FUOM (fucose mutarotase) - Rat Genome Database

Name: FUOM
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: FUOM (fucose mutarotase) Homo sapiens

Analyze

Symbol:

FUOM

Name:

fucose mutarotase

RGD ID:

1322512

HGNC Page

HGNC:24733

Description:

Predicted to enable L-fucose mutarotase activity and fucose binding activity. Predicted to be involved in fucose metabolic process and fucosylation. Predicted to act upstream of or within female mating behavior and negative regulation of neuron differentiation. Predicted to be located in cytosol.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C10orf125; FLJ26016; FucM; FUCU; MGC149258; protein fucU homolog

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Fuom (fucose mutarotase)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Fuom (fucose mutarotase)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Fuom (fucose mutarotase)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	FUOM (fucose mutarotase)	NCBI	Ortholog
Canis lupus familiaris (dog):	FUOM (fucose mutarotase)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Sus scrofa (pig):	FUOM (fucose mutarotase)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	FUOM (fucose mutarotase)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Fuom (fucose mutarotase)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Fuom (fucose mutarotase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Fuom (fucose mutarotase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	fuom (fucose mutarotase)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)

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	10	133,352,773 - 133,358,019 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	133,355,158 - 133,358,025 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	135,168,662 - 135,171,523 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	135,018,648 - 135,021,519 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	135,057,544 - 135,060,410	NCBI
Celera	10	128,345,999 - 128,348,870 (+)	NCBI		Celera
Cytogenetic Map	10	q26.3	NCBI
HuRef	10	128,712,773 - 128,715,644 (-)	NCBI		HuRef
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	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

distal 10q deletion syndrome (IAGP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

2-hydroxypropanoic acid (EXP)

3-chloropropane-1,2-diol (ISO)

6-propyl-2-thiouracil (ISO)

acrylamide (EXP)

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP,ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

butanal (EXP)

carbon nanotube (ISO)

chlorpyrifos (ISO)

cobalt dichloride (ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

diazinon (EXP)

diethylstilbestrol (ISO)

diquat (ISO)

folic acid (ISO)

gentamycin (ISO)

inulin (ISO)

lead(0) (EXP)

menadione (EXP)

methidathion (ISO)

N-Nitrosopyrrolidine (EXP)

O-methyleugenol (EXP)

ozone (ISO)

paracetamol (EXP)

PCB138 (ISO)

pentanal (EXP)

perfluorooctane-1-sulfonic acid (ISO)

pregnenolone 16alpha-carbonitrile (ISO)

propanal (EXP)

rac-lactic acid (EXP)

silver atom (ISO)

silver(0) (ISO)

sodium arsenite (EXP)

sulforaphane (ISO)

sunitinib (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

tris(2-butoxyethyl) phosphate (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

female mating behavior (ISO)

fucose metabolic process (IBA,IEA,ISS)

fucosylation (IBA,ISO)

monosaccharide metabolic process (IEA)

negative regulation of neuron differentiation (ISO)

neuron differentiation (ISO)

Cellular Component

cytosol (TAS)

Molecular Function

fucose binding (IBA,ISS)

isomerase activity (IEA)

L-fucose mutarotase activity (IEA,ISS)

monosaccharide binding (IEA)

racemase and epimerase activity, acting on carbohydrates and derivatives (IBA,ISS)

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:12477932	PMID:15146197	PMID:16385451	PMID:17602138	PMID:19524593	PMID:21873635	PMID:25036637	PMID:28514442	PMID:28675297	PMID:33961781

Genomics

Comparative Map Data

FUOM
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	133,352,773 - 133,358,019 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	133,355,158 - 133,358,025 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	135,168,662 - 135,171,523 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	135,018,648 - 135,021,519 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	135,057,544 - 135,060,410	NCBI
Celera	10	128,345,999 - 128,348,870 (+)	NCBI		Celera
Cytogenetic Map	10	q26.3	NCBI
HuRef	10	128,712,773 - 128,715,644 (-)	NCBI		HuRef
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI		T2T-CHM13v2.0

Fuom
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	139,677,724 - 139,684,745 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	139,676,683 - 139,682,354 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	140,097,811 - 140,104,832 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	140,096,770 - 140,102,441 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	147,285,369 - 147,288,305 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	139,950,790 - 139,953,639 (-)	NCBI		MGSCv36	mm8
Celera	7	139,897,533 - 139,900,469 (-)	NCBI		Celera
Cytogenetic Map	7	F4	NCBI
cM Map	7	85.11	NCBI

Fuom
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	204,318,180 - 204,322,690 (-)	NCBI		GRCr8
mRatBN7.2	1	194,888,535 - 194,893,046 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	194,886,709 - 194,893,046 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	203,249,400 - 203,253,911 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	210,384,437 - 210,388,964 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	203,058,268 - 203,062,792 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	212,563,714 - 212,568,224 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	212,563,714 - 212,568,224 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_6.0 Ensembl	1	141,832,774 - 141,836,250 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	219,478,363 - 219,482,873 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	199,895,086 - 199,899,596 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	200,046,108 - 200,049,153 (-)	NCBI
Celera	1	192,565,599 - 192,570,109 (-)	NCBI		Celera
Cytogenetic Map	1	q41	NCBI

Fuom
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955477	11,002,591 - 11,008,478 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955477	11,004,871 - 11,008,479 (-)	NCBI	ChiLan1.0	ChiLan1.0

FUOM
(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	8	145,483,786 - 145,486,677 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	10	145,489,143 - 145,492,034 (-)	NCBI		NHGRI_mPanPan1
PanPan1.1	10	134,270,956 - 134,273,834 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	10	134,267,265 - 134,274,665 (-)	Ensembl	panpan1.1		panPan2

FUOM
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	28	40,933,140 - 40,936,722 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
Dog10K_Boxer_Tasha	28	40,988,233 - 40,991,798 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	28	41,568,107 - 41,571,678 (-)	NCBI		ROS_Cfam_1.0
UMICH_Zoey_3.1	28	41,052,196 - 41,055,766 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	28	41,041,790 - 41,045,361 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	28	41,444,691 - 41,448,263 (-)	NCBI		UU_Cfam_GSD_1.0

FUOM
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	14	141,331,810 - 141,336,633 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	14	141,331,801 - 141,336,628 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	14	153,788,697 - 153,792,961 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

