 13H1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:173,064...173,990
Ensembl chrNW_004936479:173,064...173,990

G

cytochrome b-245 heavy chain

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,631,750...4,676,686
Ensembl chrNW_004936502:4,635,149...4,676,904

G

cytochrome c oxidase subunit 7B, mitochondrial

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,781,614...2,787,570
Ensembl chrNW_004936683:2,781,623...2,787,570

G

G-protein coupled receptor-associated sorting protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:1,134,420...1,139,513
Ensembl chrNW_004936813:1,134,762...1,137,290

G

transcription elongation factor A protein-like 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:7,867,398...7,869,414

G

transcription elongation factor A protein-like 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:7,957,730...7,960,984

G

small integral membrane protein 10-like protein 2A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:112,114...115,857

G

X antigen family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936873:624,373...625,817

G

uncharacterized LOC110599509

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,347,679...1,350,598

G

huntingtin-interacting protein M

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

G

sperm protein associated with the nucleus on the X chromosome N2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

G

LON peptidase N-terminal domain and ring finger 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,840,630...10,880,494
Ensembl chrNW_004936479:10,840,448...10,879,906

G

lysophosphatidic acid receptor 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:821,950...834,069
Ensembl chrNW_004936547:750,947...834,069

G

leucine rich repeats and calponin homology domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:673,276...775,860
Ensembl chrNW_004936499:673,274...775,868

G

leucine zipper protein 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:588,532...603,280

G

MAGE family member A10

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:717,931...719,028
Ensembl chrNW_004936714:717,931...718,967

G

MAGE family member B17

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,582,981...5,584,009

G

MAGE family member D1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936909:493,998...592,649
Ensembl chrNW_004936909:585,206...592,644

G

MAGE family member D2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,639,276...1,647,494
Ensembl chrNW_004936751:1,639,276...1,647,180

G

MAGE family member E1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,008,949...2,013,104
Ensembl chrNW_004936683:2,009,167...2,012,570

G

MAGE family member E2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,688,981...1,691,250
Ensembl chrNW_004936683:1,689,463...1,691,034

G

MAGE family member H1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:1,086,655...1,088,123

G

MAGI family member, X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,039,098...1,044,286
Ensembl chrNW_004936721:1,039,481...1,044,030

G

magnesium transporter 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:2,737,545...2,775,679
Ensembl chrNW_004936683:2,735,217...2,775,679

G

mastermind like domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,941,974...2,042,246
Ensembl chrNW_004936714:1,951,966...2,042,394

G

monoamine oxidase A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:9,816,443...9,888,002
Ensembl chrNW_004936502:9,815,319...9,888,026

G

monoamine oxidase B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:9,907,181...10,014,756
Ensembl chrNW_004936502:9,907,180...10,014,773

G

mitogen-activated protein kinase kinase kinase 15

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:905,249...958,946
Ensembl chrNW_004936844:905,658...956,879

G

MAP7 domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:4,038,854...4,150,495
Ensembl chrNW_004936624:4,087,099...4,147,167

G

MAP7 domain containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,989,123...11,021,086

G

muscleblind like splicing regulator 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:2,460,409...2,526,179
Ensembl chrNW_004936691:2,460,717...2,526,437

G

membrane bound transcription factor peptidase, site 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,464,152...2,510,984
Ensembl chrNW_004936624:2,463,909...2,511,158

G

MCF.2 cell line derived transforming sequence

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:7,950,082...8,035,421
Ensembl chrNW_004936513:7,922,700...8,034,793

G

MCTS1 re-initiation and release factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,432,817...9,491,615

G

methyl-CpG binding protein 2

susceptibility

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE | ClinVar Annotator: match by term: MECP2 duplication syndrome | ClinVar Annotator: match by term: Mental retardation, X-linked, Lubs type | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:1057790 PMID:1105898 PMID:1191367 PMID:1241840 PMID:2323808 More...

NCBI chrNW_004936809:902,938...967,771
Ensembl chrNW_004936809:911,764...966,839

G

mediator complex subunit 12

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:460,342...483,264
Ensembl chrNW_004936762:460,342...483,195

G

mediator complex subunit 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,280,606...7,350,750
Ensembl chrNW_004936502:7,280,534...7,350,435

G

MID1 interacting protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:5,634,319...5,638,869
Ensembl chrNW_004936502:5,636,564...5,638,869

G

midline 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,833,328...6,926,531
Ensembl chrNW_004936499:6,829,729...6,926,571

G

membrane magnesium transporter 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,229,354...11,239,152
Ensembl chrNW_004936513:11,229,506...11,239,525

G

MORC family CW-type zinc finger 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,755,405...7,811,718
Ensembl chrNW_004936499:7,755,368...7,811,282

G

mortality factor 4 like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,636,711...10,647,442
Ensembl chrNW_004936499:10,636,776...10,647,442

G

motile sperm domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:273,490...297,290
Ensembl chrNW_004936691:273,454...298,533

G

mitochondrial pyruvate carrier 1 like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,256,149...7,256,553
Ensembl chrNW_004936502:7,256,149...7,256,553

G

moesin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:2,390,390...2,461,870
Ensembl chrNW_004936635:2,389,823...2,461,930

G

myotubularin 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,792,893...1,870,338
Ensembl chrNW_004936714:1,792,845...1,870,389

G

myotubularin related protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,693,919...1,772,974
Ensembl chrNW_004936714:1,693,935...1,772,978

G

myotubularin related protein 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:3,336,218...3,415,998
Ensembl chrNW_004936635:3,336,148...3,415,166

G

N-alpha-acetyltransferase 10, NatA catalytic subunit

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:812,454...817,226
Ensembl chrNW_004936809:812,390...817,288

G

NALCN channel auxiliary factor 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:1,100,109...1,143,753
Ensembl chrNW_004936777:1,116,759...1,143,766

G

nucleosome assembly protein 1 like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:125,645...128,213
Ensembl chrNW_004936683:126,425...127,801

G

nucleosome assembly protein 1 like 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936649:274,677...277,545
Ensembl chrNW_004936649:275,068...276,681

G

norrin cystine knot growth factor NDP

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:10,080,169...10,105,155
Ensembl chrNW_004936502:10,080,145...10,105,328

G

NADH:ubiquinone oxidoreductase subunit A1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,074,290...10,078,072
Ensembl chrNW_004936479:10,074,307...10,078,066

G

NADH:ubiquinone oxidoreductase subunit B11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,921,371...12,923,702
Ensembl chrNW_004936502:12,921,370...12,923,683

G

neurite extension and migration factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,041,739...1,157,382
Ensembl chrNW_004936683:1,042,288...1,157,377

G

NHS actin remodeling regulator

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:6,632,724...6,967,878
Ensembl chrNW_004936470:6,919,623...6,971,125

G

NHS like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936959:78,505...97,228
Ensembl chrNW_004936959:83,744...354,556

G

NFKB activating protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,024,674...10,041,738
Ensembl chrNW_004936479:10,024,705...10,041,590

G

NFKB repressing factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,312,061...10,327,970
Ensembl chrNW_004936479:10,311,996...10,328,393

G

neuroligin 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:435,729...458,261
Ensembl chrNW_004936762:435,729...458,423

G

non-POU domain containing octamer binding

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:322,413...343,126
Ensembl chrNW_004936762:321,280...341,537

G

NADPH oxidase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:6,023,960...6,040,041
Ensembl chrNW_004936584:6,024,008...6,039,866

G

nuclear receptor subfamily 0 group B member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:6,436,371...6,440,141
Ensembl chrNW_004936553:6,436,371...6,440,141

G

Nik related kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:8,629,563...8,747,858

