FBXW10 (F-box and WD repeat domain containing 10)

Gene: FBXW10 (F-box and WD repeat domain containing 10) Homo sapiens

Analyze

Symbol:

FBXW10

Name:

F-box and WD repeat domain containing 10

RGD ID:

1344414

HGNC Page

HGNC:1211

Description:

Predicted to be located in cytosol.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

F-box and WD-40 domain protein 10; F-box and WD-40 domain-containing protein 10; F-box protein; F-box/WD repeat-containing protein 10; Fbw10; HREP; SM25H2; SM2SH2; testicular tissue protein Li 69; ubiquitin ligase specificity factor; ubiquitin ligase-specificity factor

RGD Orthologs

Mouse

Rat

Bonobo

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	18,744,026 - 18,779,349 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	18,647,367 - 18,682,662 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	18,588,051 - 18,623,387 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	18,588,063 - 18,623,386	NCBI
Cytogenetic Map	17	p11.2	NCBI
HuRef	17	18,230,526 - 18,264,647 (+)	NCBI		HuRef
CHM1_1	17	18,656,781 - 18,692,149 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

autistic disorder (IAGP)

common variable immunodeficiency 2 (IAGP)

Joubert syndrome 1 (IAGP)

Potocki-Lupski syndrome (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

2,3,7,8-tetrachlorodibenzodioxine (EXP)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

carbon nanotube (ISO)

CGP 52608 (EXP)

cobalt atom (EXP)

copper atom (EXP)

copper(0) (EXP)

dioxygen (ISO)

endosulfan (EXP)

epoxiconazole (ISO)

lipopolysaccharide (EXP)

methapyrilene (EXP)

methylisothiazolinone (EXP)

phenobarbital (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

triptonide (ISO)

trovafloxacin (ISO)

Tungsten carbide (EXP)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Cellular Component

cytosol (TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Agenesis of cerebellar vermis (IAGP)

Autism (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:11230166	PMID:12477932	PMID:15520277	PMID:16344560	PMID:19028597	PMID:20498703	PMID:21145461	PMID:23899520	PMID:26673895	PMID:31400758	PMID:34857952	PMID:36215168
PMID:36990424	PMID:37775405

Genomics

Comparative Map Data

FBXW10
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	18,744,026 - 18,779,349 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	18,647,367 - 18,682,662 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	18,588,051 - 18,623,387 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	17	18,588,063 - 18,623,386	NCBI
Cytogenetic Map	17	p11.2	NCBI
HuRef	17	18,230,526 - 18,264,647 (+)	NCBI		HuRef
CHM1_1	17	18,656,781 - 18,692,149 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI		T2T-CHM13v2.0

Fbxw10
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	62,737,893 - 62,768,290 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	62,737,895 - 62,768,291 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	62,847,067 - 62,877,464 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	62,847,069 - 62,877,465 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	62,660,625 - 62,690,964 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	62,663,264 - 62,693,660 (+)	NCBI		MGSCv36	mm8
Celera	11	69,772,318 - 69,802,562 (+)	NCBI		Celera
Cytogenetic Map	11	B2	NCBI
cM Map	11	38.78	NCBI

Fbxw10
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	48,012,555 - 48,051,136 (+)	NCBI		GRCr8
mRatBN7.2	10	47,513,313 - 47,551,909 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	47,486,297 - 47,551,907 (+)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	10	49,259,050 - 49,296,714 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	49,259,194 - 49,296,663 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	49,029,089 - 49,075,338 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Celera	10	46,758,482 - 46,795,881 (+)	NCBI		Celera
Cytogenetic Map	10	q23	NCBI

FBXW10
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	19	53,807,047 - 53,842,562 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	58,428,799 - 58,464,666 (+)	NCBI		NHGRI_mPanPan1