FUOM
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	26	53,204,739 - 53,209,037 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666054	41,341,450 - 41,345,715 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Fuom
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624737	13,338,974 - 13,346,986 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624737	13,341,094 - 13,343,834 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in FUOM
9 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	copy number gain	See cases [RCV000051218]	Chr10:111313099..133620674 [GRCh38] Chr10:113072857..135434178 [GRCh37] Chr10:113062847..135284168 [NCBI36] Chr10:10q25.2-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:122265252-133620674)x1	copy number loss	See cases [RCV000051069]	Chr10:122265252..133620674 [GRCh38] Chr10:124024767..135434178 [GRCh37] Chr10:124014757..135284168 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1	copy number loss	See cases [RCV000051103]	Chr10:120454430..133620674 [GRCh38] Chr10:122213942..135434178 [GRCh37] Chr10:122203932..135284168 [NCBI36] Chr10:10q26.12-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123307835-133620674)x1	copy number loss	See cases [RCV000051150]	Chr10:123307835..133620674 [GRCh38] Chr10:125067351..135434178 [GRCh37] Chr10:125057341..135284168 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:133001134-133620674)x1	copy number loss	See cases [RCV000051165]	Chr10:133001134..133620674 [GRCh38] Chr10:134814638..135434178 [GRCh37] Chr10:134664628..135284168 [NCBI36] Chr10:10q26.3	uncertain significance
GRCh38/hg38 10q26.3(chr10:131457361-133620674)x1	copy number loss	See cases [RCV000050997]	Chr10:131457361..133620674 [GRCh38] Chr10:133255624..135434178 [GRCh37] Chr10:133145614..135284168 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:132445383-133398465)x3	copy number gain	See cases [RCV000051692]	Chr10:132445383..133398465 [GRCh38] Chr10:134258887..135211969 [GRCh37] Chr10:134108877..135061959 [NCBI36] Chr10:10q26.3	uncertain significance
GRCh38/hg38 10q26.3(chr10:131914873-133613938)x1	copy number loss	See cases [RCV000052643]	Chr10:131914873..133613938 [GRCh38] Chr10:133728377..135427442 [GRCh37] Chr10:133578367..135277432 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:132475849-133620674)x1	copy number loss	See cases [RCV000052644]	Chr10:132475849..133620674 [GRCh38] Chr10:134289353..135434178 [GRCh37] Chr10:134139343..135284168 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:126256585-133613938)x1	copy number loss	See cases [RCV000052612]	Chr10:126256585..133613938 [GRCh38] Chr10:127945154..135427442 [GRCh37] Chr10:127935144..135277432 [NCBI36] Chr10:10q26.2-26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127500483-133620674)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]\|See cases [RCV000052613]	Chr10:127500483..133620674 [GRCh38] Chr10:129298747..135434178 [GRCh37] Chr10:129188737..135284168 [NCBI36] Chr10:10q26.2-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:129673966-133613938)x1	copy number loss	See cases [RCV000052614]	Chr10:129673966..133613938 [GRCh38] Chr10:131472230..135427442 [GRCh37] Chr10:131362220..135277432 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:129758596-133620674)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052615]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052615]\|See cases [RCV000052615]	Chr10:129758596..133620674 [GRCh38] Chr10:131556860..135434178 [GRCh37] Chr10:131446850..135284168 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123580320-133558988)x1	copy number loss	See cases [RCV000052611]	Chr10:123580320..133558988 [GRCh38] Chr10:125339836..135372492 [GRCh37] Chr10:125329826..135222482 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q23.31-26.3(chr10:91048545-133620674)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]\|See cases [RCV000053560]	Chr10:91048545..133620674 [GRCh38] Chr10:92808302..135434178 [GRCh37] Chr10:92798282..135284168 [NCBI36] Chr10:10q23.31-26.3	pathogenic
GRCh38/hg38 10q25.1-26.3(chr10:106925303-133620815)x3	copy number gain	See cases [RCV000053588]	Chr10:106925303..133620815 [GRCh38] Chr10:108685061..135434319 [GRCh37] Chr10:108675051..135284309 [NCBI36] Chr10:10q25.1-26.3	pathogenic
GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	copy number gain	See cases [RCV000053589]	Chr10:117866565..133554210 [GRCh38] Chr10:119626076..135367714 [GRCh37] Chr10:119616066..135217704 [NCBI36] Chr10:10q26.11-26.3	pathogenic
GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	copy number gain	See cases [RCV000133688]	Chr10:108102587..133620674 [GRCh38] Chr10:109862345..135434178 [GRCh37] Chr10:109852335..135284168 [NCBI36] Chr10:10q25.1-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125657472-133620674)x1	copy number loss	See cases [RCV000133741]	Chr10:125657472..133620674 [GRCh38] Chr10:127346041..135434178 [GRCh37] Chr10:127336031..135284168 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:133134279-133400512)x1	copy number loss	See cases [RCV000134391]	Chr10:133134279..133400512 [GRCh38] Chr10:134947783..135214016 [GRCh37] Chr10:134797773..135064006 [NCBI36] Chr10:10q26.3	benign
GRCh38/hg38 10q26.2-26.3(chr10:126730896-133620609)x1	copy number loss	See cases [RCV000134040]	Chr10:126730896..133620609 [GRCh38] Chr10:128419465..135434113 [GRCh37] Chr10:128409455..135284103 [NCBI36] Chr10:10q26.2-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:132178475-133620674)x1	copy number loss	See cases [RCV000135399]	Chr10:132178475..133620674 [GRCh38] Chr10:133991979..135434178 [GRCh37] Chr10:133841969..135284168 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:129549258-133620674)x1	copy number loss	See cases [RCV000135547]	Chr10:129549258..133620674 [GRCh38] Chr10:131347522..135434178 [GRCh37] Chr10:131237512..135284168 [NCBI36] Chr10:10q26.3	pathogenic\|likely benign
GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1	copy number loss	See cases [RCV000136028]	Chr10:124473108..133620609 [GRCh38] Chr10:126161677..135434113 [GRCh37] Chr10:126151667..135284103 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:128872419-133564028)x3	copy number gain	See cases [RCV000136888]	Chr10:128872419..133564028 [GRCh38] Chr10:130670683..135377532 [GRCh37] Chr10:130560673..135227522 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1	copy number loss	See cases [RCV000137653]	Chr10:124834858..133622588 [GRCh38] Chr10:126523427..135436092 [GRCh37] Chr10:126513417..135286082 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:128549913-133622588)x1	copy number loss	See cases [RCV000138159]	Chr10:128549913..133622588 [GRCh38] Chr10:130348177..135436092 [GRCh37] Chr10:130238167..135286082 [NCBI36] Chr10:10q26.2-26.3	pathogenic\|uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:127849717-133622588)x1	copy number loss	See cases [RCV000138160]	Chr10:127849717..133622588 [GRCh38] Chr10:129647981..135436092 [GRCh37] Chr10:129537971..135286082 [NCBI36] Chr10:10q26.2-26.3	pathogenic\|likely benign
GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	copy number gain	See cases [RCV000137747]	Chr10:100600492..133622588 [GRCh38] Chr10:102360249..135436092 [GRCh37] Chr10:102350239..135286082 [NCBI36] Chr10:10q24.31-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:129427520-133622588)x1	copy number loss	See cases [RCV000137959]	Chr10:129427520..133622588 [GRCh38] Chr10:131225784..135436092 [GRCh37] Chr10:131115774..135286082 [NCBI36] Chr10:10q26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:132962729-133622588)x1	copy number loss	See cases [RCV000138257]	Chr10:132962729..133622588 [GRCh38] Chr10:134776233..135436092 [GRCh37] Chr10:134626223..135286082 [NCBI36] Chr10:10q26.3	pathogenic\|uncertain significance
GRCh38/hg38 10q26.13-26.3(chr10:122881207-133620609)x1	copy number loss	See cases [RCV000138435]	Chr10:122881207..133620609 [GRCh38] Chr10:124640723..135434113 [GRCh37] Chr10:124630713..135284103 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1	copy number loss	See cases [RCV000139344]	Chr10:120970558..133622588 [GRCh38] Chr10:122730071..135436092 [GRCh37] Chr10:122720061..135286082 [NCBI36] Chr10:10q26.12-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:133001075-133622588)x3	copy number gain	See cases [RCV000139912]	Chr10:133001075..133622588 [GRCh38] Chr10:134814579..135436092 [GRCh37] Chr10:134664569..135286082 [NCBI36] Chr10:10q26.3	uncertain significance
GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1	copy number loss	See cases [RCV000139588]	Chr10:125021995..133620609 [GRCh38] Chr10:126710564..135434113 [GRCh37] Chr10:126700554..135284103 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125452905-133785874)x3	copy number gain	See cases [RCV000141337]	Chr10:125452905..133785874 [GRCh38] Chr10:127141474..135523199 [GRCh37] Chr10:127131464..135373189 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127664168-133622588)x3	copy number gain	See cases [RCV000140974]	Chr10:127664168..133622588 [GRCh38] Chr10:129462432..135436092 [GRCh37] Chr10:129352422..135286082 [NCBI36] Chr10:10q26.2-26.3	likely pathogenic
GRCh38/hg38 10q26.3(chr10:133059029-133622588)x3	copy number gain	See cases [RCV000140708]	Chr10:133059029..133622588 [GRCh38] Chr10:134872533..135436092 [GRCh37] Chr10:134722523..135286082 [NCBI36] Chr10:10q26.3	uncertain significance
GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3	copy number gain	See cases [RCV000142005]	Chr10:119707856..133613639 [GRCh38] Chr10:121467368..135427143 [GRCh37] Chr10:121457358..135277133 [NCBI36] Chr10:10q26.11-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1	copy number loss	See cases [RCV000142441]	Chr10:121588992..133620674 [GRCh38] Chr10:123348506..135434178 [GRCh37] Chr10:123338496..135284168 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1	copy number loss	See cases [RCV000142737]	Chr10:121918547..133620674 [GRCh38] Chr10:123678062..135434178 [GRCh37] Chr10:123668052..135284168 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127435985-133622588)x1	copy number loss	See cases [RCV000143241]	Chr10:127435985..133622588 [GRCh38] Chr10:129234249..135436092 [GRCh37] Chr10:129124239..135286082 [NCBI36] Chr10:10q26.2-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:131424682-133613639)x1	copy number loss	See cases [RCV000143762]	Chr10:131424682..133613639 [GRCh38] Chr10:133222945..135427143 [GRCh37] Chr10:133112935..135277133 [NCBI36] Chr10:10q26.3	likely pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123986772-133613639)x1	copy number loss	See cases [RCV000143623]	Chr10:123986772..133613639 [GRCh38] Chr10:125746288..135427143 [GRCh37] Chr10:125736278..135277133 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123576393-133613639)x1	copy number loss	See cases [RCV000143544]	Chr10:123576393..133613639 [GRCh38] Chr10:125335909..135427143 [GRCh37] Chr10:125325899..135277133 [NCBI36] Chr10:10q26.13-26.3	pathogenic
GRCh38/hg38 10q26.3(chr10:130625650-133613639)x1	copy number loss	See cases [RCV000143554]	Chr10:130625650..133613639 [GRCh38] Chr10:132423914..135427143 [GRCh37] Chr10:132313904..135277133 [NCBI36] Chr10:10q26.3	uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:126794646-133613639)x1	copy number loss	See cases [RCV000143615]	Chr10:126794646..133613639 [GRCh38] Chr10:128483215..135427143 [GRCh37] Chr10:128473205..135277133 [NCBI36] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123731209-135353867)x1	copy number loss	See cases [RCV000203440]	Chr10:123731209..135353867 [GRCh37] Chr10:10q26.13-26.3	pathogenic\|likely pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	copy number gain	See cases [RCV000240457]	Chr10:103288313..135512075 [GRCh37] Chr10:10q24.32-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124147428-135370736)x1	copy number loss	See cases [RCV000449336]	Chr10:124147428..135370736 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:104633712-135427143)x3	copy number gain	See cases [RCV000449386]	Chr10:104633712..135427143 [GRCh37] Chr10:10q24.32-26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)x1	copy number loss	See cases [RCV000446095]	Chr10:122343861..135427143 [GRCh37] Chr10:10q26.12-26.3	pathogenic
GRCh37/hg19 10q24.2-26.3(chr10:100780957-135427143)x3	copy number gain	See cases [RCV000446733]	Chr10:100780957..135427143 [GRCh37] Chr10:10q24.2-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)x1	copy number loss	See cases [RCV000447132]	Chr10:128465436..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:132468363-135367666)x1	copy number loss	See cases [RCV000446777]	Chr10:132468363..135367666 [GRCh37] Chr10:10q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	copy number gain	See cases [RCV000448750]	Chr10:93297..135378918 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:133965613-135427143)x1	copy number loss	See cases [RCV000448088]	Chr10:133965613..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.3(chr10:134593406-135427143)x1	copy number loss	See cases [RCV000510608]	Chr10:134593406..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.3(chr10:132354150-135427143)x3	copy number gain	See cases [RCV000510589]	Chr10:132354150..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:129825453-135427143)x1	copy number loss	See cases [RCV000511570]	Chr10:129825453..135427143 [GRCh37] Chr10:10q26.2-26.3	likely pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:127658004-135427143)x1	copy number loss	See cases [RCV000511813]	Chr10:127658004..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	copy number gain	See cases [RCV000511389]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic\|uncertain significance
GRCh37/hg19 10q26.3(chr10:134624870-135427143)x1	copy number loss	See cases [RCV000511601]	Chr10:134624870..135427143 [GRCh37] Chr10:10q26.3	likely pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3	copy number gain	See cases [RCV000510813]	Chr10:106003533..135427143 [GRCh37] Chr10:10q25.1-26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	copy number gain	See cases [RCV000510861]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3	copy number gain	See cases [RCV000510972]	Chr10:93283493..135427143 [GRCh37] Chr10:10q23.32-26.3	pathogenic
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438]	Chr10:42347406..135534747 [GRCh37] Chr10:10q11.21-26.3	drug response
GRCh37/hg19 10q26.2-26.3(chr10:129007673-135427143)x3	copy number gain	See cases [RCV000512398]	Chr10:129007673..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:134615768-135184126)x3	copy number gain	See cases [RCV000512163]	Chr10:134615768..135184126 [GRCh37] Chr10:10q26.3	likely benign
GRCh37/hg19 10q26.3(chr10:133574560-135296619)x4	copy number gain	not provided [RCV000683265]	Chr10:133574560..135296619 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.13-26.3(chr10:127375792-135427143)x1	copy number loss	not provided [RCV000683283]	Chr10:127375792..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.11-26.3(chr10:121269222-135427143)x3	copy number gain	not provided [RCV000683288]	Chr10:121269222..135427143 [GRCh37] Chr10:10q26.11-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125450893-135427143)x1	copy number loss	not provided [RCV000683285]	Chr10:125450893..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:123019239-135427143)x1	copy number loss	not provided [RCV000683286]	Chr10:123019239..135427143 [GRCh37] Chr10:10q26.12-26.3	pathogenic
GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3	copy number gain	not provided [RCV000683290]	Chr10:105613040..135427143 [GRCh37] Chr10:10q24.33-26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122509781-135427143)x1	copy number loss	not provided [RCV000683287]	Chr10:122509781..135427143 [GRCh37] Chr10:10q26.12-26.3	pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	copy number gain	not provided [RCV000683291]	Chr10:94346520..135427143 [GRCh37] Chr10:10q23.33-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:131949020-135427143)x1	copy number loss	not provided [RCV000683274]	Chr10:131949020..135427143 [GRCh37] Chr10:10q26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122443197-135477883)x1	copy number loss	not provided [RCV000737305]	Chr10:122443197..135477883 [GRCh37] Chr10:10q26.12-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129454892-135447971)x1	copy number loss	not provided [RCV000737323]	Chr10:129454892..135447971 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:134589631-135244723)x1	copy number loss	not provided [RCV000737342]	Chr10:134589631..135244723 [GRCh37] Chr10:10q26.3	benign
GRCh37/hg19 10q26.3(chr10:134777671-135434303)x1	copy number loss	not provided [RCV000749862]	Chr10:134777671..135434303 [GRCh37] Chr10:10q26.3	benign
GRCh37/hg19 10q26.3(chr10:134889866-135379710)x3	copy number gain	not provided [RCV000749866]	Chr10:134889866..135379710 [GRCh37] Chr10:10q26.3	benign
GRCh37/hg19 10q26.3(chr10:135012384-135278193)x3	copy number gain	not provided [RCV000749873]	Chr10:135012384..135278193 [GRCh37] Chr10:10q26.3	benign