G

NAD(P) dependent steroid dehydrogenase-like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:246,574...273,930
Ensembl chrNW_004936714:246,551...273,912

G

nucleoporin 62 C-terminal like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,503,475...7,579,453

G

nuclear RNA export factor 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:8,066,413...8,084,756

G

nuclear RNA export factor 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:733,393...874,254

G

nuclear transport factor 2 like export factor 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:5,604,376...5,610,972
Ensembl chrNW_004936499:5,603,805...5,611,029

G

nyctalopin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,890,582...7,909,157
Ensembl chrNW_004936502:7,890,535...7,910,986

G

OCRL inositol polyphosphate-5-phosphatase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,955,362...2,011,608
Ensembl chrNW_004936479:1,953,488...2,012,018

G

O-linked N-acetylglucosamine (GlcNAc) transferase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:99,335...137,833
Ensembl chrNW_004936762:99,293...137,874

G

oligophrenin 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:6,966...243,209
Ensembl chrNW_004936635:6,923...244,408

G

ornithine transcarbamylase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:5,234,253...5,291,891
Ensembl chrNW_004936502:5,234,253...5,291,891

G

OTU deubiquitinase 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:847,360...876,912
Ensembl chrNW_004936721:848,324...877,068

G

OTU deubiquitinase 6A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:1,616,038...1,616,913

G

pyrimidinergic receptor P2Y4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,217,858...1,218,948
Ensembl chrNW_004936762:1,217,858...1,218,950

G

PABIR family member 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:383,976...426,911
Ensembl chrNW_004936691:383,986...410,875

G

poly(A) binding protein cytoplasmic 1 like 2A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004937508:12...2,177

G

poly(A) binding protein cytoplasmic 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936649:2,195,918...2,201,480

G

p21 (RAC1) activated kinase 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:4,079,127...4,328,580
Ensembl chrNW_004936499:4,079,103...4,188,774

G

PAS domain containing repressor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

G

polysaccharide biosynthesis domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,922,633...1,928,510
Ensembl chrNW_004936683:1,922,346...1,930,163

G

protocadherin 11 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936649:1,843,290...1,893,991

G

protocadherin 19

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:5,568,740...5,668,095
Ensembl chrNW_004936584:5,568,728...5,668,116

G

proprotein convertase subtilisin/kexin type 1 inhibitor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:783,973...787,712
Ensembl chrNW_004936721:782,032...787,952

G

phosphate cytidylyltransferase 1B, choline

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:31,678...125,318
Ensembl chrNW_004936624:58,792...125,338

G

pyruvate dehydrogenase E1 subunit alpha 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:889,720...906,631
Ensembl chrNW_004936844:889,635...909,586

G

pyruvate dehydrogenase kinase 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:141,745...213,495
Ensembl chrNW_004936624:142,402...213,528

G

PDZ domain containing 11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,188,394...1,191,368
Ensembl chrNW_004936762:1,188,568...1,194,306

G

PDZ domain containing 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:681,412...707,932
Ensembl chrNW_004936809:679,938...707,938

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6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,753,627...1,806,315
Ensembl chrNW_004936751:1,753,627...1,806,294

G

phosphoglycerate kinase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:286,267...310,062
Ensembl chrNW_004936547:286,267...310,062

G

progesterone receptor membrane component 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,625,989...10,634,058
Ensembl chrNW_004936479:10,625,889...10,634,136

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phosphate regulating endopeptidase X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,124,479...2,312,847
Ensembl chrNW_004936624:2,126,253...2,312,847

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PHD finger protein 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:716,723...767,960
Ensembl chrNW_004936691:716,697...768,016

G

PHD finger protein 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:850,630...935,382
Ensembl chrNW_004936751:850,237...934,586

G

phosphorylase kinase regulatory subunit alpha 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,657,778...1,766,592
Ensembl chrNW_004936762:1,657,781...1,766,605

G

phosphorylase kinase regulatory subunit alpha 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:478,773...548,565
Ensembl chrNW_004936844:478,809...548,196

G

phosphatidylinositol glycan anchor biosynthesis class A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,730,955...4,746,958
Ensembl chrNW_004936470:4,730,961...4,746,985

G

Pim-2 proto-oncogene, serine/threonine kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:839,876...844,488
Ensembl chrNW_004936721:839,874...844,488

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peptidylprolyl cis/trans isomerase, NIMA-interacting 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936959:36,374...48,480
Ensembl chrNW_004936959:36,136...48,508

G

pirin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,794,803...4,902,211
Ensembl chrNW_004936470:4,793,823...4,902,471

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praja ring finger ubiquitin ligase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:796,101...801,111
Ensembl chrNW_004936777:796,756...798,726

G

placenta enriched 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:602,707...603,342

G

proteolipid protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,534,953...10,553,411
Ensembl chrNW_004936499:10,534,950...10,551,012

G

proteolipid protein 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,047,261...1,050,647
Ensembl chrNW_004936721:1,042,171...1,050,661

G

plastin 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:246,042...335,440
Ensembl chrNW_004936499:246,042...335,440

G

plexin A3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,209,787...1,226,726
Ensembl chrNW_004936809:1,209,743...1,226,728

G

plexin B3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:645,569...659,850
Ensembl chrNW_004936809:644,049...659,859

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pregnancy up-regulated nonubiquitous CaM kinase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:553,438...557,385
Ensembl chrNW_004936809:553,431...557,427

G

PNMA family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:90,133...93,805
Ensembl chrNW_004936714:92,269...93,660

G

PNMA family member 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:155,618...156,955
Ensembl chrNW_004936714:155,618...157,563

G

PNMA family member 6A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:76,508...79,485
Ensembl chrNW_004936714:77,885...79,336

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PNMA family member 6E

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:266,367...269,248

G

POF1B actin binding protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:6,031,281...6,101,451
Ensembl chrNW_004936547:6,029,831...6,101,451

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DNA polymerase alpha 1, catalytic subunit

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936836:1,151...287,438

G

porcupine O-acyltransferase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:495,132...508,341
Ensembl chrNW_004936721:495,093...508,347

G

POU class 3 homeobox 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:4,454,239...4,455,460
Ensembl chrNW_004936547:4,454,297...4,455,382

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protein phosphatase with EF-hand domain 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:316,889...444,043
Ensembl chrNW_004936844:318,367...445,183

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protein phosphatase 1 regulatory subunit 3F

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,137,998...1,153,243
Ensembl chrNW_004936721:1,137,916...1,156,151

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polyglutamine binding protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:825,171...830,010
Ensembl chrNW_004936721:825,075...832,755

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PRA1 domain family member 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:972,095...974,738
Ensembl chrNW_004936721:971,744...975,580

G

peroxiredoxin 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:859,281...873,784
Ensembl chrNW_004936624:859,276...873,860

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prickle planar cell polarity protein 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,050,755...1,060,603
Ensembl chrNW_004936721:1,050,801...1,060,574

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phosphoribosyl pyrophosphate synthetase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,114,838...7,136,468
Ensembl chrNW_004936499:7,115,780...7,136,449

G

proline rich 32

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:4,249,494...4,251,514
Ensembl chrNW_004936479:4,249,465...4,251,586

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proline rich and Gla domain 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,189,283...4,288,089
Ensembl chrNW_004936502:4,189,254...4,291,140

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proline rich and Gla domain 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,045,541...1,055,548
Ensembl chrNW_004936714:1,050,454...1,052,593

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proteasome 26S subunit, non-ATPase 10

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,691,758...6,698,515
Ensembl chrNW_004936499:6,691,476...6,702,986

G

patched domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:1,072,857...1,125,962
Ensembl chrNW_004936624:1,072,857...1,125,994