Variants

Variants in FBXW10
2 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17p11.2(chr17:16879232-18970941)x3	copy number gain	See cases [RCV000050888]	Chr17:16879232..18970941 [GRCh38] Chr17:16782546..18874254 [GRCh37] Chr17:16723271..18814979 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15776915-18771753)x1	copy number loss	See cases [RCV000050513]	Chr17:15776915..18771753 [GRCh38] Chr17:15680229..18675066 [GRCh37] Chr17:15620954..18615791 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15898032-20620700)x1	copy number loss	See cases [RCV000050602]	Chr17:15898032..20620700 [GRCh38] Chr17:15801346..20524013 [GRCh37] Chr17:15742071..20464605 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16879232-20390725)x3	copy number gain	See cases [RCV000050622]	Chr17:16879232..20390725 [GRCh38] Chr17:16782546..20294038 [GRCh37] Chr17:16723271..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16879232-20390725)x1	copy number loss	See cases [RCV000050624]	Chr17:16879232..20390725 [GRCh38] Chr17:16782546..20294038 [GRCh37] Chr17:16723271..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15259164-20925299)x3	copy number gain	See cases [RCV000051852]	Chr17:15259164..20925299 [GRCh38] Chr17:15162481..20828612 [GRCh37] Chr17:15103206..20769204 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15897832-20620841)x3	copy number gain	See cases [RCV000051853]	Chr17:15897832..20620841 [GRCh38] Chr17:15801146..20524154 [GRCh37] Chr17:15741871..20464746 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16836827-20340442)x3	copy number gain	See cases [RCV000051876]	Chr17:16836827..20340442 [GRCh38] Chr17:16740141..20243755 [GRCh37] Chr17:16680866..20184347 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16656168-20390725)x3	copy number gain	See cases [RCV000051855]	Chr17:16656168..20390725 [GRCh38] Chr17:16559482..20294038 [GRCh37] Chr17:16500207..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16836827-20504849)x3	copy number gain	See cases [RCV000051877]	Chr17:16836827..20504849 [GRCh38] Chr17:16740141..20408162 [GRCh37] Chr17:16680866..20348754 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16919369-20289856)x3	copy number gain	See cases [RCV000051879]	Chr17:16919369..20289856 [GRCh38] Chr17:16822683..20193169 [GRCh37] Chr17:16763408..20133761 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16692462-20390725)x3	copy number gain	See cases [RCV000051858]	Chr17:16692462..20390725 [GRCh38] Chr17:16595776..20294038 [GRCh37] Chr17:16536501..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16713514-20582527)x3	copy number gain	See cases [RCV000051860]	Chr17:16713514..20582527 [GRCh38] Chr17:16616828..20485840 [GRCh37] Chr17:16557553..20426432 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16713515-20340442)x3	copy number gain	See cases [RCV000051871]	Chr17:16713515..20340442 [GRCh38] Chr17:16616829..20243755 [GRCh37] Chr17:16557554..20184347 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15234685-20620700)x3	copy number gain	See cases [RCV000051849]	Chr17:15234685..20620700 [GRCh38] Chr17:15138002..20524013 [GRCh37] Chr17:15078727..20464605 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16760817-20429770)x3	copy number gain	See cases [RCV000051872]	Chr17:16760817..20429770 [GRCh38] Chr17:16664131..20333083 [GRCh37] Chr17:16604856..20273675 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16760818-20504849)x3	copy number gain	See cases [RCV000051873]	Chr17:16760818..20504849 [GRCh38] Chr17:16664132..20408162 [GRCh37] Chr17:16604857..20348754 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:16060129-20620841)x1	copy number loss	See cases [RCV000054330]	Chr17:16060129..20620841 [GRCh38] Chr17:15963443..20524154 [GRCh37] Chr17:15904168..20464746 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16760818-20390725)x1	copy number loss	See cases [RCV000054337]	Chr17:16760818..20390725 [GRCh38] Chr17:16664132..20294038 [GRCh37] Chr17:16604857..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16836827-20465067)x1	copy number loss	See cases [RCV000054355]	Chr17:16836827..20465067 [GRCh38] Chr17:16740141..20368380 [GRCh37] Chr17:16680866..20308972 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16858444-20340442)x1	copy number loss	See cases [RCV000054356]	Chr17:16858444..20340442 [GRCh38] Chr17:16761758..20243755 [GRCh37] Chr17:16702483..20184347 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16858444-20465067)x1	copy number loss	See cases [RCV000054357]	Chr17:16858444..20465067 [GRCh38] Chr17:16761758..20368380 [GRCh37] Chr17:16702483..20308972 [NCBI36] Chr17:17p11.2	pathogenic
Single allele	complex	PMP22-RAI1 contiguous gene duplication syndrome [RCV002280690]	Chr17:14876984..22124952 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16879232-20316151)x3	copy number gain	See cases [RCV000133695]	Chr17:16879232..20316151 [GRCh38] Chr17:16782546..20219464 [GRCh37] Chr17:16723271..20160056 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16854250-20492169)x3	copy number gain	See cases [RCV000134467]	Chr17:16854250..20492169 [GRCh38] Chr17:16757564..20395482 [GRCh37] Chr17:16698289..20336074 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:17331511-20022528)x1	copy number loss	See cases [RCV000135874]	Chr17:17331511..20022528 [GRCh38] Chr17:17234825..19925841 [GRCh37] Chr17:17175550..19866433 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:18701974-18954766)x3	copy number gain	See cases [RCV000135913]	Chr17:18701974..18954766 [GRCh38] Chr17:18605287..18858079 [GRCh37] Chr17:18546012..18798804 [NCBI36] Chr17:17p11.2	benign
GRCh38/hg38 17p11.2(chr17:16879233-20390697)x1	copy number loss	See cases [RCV000135996]	Chr17:16879233..20390697 [GRCh38] Chr17:16782547..20294010 [GRCh37] Chr17:16723272..20234602 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16734558-20390697)x3	copy number gain	See cases [RCV000135997]	Chr17:16734558..20390697 [GRCh38] Chr17:16637872..20294010 [GRCh37] Chr17:16578597..20234602 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16734558-20390697)x1	copy number loss	See cases [RCV000135998]	Chr17:16734558..20390697 [GRCh38] Chr17:16637872..20294010 [GRCh37] Chr17:16578597..20234602 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16734588-20390725)x1	copy number loss	See cases [RCV000136906]	Chr17:16734588..20390725 [GRCh38] Chr17:16637902..20294038 [GRCh37] Chr17:16578627..20234630 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16734588-20316151)x1	copy number loss	See cases [RCV000136951]	Chr17:16734588..20316151 [GRCh38] Chr17:16637902..20219464 [GRCh37] Chr17:16578627..20160056 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16699816-20390725)x1	copy number loss	See cases [RCV000137974]	Chr17:16699816..20390725 [GRCh38] Chr17:16603130..20294038 [GRCh37] Chr17:16543855..20234630 [NCBI36] Chr17:17p11.2	pathogenic\|likely benign
GRCh38/hg38 17p11.2(chr17:16854250-20492214)x3	copy number gain	See cases [RCV000138255]	Chr17:16854250..20492214 [GRCh38] Chr17:16757564..20395527 [GRCh37] Chr17:16698289..20336119 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:17331511-19017784)x3	copy number gain	See cases [RCV000138572]	Chr17:17331511..19017784 [GRCh38] Chr17:17234825..18921097 [GRCh37] Chr17:17175550..18861822 [NCBI36] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:16989087-20370816)x1	copy number loss	See cases [RCV000139239]	Chr17:16989087..20370816 [GRCh38] Chr17:16892401..20274129 [GRCh37] Chr17:16833126..20214721 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16854250-20560048)x3	copy number gain	See cases [RCV000139188]	Chr17:16854250..20560048 [GRCh38] Chr17:16757564..20463361 [GRCh37] Chr17:16698289..20403953 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15883037-20620700)x1	copy number loss	See cases [RCV000139510]	Chr17:15883037..20620700 [GRCh38] Chr17:15786351..20524013 [GRCh37] Chr17:15727076..20464605 [NCBI36] Chr17:17p12-11.2	pathogenic\|likely pathogenic
GRCh38/hg38 17p11.2(chr17:16656162-20390697)x1	copy number loss	See cases [RCV000139558]	Chr17:16656162..20390697 [GRCh38] Chr17:16559476..20294010 [GRCh37] Chr17:16500201..20234602 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:17018951-20148630)x1	copy number loss	See cases [RCV000141105]	Chr17:17018951..20148630 [GRCh38] Chr17:16922265..20051943 [GRCh37] Chr17:16862990..19992535 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16699816-20492214)x3	copy number gain	See cases [RCV000140852]	Chr17:16699816..20492214 [GRCh38] Chr17:16603130..20395527 [GRCh37] Chr17:16543855..20336119 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16838097-20436415)x1	copy number loss	See cases [RCV000141975]	Chr17:16838097..20436415 [GRCh38] Chr17:16741411..20339728 [GRCh37] Chr17:16682136..20280320 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:17067833-19019419)x1	copy number loss	See cases [RCV000141729]	Chr17:17067833..19019419 [GRCh38] Chr17:16971147..18922732 [GRCh37] Chr17:16911872..18863457 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16858500-20570955)x3	copy number gain	See cases [RCV000142075]	Chr17:16858500..20570955 [GRCh38] Chr17:16761814..20474268 [GRCh37] Chr17:16702539..20414860 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15552362-19014200)x3	copy number gain	See cases [RCV000142169]	Chr17:15552362..19014200 [GRCh38] Chr17:15455676..18917513 [GRCh37] Chr17:15396401..18858238 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16734588-18834703)x1	copy number loss	See cases [RCV000142986]	Chr17:16734588..18834703 [GRCh38] Chr17:16637902..18738016 [GRCh37] Chr17:16578627..18678741 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16696708-20492860)x3	copy number gain	See cases [RCV000143381]	Chr17:16696708..20492860 [GRCh38] Chr17:16600022..20396173 [GRCh37] Chr17:16540747..20336765 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16718415-20546210)x3	copy number gain	See cases [RCV000143417]	Chr17:16718415..20546210 [GRCh38] Chr17:16621729..20449523 [GRCh37] Chr17:16562454..20390115 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16858500-20559337)x1	copy number loss	See cases [RCV000143210]	Chr17:16858500..20559337 [GRCh38] Chr17:16761814..20462650 [GRCh37] Chr17:16702539..20403242 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15883037-20658018)x1	copy number loss	See cases [RCV000143177]	Chr17:15883037..20658018 [GRCh38] Chr17:15786351..20561331 [GRCh37] Chr17:15727076..20501923 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16699816-20428292)x1	copy number loss	See cases [RCV000143181]	Chr17:16699816..20428292 [GRCh38] Chr17:16603130..20331605 [GRCh37] Chr17:16543855..20272197 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16426633-20998588)x3	copy number gain	See cases [RCV000143715]	Chr17:16426633..20998588 [GRCh38] Chr17:16329947..20901901 [GRCh37] Chr17:16270672..20842493 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15850859-20649235)x1	copy number loss	See cases [RCV000143650]	Chr17:15850859..20649235 [GRCh38] Chr17:15754173..20552548 [GRCh37] Chr17:15694898..20493140 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh38/hg38 17p11.2(chr17:16853120-20436482)x1	copy number loss	See cases [RCV000143596]	Chr17:16853120..20436482 [GRCh38] Chr17:16756434..20339795 [GRCh37] Chr17:16697159..20280387 [NCBI36] Chr17:17p11.2	pathogenic
GRCh38/hg38 17p12-11.2(chr17:15729893-20510251)x1	copy number loss	See cases [RCV000143485]	Chr17:15729893..20510251 [GRCh38] Chr17:15633207..20413564 [GRCh37] Chr17:15573932..20354156 [NCBI36] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16603130-20261191)x1	copy number loss	See cases [RCV000449069]	Chr17:16603130..20261191 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p12-11.2(chr17:15767020-20261250)x3	copy number gain	See cases [RCV000240104]	Chr17:15767020..20261250 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:17053390-19893098)x1	copy number loss	See cases [RCV000239910]	Chr17:17053390..19893098 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16654302-20261250)x1	copy number loss	See cases [RCV000240274]	Chr17:16654302..20261250 [GRCh37] Chr17:17p11.2	pathogenic
arr[hg19]17p11.2(16,757,111-20,219,651)x3	duplication	Potocki-Lupski syndrome [RCV000591005]	Chr17:16757111..20219651 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16740141-20261191)x3	copy number gain	See cases [RCV000449384]	Chr17:16740141..20261191 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16651292-18722974)x1	copy number loss	See cases [RCV000449355]	Chr17:16651292..18722974 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p12-11.2(chr17:10771948-21510992)x1	copy number loss	See cases [RCV000447345]	Chr17:10771948..21510992 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p12-11.2(chr17:15745315-20261191)x1	copy number loss	See cases [RCV000446498]	Chr17:15745315..20261191 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16761814-20304295)x1	copy number loss	See cases [RCV000446300]	Chr17:16761814..20304295 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16637902-20261250)x1	copy number loss	See cases [RCV000446465]	Chr17:16637902..20261250 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16741771-20430791)x3	copy number gain	See cases [RCV000445753]	Chr17:16741771..20430791 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16757564-20261191)x1	copy number loss	See cases [RCV000448145]	Chr17:16757564..20261191 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18465463-19149350)x1	copy number loss	See cases [RCV000448508]	Chr17:18465463..19149350 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:16741411-20304154)x1	copy number loss	See cases [RCV000448636]	Chr17:16741411..20304154 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16741411-20449523)x1	copy number loss	See cases [RCV000448404]	Chr17:16741411..20449523 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16741411-20408379)x1	copy number loss	See cases [RCV000447955]	Chr17:16741411..20408379 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16761814-20462723)x1	copy number loss	See cases [RCV000448752]	Chr17:16761814..20462723 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16772264-20433502)x3	copy number gain	See cases [RCV000448097]	Chr17:16772264..20433502 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16745600-20396173)x1	copy number loss	See cases [RCV000510506]	Chr17:16745600..20396173 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16761814-20339795)x3	copy number gain	See cases [RCV000510267]	Chr17:16761814..20339795 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16727264-20413564)x1	copy number loss	See cases [RCV000511412]	Chr17:16727264..20413564 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16772264-20297091)x1	copy number loss	See cases [RCV000511915]	Chr17:16772264..20297091 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16741411-20410218)x1	copy number loss	See cases [RCV000511460]	Chr17:16741411..20410218 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16738161-20338182)x3	copy number gain	See cases [RCV000511433]	Chr17:16738161..20338182 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p11.2(chr17:16727264-20395889)x1	copy number loss	See cases [RCV000511111]	Chr17:16727264..20395889 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16651292-20437532)x3	copy number gain	See cases [RCV000511042]	Chr17:16651292..20437532 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18465208-18922732)x1	copy number loss	See cases [RCV000512184]	Chr17:18465208..18922732 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:16591260-20473937)x3	copy number gain	See cases [RCV000512356]	Chr17:16591260..20473937 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16741411-20489023)x1	copy number loss	See cases [RCV000512446]	Chr17:16741411..20489023 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p11.2(chr17:16842163-20217777)	copy number gain	Delayed speech and language development [RCV000626511]	Chr17:16842163..20217777 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16727264-20310241)x1	copy number loss	not provided [RCV000683897]	Chr17:16727264..20310241 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16761814-20292897)x3	copy number gain	not provided [RCV000683900]	Chr17:16761814..20292897 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16999980-20298979)x1	copy number loss	not provided [RCV000683901]	Chr17:16999980..20298979 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18615096-18917513)x3	copy number gain	not provided [RCV000683906]	Chr17:18615096..18917513 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:16741411-20430791)x1	copy number loss	not provided [RCV000683898]	Chr17:16741411..20430791 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:17021607-20015978)x1	copy number loss	not provided [RCV000683902]	Chr17:17021607..20015978 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p11.2(chr17:18596126-19180190)x3	copy number gain	not provided [RCV000739427]	Chr17:18596126..19180190 [GRCh37] Chr17:17p11.2	benign
NC_000017.11:g.(?_16770855)_(20585863_?)del	deletion	Autism [RCV000754202]	Chr17:16770855..20585863 [GRCh38] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16660721-20417975)x1	copy number loss	not provided [RCV000739417]	Chr17:16660721..20417975 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p12-11.2(chr17:15796140-20331131)x3	copy number gain	not provided [RCV000751941]	Chr17:15796140..20331131 [GRCh37] Chr17:17p12-11.2	pathogenic
NM_001267585.2(FBXW10):c.824G>T (p.Arg275Leu)	single nucleotide variant	not provided [RCV000948449]	Chr17:18749875 [GRCh38] Chr17:18653188 [GRCh37] Chr17:17p11.2	benign
GRCh37/hg19 17p11.2(chr17:16842991-20217316)	copy number loss	Smith-Magenis syndrome [RCV000767738]	Chr17:16842991..20217316 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18529674-18923470)x1	copy number loss	not provided [RCV000848947]	Chr17:18529674..18923470 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p12-11.2(chr17:15632431-18726389)x1	copy number loss	not provided [RCV001006874]	Chr17:15632431..18726389 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16664739-20370783)	copy number gain	Potocki-Lupski syndrome [RCV003236713]	Chr17:16664739..20370783 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18484296-18696073)x3	copy number gain	not provided [RCV001006880]	Chr17:18484296..18696073 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:18537316-18686905)x3	copy number gain	not provided [RCV001006881]	Chr17:18537316..18686905 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:18599743-18876835)x3	copy number gain	not provided [RCV001259294]	Chr17:18599743..18876835 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:16651292-20286898)	copy number loss	Smith-Magenis syndrome [RCV002280651]	Chr17:16651292..20286898 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16761814-20330062)x3	copy number gain	not provided [RCV001259290]	Chr17:16761814..20330062 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16763370-20395611)x1	copy number loss	not provided [RCV001259291]	Chr17:16763370..20395611 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18509439-19143976)x3	copy number gain	not provided [RCV001259293]	Chr17:18509439..19143976 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:17145361-20137943)	copy number loss	Smith-Magenis syndrome [RCV001352632]	Chr17:17145361..20137943 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16601603-20063369)	copy number gain	Potocki-Lupski syndrome [RCV001352635]	Chr17:16601603..20063369 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16829153-20361747)x3	copy number gain	Potocki-Lupski syndrome [RCV001801179]	Chr17:16829153..20361747 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:17151140-20187953)	copy number loss	Smith-Magenis syndrome [RCV002280652]	Chr17:17151140..20187953 [GRCh37] Chr17:17p11.2	pathogenic
NC_000017.10:g.(?_16842861)_(19578885_?)del	deletion	Immunodeficiency, common variable, 2 [RCV002049406]\|Joubert syndrome [RCV002047402]	Chr17:16842861..19578885 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16664739-20217378)x1	copy number loss	not provided [RCV002211424]	Chr17:16664739..20217378 [GRCh37] Chr17:17p11.2	pathogenic
NC_000017.10:g.(?_16842861)_(19578885_?)dup	duplication	Familial aplasia of the vermis [RCV003116613]\|Immunodeficiency, common variable, 2 [RCV003116614]	Chr17:16842861..19578885 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:16736709-20339460)x3	copy number gain	See cases [RCV002292216]	Chr17:16736709..20339460 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:17103571-19331028)x3	copy number gain	not provided [RCV002474502]	Chr17:17103571..19331028 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18599744-18882395)x3	copy number gain	not provided [RCV002473581]	Chr17:18599744..18882395 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh37/hg19 17p11.2(chr17:17116969-20217378)x1	copy number loss	not provided [RCV003222939]	Chr17:17116969..20217378 [GRCh37] Chr17:17p11.2	pathogenic
Single allele	duplication	not provided [RCV003448668]	Chr17:16757513..18772328 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16651293-20450566)x1	copy number loss	not provided [RCV003483315]	Chr17:16651293..20450566 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p12-11.2(chr17:15694772-20582794)x1	copy number loss	not provided [RCV003483314]	Chr17:15694772..20582794 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p11.2-11.1(chr17:18614422-22227823)x3	copy number gain	not provided [RCV003485147]	Chr17:18614422..22227823 [GRCh37] Chr17:17p11.2-11.1	uncertain significance
NM_001267585.2(FBXW10):c.2256G>A (p.Leu752=)	single nucleotide variant	not provided [RCV003413170]	Chr17:18772661 [GRCh38] Chr17:18675974 [GRCh37] Chr17:17p11.2	likely benign
GRCh37/hg19 17p12-11.2(chr17:15759103-20564268)x1	copy number loss	not specified [RCV003987246]	Chr17:15759103..20564268 [GRCh37] Chr17:17p12-11.2	pathogenic
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	copy number gain	not specified [RCV003987215]	Chr17:525..21510992 [GRCh37] Chr17:17p13.3-11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:18509272-18917513)x3	copy number gain	not provided [RCV003485146]	Chr17:18509272..18917513 [GRCh37] Chr17:17p11.2	uncertain significance
GRCh38/hg38 17p11.2(chr17:16699694-20530646)x3	copy number gain	See cases [RCV000140217]	Chr17:16699694..20530646 [GRCh38] Chr17:16603008..20433959 [GRCh37] Chr17:16543733..20374551 [NCBI36] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:17200426-21900910)x1	copy number loss	See cases [RCV000510254]	Chr17:17200426..21900910 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16782546-20294038)	copy number loss	Sleep abnormality [RCV000626510]	Chr17:16782546..20294038 [GRCh37] Chr17:17p11.2	pathogenic
GRCh37/hg19 17p11.2(chr17:16768248-20391959)x1	copy number loss	not provided [RCV000739423]	Chr17:16768248..20391959 [GRCh37] Chr17:17p11.2	pathogenic
Single allele	duplication	Autism [RCV000754201]	Chr17:16770855..20422847 [GRCh38] Chr17:17p11.2	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1644
Count of miRNA genes:	836
Interacting mature miRNAs:	978
Transcripts:	ENST00000301938, ENST00000308799, ENST00000395665, ENST00000395667, ENST00000573605, ENST00000574478
Prediction methods:	Microtar, Miranda, Pita, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