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3	copy number gain	not provided [RCV000749464]	Chr10:73232..135524321 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3	copy number gain	not provided [RCV000749465]	Chr10:98087..135477883 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095)	copy number gain	not provided [RCV000767665]	Chr10:110022170..135439095 [GRCh37] Chr10:10q25.1-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:135079677-135427143)x4	copy number gain	not provided [RCV000848040]	Chr10:135079677..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.13-26.3(chr10:124988334-135427143)x3	copy number gain	not provided [RCV000848791]	Chr10:124988334..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3	copy number gain	not provided [RCV000847820]	Chr10:114544537..135427143 [GRCh37] Chr10:10q25.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:135158728-135427143)x1	copy number loss	not provided [RCV000847103]	Chr10:135158728..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.3(chr10:135111843-135427143)x1	copy number loss	not provided [RCV000848506]	Chr10:135111843..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:129009772-135427143)x1	copy number loss	not provided [RCV001006362]	Chr10:129009772..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129381095-135427143)x1	copy number loss	not provided [RCV001006364]	Chr10:129381095..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.11-26.3(chr10:119996339-135427143)x3	copy number gain	not provided [RCV001006356]	Chr10:119996339..135427143 [GRCh37] Chr10:10q26.11-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:135165733-135427143)x3	copy number gain	not provided [RCV001259088]	Chr10:135165733..135427143 [GRCh37] Chr10:10q26.3	likely benign
GRCh37/hg19 10q26.2-26.3(chr10:129605105-135427143)x1	copy number loss	See cases [RCV002285041]	Chr10:129605105..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129031265-135427143)x1	copy number loss	not provided [RCV001259085]	Chr10:129031265..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q25.3-26.3(chr10:118247181-135435319)x3	copy number gain	not provided [RCV001537903]	Chr10:118247181..135435319 [GRCh37] Chr10:10q25.3-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129483682-135434178)	copy number loss	Global developmental delay [RCV001352664]	Chr10:129483682..135434178 [GRCh37] Chr10:10q26.2-26.3	pathogenic
Single allele	deletion	Distal 10q deletion syndrome [RCV001391670]	Chr10:127548166..135440251 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122785023-135457222)x1	copy number loss	See cases [RCV001526488]	Chr10:122785023..135457222 [GRCh37] Chr10:10q26.12-26.3	pathogenic
NC_000010.11:g.133346605_133601248dup	duplication	not provided [RCV001839379]	Chr10:133346605..133601248 [GRCh38] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143)	copy number gain	not specified [RCV002052891]	Chr10:108455687..135427143 [GRCh37] Chr10:10q25.1-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)	copy number loss	not specified [RCV002052902]	Chr10:128465436..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)	copy number loss	not specified [RCV002052895]	Chr10:122343861..135427143 [GRCh37] Chr10:10q26.12-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129914228-135427143)	copy number loss	not specified [RCV002052908]	Chr10:129914228..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
NC_000010.10:g.(?_134916201)_(135439108_?)del	deletion	not provided [RCV001972520]	Chr10:134916201..135439108 [GRCh37] Chr10:10q26.3	pathogenic
NC_000010.10:g.(?_134598420)_(135373622_?)del	deletion	not provided [RCV001975099]	Chr10:134598420..135373622 [GRCh37] Chr10:10q26.3	pathogenic
NC_000010.10:g.(?_134598420)_(135373622_?)dup	duplication	not provided [RCV003113881]	Chr10:134598420..135373622 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.13-26.3(chr10:127198625-135427143)x3	copy number gain	See cases [RCV002292400]	Chr10:127198625..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1	copy number loss	See cases [RCV002292397]	Chr10:126914469..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:130043370-135345340)x1	copy number loss	not provided [RCV002473957]	Chr10:130043370..135345340 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:132631529-135354972)x1	copy number loss	not provided [RCV002475809]	Chr10:132631529..135354972 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.357T>A (p.Phe119Leu)	single nucleotide variant	Inborn genetic diseases [RCV002761773]	Chr10:133355779 [GRCh38] Chr10:135169283 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.116C>T (p.Ser39Phe)	single nucleotide variant	Inborn genetic diseases [RCV002798474]	Chr10:133357225 [GRCh38] Chr10:135170729 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.436G>A (p.Gly146Arg)	single nucleotide variant	Inborn genetic diseases [RCV003001215]	Chr10:133355399 [GRCh38] Chr10:135168903 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.394A>G (p.Thr132Ala)	single nucleotide variant	Inborn genetic diseases [RCV002827040]	Chr10:133355742 [GRCh38] Chr10:135169246 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.364C>T (p.Arg122Trp)	single nucleotide variant	Inborn genetic diseases [RCV002769470]	Chr10:133355772 [GRCh38] Chr10:135169276 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.436G>C (p.Gly146Arg)	single nucleotide variant	Inborn genetic diseases [RCV002964937]	Chr10:133355399 [GRCh38] Chr10:135168903 [GRCh37] Chr10:10q26.3	uncertain significance
NM_001098483.3(FUOM):c.7G>T (p.Ala3Ser)	single nucleotide variant	Inborn genetic diseases [RCV003280556]	Chr10:133358001 [GRCh38] Chr10:135171505 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.12-26.3(chr10:122610933-135439810)x1	copy number loss	not provided [RCV003222684]	Chr10:122610933..135439810 [GRCh37] Chr10:10q26.12-26.3	pathogenic
NM_001098483.3(FUOM):c.386T>C (p.Val129Ala)	single nucleotide variant	Inborn genetic diseases [RCV003203788]	Chr10:133355750 [GRCh38] Chr10:135169254 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	copy number gain	Distal trisomy 10q [RCV003319593]	Chr10:11138692..135427143 [GRCh37] Chr10:10p14-q26.3	pathogenic
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319583]	Chr10:12829206..135427143 [GRCh37] Chr10:10p13-q26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123477898-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319590]	Chr10:123477898..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124895517-135440296)x1	copy number loss	Distal 10q deletion syndrome [RCV003329543]	Chr10:124895517..135440296 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128289206-135427143)x1	copy number loss	Distal 10q deletion syndrome [RCV003458182]	Chr10:128289206..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
NM_001098483.3(FUOM):c.266G>T (p.Gly89Val)	single nucleotide variant	Inborn genetic diseases [RCV003377341]	Chr10:133356698 [GRCh38] Chr10:135170202 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.3(chr10:133435524-135427143)x1	copy number loss	not provided [RCV003483110]	Chr10:133435524..135427143 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:128925940-135427143)x1	copy number loss	not provided [RCV003483108]	Chr10:128925940..135427143 [GRCh37] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:135053180-135381952)x3	copy number gain	not provided [RCV003456733]	Chr10:135053180..135381952 [GRCh37] Chr10:10q26.3	uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3	copy number gain	Distal trisomy 10q [RCV003458955]	Chr10:111378692..135427143 [GRCh37] Chr10:10q25.1-26.3	pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:125976998-133427130)x1	copy number loss	Duane syndrome type 1 [RCV003984306]	Chr10:125976998..133427130 [GRCh38] Chr10:10q26.2-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:131398569-135427143)x1	copy number loss	not specified [RCV003986883]	Chr10:131398569..135427143 [GRCh37] Chr10:10q26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125987494-135427143)x1	copy number loss	not specified [RCV003986904]	Chr10:125987494..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126127397-135427143)x1	copy number loss	not specified [RCV003986878]	Chr10:126127397..135427143 [GRCh37] Chr10:10q26.13-26.3	pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	copy number gain	not specified [RCV003986893]	Chr10:95078198..135427143 [GRCh37] Chr10:10q23.33-26.3	pathogenic
GRCh37/hg19 10q26.3(chr10:131299771-135441274)x1	copy number loss	not provided [RCV003885450]	Chr10:131299771..135441274 [GRCh37] Chr10:10q26.3	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2100
Count of miRNA genes:	710
Interacting mature miRNAs:	844
Transcripts:	ENST00000278025, ENST00000368551, ENST00000368552, ENST00000447176, ENST00000465384, ENST00000478895
Prediction methods:	Miranda, 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