G

PWWP domain containing 3B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:8,459,934...8,496,670
Ensembl chrNW_004936499:8,461,475...8,463,553

G

RAB33A, member RAS oncogene family

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,425,765...1,437,338
Ensembl chrNW_004936479:1,425,722...1,437,374

G

RAB9B, member RAS oncogene family

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,501,837...10,506,793
Ensembl chrNW_004936499:10,437,611...10,504,320

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RPA1 related single stranded DNA binding protein, X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:8,058,973...8,122,332
Ensembl chrNW_004936499:8,058,972...8,122,287

G

retinoic acid induced 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:7,016,293...7,084,787
Ensembl chrNW_004936470:7,016,665...7,018,254

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RAP2C, member of RAS oncogene family

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:2,628,563...2,645,133
Ensembl chrNW_004936691:2,628,579...2,645,268

G

RB binding protein 7, chromatin remodeling factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:6,107,754...6,133,136
Ensembl chrNW_004936470:6,104,510...6,133,185

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RNA binding motif protein 10

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,923,890...12,952,179
Ensembl chrNW_004936502:12,925,910...12,955,470

G

RNA binding motif protein 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:547,751...551,273
Ensembl chrNW_004936721:547,777...551,270

G

RNA binding motif protein 41

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,585,352...7,655,419
Ensembl chrNW_004936499:7,585,324...7,655,384

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RNA binding motif protein X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,429,862...10,442,509
Ensembl chrNW_004936513:10,429,824...10,437,108

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RNA binding motif protein X-linked 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,232,921...1,245,665
Ensembl chrNW_004936479:1,233,899...1,245,619

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renin binding protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:817,392...823,926
Ensembl chrNW_004936809:817,355...823,941

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RALBP1 associated Eps domain containing 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:6,218,035...6,428,776
Ensembl chrNW_004936470:6,218,047...6,423,408

G

regucalcin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,872,938...12,891,270
Ensembl chrNW_004936502:12,872,824...12,891,506

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RIB43A domain with coiled-coils 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:388,711...399,708
Ensembl chrNW_004936751:388,231...399,612

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ripply transcriptional repressor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,845,180...7,848,954
Ensembl chrNW_004936499:7,846,041...7,848,400

G

ring finger protein, LIM domain interacting

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:930,537...961,792
Ensembl chrNW_004936683:934,338...961,863

G

ring finger protein 113A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,078,201...10,079,400
Ensembl chrNW_004936479:10,078,304...10,079,338

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ring finger protein 128

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,952,567...8,013,589
Ensembl chrNW_004936499:7,952,567...8,052,656

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RP2 activator of ARL3 GTPase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,656,187...12,701,689
Ensembl chrNW_004936502:12,656,043...12,701,742

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retinitis pigmentosa GTPase regulator

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:5,163,164...5,212,940

G

ribosomal protein L10

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,146,994...1,149,573
Ensembl chrNW_004936809:1,146,809...1,149,618

G

ribosomal protein L36a

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:467,505...470,673

G

ribosomal protein L39

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,132,965...10,136,506

G

ribosomal protein S4 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:1,364,238...1,368,858
Ensembl chrNW_004936762:1,364,318...1,367,945

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ribosomal protein S6 kinase A3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:3,897,878...4,005,664
Ensembl chrNW_004936624:3,897,791...4,000,558

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ribosomal protein S6 kinase A6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:4,846,012...4,952,773
Ensembl chrNW_004936547:4,857,685...4,975,222

G

Ras related GTP binding B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:946,874...988,531
Ensembl chrNW_004936819:955,527...988,644

G

retinoschisin 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936844:284,938...314,524
Ensembl chrNW_004936844:284,141...314,545

G

retrotransposon Gag like 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:730,937...732,945
Ensembl chrNW_004936547:731,006...732,745

G

retrotransposon Gag like 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:2,901,534...2,904,565

G

retrotransposon Gag like 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936959:96,872...101,979

G

retrotransposon Gag like 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:4,771,535...4,782,768
Ensembl chrNW_004936499:4,771,535...4,777,111

G

S100 calcium binding protein G

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,931,158...5,934,986
Ensembl chrNW_004936470:5,930,140...5,935,000

G

SAM and SH3 domain containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,752,180...1,765,330
Ensembl chrNW_004936479:1,750,746...1,765,361

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spermidine/spermine N1-acetyltransferase 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:756,761...759,979
Ensembl chrNW_004936624:756,712...759,983

G

spermidine/spermine N1-acetyl transferase like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:5,858,120...5,874,745

G

Scm polycomb group protein like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:6,978,142...6,989,145

G

Scm polycomb group protein like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:7,457,995...7,508,069
Ensembl chrNW_004936470:7,458,007...7,508,069

G

septin 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,233,035...10,305,327
Ensembl chrNW_004936479:10,233,005...10,305,392

G

serpin family A member 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:8,568,309...8,573,764

G

SH2 domain containing 1A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:6,258,953...6,281,552
Ensembl chrNW_004936479:6,258,953...6,281,552

G

SH3 domain binding glutamate rich protein like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:2,661,747...2,737,338
Ensembl chrNW_004936547:2,661,575...2,739,418

G

SH3 domain containing kinase binding protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:4,327,100...4,616,724
Ensembl chrNW_004936624:4,327,031...4,615,699

G

shroom family member 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:2,068,731...2,166,537

G

solute carrier family 10 member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,241,980...1,245,986
Ensembl chrNW_004936809:1,241,986...1,246,266

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solute carrier family 16 member 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:803,186...910,143
Ensembl chrNW_004936683:803,134...910,284

G

solute carrier family 25 member 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,272,445...1,307,358
Ensembl chrNW_004936479:1,271,402...1,307,545

G

solute carrier family 25 member 43

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,455,632...10,499,224
Ensembl chrNW_004936479:10,453,187...10,499,251

G

solute carrier family 25 member 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,432,172...10,435,154

G

solute carrier family 25 member 53

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,294,491...10,306,003

G

solute carrier family 35 member A2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:830,067...838,783
Ensembl chrNW_004936721:830,042...838,866

G

solute carrier family 38 member 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:419,286...441,224
Ensembl chrNW_004936721:419,268...441,350

G

solute carrier family 6 member 14

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:13,024,831...13,051,908

G

solute carrier family 6 member 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:571,234...578,298

G

solute carrier family 7 member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:661,532...667,277
Ensembl chrNW_004936762:661,491...667,298

G

solute carrier family 9 member A6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,158,609...11,215,477
Ensembl chrNW_004936513:11,158,730...11,215,568

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solute carrier family 9 member A7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,450,702...12,587,196
Ensembl chrNW_004936502:12,452,720...12,587,192

G

SLIT and NTRK like family member 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:2,961,842...2,969,938
Ensembl chrNW_004936513:2,961,983...2,966,439

G

SLIT and NTRK like family member 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936513:4,742,743...4,750,633
Ensembl chrNW_004936513:4,743,661...4,750,633

G

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:2,030,788...2,110,501
Ensembl chrNW_004936479:2,030,716...2,110,661

G

structural maintenance of chromosomes 1A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:332,351...388,756
Ensembl chrNW_004936751:349,597...388,755

G

small muscle protein X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,603,210...2,659,368
Ensembl chrNW_004936624:2,603,171...2,659,364

G

spermine synthase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,345,573...2,402,157
Ensembl chrNW_004936624:2,346,018...2,401,893

G

sorting nexin 12

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:523,641...534,646
Ensembl chrNW_004936762:523,564...542,757

G

sosondowah ankyrin repeat domain family member D

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,162,691...10,164,190

G

SRY-box transcription factor 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:7,218,583...7,221,085

G

spindlin family member 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:4,367,956...4,369,768
Ensembl chrNW_004936635:4,368,491...4,369,240

G

SRSF protein kinase 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:661,264...666,198
Ensembl chrNW_004936809:661,264...666,188

G

sushi repeat containing protein X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:5,010,692...5,107,221
Ensembl chrNW_004936502:5,010,682...5,107,254

G

sushi repeat containing protein X-linked 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:5,855,818...5,879,478
Ensembl chrNW_004936584:5,855,818...5,880,259

G

signal sequence receptor subunit 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:675,178...679,245
Ensembl chrNW_004936809:675,049...679,707

G

STAG2 cohesin complex component

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:6,508,539...6,635,127
Ensembl chrNW_004936479:6,508,532...6,632,627

G

StAR related lipid transfer domain containing 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:316,332...358,241
Ensembl chrNW_004936777:323,367...358,243

G

STING1 ER exit protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,351,016...10,373,416
Ensembl chrNW_004936479:10,351,059...10,404,657

G

serine/threonine kinase 26

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:2,757,934...2,811,961
Ensembl chrNW_004936691:2,757,934...2,811,937

G

SUV39H1 histone lysine methyltransferase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:646,778...661,144
Ensembl chrNW_004936721:646,772...661,091

G

synapse associated protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,994,217...6,026,057
Ensembl chrNW_004936470:5,994,177...6,028,037

G

synapsin I

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,334,998...13,387,082
Ensembl chrNW_004936502:13,334,995...13,387,172

G

synaptophysin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,062,206...1,075,935
Ensembl chrNW_004936721:1,062,217...1,075,988

G

synaptotagmin like 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:5,882,428...5,945,514
Ensembl chrNW_004936584:5,884,193...5,917,300

G

synaptotagmin like 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,873,750...4,987,742
Ensembl chrNW_004936502:4,750,233...4,987,887

G

TGF-beta activated kinase 1 (MAP3K7) binding protein 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:6,860,435...6,917,796
Ensembl chrNW_004936553:6,860,261...6,885,475

G

TATA-box binding protein associated factor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:189,710...271,759

G

TATA-box binding protein associated factor 7 like

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:357,571...378,479
Ensembl chrNW_004936813:357,571...372,736

G

TATA-box binding protein associated factor 9b

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:312,909...321,424
Ensembl chrNW_004936547:314,344...323,040

G

tafazzin, phospholipid-lysophospholipid transacylase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,160,265...1,168,956
Ensembl chrNW_004936809:1,160,247...1,171,097

G

TLR adaptor interacting with endolysosomal SLC15A4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936553:6,628,131...6,629,027
Ensembl chrNW_004936553:6,628,131...6,629,027

G

TBC1 domain family member 25

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:524,398...536,918
Ensembl chrNW_004936721:524,247...537,363

G

TBC1 domain family member 8B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:7,876,238...7,946,054
Ensembl chrNW_004936499:7,876,230...7,946,068

G

T-box transcription factor 22

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:1,645,118...1,654,332
Ensembl chrNW_004936547:1,645,118...1,654,332

G

transcription elongation factor A like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,671,607...10,673,712
Ensembl chrNW_004936499:10,671,595...10,673,431

G

transcription elongation factor A like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004937070:101,478...103,312

G

transcription elongation factor A like 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,710,694...10,712,884

G

transcription elongation factor A like 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,740,406...10,742,748
Ensembl chrNW_004936499:10,741,053...10,741,631

G

transcription elongation factor A like 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:7,916,172...7,918,010
Ensembl chrNW_004936547:7,916,292...7,917,964

G

transcription elongation factor A like 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:7,974,317...7,975,311
Ensembl chrNW_004936547:7,973,152...7,975,311

G

teneurin transmembrane protein 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:5,603,944...6,254,846
Ensembl chrNW_004936479:5,710,613...6,250,232

G

terminal nucleotidyltransferase 5D

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:1,905,253...1,906,568
Ensembl chrNW_004936547:1,905,266...1,906,438

G

testis expressed 11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:681,962...969,749
Ensembl chrNW_004936762:681,130...969,455

G

testis expressed 13A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:9,265,867...9,267,139

G

testis expressed 13B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,789,511...6,790,771

G

testis expressed 28

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:1,022,795...1,042,475
Ensembl chrNW_004936809:1,022,795...1,040,120

G

transcription factor binding to IGHM enhancer 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:933,572...945,717
Ensembl chrNW_004936721:933,404...945,725

G

TGFB induced factor homeobox 2 like X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936649:3,483,325...3,484,008

G

THO complex 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:6,855,405...6,972,256
Ensembl chrNW_004936479:6,855,411...6,972,256

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translocase of inner mitochondrial membrane 17B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:817,738...824,074
Ensembl chrNW_004936721:818,608...826,042

G

translocase of inner mitochondrial membrane 8A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:425,613...428,722
Ensembl chrNW_004936813:425,613...428,702

G

TIMP metallopeptidase inhibitor 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,345,936...13,350,170
Ensembl chrNW_004936502:13,345,832...13,350,248

G

transketolase like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:1,048,672...1,084,125
Ensembl chrNW_004936809:1,048,672...1,083,994

G

transmembrane protein 164

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:5,042,638...5,199,433

G

transmembrane protein 255A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,721,602...9,781,468
Ensembl chrNW_004936479:9,721,633...9,781,509

G

transmembrane protein 35A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:150,204...167,931
Ensembl chrNW_004936813:150,081...167,945

G

transmembrane protein 47

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:1,990,524...2,018,707
Ensembl chrNW_004936502:1,993,749...2,018,204

G

thymosin beta 15B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,315,198...10,318,382

G

tenomodulin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:5,803,309...5,818,643
Ensembl chrNW_004936584:5,803,309...5,818,647

G

three prime repair exonuclease 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:317,655...319,293
Ensembl chrNW_004936809:318,548...319,258

G

tRNA methyltransferase 2 homolog B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:93,738...130,928
Ensembl chrNW_004936813:94,441...129,010

G

trophinin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,740,804...1,752,256

G

transient receptor potential cation channel subfamily C member 5

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:3,391,386...3,541,406
Ensembl chrNW_004936499:3,343,669...3,543,035

G

TRPC5 opposite strand

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:3,443,515...3,443,966

G

TSC22 domain family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,977,924...7,044,173
Ensembl chrNW_004936499:6,977,686...7,045,294

G

tetraspanin 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936584:5,842,549...5,848,533
Ensembl chrNW_004936584:5,840,312...5,848,622

G

tetraspanin 7

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:5,416,454...5,538,870
Ensembl chrNW_004936502:5,416,454...5,538,905

G

TSPY like 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:85,104...91,596
Ensembl chrNW_004936751:85,248...91,000

G

TSR2 ribosome maturation factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,350,542...1,355,449
Ensembl chrNW_004936751:1,350,481...1,358,110

G

taxilin gamma

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:6,054,076...6,107,613
Ensembl chrNW_004936470:6,053,905...6,109,437

G

ubiquitin like modifier activating enzyme 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,961,236...12,984,235
Ensembl chrNW_004936502:12,969,145...12,984,238

G

ubiquitin conjugating enzyme E2 A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,330,666...10,340,268
Ensembl chrNW_004936479:10,330,632...10,340,367

G

ubiquitin like 4A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:1,238,459...1,241,319
Ensembl chrNW_004936809:1,238,462...1,241,318

G

ubiquilin 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:530,833...534,185
Ensembl chrNW_004936819:532,037...533,920

G

UPF3B regulator of nonsense mediated mRNA decay

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:10,093,290...10,111,293
Ensembl chrNW_004936479:10,093,290...10,111,752

G

uracil phosphoribosyltransferase homolog

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,432,004...1,454,004
Ensembl chrNW_004936683:1,431,965...1,454,991

G

ubiquitin specific peptidase 11

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,003,214...13,020,772
Ensembl chrNW_004936502:13,003,261...13,020,388

G

ubiquitin specific peptidase 26

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:1,913,416...1,916,214

G

ubiquitin specific peptidase 27 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:1,396,103...1,399,718
Ensembl chrNW_004936721:1,396,103...1,399,745

G

ubiquitin specific peptidase 51

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936819:1,115,524...1,119,083
Ensembl chrNW_004936819:1,116,447...1,118,558

G

ubiquitin specific peptidase 9 X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:7,649,808...7,732,731
Ensembl chrNW_004936502:7,649,842...7,735,382

G

UTP14A small subunit processome component

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,646,600...1,667,677

G

ubiquitously expressed prefoldin like chaperone

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,419,520...13,427,777
Ensembl chrNW_004936502:13,418,403...13,427,767

G

VCP nuclear cofactor family member 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,973,538...1,984,250

G

vascular endothelial growth factor D

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:4,761,827...4,794,751
Ensembl chrNW_004936470:4,762,332...4,793,938

G

vestigial like family member 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:10,704,343...10,742,583
Ensembl chrNW_004936513:10,721,500...10,742,670

G

vacuolar ATPase assembly factor VMA21

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:1,273,528...1,281,266
Ensembl chrNW_004936714:1,272,565...1,281,287

G

V-set and immunoglobulin domain containing 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:6,708,049...6,738,358
Ensembl chrNW_004936499:6,708,049...6,738,306

G

V-set and immunoglobulin domain containing 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:2,167,633...2,191,725
Ensembl chrNW_004936635:2,167,617...2,191,740

G

WASP actin nucleation promoting factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:634,685...641,248
Ensembl chrNW_004936721:634,706...641,082

G

WD repeat domain 13

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:566,529...594,203
Ensembl chrNW_004936721:566,520...574,934

G

WD repeat domain 44

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:11,373,781...11,465,516
Ensembl chrNW_004936479:11,373,717...11,465,607

G

WD repeat domain 45

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936721:975,113...981,149
Ensembl chrNW_004936721:975,104...981,731

G

WNK lysine deficient protein kinase 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936751:1,095,578...1,266,772
Ensembl chrNW_004936751:1,100,192...1,266,740

G

X-linked inhibitor of apoptosis

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:6,677,533...6,724,800
Ensembl chrNW_004936479:6,677,526...6,722,116

G

X-linked Kx blood group antigen, Kell and VPS13A binding protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:4,532,100...4,584,931
Ensembl chrNW_004936502:4,532,100...4,587,439

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XK related X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:22,094...34,529
Ensembl chrNW_004936813:22,094...34,529

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X-prolyl aminopeptidase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,773,797...1,883,606
Ensembl chrNW_004936479:1,773,799...1,803,104

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Yip1 domain family member 6

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936777:169,794...193,155
Ensembl chrNW_004936777:169,080...193,231

G

YY2 transcription factor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:2,487,983...2,489,630

G

zinc finger and BTB domain containing 33

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:9,781,923...9,791,000
Ensembl chrNW_004936479:9,781,952...9,790,821

G

zinc finger CCCH-type containing 12B

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:2,580,693...2,690,297
Ensembl chrNW_004936635:2,588,510...2,641,616

G

zinc finger C4H2-type containing

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936635:2,924,632...2,954,003
Ensembl chrNW_004936635:2,924,601...2,953,854

G

zinc finger CCHC-type containing 12

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:11,021,502...11,024,612

G

zinc finger CCHC-type containing 13

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:661,870...662,382
Ensembl chrNW_004936683:661,870...662,382

G

zinc finger CCHC-type containing 18

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936499:10,293,483...10,294,414

G

zinc finger DHHC-type palmitoyltransferase 15

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936683:1,482,968...1,576,969
Ensembl chrNW_004936683:1,482,950...1,577,702

G

zinc finger DHHC-type palmitoyltransferase 9

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,711,756...1,743,306
Ensembl chrNW_004936479:1,711,713...1,741,167

G

ZFP92 zinc finger protein

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936809:294,114...309,368
Ensembl chrNW_004936809:301,482...356,094

G

zinc finger protein X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936624:417,164...471,638
Ensembl chrNW_004936624:416,753...472,030

G

Zic family member 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:9,780,895...9,792,865
Ensembl chrNW_004936513:9,786,709...9,793,077

G

zinc finger matrin-type 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936813:860,397...906,448
Ensembl chrNW_004936813:860,426...906,772

G

zinc finger MYM-type containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936762:360,581...376,509
Ensembl chrNW_004936762:361,032...376,513

G

zinc finger protein 157

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,127,503...13,158,443
Ensembl chrNW_004936502:13,127,563...13,158,962

G

zinc finger protein 185 with LIM domain

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:25741868 PMID:27247049 PMID:27761913 PMID:28257338 More...

NCBI chrNW_004936714:167,552...218,785
Ensembl chrNW_004936714:152,319...218,921

G

zinc finger protein 275

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

PMID:22679399 PMID:27247049 PMID:27761913 PMID:28257338 PMID:29141583 More...

NCBI chrNW_004936809:196,939...212,587
Ensembl chrNW_004936809:196,926...212,593

G

zinc finger protein 280C

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936479:1,354,919...1,412,963
Ensembl chrNW_004936479:1,365,006...1,410,901

G

zinc finger protein 41

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,176,781...13,226,872
Ensembl chrNW_004936502:13,178,189...13,227,257

G

zinc finger protein 449

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936513:11,526,142...11,543,387
Ensembl chrNW_004936513:11,524,731...11,543,419

G

zinc finger protein 674

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:12,370,517...12,372,855

G

zinc finger protein 711

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936547:5,999,792...6,026,719
Ensembl chrNW_004936547:5,999,739...6,026,769

G

zinc finger protein 75D

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936691:4,682...25,029
Ensembl chrNW_004936691:12,958...23,033

G

zinc finger protein 81

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936502:13,468,969...13,526,510
Ensembl chrNW_004936502:13,497,078...13,526,328

G

zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type

NCBI chrNW_004936470:5,233,798...5,258,266
Ensembl chrNW_004936470:5,233,740...5,258,266

syndromic X-linked intellectual disability Najm type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ATPase H+ transporting accessory protein 2

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,206,226...7,232,798
Ensembl chrNW_004936502:7,206,172...7,233,912

G

BCL6 corepressor

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:6,764,043...6,812,194
Ensembl chrNW_004936502:6,764,907...6,792,916

G

calcium/calmodulin dependent serine protein kinase

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Najm type

PMID:9536098 PMID:16199547 PMID:17576681 PMID:18414213 PMID:19165920 More...

NCBI chrNW_004936502:7,933,312...8,281,492
Ensembl chrNW_004936502:7,937,146...8,281,492

G

chromosome X CXorf38 homolog

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,260,094...7,278,416
Ensembl chrNW_004936502:7,259,928...7,278,725

G

DEAD-box helicase 3 X-linked

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,770,896...7,820,555
Ensembl chrNW_004936502:7,804,824...7,820,569

G

G protein-coupled receptor 34

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:19165920 PMID:20029458 PMID:21735175 PMID:21954287 PMID:22452838 More...

NCBI chrNW_004936502:8,070,824...8,078,273
Ensembl chrNW_004936502:8,076,590...8,077,714

G

G protein-coupled receptor 82

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:19165920 PMID:20029458 PMID:21735175 PMID:21954287 PMID:22452838 More...

NCBI chrNW_004936502:8,100,698...8,102,349
Ensembl chrNW_004936502:8,098,580...8,102,349

G

low density lipoprotein receptor

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Najm type

PMID:1301956 PMID:9654205 PMID:9974426 PMID:11139254 PMID:11317361 More...

NCBI chrNW_004936659:1,259,405...1,300,545
Ensembl chrNW_004936659:1,259,369...1,302,294

G

mediator complex subunit 14

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,280,606...7,350,750
Ensembl chrNW_004936502:7,280,534...7,350,435

G

mitochondrial pyruvate carrier 1 like

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,256,149...7,256,553
Ensembl chrNW_004936502:7,256,149...7,256,553

G

nyctalopin

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,890,582...7,909,157
Ensembl chrNW_004936502:7,890,535...7,910,986

G

ubiquitin specific peptidase 9 X-linked

ClinVar Annotator: match by term: Intellectual disability, CASK-related, X-linked

PMID:23901204 PMID:28492532

NCBI chrNW_004936502:7,649,808...7,732,731
Ensembl chrNW_004936502:7,649,842...7,735,382

syndromic X-linked intellectual disability Nascimento type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ubiquitin conjugating enzyme E2 A

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Nascimento type

PMID:16909393 PMID:20412111 PMID:25741868 PMID:32415735

NCBI chrNW_004936479:10,330,666...10,340,268
Ensembl chrNW_004936479:10,330,632...10,340,367

syndromic X-linked intellectual disability Pilorge type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

FA complementation group B

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic, Pilorge type

PMID:20479760 PMID:25741868 PMID:28588452

NCBI chrNW_004936470:4,305,220...4,323,456
Ensembl chrNW_004936470:4,305,740...4,323,374

G

glycine receptor alpha 2

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic, Pilorge type

PMID:20479760 PMID:25741868 PMID:26370147 PMID:28135719 PMID:28492532 More...

NCBI chrNW_004936470:4,014,897...4,202,625
Ensembl chrNW_004936470:4,014,885...4,202,633

syndromic X-linked intellectual disability Raymond type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

apoptosis inducing factor mitochondria associated 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,441,508...1,477,133
Ensembl chrNW_004936479:1,441,437...1,478,107

G

apelin

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:22796527 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,889,930...1,899,811
Ensembl chrNW_004936479:1,890,229...1,899,730

G

BCL6 corepressor like 1

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,539,676...1,605,647
Ensembl chrNW_004936479:1,538,051...1,606,344

G

E74 like ETS transcription factor 4

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,519,663...1,534,510
Ensembl chrNW_004936479:1,519,874...1,530,733

G

OCRL inositol polyphosphate-5-phosphatase

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:22796527 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,955,362...2,011,608
Ensembl chrNW_004936479:1,953,488...2,012,018

G

SAM and SH3 domain containing 3

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:22796527 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,752,180...1,765,330
Ensembl chrNW_004936479:1,750,746...1,765,361

G

UTP14A small subunit processome component

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,646,600...1,667,677

G

X-prolyl aminopeptidase 2

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:17436253 PMID:22796527 PMID:24357419 PMID:28492532

NCBI chrNW_004936479:1,773,797...1,883,606
Ensembl chrNW_004936479:1,773,799...1,803,104

G

zinc finger DHHC-type palmitoyltransferase 9

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Raymond type

PMID:9536098 PMID:17436253 PMID:17576681 PMID:19377476 PMID:22796527 More...

NCBI chrNW_004936479:1,711,756...1,743,306
Ensembl chrNW_004936479:1,711,713...1,741,167

syndromic X-linked intellectual disability Shashi type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

RNA binding motif protein X-linked

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Shashi type

PMID:10677307 PMID:25256757 PMID:25741868

NCBI chrNW_004936513:10,429,862...10,442,509
Ensembl chrNW_004936513:10,429,824...10,437,108

syndromic X-linked intellectual disability Siderius type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

PHD finger protein 8

ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Siderius type

PMID:10398231 PMID:16199551 PMID:17594395 PMID:17661819 PMID:25741868 More...

NCBI chrNW_004936751:850,630...935,382
Ensembl chrNW_004936751:850,237...934,586

syndromic X-linked intellectual disability Snyder type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

spermine synthase

ClinVar Annotator: match by term: SMS-Related Disorder | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Snyder type

PMID:5823961 PMID:14508504 PMID:18550699 PMID:19206178 PMID:19377476 More...

NCBI chrNW_004936624:2,345,573...2,402,157
Ensembl chrNW_004936624:2,346,018...2,401,893

syndromic X-linked intellectual disability Turner type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ALF transcription elongation factor 2

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE

NCBI chrNW_004936513:414,839...893,670
Ensembl chrNW_004936513:414,574...893,676

G

calmodulin binding transcription activator 1

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE

NCBI chrNW_004936623:1,759,052...2,265,466
Ensembl chrNW_004936623:1,526,171...2,266,124

G

HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1

ClinVar Annotator: match by term: HUWE1-related condition | ClinVar Annotator: match by term: HUWE1-related neurodevelopmental disorder | ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE | ClinVar Annotator: match by term: Intellectual disability, X-linked syndromic, Turner type

PMID:6107045 PMID:7943042 PMID:7943044 PMID:9536098 PMID:16700052 More...

NCBI chrNW_004936751:478,978...622,818
Ensembl chrNW_004936751:478,300...622,820

G

SKI proto-oncogene

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE

PMID:25741868 PMID:28492532

NCBI chrNW_004936737:1,223,653...1,274,664
Ensembl chrNW_004936737:1,222,341...1,276,631

syndromic X-linked intellectual disability type 10

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

hydroxysteroid 17-beta dehydrogenase 10

ClinVar Annotator: match by term: CHORIOATHETOSIS WITH MENTAL RETARDATION AND ABNORMAL BEHAVIOR | ClinVar Annotator: match by term: HSD10 mitochondrial disease | ClinVar Annotator: match by term: HSD17B10-Related Disorder

PMID:10521307 PMID:11102558 PMID:12112118 PMID:12555940 PMID:12696021 More...

NCBI chrNW_004936751:399,743...402,200
Ensembl chrNW_004936751:399,701...402,344

syndromic X-linked intellectual disorder Lujan-Fryns-type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

mediator complex subunit 12

ClinVar Annotator: match by term: Lujan Syndrome | ClinVar Annotator: match by term: MED12-related intellectual disability syndrome | ClinVar Annotator: match by term: X-linked mental retardation with marfanoid habitus syndrome

PMID:6711603 PMID:10405444 PMID:16199547 PMID:17334363 PMID:17369503 More...

NCBI chrNW_004936762:460,342...483,264
Ensembl chrNW_004936762:460,342...483,195

Syndromic X-Linked Mental Retardation 33

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

TATA-box binding protein associated factor 1

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33 | ClinVar Annotator: match by term: TAF1-related syndromic intellectual disability

PMID:9536098 PMID:17576681 PMID:25741868 PMID:26637982 PMID:28492532 More...

NCBI chrNW_004936762:189,710...271,759

syndromic X-linked mental retardation 35

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ribosomal protein L10

susceptibility

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35 | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35

PMID:7626060 PMID:18258260 PMID:25316788 PMID:25741868 PMID:25846674 More...

NCBI chrNW_004936809:1,146,994...1,149,573
Ensembl chrNW_004936809:1,146,809...1,149,618

syndromic X-linked mental retardation Hough type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

connector enhancer of kinase suppressor of Ras 2

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HOUGE TYPE

PMID:25223753 PMID:25644381 PMID:25741868 PMID:28098945 PMID:28492532

NCBI chrNW_004936624:2,727,208...2,989,653
Ensembl chrNW_004936624:2,727,208...2,989,659

Tonne-Kalscheuer syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ring finger protein, LIM domain interacting

ClinVar Annotator: match by term: RLIM-related syndromic intellectual disability | ClinVar Annotator: match by term: TONNE-KALSCHEUER SYNDROME

PMID:25644381 PMID:25735484 PMID:25741868 PMID:29728705 PMID:29742418

NCBI chrNW_004936683:930,537...961,792
Ensembl chrNW_004936683:934,338...961,863

Van Esch-O'Driscoll syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

DNA polymerase alpha 1, catalytic subunit

ClinVar Annotator: match by term: X-linked intellectual disability, van Esch type

PMID:9536098 PMID:17576681 PMID:25741868 PMID:27019227 PMID:28492532 More...

NCBI chrNW_004936836:1,151...287,438

WIEACKER-WOLFF SYNDROME, FEMALE-RESTRICTED

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

zinc finger CCCH-type containing 12B

ClinVar Annotator: match by term: Wieacker-Wolff syndrome, female-restricted

NCBI chrNW_004936635:2,580,693...2,690,297
Ensembl chrNW_004936635:2,588,510...2,641,616

G

zinc finger C4H2-type containing

ClinVar Annotator: match by term: Wieacker-Wolff syndrome, female-restricted

PMID:23623388 PMID:25741868 PMID:28814648 PMID:31206972

NCBI chrNW_004936635:2,924,632...2,954,003
Ensembl chrNW_004936635:2,924,601...2,953,854

Wilson-Turner syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

histone deacetylase 8

DNA:snp:intron:c.164+5G>A (human)

NCBI chrNW_004936762:1,425,337...1,652,058
Ensembl chrNW_004936762:1,425,335...1,652,063

G

LAS1 like ribosome biogenesis factor

ClinVar Annotator: match by term: Wilson-Turner syndrome

PMID:1746601 PMID:24647030 PMID:25644381 PMID:25741868 PMID:28492532

NCBI chrNW_004936635:2,560,586...2,580,309
Ensembl chrNW_004936635:2,560,471...2,581,785

G

zinc finger CCCH-type containing 12B

ClinVar Annotator: match by term: Wilson-Turner syndrome

NCBI chrNW_004936635:2,580,693...2,690,297
Ensembl chrNW_004936635:2,588,510...2,641,616

X-linked Aarskog syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

FYVE, RhoGEF and PH domain containing 1

ClinVar Annotator: match by term: FGD1-Related Disorders | ClinVar Annotator: match by term: FGD1-related condition

PMID:11940089 PMID:14560308 PMID:21739585 PMID:23211637 PMID:25046119 More...

NCBI chrNW_004936751:1,355,606...1,397,282
Ensembl chrNW_004936751:1,351,795...1,397,288

G

TSR2 ribosome maturation factor

ClinVar Annotator: match by term: FGD1-related condition

PMID:25741868 PMID:28492532

NCBI chrNW_004936751:1,350,542...1,355,449
Ensembl chrNW_004936751:1,350,481...1,358,110

X-linked intellectual developmental disorder 108

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

IQ motif and Sec7 domain ArfGEF 2

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked 108

NCBI chrNW_004936751:210,800...294,358
Ensembl chrNW_004936751:210,761...294,399

G

solute carrier family 9 member A7

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked 108 | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED 108

PMID:25741868 PMID:28492532 PMID:30335141

NCBI chrNW_004936502:12,450,702...12,587,196
Ensembl chrNW_004936502:12,452,720...12,587,192

X-linked intellectual developmental disorder 109

term browser

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Object Name

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Evidence

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PubMed Reference(s)

RGD Reference(s)

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G

ALF transcription elongation factor 2

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 109 | ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked 109

PMID:18414213 PMID:21739600 PMID:22773736 PMID:23562910 PMID:25741868 More...

NCBI chrNW_004936513:414,839...893,670
Ensembl chrNW_004936513:414,574...893,676

X-Linked Intellectual Developmental Disorder 110

term browser

Symbol

Object Name

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Evidence

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Source

PubMed Reference(s)

RGD Reference(s)

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G

fibroblast growth factor 13

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked 110

NCBI chrNW_004936513:8,419,588...8,911,010
Ensembl chrNW_004936513:8,714,396...8,911,367

X-Linked Intellectual Developmental Disorder 112

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

zinc finger MYM-type containing 3

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked 112 | ClinVar Annotator: match by term: ZMYM3-related condition

PMID:24721225 PMID:25741868 PMID:28492532 PMID:36586412

NCBI chrNW_004936762:360,581...376,509
Ensembl chrNW_004936762:361,032...376,513

X-Linked Intellectual Developmental Disorder 113

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

cleavage stimulation factor subunit 2

ClinVar Annotator: match by term: Intellectual developmental disorder, x-linked 113

NCBI chrNW_004936584:6,042,785...6,066,758
Ensembl chrNW_004936584:6,040,336...6,066,703

X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

chloride intracellular channel 2

ClinVar Annotator: match by term: X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome

PMID:21630357 PMID:22814392 PMID:25741868 PMID:25741909

NCBI chrNW_004936927:514,989...543,691
Ensembl chrNW_004936927:514,899...543,693

X-linked intellectual disability-psychosis-macroorchidism syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

FYVE, RhoGEF and PH domain containing 1

ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic 16

PMID:25741868 PMID:28492532

NCBI chrNW_004936751:1,355,606...1,397,282
Ensembl chrNW_004936751:1,351,795...1,397,288

G

methyl-CpG binding protein 2

susceptibility

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13 | ClinVar Annotator: match by term: PPM-X syndrome | ClinVar Annotator: match by term: X-linked intellectual disability-psychosis-macroorchidism syndrome

PMID:1057790 PMID:1105898 PMID:1191367 PMID:1241840 PMID:2323808 More...

NCBI chrNW_004936809:902,938...967,771
Ensembl chrNW_004936809:911,764...966,839

X-linked intellectual disability-short stature-overweight syndrome

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

SIL1 nucleotide exchange factor

ClinVar Annotator: match by term: X-linked intellectual disability-short stature-overweight syndrome

PMID:19471582 PMID:22995991 PMID:25741868 PMID:26467025 PMID:28492532 More...

NCBI chrNW_004936531:8,062,441...8,320,287
Ensembl chrNW_004936531:8,060,787...8,320,302

G

THO complex 2

ClinVar Annotator: match by term: X-linked intellectual disability-short stature-overweight syndrome

PMID:1605217 PMID:8825049 PMID:25741868 PMID:26166480 PMID:28492532

NCBI chrNW_004936479:6,855,405...6,972,256
Ensembl chrNW_004936479:6,855,411...6,972,256

X-linked mental retardation Gustavson type

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

RNA binding motif protein X-linked

ClinVar Annotator: match by term: Mental retardation Gustavson type, X-linked

NCBI chrNW_004936513:10,429,862...10,442,509
Ensembl chrNW_004936513:10,429,824...10,437,108

X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

oligophrenin 1

ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE | ClinVar Annotator: match by term: MENTAL RETARDATION, X-LINKED 60 | ClinVar Annotator: match by term: OPHN1-related condition

PMID:9582072 PMID:10818214 PMID:12807966 PMID:16199547 PMID:16221952 More...

NCBI chrNW_004936635:6,966...243,209
Ensembl chrNW_004936635:6,923...244,408

X-linked mental retardation-hypotonic facies syndrome-1

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

ATRX chromatin remodeler

ClinVar Annotator: match by term: Carpenter-Waziri syndrome | ClinVar Annotator: match by term: HOLMES-GANG SYNDROME | ClinVar Annotator: match by term: Intellectual disability-hypotonic facies syndrome, X-linked | ClinVar Annotator: match by term: Mental retardation-hypotonic facies syndrome X-linked, 1 | ClinVar Annotator: match by term: Smith Fineman Myers syndrome 1

PMID:3239563 PMID:6682021 PMID:6711605 PMID:7697714 PMID:8630485 More...

NCBI chrNW_004936683:2,496,307...2,718,539
Ensembl chrNW_004936683:2,495,959...2,718,620

G

erythropoietin receptor

ClinVar Annotator: match by term: Carpenter-Waziri syndrome

PMID:8174675 PMID:9394420 PMID:25741868 PMID:28492532

NCBI chrNW_004936659:1,468,391...1,473,880
Ensembl chrNW_004936659:1,468,634...1,473,880

G

HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1

ClinVar Annotator: match by term: Carpenter-Waziri syndrome

NCBI chrNW_004936751:478,978...622,818
Ensembl chrNW_004936751:478,300...622,820

Term paths to the root

Path 1
Term	Annotations
disease	16465
Developmental Disease	16381
Neurodevelopmental Disorders	6302
intellectual disability	4008
syndromic intellectual disability	708
syndromic X-linked intellectual disability	575
Armfield syndrome	1
Arts syndrome	2
Basilicata-Akhtar syndrome	1
Borjeson-Forssman-Lehmann syndrome	1
Christianson syndrome	15
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE	1
MEHMO syndrome	1
Mental Retardation, X-Linked, Syndromic, Ube2a-Related	0
Miles-Carpenter syndrome +	2
Mullegama-Klein-Martinez syndrome	2
Paganini-Miozzo syndrome	1
Partington syndrome	1
Prieto syndrome	1
Raynaud-Claes syndrome	1
Renpenning syndrome	2
Schimke X-Linked Mental Retardation Syndrome	0
Stocco Dos Santos type X-linked intellectual disability	10
Syndromic X-Linked Mental Retardation 33	1
Tonne-Kalscheuer syndrome	1
Van Esch-O'Driscoll syndrome	1
Wilson-Turner syndrome	3
X-Linked Intellectual Developmental Disorder 110	1
X-Linked Intellectual Developmental Disorder 112	1
X-Linked Intellectual Developmental Disorder 113	1
X-linked Aarskog syndrome	2
X-linked intellectual developmental disorder 108	2
X-linked intellectual developmental disorder 109	1
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	1
X-linked intellectual disability-psychosis-macroorchidism syndrome	2
X-linked intellectual disability-short stature-overweight syndrome	2
X-linked mental retardation Gustavson type	1
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance	1
X-linked mental retardation-hypotonic facies syndrome-1	3
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	1
deafness-intellectual disability, Martin-Probst type syndrome	0
female-restricted syndromic X-linked intellectual disability 99	1
syndromic X-linked intellectual developmental disorder Bain type	2
syndromic X-linked intellectual disability 12	0
syndromic X-linked intellectual disability 14	17
syndromic X-linked intellectual disability 17	0
syndromic X-linked intellectual disability 34	1
syndromic X-linked intellectual disability 5	2
syndromic X-linked intellectual disability 7	0
syndromic X-linked intellectual disability 94	1
syndromic X-linked intellectual disability Abidi type	0
syndromic X-linked intellectual disability Cabezas type	26
syndromic X-linked intellectual disability Chudley-Schwartz type	0
syndromic X-linked intellectual disability Claes-Jensen type	2
syndromic X-linked intellectual disability Hedera type	12
syndromic X-linked intellectual disability Lubs type	561
syndromic X-linked intellectual disability Najm type	12
syndromic X-linked intellectual disability Nascimento type	1
syndromic X-linked intellectual disability Pilorge type	2
syndromic X-linked intellectual disability Raymond type	9
syndromic X-linked intellectual disability Shashi type	1
syndromic X-linked intellectual disability Shrimpton type	0
syndromic X-linked intellectual disability Siderius type	1
syndromic X-linked intellectual disability Snyder type	1
syndromic X-linked intellectual disability Turner type	4
syndromic X-linked intellectual disability type 10	1
syndromic X-linked intellectual disorder Lujan-Fryns-type	1
syndromic X-linked mental retardation 35	1
syndromic X-linked mental retardation Hough type	1
Path 2
Term	Annotations
disease	16465
disease of anatomical entity	14117
nervous system disease	12341
central nervous system disease	11056
brain disease	10378
disease of mental health	7458
developmental disorder of mental health	5072
specific developmental disorder	4193
intellectual disability	4008
syndromic intellectual disability	708
syndromic X-linked intellectual disability	575
Armfield syndrome	1
Arts syndrome	2
Basilicata-Akhtar syndrome	1
Borjeson-Forssman-Lehmann syndrome	1
Christianson syndrome	15
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE	1
MEHMO syndrome	1
Mental Retardation, X-Linked, Syndromic, Ube2a-Related	0
Miles-Carpenter syndrome +	2
Mullegama-Klein-Martinez syndrome	2
Paganini-Miozzo syndrome	1
Partington syndrome	1
Prieto syndrome	1
Raynaud-Claes syndrome	1
Renpenning syndrome	2
Schimke X-Linked Mental Retardation Syndrome	0
Stocco Dos Santos type X-linked intellectual disability	10
Syndromic X-Linked Mental Retardation 33	1
Tonne-Kalscheuer syndrome	1
Van Esch-O'Driscoll syndrome	1
Wilson-Turner syndrome	3
X-Linked Intellectual Developmental Disorder 110	1
X-Linked Intellectual Developmental Disorder 112	1
X-Linked Intellectual Developmental Disorder 113	1
X-linked Aarskog syndrome	2
X-linked intellectual developmental disorder 108	2
X-linked intellectual developmental disorder 109	1
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	1
X-linked intellectual disability-psychosis-macroorchidism syndrome	2
X-linked intellectual disability-short stature-overweight syndrome	2
X-linked mental retardation Gustavson type	1
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance	1
X-linked mental retardation-hypotonic facies syndrome-1	3
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	1
deafness-intellectual disability, Martin-Probst type syndrome	0
female-restricted syndromic X-linked intellectual disability 99	1
syndromic X-linked intellectual developmental disorder Bain type	2
syndromic X-linked intellectual disability 12	0
syndromic X-linked intellectual disability 14	17
syndromic X-linked intellectual disability 17	0
syndromic X-linked intellectual disability 34	1
syndromic X-linked intellectual disability 5	2
syndromic X-linked intellectual disability 7	0
syndromic X-linked intellectual disability 94	1
syndromic X-linked intellectual disability Abidi type	0
syndromic X-linked intellectual disability Cabezas type	26
syndromic X-linked intellectual disability Chudley-Schwartz type	0
syndromic X-linked intellectual disability Claes-Jensen type	2
syndromic X-linked intellectual disability Hedera type	12
syndromic X-linked intellectual disability Lubs type	561
syndromic X-linked intellectual disability Najm type	12
syndromic X-linked intellectual disability Nascimento type	1
syndromic X-linked intellectual disability Pilorge type	2
syndromic X-linked intellectual disability Raymond type	9
syndromic X-linked intellectual disability Shashi type	1
syndromic X-linked intellectual disability Shrimpton type	0
syndromic X-linked intellectual disability Siderius type	1
syndromic X-linked intellectual disability Snyder type	1
syndromic X-linked intellectual disability Turner type	4
syndromic X-linked intellectual disability type 10	1
syndromic X-linked intellectual disorder Lujan-Fryns-type	1
syndromic X-linked mental retardation 35	1
syndromic X-linked mental retardation Hough type	1

paths to the root