RH123806

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	18,653,452 - 18,653,798	UniSTS	GRCh37
GRCh37	17	15,516,581 - 15,516,927	UniSTS	GRCh37
Build 36	17	15,457,306 - 15,457,652	RGD	NCBI36
Cytogenetic Map	17	p12	UniSTS
HuRef	17	15,389,282 - 15,389,628	UniSTS
TNG Radiation Hybrid Map	17	9148.0	UniSTS

D17S1686

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	18,659,103 - 18,659,322	UniSTS	GRCh37
Build 36	17	18,599,828 - 18,600,047	RGD	NCBI36
Cytogenetic Map	17	p12	UniSTS
Whitehead-YAC Contig Map	17		UniSTS

FBXW10_9126

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	15,468,614 - 15,469,437	UniSTS	GRCh37
GRCh37	17	18,682,021 - 18,682,846	UniSTS	GRCh37
Build 36	17	15,409,339 - 15,410,162	RGD	NCBI36
HuRef	17	18,264,006 - 18,264,831	UniSTS

D17S725

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	18,657,151 - 18,657,252	UniSTS	GRCh37
GRCh37	17	15,513,108 - 15,513,228	UniSTS	GRCh37
Build 36	17	15,453,833 - 15,453,953	RGD	NCBI36
Cytogenetic Map	17	p12	UniSTS
HuRef	17	15,385,809 - 15,385,929	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

High

Medium

269

Low

957

130

110

185

172

671

184

799

168

Below cutoff

2215

2319

695

442

846

304

3749

1887

2963

268

891

689

143

1099

2485

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001267585	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001267586	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001411059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_051988	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011523626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017024020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017024021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435121	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435123	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435124	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435126	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435127	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435129	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435130	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435131	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC107982	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310383	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136822	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY729024	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC028364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI828401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB055860	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HC006954	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HM005382	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000301938 ⟹ ENSP00000306937

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	18,744,075 - 18,779,349 (+)	Ensembl

RefSeq Acc Id:

ENST00000308799 ⟹ ENSP00000310382

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	18,744,026 - 18,779,349 (+)	Ensembl

RefSeq Acc Id:

ENST00000395665 ⟹ ENSP00000379025

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	18,744,054 - 18,779,349 (+)	Ensembl

RefSeq Acc Id:

ENST00000573605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	18,769,477 - 18,772,634 (+)	Ensembl

RefSeq Acc Id:

ENST00000574478 ⟹ ENSP00000463552

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	18,744,072 - 18,779,342 (+)	Ensembl

RefSeq Acc Id:

NM_001267585 ⟹ NP_001254514

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI
GRCh37	17	18,647,326 - 18,682,662 (+)	NCBI
HuRef	17	18,230,526 - 18,264,647 (+)	NCBI
CHM1_1	17	18,656,781 - 18,692,149 (+)	NCBI
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

Sequence:

show sequence

AGACTTCTGCTGGCAGTTACTGAGAGAGATAGGCTTTCCATCCATGGCAGCCATTTACTTTTGC
TCTGGGAGACGTTTGTAATAGAAAAGGCACAACTGGGGTATTTATTCATTCCCCCCGTTCCTCT
AGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAGGGCTAAAATGGACTGGTTATCTTAGGATCA
TGGAAAACCTGGAATCAAGGCTCAAGAATGCCCCCTATTTTCGTTGTGAGAAGGGAACCGATTC
CATCCCTCTATGCCGGAAGTGTGAGACGTGTGTCTTAGCCTGGAAGATCTTCTCTACCAAAGAG
TGGTTCTGCAGGATCAATGACATATCACAGAGGAGGTTTCTAGTTGGCATTCTGAAGCAGTTAA
ATAGCTTATATTTGTTACACTATTTCCAAAATATCCTTCAGACCACACAGGGAAAGGATTTCAT
CTATAACAGGTCCCGGATCAACCTCAGCAAGAAAGAGGGGAAAGTTGTGAAGTCCTCCTTGAAC
CAAATGTTGGATAAAACAGTAGAACAGAAGATGAAAGAGATCTTGTACTGGTTTGCGAACAGCA
CCCAGTGGACCAAGGCGAATTATACTCTCTTACTGCTGCAGATGTGCAACCCCAAATTACTGCT
CACTGCTGCCAATGTGATCAGAGTCCTGTTTCTGAGAGAGGAGAACAATATCTCAGGGCTCAAT
CAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCAC
AAGTCTATTGGACAGCCAAAACTCAGCACACATCCCTTCCTTTGTCCAAAGCCCCAGAAAATGA
ACACTTGCTTGGGGCAGCATCTAACCCTGAGGAACCATGGAGGAATTCACTCCGGTGTATATCC
GAAATGAATAGGCTGTTTTCTGGAAAAGGAGACATAACCAAGCCAGGGTACGATCCCTGCAATC
TATTGGTTGACCTGGATGACATCAGAGACCTGTCTTCTGGGTTCAGCAAATACCGAGACTTCAT
CCGTTACCTGCCCATCCACCTCTCCAAGTACATTCTAAGAATGCTGGATAGACACACCCTGAAC
AAGTGCGCCTCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACTTGTCAG
CGCACGGCTTCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAATTGATCC
TAATTATGCCAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGCATGCGT
GTGAAACATCCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCATACCAGA
ACGAGGAAACGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAATGTTCG
CATTCTCTCTGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTGATAGCT
GTGTCATCTAATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCGTTGAAT
TCCGAGGCCATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCTCCTAAG
CGGGAGCTATGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGAATCTTC
GGTGGTCACCAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTGGAGGAA
GAGATTGCCAGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAA
AGACCCCATCTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTG
GTGAAAGTGTGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGGGAGCCG
TGAAATGCCTGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGTCATGGC
CTGGAGCATGGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGGAGGTGCTC
GACGTGTCCCTTCTCTTCCTCCGGGTCATCAGCGCCTGTGCAGATGGCAAGATCCGAATTTACA
ATTTCCTCAACGGGAACTGTATGAAGGTGTTAAAAGCCAATGGCAGAGGTGATCCTGTGCTGTC
CTTCTTTATTCAGGGCAACAGGATGGTGGTCAACACAGAGAGCAATGTTCTCATGTTCCAGTTT
GAGCACATAAAGTGGCAGTATGCCGTGGAAAAAACGAAACAAAAGAAGAATAAGGAGAAAGAGG
AGGAAAAAGAAGAAAATAGTCTCATGGAAATTCTCTCTAAGTGTAATATTCAGGTTCACAGCCC
AAGAGAGTCTGTATCCAGTAAACAAACTGTGATCCAAGAGCTCCTACCAGGCAAACCTCCCAAG
TCCCGAGTACTCCTGAAGCCGGCCAAGTTCTCTTCAGCAGTGTTAATAGAGGAACTTCAAAGTC
AAGGAAAGTCAAAATCACCCCGAAGAGATGCAGATGATGTGGAGAAAGCACAAAAACAAGGACA
ATTGGAAACTCCTGGAAAACTGCCCAGTCACCCAAAGAAAAAGTCTTGGAAAATCCCTATGTCA
CCTGACCAATTCCTCCTGACTGTTAGCGCCCTGCAGCACGCCCATAATTCCGGGGAATTTGCCT
ATCCCTGTAGGCCCCAAACAGAAATTACTGATGTCTGGGGACCTTCAATTTCATACCCAAGGAA
GGTCTTGAATTTCAAAGGAAAATCAATCCAACGTGCAGTTGATCGGTTGAGATTGAGCAATCCT
CCTATAGATGTGAAACGAACCAGTATTCCCCTTGAAATCCAGAAACTGCAGCCCAACTTGAAGA
TCTCTTTGCACAGTCCTAGAGTCCAGTCCACCATACCCCAGCCCATGATTATCCGCTCCAGGTT
CTCTGGCAGCTTAAAGGGTGGAGACCAAGTGACCAGTTCAATTGAAAGGGCTGTGTGCAGTACG
GGTCCCCTGACCAGTATGCAGGTCATTAAACCAAACCGCATGCTAGCTCCACAAGTGGGCACAG
CCACCCTGTCTCTTAAGAAAGAACGGCCTCGCATCTATACAGCCCTTGATCCTTTTAGAGTGAA
CACTGAGTTCGTGCTGTTGACCGTGAAGGAGGAGAAGGAGCACCAGGAAGCCAAGATGAAGGAA
TATCAGGCCAGGGAGTCCACTGGAGTGGTTGATCCAGGAAAAGTCAGCAAAGCTGCATGGATCA
GGAAGATCAAAGGCCTGCCTATTGATAATTTCACGAAGCAAGGGAAAACAGCGGCCCCTGAACT
TGGACAAAATGTATTTATCTAAACCAGCCTTGGGAAATTACAATGTTTTACAATAAACAGAAAG
CCAAGCGGA

hide sequence

RefSeq Acc Id:

NM_001267586 ⟹ NP_001254515

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI
GRCh37	17	18,647,326 - 18,682,662 (+)	NCBI
HuRef	17	18,230,526 - 18,264,647 (+)	NCBI
CHM1_1	17	18,656,781 - 18,692,149 (+)	NCBI
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

Sequence:

show sequence

AGACTTCTGCTGGCAGTTACTGAGAGAGATAGGCTTTCCATCCATGGCAGCCATTTACTTTTGC
TCTGGGAGACGTTTGTAATAGAAAAGGCACAACTGGGGTATTTATTCATTCCCCCCGTTCCTCT
AGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAGGGCTAAAATGGACTGGTTATCTTAGGATCA
TGGAAAACCTGGAATCAAGGCTCAAGAATGCCCCCTATTTTCGTTGTGAGAAGGGAACCGATTC
CATCCCTCTATGCCGGAAGTGTGAGACGTGTGTCTTAGCCTGGAAGATCTTCTCTACCAAAGAG
TGGTTCTGCAGGATCAATGACATATCACAGAGGAGGTTTCTAGTTGGCATTCTGAAGCAGTTAA
ATAGCTTATATTTGTTACACTATTTCCAAAATATCCTTCAGACCACACAGGGAAAGGATTTCAT
CTATAACAGGTCCCGGATCAACCTCAGCAAGAAAGAGGGGAAAGTTGTGAAGTCCTCCTTGAAC
CAAATGTTGGATAAAACAGTAGAACAGAAGATGAAAGAGATCTTGTACTGGTTTGCGAACAGCA
CCCAGTGGACCAAGGCGAATTATACTCTCTTACTGCTGCAGATGTGCAACCCCAAATTACTGCT
CACTGCTGCCAATGTGATCAGAGTCCTGTTTCTGAGAGAGGAGAACAATATCTCAGGGCTCAAT
CAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCAC
AAGTCTATTGGACAGCCAAAACTCAGCACACATCCCTTCCTTTGTCCAAAGCCCCAGAAAATGA
ACACTTGCTTGGGGCAGCATCTAACCCTGAGGAACCATGGAGGAATTCACTCCGGTGTATATCC
GAAATGAATAGGCTGTTTTCTGGAAAAGGAGACATAACCAAGCCAGGGTACGATCCCTGCAATC
TATTGGTTGACCTGGATGACATCAGAGACCTGTCTTCTGGGTTCAGCAAATACCGAGACTTCAT
CCGTTACCTGCCCATCCACCTCTCCAAGTACATTCTAAGAATGCTGGATAGACACACCCTGAAC
AAGTGCGCCTCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACTTGTCAG
CGCACGGCTTCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAATTGATCC
TAATTATGCCAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGCATGCGT
GTGAAACATCCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCATACCAGA
ACGAGGAAACGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAATGTTCG
CATTCTCTCTGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTGATAGCT
GTGTCATCTAATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCGTTGAAT
TCCGAGGCCATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCTCCTAAG
CGGGAGCTATGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGAATCTTC
GGTGGTCACCAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTGGAGGAA
GAGATTGCCAGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAA
AGACCCCATCTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTG
GTGAAAGTGTGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGGGAGCCG
TGAAATGCCTGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGTCATGGC
CTGGAGCATGGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGATGGTGGTC
AACACAGAGAGCAATGTTCTCATGTTCCAGTTTGAGCACATAAAGTGGCAGTATGCCGTGGAAA
AAACGAAACAAAAGAAGAATAAGGAGAAAGAGGAGGAAAAAGAAGAAAATAGTCTCATGGAAAT
TCTCTCTAAGTGTAATATTCAGGTTCACAGCCCAAGAGAGTCTGTATCCAGTAAACAAACTGTG
ATCCAAGAGCTCCTACCAGGCAAACCTCCCAAGTCCCGAGTACTCCTGAAGCCGGCCAAGTTCT
CTTCAGCAGTGTTAATAGAGGAACTTCAAAGTCAAGGAAAGTCAAAATCACCCCGAAGAGATGC
AGATGATGTGGAGAAAGCACAAAAACAAGGACAATTGGAAACTCCTGGAAAACTGCCCAGTCAC
CCAAAGAAAAAGTCTTGGAAAATCCCTATGTCACCTGACCAATTCCTCCTGACTGTTAGCGCCC
TGCAGCACGCCCATAATTCCGGGGAATTTGCCTATCCCTGTAGGCCCCAAACAGAAATTACTGA
TGTCTGGGGACCTTCAATTTCATACCCAAGGAAGGTCTTGAATTTCAAAGGAAAATCAATCCAA
CGTGCAGTTGATCGGTTGAGATTGAGCAATCCTCCTATAGATGTGAAACGAACCAGTATTCCCC
TTGAAATCCAGAAACTGCAGCCCAACTTGAAGATCTCTTTGCACAGTCCTAGAGTCCAGTCCAC
CATACCCCAGCCCATGATTATCCGCTCCAGGTTCTCTGGCAGCTTAAAGGGTGGAGACCAAGTG
ACCAGTTCAATTGAAAGGGCTGTGTGCAGTACGGGTCCCCTGACCAGTATGCAGGTCATTAAAC
CAAACCGCATGCTAGCTCCACAAGTGGGCACAGCCACCCTGTCTCTTAAGAAAGAACGGCCTCG
CATCTATACAGCCCTTGATCCTTTTAGAGTGAACACTGAGTTCGTGCTGTTGACCGTGAAGGAG
GAGAAGGAGCACCAGGAAGCCAAGATGAAGGAATATCAGGCCAGGGAGTCCACTGGAGTGGTTG
ATCCAGGAAAAGTCAGCAAAGCTGCATGGATCAGGAAGATCAAAGGCCTGCCTATTGATAATTT
CACGAAGCAAGGGAAAACAGCGGCCCCTGAACTTGGACAAAATGTATTTATCTAAACCAGCCTT
GGGAAATTACAATGTTTTACAATAAACAGAAAGCCAAGCGGA

hide sequence

RefSeq Acc Id:

NM_001411059 ⟹ NP_001397988

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

NR_051988

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI
GRCh37	17	18,647,326 - 18,682,662 (+)	NCBI
HuRef	17	18,230,526 - 18,264,647 (+)	NCBI
CHM1_1	17	18,656,781 - 18,692,149 (+)	NCBI
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