RH70279

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	135,168,775 - 135,168,927	UniSTS	GRCh37
Build 36	10	135,018,765 - 135,018,917	RGD	NCBI36
Celera	10	128,348,601 - 128,348,753	RGD
Cytogenetic Map	10	q26.3	UniSTS
HuRef	10	128,712,890 - 128,713,042	UniSTS
GeneMap99-GB4 RH Map	10	561.05	UniSTS
NCBI RH Map	10	1382.8	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

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

608

778

712

518

1077

453

1575

139

715

274

531

857

696

825

Low

1817

2206

1010

105

855

2723

1991

2943

132

913

722

508

1907

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001098483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001301827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001301828	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_198472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539670	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011539675	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024447946	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AI333356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK129527	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL360181	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC129818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC129819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM009909	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU849497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX119427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN368132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY163253	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000278025 ⟹ ENSP00000278025

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,158 - 133,358,019 (-)	Ensembl

RefSeq Acc Id:

ENST00000368551 ⟹ ENSP00000357539

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,203 - 133,357,737 (-)	Ensembl

RefSeq Acc Id:

ENST00000368552 ⟹ ENSP00000357540

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,160 - 133,358,025 (-)	Ensembl

RefSeq Acc Id:

ENST00000447176 ⟹ ENSP00000413379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,164 - 133,357,995 (-)	Ensembl

RefSeq Acc Id:

ENST00000465384

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,169 - 133,358,001 (-)	Ensembl

RefSeq Acc Id:

ENST00000478895

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	133,355,520 - 133,356,996 (-)	Ensembl

RefSeq Acc Id:

NM_001098483 ⟹ NP_001091953

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI
GRCh37	10	135,168,658 - 135,171,529 (-)	RGD
Build 36	10	135,018,785 - 135,021,519 (-)	NCBI Archive
Celera	10	128,345,999 - 128,348,870 (+)	RGD
HuRef	10	128,712,773 - 128,715,644 (-)	RGD
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

Sequence:

show sequence

GTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCGAGCTGCTCTACG
CGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTTCCCGGCCTCCTC
CATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCGCAGCTCCTGGAG
GCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAGTCATGGAGCTGG
TGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGAGTCCATCCTACG
CAGGGCCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAG
AAGGCTTTTGCTGTTGTGGCAACGGGGGAGACGGCCCTCTACGGAAACCTCATCCTCAGGAAGG
GGGTGCTTGCCCTCAACCCCCTGCTGTAGGCCTGGTGAAGACCACCTGGGCCGGAAGAGGAACT
GGGGGCACCCTGAGCTCCAGTACCACCACTCACAACAGGCCTCCCAGTGGCAGCTCCCAGACCT
GGGCCCTGGCCAGGGCTCTAGGGGCCGGCAGTCTTGGGGTGGGCCCTGCCAATTGGGACGAGTA
TCCCTGATTTGTGAAAATGATGGAAAAACGTTCAGTCTCAAGAGTCCAA

hide sequence

RefSeq Acc Id:

NM_001301827 ⟹ NP_001288756

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

Sequence:

show sequence

GTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCGAGCTGCTCTACG
CGCTGGCGCGGATGGGGCACGGGGACGAGATCGGCCTGGGCATCCCGCAGCTCCTGGAGGCCGT
GCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAGTCATGGAGCTGGTGCCC
AGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGAGTCCATCCTACGCAGGG
CCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAGAAGGC
TTTTGCTGTTGTGGCAACGGGGGAGACGGCCCTCTACGGAAACCTCATCCTCAGGAAGGGGGTG
CTTGCCCTCAACCCCCTGCTGTAGGCCTGGTGAAGACCACCTGGGCCGGAAGAGGAACTGGGGG
CACCCTGAGCTCCAGTACCACCACTCACAACAGGCCTCCCAGTGGCAGCTCCCAGACCTGGGCC
CTGGCCAGGGCTCTAGGGGCCGGCAGTCTTGGGGTGGGCCCTGCCAATTGGGACGAGTATCCCT
GATTTGTGAAAATGATGGAAAAACGTTCAGTCTCAAGAGTCCAA

hide sequence

RefSeq Acc Id:

NM_001301828 ⟹ NP_001288757

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

Sequence:

show sequence

GTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCGAGCTGCTCTACG
CGCTGGCGCGGATGGGGCACGGGGACGAGATCGGCAGGGACCTTGCCCTCCCCACCTCCCCGCG
TGGCTTCCAGCCCTGCGGATCTGACTGCGGCCGGTCGGCGGTGGGGGCGCCCAACTGGCTGACC
TGAGACCTCTTGTGACCCACGATCTGCCGCCATGACTGGGTGGGAGGACGGGCGGCGCCGACCC
CGAGGGCAGGGATAGGTGCCGACACGGGCTGTCCTCCCGGCTGTTTAGTTCTTGCGGACTTGAA
CTTCCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATC
CCGCAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTG
CAGTCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTA
CGAGTCCATCCTACGCAGGGCCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTT
TATGAACGGGCTAAGAAGGCTTTTGCTGTTGTGGCAACGGGGGAGACGGCCCTCTACGGAAACC
TCATCCTCAGGAAGGGGGTGCTTGCCCTCAACCCCCTGCTGTAGGCCTGGTGAAGACCACCTGG
GCCGGAAGAGGAACTGGGGGCACCCTGAGCTCCAGTACCACCACTCACAACAGGCCTCCCAGTG
GCAGCTCCCAGACCTGGGCCCTGGCCAGGGCTCTAGGGGCCGGCAGTCTTGGGGTGGGCCCTGC
CAATTGGGACGAGTATCCCTGATTTGTGAAAATGATGGAAAAACGTTCAGTCTCAAGAGTCCAA

hide sequence

RefSeq Acc Id:

NM_198472 ⟹ NP_940874

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI
GRCh37	10	135,168,658 - 135,171,529 (-)	RGD
Build 36	10	135,018,648 - 135,021,519 (-)	NCBI Archive
Celera	10	128,345,999 - 128,348,870 (+)	RGD
HuRef	10	128,712,773 - 128,715,644 (-)	RGD
CHM1_1	10	135,450,598 - 135,453,469 (-)	NCBI
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

Sequence:

show sequence

GTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCGAGCTGCTCTACG
CGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTTCCCGGCCTCCTC
CATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCGCAGCTCCTGGAG
GCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAGTCATGGAGCTGG
TGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGAGTCCATCCTACG
CAGGGCCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAG
AAGGCTTTTGCTGTTGTGGCAACGGGATGCTGAAGCAGGGTCTCGGCACCCTGGCCCTGCAGCC
CAGCTCAGTGCTGGGCTTGGCTCCTCTGCAGGGAGACGGCCCTCTACGGAAACCTCATCCTCAG
GAAGGGGGTGCTTGCCCTCAACCCCCTGCTGTAGGCCTGGTGAAGACCACCTGGGCCGGAAGAG
GAACTGGGGGCACCCTGAGCTCCAGTACCACCACTCACAACAGGCCTCCCAGTGGCAGCTCCCA
GACCTGGGCCCTGGCCAGGGCTCTAGGGGCCGGCAGTCTTGGGGTGGGCCCTGCCAATTGGGAC
GAGTATCCCTGATTTGTGAAAATGATGGAAAAACGTTCAGTCTCAAGAGTCCAA

hide sequence

RefSeq Acc Id:

XM_011539670 ⟹ XP_011537972

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGGGTTCCCTCCAACCCTGCCATTTTGTCTTCCAGAGA
GCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAGAAGGCTTTTGCTGTTGTGG
CAACGGGCCCAGCTCAGTGCTGGGCTTGGCTCCTCTGCAGGGAGACGGCCCTCTACGGAAACCT
CATCCTCAGGAAGGGGGTGCTTGCCCTCAACCCCCTGCTGTAGGCCTGGTGAAGACCACCTGGG
CCGGAAGAGGAACTGGGGGCACCCTGAGCTCCAGTACCACCACTCACAACAGGCCTCCCAGTGG
CAGCTCCCAGACCTGGGCCCTGGCCAGGGCTCTAGGGGCCGGCAGTCTTGGGGTGGGCCCTGCC
AATTGGGACGAGTATCCCTGATTTGTGAAAATGATGGAAAAACGTTCAGTCTCAAGAGTCCAAT
TCCA

hide sequence

RefSeq Acc Id:

XM_011539671 ⟹ XP_011537973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTTTAT
GAACGGGCTAAGAAGGCTTTTGCTGTTGTGGCAACGGGCCCAGCTCAGTGCTGGGCTTGGCTCC
TCTGCAGGGAGACGGCCCTCTACGGAAACCTCATCCTCAGGAAGGGGGTGCTTGCCCTCAACCC
CCTGCTGTAGGCCTGGTGAAGACCACCTGGGCCGGAAGAGGAACTGGGGGCACCCTGAGCTCCA
GTACCACCACTCACAACAGGCCTCCCAGTGGCAGCTCCCAGACCTGGGCCCTGGCCAGGGCTCT
AGGGGCCGGCAGTCTTGGGGTGGGCCCTGCCAATTGGGACGAGTATCCCTGATTTGTGAAAATG
ATGGAAAAACGTTCAGTCTCAAGAGTCCAATTCCA

hide sequence

RefSeq Acc Id:

XM_011539672 ⟹ XP_011537974

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGGGTTCCCTCCAACCCTGCCATTTTGTCTTCCAGAGA
GCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAGAAGGCTTTTGCTGTTGTGG
CAACGGGGGAGACGGCCCTCTACGGAAACCTCATCCTCAGGAAGGGGGTGCTTGCCCTCAACCC
CCTGCTGTAGGCCTGGTGAAGACCACCTGGGCCGGAAGAGGAACTGGGGGCACCCTGAGCTCCA
GTACCACCACTCACAACAGGCCTCCCAGTGGCAGCTCCCAGACCTGGGCCCTGGCCAGGGCTCT
AGGGGCCGGCAGTCTTGGGGTGGGCCCTGCCAATTGGGACGAGTATCCCTGATTTGTGAAAATG
ATGGAAAAACGTTCAGTCTCAAGAGTCCAATTCCA

hide sequence

RefSeq Acc Id:

XM_011539673 ⟹ XP_011537975

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,352,773 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGGGTTCCCTCCAACCCTGCCATTTTGTCTTCCAGAGA
GCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAGAAGGCTTTTGCTGTTGTGG
CAACGGGGCTTGTTTGGTGCTGAGCTCAAGGGAGGCTGCTGGCTCCAGAGTGGCCCCCACGTAC
CCTTGACGAACCTTGAGTGGGAAATCAGGCCTGGGGCCCTGGGGACTGGGCGGGGTGCCTGGTG
CCCTGGGGACACCAAGGGCTGGAGTGGGGGCAGTGGCTGCCCTGGAGGCCTTGAGAGGGGTGGG
GACTTCTGCCATAGCCCCTGGGCTGTGGACACCAAGGGGGTTCTTCACCGGGGTCCATTCCTTC
CACCCGCAGGAGGGCAGGTGGCAGGGGCTGGCCTGGACGCTTCGGGAGGAACTGTCGGCTGGAG
AGGCCTCGGTGTGGGCCATGCCCTATGCCTGTGGCATAGGTGGCCTCCCGCTGAAAGCCTCACT
TGCCCTGGCAGGCAGGGGAGGTAAAGGACACGAGGTCATTTGGAGTCCAGTGCCAGGCAGAGGT
GGGATGCAGGGGGTTCCTGAAAGGGGGTGCCTGGGAGGCTTGCCCATGGGATGCTTGGACTGGT
CCCCAAGGATGGGGAAGAATAACCACCAGCCACTGTCCGGACCCTCGTCTTGCTCCCCAGAACT
TGCTGCAGTGACAGGTACAGGAAGAAGATGGGGCAGGGCTGGAGTTTGAGGGACCAAGGGCAGG
AGTGGGGATGACAGGGGCTTCCCCCAGGGCCTGGGGCTGGTGTCCCCGGGGCTCGAGGGGGCAA
GTCCCAGGGTTCCAGACCCCCACTCCAGACCGCAGGAGAACCTTGGGGGTGCAGGCAAGCCCAC
CCCGGCTGAGATGTGGCTCCAAATCTGGGGAAGGGACCCTGTCTGGGCTTGGCTGCAGACTTTG
GGGTCCTGTCCGCCTGCTGCTCCCAGATGGTAGCCAAGGCTTTCTCTGTGCTCACTAGTGGTCA
GCCTTGGCCCCAGGGGCCTCGCACTTGCCTGGCCAATCACTGCTCATCTCTAGACCCGATGGCC
GCGTCGTGGCCTAACATCAGCGGTGTACGAGCTGGTTGCACACACCCTCGCCCATCCCCAGGCT
CAGCCCCACAGATGAGCCTCTGGGGTTAGTGTGCCCTCTCTAGCATGTTATATAAATGAAGCCA
TATATGAGCAAACTAAGTAAAATCACGAGAAAAAACAAAGTAATGGGCAAAACAAAATAAAATC
AAGATAGCTTTAAAAAAAAAAAAAAAGCCACAAACACCAGCTTGGGCTGCCTAGGGCAAGACCC
TCCTGCAACTCAGAGATCCAGGGTCTTCTACCTGCCTGGGGCTCAGGGAGTGGGGAAGGAGTTG
CCCAAATCTCAGCCCTGAGCGTGTTGATCCCTCAATGCCCTCCTACCCCATGTTCTTATCAGGA
TGACAGGGGAGGCTGCCAAGGGAGAAGCTGGCAGCCCATCTCTGGCCCTTTTAGGACAGAACCT
CAAAGGTCACTGGCCTCTCCAGCTCATCCATAAGCCAGGGTAACAGCTCTTACATTGTGGGACA
CCGTGGGGCACCCTTGGGCAGTTACTCTCAGCCGTTGGTGTCCTGGGAGAGCGGGGATTTGCTG
GCGGTGCAAGGAGCTCTTCCACACCTGGGCAAACCCTCAGCCCCCTGAGTGGCCACACGAGGGC
TGAACACGGCAGGATGAGGGACGGGTGGCCTCTCTCCCTTGCTCCGTTCTGTCTTAGCTGCTGG
AGCTGGCAAATGTGTGTGGCTCAGCCCCGGGCTTGGCACCAGGTGCTTCTCTCTCACCATAGGG
ATGAGACTGCCACGCAGGAACCCCGCCCACATTTGCATGTGCCCAGGACACATGCGGTGTGTGA
GTGACTCCAGCAGCCTGGACCTGCGCTGCAGCATTGGGCCTGCTGGGCCAGGAGGACAGGATGG
GCACCCAGAGTGGGAGCTGCACAGAACGTCAGGAGGGCAGAAAGGCCATGTCCTGGGCCTGGGT
CTACCCGCCCTCACCTGAGACCTGTGCACTTTCCACCTGAGCACATGCACGTCCGTTCAGCTGG
GCCCTGAGCCCCAGGCACTCGGCCACCCTCCTCCCCGACCCTGTCTCAGGCTCCTGCTGTAGGG
AGCCCAGGGTGGGTTCTGTTTCTCAGCTGAGACTGGTCCCAGGGTGCCCTCTGGTCCCATCCCC
TAACTGCTGCCACACCCCTCACCATCCCGGTATACAAGGAGGAGGGCCTGGGGGTAGTGCAACC
TTCTGGGAGCCAAGGGTCACCTGGGCCTTGTGCAGCCCTTGATTCTCCTAGGCAGGGCAGGCTG
GGCCCCGGTCATCGGTCTTCTGGGGCATGTGGCCTCCCACCTGTTTGCAGGGGTTGATTGATTG
ATTGATTGATCGATTGAGATGGAGTCTTGCTCTGTCGCCCAGCCTGGAGTGCAATGGCACGATC
TC

hide sequence

RefSeq Acc Id:

XM_011539674 ⟹ XP_011537976

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGGGTTCCCTCCAACCCTGCCATTTTGTCTTCCAGAGA
GCCCTGGCAAAGATAGAGAGGTTTGAGTTTTATGAACGGGCTAAGAAGGCTTTTGCTGTTGTGG
CAACGGGATGCTGAAGCAGGGTCTCGGCACCCTGGCCCTGCAGCCCAGCTCAGTGCTGGGCTTG
GCTCCTCTGCAGGGAGACGGCCCTCTACGGAAACCTCATCCTCAGGAAGGGGGTGCTTGCCCTC
AACCCCCTGCTGTAGG

hide sequence

RefSeq Acc Id:

XM_011539675 ⟹ XP_011537977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,352,773 - 133,358,019 (-)	NCBI

Sequence:

show sequence

CCCGCCCGCCCCGTCTGCCGGGCCATGGTGGCGCTGAAGGGTGTCCCCGCACTGCTGTCCCCCG
AGCTGCTCTACGCGCTGGCGCGGATGGGGCACGGGGACGAGATCGTTCTTGCGGACTTGAACTT
CCCGGCCTCCTCCATCTGCCAGTGTGGGCCCATGGAGATCCGTGCAGACGGCCTGGGCATCCCG
CAGCTCCTGGAGGCCGTGCTGAAGCTGCTGCCCCTGGACACCTATGTGGAGAGTCCGGCTGCAG
TCATGGAGCTGGTGCCCAGCGACAAGGAGAGGGGCCTGCAGACCCCAGTGTGGACGGAGTACGA
GTCCATCCTACGCAGGGCCGGCTGTGTGAGAGCCCTGGCAAAGATAGAGAGGTTTGAGTTTTAT
GAACGGGCTAAGAAGGCTTTTGCTGTTGTGGCAACGGGGCTTGTTTGGTGCTGAGCTCAAGGGA
GGCTGCTGGCTCCAGAGTGGCCCCCACGTACCCTTGACGAACCTTGAGTGGGAAATCAGGCCTG
GGGCCCTGGGGACTGGGCGGGGTGCCTGGTGCCCTGGGGACACCAAGGGCTGGAGTGGGGGCAG
TGGCTGCCCTGGAGGCCTTGAGAGGGGTGGGGACTTCTGCCATAGCCCCTGGGCTGTGGACACC
AAGGGGGTTCTTCACCGGGGTCCATTCCTTCCACCCGCAGGAGGGCAGGTGGCAGGGGCTGGCC
TGGACGCTTCGGGAGGAACTGTCGGCTGGAGAGGCCTCGGTGTGGGCCATGCCCTATGCCTGTG
GCATAGGTGGCCTCCCGCTGAAAGCCTCACTTGCCCTGGCAGGCAGGGGAGGTAAAGGACACGA
GGTCATTTGGAGTCCAGTGCCAGGCAGAGGTGGGATGCAGGGGGTTCCTGAAAGGGGGTGCCTG
GGAGGCTTGCCCATGGGATGCTTGGACTGGTCCCCAAGGATGGGGAAGAATAACCACCAGCCAC
TGTCCGGACCCTCGTCTTGCTCCCCAGAACTTGCTGCAGTGACAGGTACAGGAAGAAGATGGGG
CAGGGCTGGAGTTTGAGGGACCAAGGGCAGGAGTGGGGATGACAGGGGCTTCCCCCAGGGCCTG
GGGCTGGTGTCCCCGGGGCTCGAGGGGGCAAGTCCCAGGGTTCCAGACCCCCACTCCAGACCGC
AGGAGAACCTTGGGGGTGCAGGCAAGCCCACCCCGGCTGAGATGTGGCTCCAAATCTGGGGAAG
GGACCCTGTCTGGGCTTGGCTGCAGACTTTGGGGTCCTGTCCGCCTGCTGCTCCCAGATGGTAG
CCAAGGCTTTCTCTGTGCTCACTAGTGGTCAGCCTTGGCCCCAGGGGCCTCGCACTTGCCTGGC
CAATCACTGCTCATCTCTAGACCCGATGGCCGCGTCGTGGCCTAACATCAGCGGTGTACGAGCT
GGTTGCACACACCCTCGCCCATCCCCAGGCTCAGCCCCACAGATGAGCCTCTGGGGTTAGTGTG
CCCTCTCTAGCATGTTATATAAATGAAGCCATATATGAGCAAACTAAGTAAAATCACGAGAAAA
AACAAAGTAATGGGCAAAACAAAATAAAATCAAGATAGCT

hide sequence

RefSeq Acc Id:

XM_047425101 ⟹ XP_047281057

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,357,696 (-)	NCBI

RefSeq Acc Id:

XM_047425102 ⟹ XP_047281058

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,357,696 (-)	NCBI

RefSeq Acc Id:

XM_047425103 ⟹ XP_047281059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,357,696 (-)	NCBI

RefSeq Acc Id:

XM_047425104 ⟹ XP_047281060

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,356,640 - 133,358,019 (-)	NCBI

RefSeq Acc Id:

XM_047425105 ⟹ XP_047281061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	133,355,158 - 133,357,696 (-)	NCBI

RefSeq Acc Id:

XM_054365619 ⟹ XP_054221594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,280 - 134,313,135 (-)	NCBI

RefSeq Acc Id:

XM_054365620 ⟹ XP_054221595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,280 - 134,313,135 (-)	NCBI

RefSeq Acc Id:

XM_054365621 ⟹ XP_054221596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

RefSeq Acc Id:

XM_054365622 ⟹ XP_054221597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,274 - 134,313,135 (-)	NCBI

RefSeq Acc Id:

XM_054365623 ⟹ XP_054221598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,280 - 134,312,890 (-)	NCBI

RefSeq Acc Id:

XM_054365624 ⟹ XP_054221599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,280 - 134,312,864 (-)	NCBI

RefSeq Acc Id:

XM_054365625 ⟹ XP_054221600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,274 - 134,312,874 (-)	NCBI

RefSeq Acc Id:

XM_054365626 ⟹ XP_054221601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,311,756 - 134,313,135 (-)	NCBI

RefSeq Acc Id:

XM_054365627 ⟹ XP_054221602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	134,310,274 - 134,312,864 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001091953	(Get FASTA)	NCBI Sequence Viewer
	NP_001288756	(Get FASTA)	NCBI Sequence Viewer
	NP_001288757	(Get FASTA)	NCBI Sequence Viewer
	NP_940874	(Get FASTA)	NCBI Sequence Viewer
	XP_011537972	(Get FASTA)	NCBI Sequence Viewer
	XP_011537973	(Get FASTA)	NCBI Sequence Viewer
	XP_011537974	(Get FASTA)	NCBI Sequence Viewer
	XP_011537975	(Get FASTA)	NCBI Sequence Viewer
	XP_011537976	(Get FASTA)	NCBI Sequence Viewer
	XP_011537977	(Get FASTA)	NCBI Sequence Viewer
	XP_047281057	(Get FASTA)	NCBI Sequence Viewer
	XP_047281058	(Get FASTA)	NCBI Sequence Viewer
	XP_047281059	(Get FASTA)	NCBI Sequence Viewer
	XP_047281060	(Get FASTA)	NCBI Sequence Viewer
	XP_047281061	(Get FASTA)	NCBI Sequence Viewer
	XP_054221594	(Get FASTA)	NCBI Sequence Viewer
	XP_054221595	(Get FASTA)	NCBI Sequence Viewer
	XP_054221596	(Get FASTA)	NCBI Sequence Viewer
	XP_054221597	(Get FASTA)	NCBI Sequence Viewer
	XP_054221598	(Get FASTA)	NCBI Sequence Viewer
	XP_054221599	(Get FASTA)	NCBI Sequence Viewer
	XP_054221600	(Get FASTA)	NCBI Sequence Viewer
	XP_054221601	(Get FASTA)	NCBI Sequence Viewer
	XP_054221602	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	A2VDF0	(Get FASTA)	NCBI Sequence Viewer
	AAI29819	(Get FASTA)	NCBI Sequence Viewer
	AAI29820	(Get FASTA)	NCBI Sequence Viewer
	BAC85178	(Get FASTA)	NCBI Sequence Viewer
	EAW61337	(Get FASTA)	NCBI Sequence Viewer
	EAW61338	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000278025
	ENSP00000278025.5
	ENSP00000357539
	ENSP00000357539.1
	ENSP00000357540
	ENSP00000357540.5
	ENSP00000413379
	ENSP00000413379.2

RefSeq Acc Id:	NP_940874 ⟸ NM_198472
- Peptide Label:	isoform 2
- UniProtKB:	A2VDF0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVRALAKIERFEFYERAKKAFA VVATGC hide sequence

RefSeq Acc Id:	NP_001091953 ⟸ NM_001098483
- Peptide Label:	isoform 1
- UniProtKB:	Q5VWY3 (UniProtKB/Swiss-Prot), Q5VWY2 (UniProtKB/Swiss-Prot), A1L300 (UniProtKB/Swiss-Prot), Q6ZPD2 (UniProtKB/Swiss-Prot), A2VDF0 (UniProtKB/Swiss-Prot), X6RK00 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVRALAKIERFEFYERAKKAFA VVATGETALYGNLILRKGVLALNPLL hide sequence

RefSeq Acc Id:	NP_001288756 ⟸ NM_001301827
- Peptide Label:	isoform 3
- UniProtKB:	X6RK00 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIGLGIPQLLEAVLKLLPLDTYVESPAAVMELVPSDKE RGLQTPVWTEYESILRRAGCVRALAKIERFEFYERAKKAFAVVATGETALYGNLILRKGVLALN PLL hide sequence

RefSeq Acc Id:	NP_001288757 ⟸ NM_001301828
- Peptide Label:	isoform 4
- UniProtKB:	X6R6T9 (UniProtKB/TrEMBL), X6RK00 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEIRADGLGIPQLLEAVLKLLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVR ALAKIERFEFYERAKKAFAVVATGETALYGNLILRKGVLALNPLL hide sequence

RefSeq Acc Id:	XP_011537977 ⟸ XM_011539675
- Peptide Label:	isoform X11
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVRALAKIERFEFYERAKKAFA VVATGLVWC hide sequence

RefSeq Acc Id:	XP_011537975 ⟸ XM_011539673
- Peptide Label:	isoform X10
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVGSLQPCHFVFQRALAKIERF EFYERAKKAFAVVATGLVWC hide sequence

RefSeq Acc Id:	XP_011537973 ⟸ XM_011539671
- Peptide Label:	isoform X2
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVRALAKIERFEFYERAKKAFA VVATGPAQCWAWLLCRETALYGNLILRKGVLALNPLL hide sequence

RefSeq Acc Id:	XP_011537974 ⟸ XM_011539672
- Peptide Label:	isoform X3
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVGSLQPCHFVFQRALAKIERF EFYERAKKAFAVVATGETALYGNLILRKGVLALNPLL hide sequence

RefSeq Acc Id:	XP_011537972 ⟸ XM_011539670
- Peptide Label:	isoform X1
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVGSLQPCHFVFQRALAKIERF EFYERAKKAFAVVATGPAQCWAWLLCRETALYGNLILRKGVLALNPLL hide sequence

RefSeq Acc Id:	XP_011537976 ⟸ XM_011539674
- Peptide Label:	isoform X4
- Sequence:	show sequence MVALKGVPALLSPELLYALARMGHGDEIVLADLNFPASSICQCGPMEIRADGLGIPQLLEAVLK LLPLDTYVESPAAVMELVPSDKERGLQTPVWTEYESILRRAGCVGSLQPCHFVFQRALAKIERF EFYERAKKAFAVVATGC hide sequence

RefSeq Acc Id:

ENSP00000357540 ⟸ ENST00000368552

RefSeq Acc Id:

ENSP00000357539 ⟸ ENST00000368551

RefSeq Acc Id:

ENSP00000413379 ⟸ ENST00000447176

RefSeq Acc Id:

ENSP00000278025 ⟸ ENST00000278025

RefSeq Acc Id:	XP_047281061 ⟸ XM_047425105
- Peptide Label:	isoform X9
- UniProtKB:	X6R6T9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047281058 ⟸ XM_047425102
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047281059 ⟸ XM_047425103
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047281057 ⟸ XM_047425101
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047281060 ⟸ XM_047425104
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054221596 ⟸ XM_054365621
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054221597 ⟸ XM_054365622
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054221600 ⟸ XM_054365625
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054221602 ⟸ XM_054365627
- Peptide Label:	isoform X9
- UniProtKB:	X6R6T9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054221595 ⟸ XM_054365620
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054221594 ⟸ XM_054365619
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054221598 ⟸ XM_054365623
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054221599 ⟸ XM_054365624
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054221601 ⟸ XM_054365626
- Peptide Label:	isoform X8

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-A2VDF0-F1-model_v2	AlphaFold	A2VDF0	1-154	view protein structure

Promoters

RGD ID:

7219063

Promoter ID:

EPDNEW_H15277

Type:

initiation region

Name:

FUOM_1

Description:

fucose mutarotase

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	10	133,358,019 - 133,358,079	EPDNEW

RGD ID:

6787405

Promoter ID:

HG_KWN:11760

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell_12Hour

Transcripts:

OTTHUMT00000051139

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	135,020,691 - 135,021,191 (-)	MPROMDB

RGD ID:

6787398

Promoter ID:

HG_KWN:11761

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000368551, NM_001098483, NM_198472, OTTHUMT00000051136, OTTHUMT00000051138

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	135,021,106 - 135,021,606 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:24733	AgrOrtholog
COSMIC	FUOM	COSMIC
Ensembl Genes	ENSG00000148803	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000278025	ENTREZGENE
	ENST00000278025.9	UniProtKB/Swiss-Prot
	ENST00000368551	ENTREZGENE
	ENST00000368551.1	UniProtKB/TrEMBL
	ENST00000368552	ENTREZGENE
	ENST00000368552.7	UniProtKB/Swiss-Prot
	ENST00000447176	ENTREZGENE
	ENST00000447176.5	UniProtKB/TrEMBL
	ENST00000465384	ENTREZGENE
Gene3D-CATH	3.40.1650.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000148803	GTEx
HGNC ID	HGNC:24733	ENTREZGENE
Human Proteome Map	FUOM	Human Proteome Map
InterPro	RbsD-like_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	RbsD_FucU	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:282969	UniProtKB/Swiss-Prot
NCBI Gene	282969	ENTREZGENE
OMIM	617725	OMIM
PANTHER	FUCOSE MUTAROTASE	UniProtKB/Swiss-Prot
	FUCOSE MUTAROTASE	UniProtKB/Swiss-Prot
	FUCOSE MUTAROTASE	UniProtKB/TrEMBL
	FUCOSE MUTAROTASE	UniProtKB/TrEMBL
Pfam	RbsD_FucU	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134972390	PharmGKB
Superfamily-SCOP	SSF102546	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A1L300	ENTREZGENE
	A2VDF0	ENTREZGENE, UniProtKB/Swiss-Prot
	Q5VWY2	ENTREZGENE
	Q5VWY3	ENTREZGENE
	Q6ZPD2	ENTREZGENE
	X6R6T9	ENTREZGENE, UniProtKB/TrEMBL
	X6RK00	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	A1L300	UniProtKB/Swiss-Prot
	Q5VWY2	UniProtKB/Swiss-Prot
	Q5VWY3	UniProtKB/Swiss-Prot
	Q6ZPD2	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2012-07-13	FUOM	fucose mutarotase	C10orf125	chromosome 10 open reading frame 125	Symbol and/or name change	5135510	APPROVED

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)

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Imported Disease Annotations - ClinVar