Sequence:

show sequence

AGACTTCTGCTGGCAGTTACTGAGAGAGATAGGCTTTCCATCCATGGCAGCCATTTACTTTTGC
TCTGGGAGACGTTTGTAATAGAAAAGGCACAACTGGGGTATTTATTCATTCCCCCCGTTCCTCT
AGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAGGGCTAAAATGGACTGGTTATCTTAGGATCA
TGGAAAACCTGGAATCAAGGCTCAAGAATGCCCCCTATTTTCGTTGTGAGAAGGGAACCGATTC
CATCCCTCTATGCCGGAAGTGTGAGACGTGTGTCTTAGCCTGGAAGATCTTCTCTACCAAAGAG
TGGTTCTGCAGGATCAATGACATATCACAGAGGAGGTTTCTAGTTGGCATTCTGAAGCAGTTAA
ATAGCTTATATTTGTTACACTATTTCCAAAATATCCTTCAGACCACACAGGGAAAGGATTTCAT
CTATAACAGGTCCCGGATCAACCTCAGCAAGAAAGAGGGGAAAGTTGTGAAGTCCTCCTTGAAC
CAAATGTTGGATAAAACAGTAGAACAGAAGATGAAAGAGATCTTGTACTGGTTTGCGAACAGCA
CCCAGTGGACCAAGGCGAATTATACTCTCTTACTGCTGCAGATGTGCAACCCCAAATTACTGCT
CACTGCTGCCAATGTGATCAGAGTCCTGTTTCTGAGAGAGGAGAACAATATCTCAGGTAAACAA
GGCCACAGGCAGAGACTAGAGGGCCCCCGAAGACCAGAAGGCAAGGCTTCAGAAATCTGTAAGG
AACTGCAGTTGTAGACAACATAGGTAGACAGAGATTGCACAGAACTCAGCATAGGTTTTTTGAA
CTGACACCTTGTCCTGACACCCGATCCTGTTTACCAAAGGAGAAATGACTGAGTGTAACTTCCT
TCTTGAAAATGATCAATGCAGGAGGAAGTACACAACTTTTAACTCACAAGCATTTATCATGGAT
TTCTGCATCTCATAGGCCCAGAAATGGCTGGTCCCTGCCCCTGACCCCTTAATGCTGGTGTCGT
TCCTGCTTTAGGGATTGGACTGAGCTCGAGAGGGTTGTAAAGGGGAAGCTTTTGTTTTTCTCTT
CAGCTGCCCTGCACAGAAACCAGACCAAGAAGTCAAAACTTAGGGCTTTTTTTTTTTTTTTCAT
TCACTCTACCATGCTCCTTGCTTATCCATGAAATGAAACCTTAAAGTAGAGTTTCTCCAAGGCT
GGAGATAGCTTAAGGGCCAAATAAGTCTAGGGTGGTAGTTCTCCAGCTGTGGCTTGTATCAGGA
TCTCCAGCAGGACCTGTTAAAACAAGCTCCTCCCCCAGAACTTCGGACTCAGCAGGTCTGAGGG
CTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGA
CCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACATCCCTTCCTTTGTCCAAAGCCCCAGA
AAATGAACACTTGCTTGGGGCAGCATCTAACCCTGAGGAACCATGGAGGAATTCACTCCGGTGT
ATATCCGAAATGAATAGGCTGTTTTCTGGAAAAGGAGACATAACCAAGCCAGGGTACGATCCCT
GCAATCTATTGGTTGACCTGGATGACATCAGAGACCTGTCTTCTGGGTTCAGCAAATACCGAGA
CTTCATCCGTTACCTGCCCATCCACCTCTCCAAGTACATTCTAAGAATGCTGGATAGACACACC
CTGAACAAGTGCGCCTCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACT
TGTCAGCGCACGGCTTCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAAT
TGATCCTAATTATGCCAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGC
ATGCGTGTGAAACATCCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCAT
ACCAGAACGAGGAAACGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAA
TGTTCGCATTCTCTCTGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTG
ATAGCTGTGTCATCTAATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCG
TTGAATTCCGAGGCCATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCT
CCTAAGCGGGAGCTATGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGA
ATCTTCGGTGGTCACCAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTG
GAGGAAGAGATTGCCAGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAG
ACACAAAGACCCCATCTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGA
GGGCTGGTGAAAGTGTGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGG
GAGCCGTGAAATGCCTGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGT
CATGGCCTGGAGCATGGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGGAG
GTGCTCGACGTGTCCCTTCTCTTCCTCCGGGTCATCAGCGCCTGTGCAGATGGCAAGATCCGAA
TTTACAATTTCCTCAACGGGAACTGTATGAAGGTGTTAAAAGCCAATGGCAGAGGTGATCCTGT
GCTGTCCTTCTTTATTCAGGGCAACAGGATGGTGGTCAACACAGAGAGCAATGTTCTCATGTTC
CAGTTTGAGCACATAAAGTGGCAGTATGCCGTGGAAAAAACGAAACAAAAGAAGAATAAGGAGA
AAGAGGAGGAAAAAGAAGAAAATAGTCTCATGGAAATTCTCTCTAAGTGTAATATTCAGGTTCA
CAGCCCAAGAGAGTCTGTATCCAGTAAACAAACTGTGATCCAAGAGCTCCTACCAGGCAAACCT
CCCAAGTCCCGAGTACTCCTGAAGCCGGCCAAGTTCTCTTCAGCAGTGTTAATAGAGGAACTTC
AAAGTCAAGGAAAGTCAAAATCACCCCGAAGAGATGAGTGAACACTGAGTTCGTGCTGTTGACC
GTGAAGGAGGAGAAGGAGCACCAGGAAGCCAAGATGAAGGAATATCAGGCCAGGGAGTCCACTG
GAGTGGTTGATCCAGGAAAAGTCAGCAAAGCTGCATGGATCAGGAAGATCAAAGGCCTGCCTAT
TGATAATTTCACGAAGCAAGGGAAAACAGCGGCCCCTGAACTTGGACAAAATGTATTTATCTAA
ACCAGCCTTGGGAAATTACAATGTTTTACAATAAACAGAAAGCCAAGCGGA

hide sequence

RefSeq Acc Id:

XM_011523625 ⟹ XP_011521927

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,778,564 (+)	NCBI

Sequence:

show sequence

ATGTTTCCAAGGAGGTCTGTACAAAAAGCCAGACTTCTGCTGGCAGTTACTGAGAGAGATAGGC
TTTCCATCCATGGCAGCCATTTACTTTTGCTCTGGGAGACGTTTGTAATAGAAAAGGCACAACT
GGGGTATTTATTCATTCCCCCCGTTCCTCTAGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAG
GGCTAAAATGGACTGGTTATCTTAGGATCATGGAAAACCTGGAATCAAGGCTCAAGAATGCCCC
CTATTTTCGTTGTGAGAAGGGAACCGATTCCATCCCTCTATGCCGGAAGTGTGAGACGTGTGTC
TTAGCCTGGAAGATCTTCTCTACCAAAGAGTGGTTCTGCAGGATCAATGACATATCACAGAGGA
GGTTTCTAGTTGGCATTCTGAAGCAGTTAAATAGCTTATATTTGTTACACTATTTCCAAAATAT
CCTTCAGACCACACAGGGAAAGGATTTCATCTATAACAGGTCCCGGATCAACCTCAGCAAGAAA
GAGGGGAAAGTTGTGAAGTCCTCCTTGAACCAAATGTTGGATAAAACAGTAGAACAGAAGATGA
AAGAGATCTTGTACTGGTTTGCGAACAGCACCCAGTGGACCAAGGCGAATTATACTCTCTTACT
GCTGCAGATGTGCAACCCCAAATTACTGCTCACTGCTGCCAATGTGATCAGAGTCCTGTTTCTG
AGAGAGGAGAACAATATCTCAGGTAAACAAGGCCACAGGCAGAGACTAGAGGGCCCCCGAAGAC
CAGAAGGCAAGGCTTCAGAAATCTGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGA
GAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACA
TCCCTTCCTTTGTCCAAAGCCCCAGAAAATGAACACTTGCTTGGGGCAGCATCTAACCCTGAGG
AACCATGGAGGAATTCACTCCGGTGTATATCCGAAATGAATAGGCTGTTTTCTGGAAAAGGAGA
CATAACCAAGCCAGGGTACGATCCCTGCAATCTATTGGTTGACCTGGATGACATCAGAGACCTG
TCTTCTGGGTTCAGCAAATACCGAGACTTCATCCGTTACCTGCCCATCCACCTCTCCAAGTACA
TTCTAAGTATGCTGGGGTGTATGAGGGGATTTCCCAGACACCTCCCCTCTTGGCCCAGTTCTGG
GGTTTCTGGGTCCATCTTTTTTTTTCCAGGAATGCTGGATAGACACACCCTGAACAAGTGCGCC
TCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACTTGTCAGCGCACGGCT
TCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAATTGATCCTAATTATGC
CAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGCATGCGTGTGAAACAT
CCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCATACCAGAACGAGGAAA
CGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAATGTTCGCATTCTCTC
TGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTGATAGCTGTGTCATCT
AATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCGTTGAATTCCGAGGCC
ATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCTCCTAAGCGGGAGCTA
TGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGAATCTTCGGTGGTCAC
CAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTGGAGGAAGAGATTGCC
AGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAAAGACCCCAT
CTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTGGTGAAAGTG
TGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGGGAGCCGTGAAATGCC
TGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGTCATGGCCTGGAGCAT
GGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGGAGGTGCTCGACGTGTCC
CTTCTCTTCCTCCGGGTCATCAGCGCCTGTGCAGATGGCAAGATCCGAATTTACAATTTCCTCA
ACGGGAACTGTATGAAGGTGTTAAAAGCCAATGGCAGAGGTGATCCTGTGCTGTCCTTCTTTAT
TCAGGGCAACAGGATGGTGGTCAACACAGAGAGCAATGTTCTCATGTTCCAGTTTGAGCACATA
AAGTGGCAGTATGCCGTGGAAAAAACGAAACAAAAGAAGAATAAGGAGAAAGAGGAGGAAAAAG
AAGAAAATAGTCTCATGGAAATTCTCTCTAAGTGTAATATTCAGGTTCACAGCCCAAGAGAGTC
TGTATCCAGTAAACAAACTGTGATCCAAGAGCTCCTACCAGGCAAACCTCCCAAGTCCCGAGTA
CTCCTGAAGCCGGCCAAGTTCTCTTCAGCAGTGTTAATAGAGGAACTTCAAAGTCAAGGAAAGT
CAAAATCACCCCGAAGAGATGCAGGCCACTACCTTTGCTTGTCTTTGAGAAACTGGAATGAATA
CAATGCCTGGCTTCTCCCAAGAGTGACTGGTTTTCCTTAATTGTCCCTTTTCTGACTTGAGGCC
ACAGAGGGAGAACCTTTCTAAGATGATGTGGAGAAAGCACAAAAACAAGGACAATTGGAAACTC
CTGGAAAACTGCCCAGTCACCCAAAGAAAAAGTCTTGGAAAATCC

hide sequence

RefSeq Acc Id:

XM_017024020 ⟹ XP_016879509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

Sequence:

show sequence

ATGTTTCCAAGGAGGTCTGTACAAAAAGCCAGACTTCTGCTGGCAGTTACTGAGAGAGATAGGC
TTTCCATCCATGGCAGCCATTTACTTTTGCTCTGGGAGACGTTTGTAATAGAAAAGGCACAACT
GGGGTATTTATTCATTCCCCCCGTTCCTCTAGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAG
GGCTAAAATGGACTGGTTATCTTAGGATCATGGAAAACCTGGAATCAAGGCTCAAGAATGCCCC
CTATTTTCGTTGTGAGAAGGGAACCGATTCCATCCCTCTATGCCGGAAGTGTGAGACGTGTGTC
TTAGCCTGGAAGATCTTCTCTACCAAAGAGTGGTTCTGCAGGATCAATGACATATCACAGAGGA
GGTTTCTAGTTGGCATTCTGAAGCAGTTAAATAGCTTATATTTGTTACACTATTTCCAAAATAT
CCTTCAGACCACACAGGGAAAGGATTTCATCTATAACAGGTCCCGGATCAACCTCAGCAAGAAA
GAGGGGAAAGTTGTGAAGTCCTCCTTGAACCAAATGTTGGATAAAACAGTAGAACAGAAGATGA
AAGAGATCTTGTACTGGTTTGCGAACAGCACCCAGTGGACCAAGGCGAATTATACTCTCTTACT
GCTGCAGATGTGCAACCCCAAATTACTGCTCACTGCTGCCAATGTGATCAGAGTCCTGTTTCTG
AGAGAGGAGAACAATATCTCAGGTAAACAAGGCCACAGGCAGAGACTAGAGGGCCCCCGAAGAC
CAGAAGGCAAGGCTTCAGAAATCTGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGA
GAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACA
TCCCTTCCTTTGTCCAAAGCCCCAGAAAATGAACACTTGCTTGGGGCAGCATCTAACCCTGAGG
AACCATGGAGGAATTCACTCCGGTGTATATCCGAAATGAATAGGCTGTTTTCTGGAAAAGGAGA
CATAACCAAGCCAGGGTACGATCCCTGCAATCTATTGGTTGACCTGGATGACATCAGAGACCTG
TCTTCTGGGTTCAGCAAATACCGAGACTTCATCCGTTACCTGCCCATCCACCTCTCCAAGTACA
TTCTAAGTATGCTGGGGTGTATGAGGGGATTTCCCAGACACCTCCCCTCTTGGCCCAGTTCTGG
GGTTTCTGGGTCCATCTTTTTTTTTCCAGGAATGCTGGATAGACACACCCTGAACAAGTGCGCC
TCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACTTGTCAGCGCACGGCT
TCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAATTGATCCTAATTATGC
CAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGCATGCGTGTGAAACAT
CCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCATACCAGAACGAGGAAA
CGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAATGTTCGCATTCTCTC
TGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTGATAGCTGTGTCATCT
AATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCGTTGAATTCCGAGGCC
ATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCTCCTAAGCGGGAGCTA
TGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGAATCTTCGGTGGTCAC
CAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTGGAGGAAGAGATTGCC
AGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAAAGACCCCAT
CTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTGGTGAAAGTG
TGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGGGAGCCGTGAAATGCC
TGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGTCATGGCCTGGAGCAT
GGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGGAGGTGCTCGACGTGTCC
CTTCTCTTCCTCCGGGTCATCAGCGCCTGTGCAGATGGCAAGATCCGAATTTACAATTTCCTCA
ACGGGAACTGTATGAAGGTGTTAAAAGCCAATGGCAGAGGTGATCCTGTGCTGTCCTTCTTTAT
TCAGGGCAACAGGATGGTGGTCAACACAGAGAGCAATGTTCTCATGTTCCAGTTTGAGCACATA
AAGTGGCAGTATGCCGTGGAAAAAACGAAACAAAAGAAGAATAAGGAGAAAGAGGAGGAAAAAG
AAGAAAATAGTCTCATGGAAATTCTCTCTAAGTGTAATATTCAGGTTCACAGCCCAAGAGAGTC
TGTATCCAGTAAACAAACTGTGATCCAAGAGCTCCTACCAGGCAAACCTCCCAAGTCCCGAGTA
CTCCTGAAGCCGGCCAAGTTCTCTTCAGCAGTGTTAATAGAGGAACTTCAAAGTCAAGGAAAGT
CAAAATCACCCCGAAGAGATGCAGGCCACTACCTTTGCTTGTCTTTGAGAAACTGGAATGAATA
CAATGCCTGGCTTCTCCCAAGAGTGACTGGTTTTCCTTAATTGTCCCTTTTCTGACTTGAGGCC
ACAGAGGGAGAACCTTTCTAAGCAGATGATGTGGAGAAAG

hide sequence

RefSeq Acc Id:

XM_017024021 ⟹ XP_016879510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,772,566 (+)	NCBI

Sequence:

show sequence

ATGTTTCCAAGGAGGTCTGTACAAAAAGCCAGACTTCTGCTGGCAGTTACTGAGAGAGATAGGC
TTTCCATCCATGGCAGCCATTTACTTTTGCTCTGGGAGACGTTTGTAATAGAAAAGGCACAACT
GGGGTATTTATTCATTCCCCCCGTTCCTCTAGTGTTTGGTGGCGTTGCCGTTGCAAGTGCGCAG
GGCTAAAATGGACTGGTTATCTTAGGATCATGGAAAACCTGGAATCAAGGCTCAAGAATGCCCC
CTATTTTCGTTGTGAGAAGGGAACCGATTCCATCCCTCTATGCCGGAAGTGTGAGACGTGTGTC
TTAGCCTGGAAGATCTTCTCTACCAAAGAGTGGTTCTGCAGGATCAATGACATATCACAGAGGA
GGTTTCTAGTTGGCATTCTGAAGCAGTTAAATAGCTTATATTTGTTACACTATTTCCAAAATAT
CCTTCAGACCACACAGGGAAAGGATTTCATCTATAACAGGTCCCGGATCAACCTCAGCAAGAAA
GAGGGGAAAGTTGTGAAGTCCTCCTTGAACCAAATGTTGGATAAAACAGTAGAACAGAAGATGA
AAGAGATCTTGTACTGGTTTGCGAACAGCACCCAGTGGACCAAGGCGAATTATACTCTCTTACT
GCTGCAGATGTGCAACCCCAAATTACTGCTCACTGCTGCCAATGTGATCAGAGTCCTGTTTCTG
AGAGAGGAGAACAATATCTCAGGTAAACAAGGCCACAGGCAGAGACTAGAGGGCCCCCGAAGAC
CAGAAGGCAAGGCTTCAGAAATCTGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGA
GAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACA
TCCCTTCCTTTGTCCAAAGCCCCAGAAAATGAACACTTGCTTGGGGCAGCATCTAACCCTGAGG
AACCATGGAGGAATTCACTCCGGTGTATATCCGAAATGAATAGGCTGTTTTCTGGAAAAGGAGA
CATAACCAAGCCAGGGTACGATCCCTGCAATCTATTGGTTGACCTGGATGACATCAGAGACCTG
TCTTCTGGGTTCAGCAAATACCGAGACTTCATCCGTTACCTGCCCATCCACCTCTCCAAGTACA
TTCTAAGTATGCTGGGGTGTATGAGGGGATTTCCCAGACACCTCCCCTCTTGGCCCAGTTCTGG
GGTTTCTGGGTCCATCTTTTTTTTTCCAGGAATGCTGGATAGACACACCCTGAACAAGTGCGCC
TCTGTGAGCCAGCACTGGGCCGCCATGGCTCAACAGGTCAAGATGGACTTGTCAGCGCACGGCT
TCATTCAGAACCAGATTACCTTCTTGCAGGGGTCCTACACAAGAGGAATTGATCCTAATTATGC
CAATAAGGTTTCTATCCCAGTTCCTAAAATGGTAGATGACGGGAAGAGCATGCGTGTGAAACAT
CCGAAGTGGAAGCTGAGAACGAAGAATGAGTACAACCTGTGGACTGCATACCAGAACGAGGAAA
CGCAGCAGGTCCTGATAGAGGAGAGAAATGTTTTCTGTGGGACCTACAATGTTCGCATTCTCTC
TGACACGTGGGATCAAAACCGAGTCATCCACTATTCCGGGGGAGATCTGATAGCTGTGTCATCT
AATCGAAAGATCCATCTTCTGGACATCATACAAGTGAAAGCGATACCCGTTGAATTCCGAGGCC
ATGCTGGGAGTGTCCGGGCCCTCTTCCTGTGTGAGGAGGAAAACTTTCTCCTAAGCGGGAGCTA
TGACCTAAGTATCAGATACTGGGATCTGAAAAGTGGGGTTTGCACACGAATCTTCGGTGGTCAC
CAGGGGACTATCACTTGCATGGACTTGTGTAAGAACAGGCTCGTATCTGGAGGAAGAGATTGCC
AGGTAAAAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAAAGACCCCAT
CTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTGGTGAAAGTG
TGGCACATTGCCATGGCCCAGTTGGTAAAGACTCTCAGTGGCCATGAGGGAGCCGTGAAATGCC
TGTTCTTTGACCAGTGGCATCTCCTCTCAGGAAGTACTGATGGCCTGGTCATGGCCTGGAGCAT
GGTGGGGAAGTACGAGCGCTGCCTGATGGCCTTCAAGCATCCCAAGGAGGTGCTCGACGTGTCC
CTTCTCTTCCTCCGGGTCATCAGCGCCTGTGCAGATGGCAAGATCCGAATTTACAATTTCCTCA
ACGGGAACTGTATGAAGGTGTTAAAAGCCAATGGCAGAGGATGGTGGTCAACACAGAGAGCAAT
GTTCTCATGTTCCAGTTTGAGCACATAAAGTGGCAGTATGCCGTGGAAAAAACGAAACAAAAGA
AGAATAAGGAGAAAGAGGAGGAAAAAGAAGAAAATAGTCTCATGGAAATTCTCTCTAAGTGTAA
TATTCAGGTTCACAGCCCAAGAGAGTCTGTATCCAGTAAACAAACTGTGATCCAAGAGCTCCTA
CCAGGCAAACCTCCCAAGTCCCGAGTACTCCTGAAGCCGGCCAAGTTCTCTTCAGCAGTGTTAA
TAGAGGAACTTCAAAGTCAAGGAAAGTCAAAATCAC

hide sequence

RefSeq Acc Id:

XM_047435121 ⟹ XP_047291077

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435122 ⟹ XP_047291078

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435123 ⟹ XP_047291079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435124 ⟹ XP_047291080

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435125 ⟹ XP_047291081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435126 ⟹ XP_047291082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435127 ⟹ XP_047291083

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435129 ⟹ XP_047291085

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435130 ⟹ XP_047291086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435131 ⟹ XP_047291087

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435132 ⟹ XP_047291088

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_047435133 ⟹ XP_047291089

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,763,471 - 18,779,349 (+)	NCBI

RefSeq Acc Id:

XM_054314707 ⟹ XP_054170682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,048 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314708 ⟹ XP_054170683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,048 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314709 ⟹ XP_054170684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314710 ⟹ XP_054170685

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314711 ⟹ XP_054170686

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314712 ⟹ XP_054170687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314713 ⟹ XP_054170688

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,049 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314714 ⟹ XP_054170689

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314715 ⟹ XP_054170690

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,048 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314716 ⟹ XP_054170691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,208 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314717 ⟹ XP_054170692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,047 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314718 ⟹ XP_054170693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,048 - 18,724,713 (+)	NCBI

RefSeq Acc Id:

XM_054314719 ⟹ XP_054170694

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,048 - 18,725,498 (+)	NCBI

RefSeq Acc Id:

XM_054314720 ⟹ XP_054170695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,690,049 - 18,718,715 (+)	NCBI

RefSeq Acc Id:

XM_054314721 ⟹ XP_054170696

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	18,709,624 - 18,725,498 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001254514	(Get FASTA)	NCBI Sequence Viewer
	NP_001254515	(Get FASTA)	NCBI Sequence Viewer
	NP_001397988	(Get FASTA)	NCBI Sequence Viewer
	XP_011521927	(Get FASTA)	NCBI Sequence Viewer
	XP_016879509	(Get FASTA)	NCBI Sequence Viewer
	XP_016879510	(Get FASTA)	NCBI Sequence Viewer
	XP_047291077	(Get FASTA)	NCBI Sequence Viewer
	XP_047291078	(Get FASTA)	NCBI Sequence Viewer
	XP_047291079	(Get FASTA)	NCBI Sequence Viewer
	XP_047291080	(Get FASTA)	NCBI Sequence Viewer
	XP_047291081	(Get FASTA)	NCBI Sequence Viewer
	XP_047291082	(Get FASTA)	NCBI Sequence Viewer
	XP_047291083	(Get FASTA)	NCBI Sequence Viewer
	XP_047291085	(Get FASTA)	NCBI Sequence Viewer
	XP_047291086	(Get FASTA)	NCBI Sequence Viewer
	XP_047291087	(Get FASTA)	NCBI Sequence Viewer
	XP_047291088	(Get FASTA)	NCBI Sequence Viewer
	XP_047291089	(Get FASTA)	NCBI Sequence Viewer
	XP_054170682	(Get FASTA)	NCBI Sequence Viewer
	XP_054170683	(Get FASTA)	NCBI Sequence Viewer
	XP_054170684	(Get FASTA)	NCBI Sequence Viewer
	XP_054170685	(Get FASTA)	NCBI Sequence Viewer
	XP_054170686	(Get FASTA)	NCBI Sequence Viewer
	XP_054170687	(Get FASTA)	NCBI Sequence Viewer
	XP_054170688	(Get FASTA)	NCBI Sequence Viewer
	XP_054170689	(Get FASTA)	NCBI Sequence Viewer
	XP_054170690	(Get FASTA)	NCBI Sequence Viewer
	XP_054170691	(Get FASTA)	NCBI Sequence Viewer
	XP_054170692	(Get FASTA)	NCBI Sequence Viewer
	XP_054170693	(Get FASTA)	NCBI Sequence Viewer
	XP_054170694	(Get FASTA)	NCBI Sequence Viewer
	XP_054170695	(Get FASTA)	NCBI Sequence Viewer
	XP_054170696	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH28364	(Get FASTA)	NCBI Sequence Viewer
	AAU43731	(Get FASTA)	NCBI Sequence Viewer
	AEE60982	(Get FASTA)	NCBI Sequence Viewer
	CAB66756	(Get FASTA)	NCBI Sequence Viewer
	CBH19282	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000306937
	ENSP00000306937.4
	ENSP00000310382
	ENSP00000310382.4
	ENSP00000379025
	ENSP00000379025.4
	ENSP00000463552.1
GenBank Protein	Q5XX13	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001254514 ⟸ NM_001267585
- Peptide Label:	isoform 1
- UniProtKB:	Q8TC00 (UniProtKB/Swiss-Prot), C9JZD7 (UniProtKB/Swiss-Prot), C9JRY8 (UniProtKB/Swiss-Prot), Q9H0F0 (UniProtKB/Swiss-Prot), Q5XX13 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MENLESRLKNAPYFRCEKGTDSIPLCRKCETCVLAWKIFSTKEWFCRINDISQRRFLVGILKQL NSLYLLHYFQNILQTTQGKDFIYNRSRINLSKKEGKVVKSSLNQMLDKTVEQKMKEILYWFANS TQWTKANYTLLLLQMCNPKLLLTAANVIRVLFLREENNISGLNQDITDVCFSPEKDHSSKSATS QVYWTAKTQHTSLPLSKAPENEHLLGAASNPEEPWRNSLRCISEMNRLFSGKGDITKPGYDPCN LLVDLDDIRDLSSGFSKYRDFIRYLPIHLSKYILRMLDRHTLNKCASVSQHWAAMAQQVKMDLS AHGFIQNQITFLQGSYTRGIDPNYANKVSIPVPKMVDDGKSMRVKHPKWKLRTKNEYNLWTAYQ NEETQQVLIEERNVFCGTYNVRILSDTWDQNRVIHYSGGDLIAVSSNRKIHLLDIIQVKAIPVE FRGHAGSVRALFLCEEENFLLSGSYDLSIRYWDLKSGVCTRIFGGHQGTITCMDLCKNRLVSGG RDCQVKVWDVDTGKCLKTFRHKDPILATRINDTYIVSSCERGLVKVWHIAMAQLVKTLSGHEGA VKCLFFDQWHLLSGSTDGLVMAWSMVGKYERCLMAFKHPKEVLDVSLLFLRVISACADGKIRIY NFLNGNCMKVLKANGRGDPVLSFFIQGNRMVVNTESNVLMFQFEHIKWQYAVEKTKQKKNKEKE EEKEENSLMEILSKCNIQVHSPRESVSSKQTVIQELLPGKPPKSRVLLKPAKFSSAVLIEELQS QGKSKSPRRDADDVEKAQKQGQLETPGKLPSHPKKKSWKIPMSPDQFLLTVSALQHAHNSGEFA YPCRPQTEITDVWGPSISYPRKVLNFKGKSIQRAVDRLRLSNPPIDVKRTSIPLEIQKLQPNLK ISLHSPRVQSTIPQPMIIRSRFSGSLKGGDQVTSSIERAVCSTGPLTSMQVIKPNRMLAPQVGT ATLSLKKERPRIYTALDPFRVNTEFVLLTVKEEKEHQEAKMKEYQARESTGVVDPGKVSKAAWI RKIKGLPIDNFTKQGKTAAPELGQNVFI hide sequence

RefSeq Acc Id:	NP_001254515 ⟸ NM_001267586
- Peptide Label:	isoform 2
- UniProtKB:	Q5XX13 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MENLESRLKNAPYFRCEKGTDSIPLCRKCETCVLAWKIFSTKEWFCRINDISQRRFLVGILKQL NSLYLLHYFQNILQTTQGKDFIYNRSRINLSKKEGKVVKSSLNQMLDKTVEQKMKEILYWFANS TQWTKANYTLLLLQMCNPKLLLTAANVIRVLFLREENNISGLNQDITDVCFSPEKDHSSKSATS QVYWTAKTQHTSLPLSKAPENEHLLGAASNPEEPWRNSLRCISEMNRLFSGKGDITKPGYDPCN LLVDLDDIRDLSSGFSKYRDFIRYLPIHLSKYILRMLDRHTLNKCASVSQHWAAMAQQVKMDLS AHGFIQNQITFLQGSYTRGIDPNYANKVSIPVPKMVDDGKSMRVKHPKWKLRTKNEYNLWTAYQ NEETQQVLIEERNVFCGTYNVRILSDTWDQNRVIHYSGGDLIAVSSNRKIHLLDIIQVKAIPVE FRGHAGSVRALFLCEEENFLLSGSYDLSIRYWDLKSGVCTRIFGGHQGTITCMDLCKNRLVSGG RDCQVKVWDVDTGKCLKTFRHKDPILATRINDTYIVSSCERGLVKVWHIAMAQLVKTLSGHEGA VKCLFFDQWHLLSGSTDGLVMAWSMVGKYERCLMAFKHPKMVVNTESNVLMFQFEHIKWQYAVE KTKQKKNKEKEEEKEENSLMEILSKCNIQVHSPRESVSSKQTVIQELLPGKPPKSRVLLKPAKF SSAVLIEELQSQGKSKSPRRDADDVEKAQKQGQLETPGKLPSHPKKKSWKIPMSPDQFLLTVSA LQHAHNSGEFAYPCRPQTEITDVWGPSISYPRKVLNFKGKSIQRAVDRLRLSNPPIDVKRTSIP LEIQKLQPNLKISLHSPRVQSTIPQPMIIRSRFSGSLKGGDQVTSSIERAVCSTGPLTSMQVIK PNRMLAPQVGTATLSLKKERPRIYTALDPFRVNTEFVLLTVKEEKEHQEAKMKEYQARESTGVV DPGKVSKAAWIRKIKGLPIDNFTKQGKTAAPELGQNVFI hide sequence

RefSeq Acc Id:

XP_011521927 ⟸ XM_011523625

- Peptide Label:

isoform X12

- Sequence:

show sequence

MENLESRLKNAPYFRCEKGTDSIPLCRKCETCVLAWKIFSTKEWFCRINDISQRRFLVGILKQL
NSLYLLHYFQNILQTTQGKDFIYNRSRINLSKKEGKVVKSSLNQMLDKTVEQKMKEILYWFANS
TQWTKANYTLLLLQMCNPKLLLTAANVIRVLFLREENNISGKQGHRQRLEGPRRPEGKASEIWL
NQDITDVCFSPEKDHSSKSATSQVYWTAKTQHTSLPLSKAPENEHLLGAASNPEEPWRNSLRCI
SEMNRLFSGKGDITKPGYDPCNLLVDLDDIRDLSSGFSKYRDFIRYLPIHLSKYILSMLGCMRG
FPRHLPSWPSSGVSGSIFFFPGMLDRHTLNKCASVSQHWAAMAQQVKMDLSAHGFIQNQITFLQ
GSYTRGIDPNYANKVSIPVPKMVDDGKSMRVKHPKWKLRTKNEYNLWTAYQNEETQQVLIEERN
VFCGTYNVRILSDTWDQNRVIHYSGGDLIAVSSNRKIHLLDIIQVKAIPVEFRGHAGSVRALFL
CEEENFLLSGSYDLSIRYWDLKSGVCTRIFGGHQGTITCMDLCKNRLVSGGRDCQVKVWDVDTG
KCLKTFRHKDPILATRINDTYIVSSCERGLVKVWHIAMAQLVKTLSGHEGAVKCLFFDQWHLLS
GSTDGLVMAWSMVGKYERCLMAFKHPKEVLDVSLLFLRVISACADGKIRIYNFLNGNCMKVLKA
NGRGDPVLSFFIQGNRMVVNTESNVLMFQFEHIKWQYAVEKTKQKKNKEKEEEKEENSLMEILS
KCNIQVHSPRESVSSKQTVIQELLPGKPPKSRVLLKPAKFSSAVLIEELQSQGKSKSPRRDAGH
YLCLSLRNWNEYNAWLLPRVTGFP

hide sequence

RefSeq Acc Id:

XP_016879509 ⟸ XM_017024020

- Peptide Label:

isoform X12

- Sequence:

show sequence

MENLESRLKNAPYFRCEKGTDSIPLCRKCETCVLAWKIFSTKEWFCRINDISQRRFLVGILKQL
NSLYLLHYFQNILQTTQGKDFIYNRSRINLSKKEGKVVKSSLNQMLDKTVEQKMKEILYWFANS
TQWTKANYTLLLLQMCNPKLLLTAANVIRVLFLREENNISGKQGHRQRLEGPRRPEGKASEIWL
NQDITDVCFSPEKDHSSKSATSQVYWTAKTQHTSLPLSKAPENEHLLGAASNPEEPWRNSLRCI
SEMNRLFSGKGDITKPGYDPCNLLVDLDDIRDLSSGFSKYRDFIRYLPIHLSKYILSMLGCMRG
FPRHLPSWPSSGVSGSIFFFPGMLDRHTLNKCASVSQHWAAMAQQVKMDLSAHGFIQNQITFLQ
GSYTRGIDPNYANKVSIPVPKMVDDGKSMRVKHPKWKLRTKNEYNLWTAYQNEETQQVLIEERN
VFCGTYNVRILSDTWDQNRVIHYSGGDLIAVSSNRKIHLLDIIQVKAIPVEFRGHAGSVRALFL
CEEENFLLSGSYDLSIRYWDLKSGVCTRIFGGHQGTITCMDLCKNRLVSGGRDCQVKVWDVDTG
KCLKTFRHKDPILATRINDTYIVSSCERGLVKVWHIAMAQLVKTLSGHEGAVKCLFFDQWHLLS
GSTDGLVMAWSMVGKYERCLMAFKHPKEVLDVSLLFLRVISACADGKIRIYNFLNGNCMKVLKA
NGRGDPVLSFFIQGNRMVVNTESNVLMFQFEHIKWQYAVEKTKQKKNKEKEEEKEENSLMEILS
KCNIQVHSPRESVSSKQTVIQELLPGKPPKSRVLLKPAKFSSAVLIEELQSQGKSKSPRRDAGH
YLCLSLRNWNEYNAWLLPRVTGFP

hide sequence

RefSeq Acc Id:

XP_016879510 ⟸ XM_017024021

- Peptide Label:

isoform X13

- Sequence:

show sequence

MENLESRLKNAPYFRCEKGTDSIPLCRKCETCVLAWKIFSTKEWFCRINDISQRRFLVGILKQL
NSLYLLHYFQNILQTTQGKDFIYNRSRINLSKKEGKVVKSSLNQMLDKTVEQKMKEILYWFANS
TQWTKANYTLLLLQMCNPKLLLTAANVIRVLFLREENNISGKQGHRQRLEGPRRPEGKASEIWL
NQDITDVCFSPEKDHSSKSATSQVYWTAKTQHTSLPLSKAPENEHLLGAASNPEEPWRNSLRCI
SEMNRLFSGKGDITKPGYDPCNLLVDLDDIRDLSSGFSKYRDFIRYLPIHLSKYILSMLGCMRG
FPRHLPSWPSSGVSGSIFFFPGMLDRHTLNKCASVSQHWAAMAQQVKMDLSAHGFIQNQITFLQ
GSYTRGIDPNYANKVSIPVPKMVDDGKSMRVKHPKWKLRTKNEYNLWTAYQNEETQQVLIEERN
VFCGTYNVRILSDTWDQNRVIHYSGGDLIAVSSNRKIHLLDIIQVKAIPVEFRGHAGSVRALFL
CEEENFLLSGSYDLSIRYWDLKSGVCTRIFGGHQGTITCMDLCKNRLVSGGRDCQVKVWDVDTG
KCLKTFRHKDPILATRINDTYIVSSCERGLVKVWHIAMAQLVKTLSGHEGAVKCLFFDQWHLLS
GSTDGLVMAWSMVGKYERCLMAFKHPKEVLDVSLLFLRVISACADGKIRIYNFLNGNCMKVLKA
NGRGWWSTQRAMFSCSSLST

hide sequence

RefSeq Acc Id:

ENSP00000310382 ⟸ ENST00000308799

RefSeq Acc Id:

ENSP00000463552 ⟸ ENST00000574478

RefSeq Acc Id:

ENSP00000306937 ⟸ ENST00000301938

RefSeq Acc Id:

ENSP00000379025 ⟸ ENST00000395665

RefSeq Acc Id:	XP_047291077 ⟸ XM_047435121
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047291078 ⟸ XM_047435122
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047291079 ⟸ XM_047435123
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047291080 ⟸ XM_047435124
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047291081 ⟸ XM_047435125
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047291088 ⟸ XM_047435132
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_047291086 ⟸ XM_047435130
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_047291083 ⟸ XM_047435127
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047291082 ⟸ XM_047435126
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047291085 ⟸ XM_047435129
- Peptide Label:	isoform X8
- UniProtKB:	A0A140VJJ5 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047291087 ⟸ XM_047435131
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047291089 ⟸ XM_047435133
- Peptide Label:	isoform X14

RefSeq Acc Id:	NP_001397988 ⟸ NM_001411059
- Peptide Label:	isoform 3

RefSeq Acc Id:	XP_054170684 ⟸ XM_054314709
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054170685 ⟸ XM_054314710
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054170686 ⟸ XM_054314711
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054170692 ⟸ XM_054314717
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_054170694 ⟸ XM_054314719
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054170682 ⟸ XM_054314707
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054170683 ⟸ XM_054314708
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054170690 ⟸ XM_054314715
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054170693 ⟸ XM_054314718
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054170688 ⟸ XM_054314713
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054170695 ⟸ XM_054314720
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054170687 ⟸ XM_054314712
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054170689 ⟸ XM_054314714
- Peptide Label:	isoform X8
- UniProtKB:	A0A140VJJ5 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054170691 ⟸ XM_054314716
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054170696 ⟸ XM_054314721
- Peptide Label:	isoform X14

Protein Domains

F-box

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q5XX13-F1-model_v2	AlphaFold	Q5XX13	1-1052	view protein structure

Promoters

RGD ID:

7234233

Promoter ID:

EPDNEW_H22862

Type:

initiation region

Name:

FBXW10_1

Description:

F-box and WD repeat domain containing 10

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	18,744,054 - 18,744,114	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:1211	AgrOrtholog
COSMIC	FBXW10	COSMIC
Ensembl Genes	ENSG00000171931	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000301938	ENTREZGENE
	ENST00000301938.4	UniProtKB/Swiss-Prot
	ENST00000308799	ENTREZGENE
	ENST00000308799.8	UniProtKB/Swiss-Prot
	ENST00000395665	ENTREZGENE
	ENST00000395665.9	UniProtKB/Swiss-Prot
	ENST00000574478	ENTREZGENE
	ENST00000574478.1	UniProtKB/TrEMBL
Gene3D-CATH	1.20.1280.50	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	2.130.10.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000171931	GTEx
HGNC ID	HGNC:1211	ENTREZGENE
Human Proteome Map	FBXW10	Human Proteome Map
InterPro	F-box-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G-protein_beta_WD-40_rep	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40/YVTN_repeat-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD40_repeat_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:10517	UniProtKB/Swiss-Prot
NCBI Gene	10517	ENTREZGENE
OMIM	611679	OMIM
PANTHER	CMT1A DUPLICATED REGION TRANSCRIPT 1 PROTEIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	UBIQUITIN LIGASE SPECIFICITY FACTOR/HREP PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA25575	PharmGKB
PRINTS	GPROTEINBRPT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	WD_REPEATS_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD_REPEATS_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WD_REPEATS_REGION	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	WD40	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF50978	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF81383	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A140VJJ5	ENTREZGENE, UniProtKB/TrEMBL
	C9JRY8	ENTREZGENE
	C9JZD7	ENTREZGENE
	FBW10_HUMAN	UniProtKB/Swiss-Prot
	J3QLH9_HUMAN	UniProtKB/TrEMBL
	Q5XX13	ENTREZGENE
	Q8TC00	ENTREZGENE
	Q9H0F0	ENTREZGENE
UniProt Secondary	C9JRY8	UniProtKB/Swiss-Prot
	C9JZD7	UniProtKB/Swiss-Prot
	Q8TC00	UniProtKB/Swiss-Prot
	Q9H0F0	UniProtKB/Swiss-Prot

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

Send us a Message

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar