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Gene: WSCD1 (WSC domain containing 1) Homo sapiens

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Symbol:

WSCD1

Name:

WSC domain containing 1

RGD ID:

1603698

HGNC Page

HGNC:29060

Description:

Predicted to enable sulfotransferase activity. Predicted to be located in Golgi membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

KIAA0523; sialate:O-sulfotransferase 1; WSC domain-containing protein 1

RGD Orthologs

Alliance Orthologs

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):	Wscd1 (WSC domain containing 1)	HGNC	HGNC, HomoloGene, NCBI, Panther
Rattus norvegicus (Norway rat):	Wscd1 (WSC domain containing 1)	HGNC	HomoloGene, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Wscd1 (WSC domain containing 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	WSCD1 (WSC domain containing 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	WSCD1 (WSC domain containing 1)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Wscd1 (WSC domain containing 1)	NCBI	Ortholog
Sus scrofa (pig):	WSCD1 (WSC domain containing 1)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	WSCD1 (WSC domain containing 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Wscd1 (WSC domain containing 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Fads1 (fatty acid desaturase 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Wscd1 (WSC domain containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Wscd1 (WSC domain containing 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	wscd1a (WSC domain containing 1a)	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Danio rerio (zebrafish):	wscd1b (WSC domain containing 1b)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|ZFIN)
Drosophila melanogaster (fruit fly):	CG9164	Alliance	DIOPT (OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	wscd1.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	wscd1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	wscd1.L	Alliance	DIOPT (Xenbase)

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	6,069,116 - 6,124,427 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	6,057,807 - 6,124,427 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	5,972,436 - 6,027,747 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	5,914,658 - 5,968,471 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	5,989,799 - 6,043,603 (+)	NCBI		Celera
Cytogenetic Map	17	p13.2	NCBI
HuRef	17	5,875,040 - 5,919,106 (+)	NCBI		HuRef
CHM1_1	17	5,983,259 - 6,037,060 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	5,963,314 - 6,018,611 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
WSCD1	Human	developmental and epileptic encephalopathy 25		IAGP	RGD:156443507	8554872	ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 25	ClinVar	PMID:28492532

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
WSCD1	Human	Liver Neoplasms		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:19233941
WSCD1	Human	pre-malignant neoplasm		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:19233941

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
WSCD1	Human	17beta-estradiol	decreases expression	ISO	RGD:1317859	6480464	Estradiol results in decreased expression of WSCD1 mRNA	CTD	PMID:39298647
WSCD1	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	ISO	RGD:1317859	6480464	[Tetrachlorodibenzodioxin co-treated with Lipopolysaccharides] results in increased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	EXP		6480464	[Tetrachlorodibenzodioxin co-treated with 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide] results in increased expression of WSCD1 mRNA	CTD	PMID:29704546
WSCD1	Human	2,3,7,8-tetrachlorodibenzodioxine	increases methylation	ISO	RGD:1317859	6480464	Tetrachlorodibenzodioxin results in increased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases methylation	ISO	RGD:1317859	6480464	Tetrachlorodibenzodioxin results in decreased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	4,4'-sulfonyldiphenol	decreases expression	ISO	RGD:1317859	6480464	bisphenol S results in decreased expression of WSCD1 mRNA	CTD	PMID:30951980
WSCD1	Human	6-propyl-2-thiouracil	decreases expression	ISO	RGD:1308212	6480464	Propylthiouracil results in decreased expression of WSCD1 mRNA	CTD	PMID:24780913
WSCD1	Human	6-propyl-2-thiouracil	increases expression	ISO	RGD:1308212	6480464	Propylthiouracil results in increased expression of WSCD1 mRNA	CTD	PMID:30047161
WSCD1	Human	aflatoxin B1	increases methylation	EXP		6480464	Aflatoxin B1 results in increased methylation of WSCD1 intron	CTD	PMID:30157460
WSCD1	Human	amitrole	increases expression	ISO	RGD:1308212	6480464	Amitrole results in increased expression of WSCD1 mRNA	CTD	PMID:30047161
WSCD1	Human	antirheumatic drug	increases expression	EXP		6480464	Antirheumatic Agents results in increased expression of WSCD1 mRNA	CTD	PMID:24449571
WSCD1	Human	aristolochic acid A	increases expression	EXP		6480464	aristolochic acid I results in increased expression of WSCD1 mRNA	CTD	PMID:33212167
WSCD1	Human	benzo[a]pyrene	increases expression	ISO	RGD:1317859	6480464	Benzo(a)pyrene results in increased expression of WSCD1 mRNA	CTD	PMID:22228805
WSCD1	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of WSCD1 3' UTR; Benzo(a)pyrene affects the methylation of WSCD1 5' more ...	CTD	PMID:27901495\|PMID:30157460
WSCD1	Human	bis(2-ethylhexyl) phthalate	decreases expression	EXP		6480464	Diethylhexyl Phthalate results in decreased expression of WSCD1 mRNA	CTD	PMID:31163220
WSCD1	Human	bisphenol A	decreases expression	ISO	RGD:1308212	6480464	bisphenol A results in decreased expression of WSCD1 mRNA	CTD	PMID:25181051
WSCD1	Human	bisphenol A	increases expression	ISO	RGD:1317859	6480464	bisphenol A results in increased expression of WSCD1 mRNA	CTD	PMID:32156529
WSCD1	Human	bisphenol A	increases methylation	EXP		6480464	bisphenol A results in increased methylation of WSCD1 gene	CTD	PMID:31601247
WSCD1	Human	bisphenol A	increases expression	ISO	RGD:1308212	6480464	bisphenol A results in increased expression of WSCD1 mRNA	CTD	PMID:34947998
WSCD1	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of WSCD1 mRNA	CTD	PMID:31715268
WSCD1	Human	bisphenol F	decreases expression	ISO	RGD:1317859	6480464	bisphenol F results in decreased expression of WSCD1 mRNA	CTD	PMID:30951980
WSCD1	Human	butanal	increases expression	EXP		6480464	butyraldehyde results in increased expression of WSCD1 mRNA	CTD	PMID:26079696
WSCD1	Human	C60 fullerene	increases expression	ISO	RGD:1308212	6480464	fullerene C60 results in increased expression of WSCD1 mRNA	CTD	PMID:19167457
WSCD1	Human	cadmium atom	increases expression	EXP		6480464	Cadmium results in increased expression of WSCD1 mRNA	CTD	PMID:31082426
WSCD1	Human	chloroprene	decreases expression	ISO	RGD:1317859	6480464	Chloroprene results in decreased expression of WSCD1 mRNA	CTD	PMID:23125180
WSCD1	Human	chlorpyrifos	increases expression	ISO	RGD:1317859	6480464	Chlorpyrifos results in increased expression of WSCD1 mRNA	CTD	PMID:37019170
WSCD1	Human	clobetasol	decreases expression	ISO	RGD:1317859	6480464	Clobetasol results in decreased expression of WSCD1 mRNA	CTD	PMID:27462272
WSCD1	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with p-Chloromercuribenzoic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	endosulfan	increases expression	ISO	RGD:1308212	6480464	Endosulfan results in increased expression of WSCD1 mRNA	CTD	PMID:29391264
WSCD1	Human	gentamycin	decreases expression	ISO	RGD:1308212	6480464	Gentamicins results in decreased expression of WSCD1 mRNA	CTD	PMID:22061828
WSCD1	Human	lipopolysaccharide	decreases methylation	ISO	RGD:1317859	6480464	Lipopolysaccharides results in decreased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	lipopolysaccharide	multiple interactions	ISO	RGD:1317859	6480464	[Tetrachlorodibenzodioxin co-treated with Lipopolysaccharides] results in increased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	lipopolysaccharide	increases methylation	ISO	RGD:1317859	6480464	Lipopolysaccharides results in increased methylation of WSCD1 gene	CTD	PMID:21212295
WSCD1	Human	methimazole	increases expression	ISO	RGD:1308212	6480464	Methimazole results in increased expression of WSCD1 mRNA	CTD	PMID:30047161
WSCD1	Human	methylmercury chloride	decreases expression	EXP		6480464	methylmercuric chloride results in decreased expression of WSCD1 mRNA	CTD	PMID:28001369
WSCD1	Human	miconazole	decreases expression	ISO	RGD:1317859	6480464	Miconazole results in decreased expression of WSCD1 mRNA	CTD	PMID:27462272
WSCD1	Human	N,N-diethyl-m-toluamide	multiple interactions	ISO	RGD:1308212	6480464	[Permethrin co-treated with DEET] results in decreased methylation of WSCD1 gene	CTD	PMID:33148267
WSCD1	Human	N-methyl-4-phenylpyridinium	increases expression	EXP		6480464	1-Methyl-4-phenylpyridinium results in increased expression of WSCD1 mRNA	CTD	PMID:24810058
WSCD1	Human	oxaliplatin	multiple interactions	ISO	RGD:1308212	6480464	[oxaliplatin co-treated with Topotecan] results in decreased expression of WSCD1 mRNA	CTD	PMID:25729387
WSCD1	Human	ozone	multiple interactions	ISO	RGD:1317859	6480464	[Air Pollutants results in increased abundance of [Ozone co-treated with Soot]] which results in decreased more ...	CTD	PMID:34911549
WSCD1	Human	p-chloromercuribenzoic acid	decreases expression	EXP		6480464	p-Chloromercuribenzoic Acid results in decreased expression of WSCD1 mRNA	CTD	PMID:26272509
WSCD1	Human	p-chloromercuribenzoic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with p-Chloromercuribenzoic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	paracetamol	affects expression	ISO	RGD:1317859	6480464	Acetaminophen affects the expression of WSCD1 mRNA	CTD	PMID:17562736
WSCD1	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of WSCD1 mRNA	CTD	PMID:26690555
WSCD1	Human	pentanal	increases expression	EXP		6480464	pentanal results in increased expression of WSCD1 mRNA	CTD	PMID:26079696
WSCD1	Human	perfluorooctane-1-sulfonic acid	multiple interactions	ISO	RGD:1317859	6480464	[perfluorooctane sulfonic acid co-treated with Pectins] results in decreased expression of WSCD1 mRNA	CTD	PMID:36331819
WSCD1	Human	permethrin	multiple interactions	ISO	RGD:1308212	6480464	[Permethrin co-treated with DEET] results in decreased methylation of WSCD1 gene	CTD	PMID:33148267
WSCD1	Human	phenobarbital	affects methylation	ISO	RGD:1317859	6480464	Phenobarbital affects the methylation of WSCD1 gene	CTD	PMID:19233941
WSCD1	Human	phenylmercury acetate	decreases expression	EXP		6480464	Phenylmercuric Acetate results in decreased expression of WSCD1 mRNA	CTD	PMID:26272509
WSCD1	Human	phenylmercury acetate	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	potassium dichromate	decreases expression	ISO	RGD:1317859	6480464	Potassium Dichromate results in decreased expression of WSCD1 mRNA	CTD	PMID:23608068
WSCD1	Human	propanal	increases expression	EXP		6480464	propionaldehyde results in increased expression of WSCD1 mRNA	CTD	PMID:26079696
WSCD1	Human	resveratrol	multiple interactions	EXP		6480464	[Plant Extracts co-treated with Resveratrol] results in decreased expression of WSCD1 mRNA	CTD	PMID:23557933
WSCD1	Human	rotenone	increases expression	EXP		6480464	Rotenone results in increased expression of WSCD1 mRNA	CTD	PMID:29955902
WSCD1	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with p-Chloromercuribenzoic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of WSCD1 mRNA	CTD	PMID:29301061
WSCD1	Human	Soman	increases expression	ISO	RGD:1308212	6480464	Soman results in increased expression of WSCD1 mRNA	CTD	PMID:19281266
WSCD1	Human	sulfadimethoxine	increases expression	ISO	RGD:1308212	6480464	Sulfadimethoxine results in increased expression of WSCD1 mRNA	CTD	PMID:30047161
WSCD1	Human	testosterone	increases expression	EXP		6480464	Testosterone results in increased expression of WSCD1 mRNA	CTD	PMID:33359661
WSCD1	Human	testosterone	increases expression	ISO	RGD:1317859	6480464	Testosterone deficiency results in increased expression of WSCD1 mRNA	CTD	PMID:33848595
WSCD1	Human	titanium dioxide	decreases expression	ISO	RGD:1317859	6480464	titanium dioxide results in decreased expression of WSCD1 mRNA	CTD	PMID:23557971
WSCD1	Human	titanium dioxide	increases methylation	ISO	RGD:1317859	6480464	titanium dioxide results in increased methylation of WSCD1 gene	CTD	PMID:35295148
WSCD1	Human	topotecan	multiple interactions	ISO	RGD:1308212	6480464	[oxaliplatin co-treated with Topotecan] results in decreased expression of WSCD1 mRNA	CTD	PMID:25729387
WSCD1	Human	topotecan	decreases expression	ISO	RGD:1308212	6480464	Topotecan results in decreased expression of WSCD1 mRNA	CTD	PMID:25729387
WSCD1	Human	trichostatin A	increases expression	EXP		6480464	trichostatin A results in increased expression of WSCD1 mRNA	CTD	PMID:24935251
WSCD1	Human	trichostatin A	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	trichostatin A	decreases expression	EXP		6480464	trichostatin A results in decreased expression of WSCD1 mRNA	CTD	PMID:24935251\|PMID:26272509
WSCD1	Human	trimellitic anhydride	decreases expression	ISO	RGD:1317859	6480464	trimellitic anhydride results in decreased expression of WSCD1 mRNA	CTD	PMID:19042947
WSCD1	Human	valproic acid	affects expression	ISO	RGD:1317859	6480464	Valproic Acid affects the expression of WSCD1 mRNA	CTD	PMID:17963808
WSCD1	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of WSCD1 mRNA	CTD	PMID:25979313
WSCD1	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of WSCD1 mRNA	CTD	PMID:24935251\|PMID:25716160\|PMID:29154799
WSCD1	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of WSCD1 mRNA	CTD	PMID:23179753\|PMID:26272509
WSCD1	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
WSCD1	Human	vitamin E	decreases expression	EXP		6480464	Vitamin E results in decreased expression of WSCD1 mRNA	CTD	PMID:19244175
WSCD1	Human	zoledronic acid	decreases expression	EXP		6480464	zoledronic acid results in decreased expression of WSCD1 mRNA	CTD	PMID:24714768

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
WSCD1	Human	Golgi apparatus	located_in	IEA	UniProtKB-KW:KW-0333	150520179		UniProt	GO_REF:0000043
WSCD1	Human	Golgi membrane	located_in	ISS	UniProtKB:Q80XH4	150520179		UniProt	GO_REF:0000024
WSCD1	Human	Golgi membrane	located_in	IEA	UniProtKB-SubCell:SL-0134	150520179		UniProt	GO_REF:0000044
WSCD1	Human	Golgi membrane	located_in	IEA	UniProtKB:Q80XH4\|ensembl:ENSMUSP00000104150	150520179		Ensembl	GO_REF:0000107
WSCD1	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
WSCD1	Human	sulfotransferase activity	enables	IEA	InterPro:IPR000863	150520179		InterPro	GO_REF:0000002
WSCD1	Human	sulfotransferase activity	enables	IEA	UniProtKB:Q80XH4\|ensembl:ENSMUSP00000104150	150520179		Ensembl	GO_REF:0000107
WSCD1	Human	sulfotransferase activity	enables	ISS	UniProtKB:Q80XH4	150520179		UniProt	GO_REF:0000024

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:9628581	PMID:12477932	PMID:19460752	PMID:23740775	PMID:25231870

WSCD1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	6,069,116 - 6,124,427 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	6,057,807 - 6,124,427 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	5,972,436 - 6,027,747 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	5,914,658 - 5,968,471 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	5,989,799 - 6,043,603 (+)	NCBI		Celera
Cytogenetic Map	17	p13.2	NCBI
HuRef	17	5,875,040 - 5,919,106 (+)	NCBI		HuRef
CHM1_1	17	5,983,259 - 6,037,060 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	5,963,314 - 6,018,611 (+)	NCBI		T2T-CHM13v2.0

Wscd1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	71,640,719 - 71,680,475 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	71,640,746 - 71,680,473 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	71,749,893 - 71,789,649 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	71,749,920 - 71,789,647 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	71,564,205 - 71,603,149 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	71,566,898 - 71,605,842 (+)	NCBI		MGSCv36	mm8
Celera	11	79,281,706 - 79,320,674 (+)	NCBI		Celera
Cytogenetic Map	11	B4	NCBI
cM Map	11	43.62	NCBI

Wscd1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	56,884,404 - 56,924,013 (+)	NCBI		GRCr8
mRatBN7.2	10	56,385,858 - 56,426,442 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	56,395,874 - 56,424,677 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	61,060,037 - 61,088,751 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	60,548,533 - 60,577,247 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	56,047,592 - 56,076,306 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	58,330,711 - 58,372,966 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	58,332,588 - 58,371,196 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	58,084,069 - 58,112,875 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	58,616,509 - 58,645,325 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	58,630,131 - 58,658,949 (+)	NCBI
Celera	10	55,530,183 - 55,558,989 (+)	NCBI		Celera
Cytogenetic Map	10	q24	NCBI

Wscd1
(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_004955467	11,642,280 - 11,684,265 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955467	11,642,318 - 11,684,265 (+)	NCBI	ChiLan1.0	ChiLan1.0

WSCD1
(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	13,681,558 - 13,737,681 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	15,647,260 - 15,703,647 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	6,119,168 - 6,175,306 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	6,109,432 - 6,165,369 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	6,109,559 - 6,165,369 (+)	Ensembl	panpan1.1		panPan2

WSCD1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	5	30,992,773 - 31,023,526 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	5	30,995,909 - 31,023,536 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	5	31,124,007 - 31,154,807 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	5	31,094,030 - 31,124,869 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	5	31,094,030 - 31,124,880 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	5	31,059,098 - 31,089,543 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	5	31,017,809 - 31,048,589 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	5	31,191,293 - 31,222,141 (-)	NCBI		UU_Cfam_GSD_1.0

Wscd1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405602	54,069,331 - 54,112,108 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936677	1,767,095 - 1,821,175 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936677	1,788,867 - 1,831,584 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

WSCD1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	51,154,478 - 51,196,933 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	51,152,568 - 51,198,302 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	53,228,272 - 53,272,101 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

WSCD1
(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	16	5,452,255 - 5,504,686 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	5,318,532 - 5,507,872 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666059	16,009,823 - 16,063,791 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Wscd1
(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_004624786	7,879,985 - 7,931,906 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624786	7,884,450 - 7,933,275 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in WSCD1
91 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17p13.2-13.1(chr17:5732977-8038822)x1	copy number loss	See cases [RCV000051043]	Chr17:5732977..8038822 [GRCh38] Chr17:5636297..7942140 [GRCh37] Chr17:5577021..7882865 [NCBI36] Chr17:17p13.2-13.1	pathogenic
GRCh38/hg38 17p13.2-13.1(chr17:3601515-7178024)x1	copy number loss	See cases [RCV000053406]	Chr17:3601515..7178024 [GRCh38] Chr17:3504809..7081343 [GRCh37] Chr17:3451558..7022067 [NCBI36] Chr17:17p13.2-13.1	pathogenic
NM_015253.1(WSCD1):c.878G>A (p.Trp293Ter)	single nucleotide variant	Malignant melanoma [RCV000071609]	Chr17:6109635 [GRCh38] Chr17:6012955 [GRCh37] Chr17:5953679 [NCBI36] Chr17:17p13.2	not provided
NM_015253.1(WSCD1):c.1589G>A (p.Arg530Gln)	single nucleotide variant	Malignant melanoma [RCV000071610]	Chr17:6120522 [GRCh38] Chr17:6023842 [GRCh37] Chr17:5964566 [NCBI36] Chr17:17p13.2	not provided
NM_015253.1(WSCD1):c.1590G>A (p.Arg530=)	single nucleotide variant	Malignant melanoma [RCV000071611]	Chr17:6120523 [GRCh38] Chr17:6023843 [GRCh37] Chr17:5964567 [NCBI36] Chr17:17p13.2	not provided
GRCh38/hg38 17p13.3-13.1(chr17:162088-6959050)x1	copy number loss	See cases [RCV000134135]	Chr17:162088..6959050 [GRCh38] Chr17:45835..6862369 [GRCh37] Chr17:11879..6803093 [NCBI36] Chr17:17p13.3-13.1	pathogenic
GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3	copy number gain	See cases [RCV000134851]	Chr17:5732953..12095349 [GRCh38] Chr17:5636273..11998666 [GRCh37] Chr17:5576997..11939391 [NCBI36] Chr17:17p13.2-12	pathogenic
GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1	copy number loss	See cases [RCV000138214]	Chr17:162016..7697012 [GRCh38] Chr17:45835..7600330 [GRCh37] Chr17:11807..7541055 [NCBI36] Chr17:17p13.3-13.1	pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3	copy number gain	See cases [RCV000138531]	Chr17:162016..12343901 [GRCh38] Chr17:45835..12247218 [GRCh37] Chr17:11807..12187943 [NCBI36] Chr17:17p13.3-12	pathogenic
GRCh38/hg38 17p13.2(chr17:5695008-6341442)x1	copy number loss	See cases [RCV000139189]	Chr17:5695008..6341442 [GRCh38] Chr17:5598328..6244762 [GRCh37] Chr17:5539052..6185486 [NCBI36] Chr17:17p13.2	uncertain significance
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	copy number gain	See cases [RCV000142236]	Chr17:150732..14764202 [GRCh38] Chr17:525..14667519 [GRCh37] Chr17:525..14608244 [NCBI36] Chr17:17p13.3-12	pathogenic
GRCh37/hg19 17p13.3-13.1(chr17:1113102-6742486)	copy number gain	See cases [RCV000445679]	Chr17:1113102..6742486 [GRCh37] Chr17:17p13.3-13.1	pathogenic
GRCh37/hg19 17p13.2(chr17:5871307-6472074)x4	copy number gain	See cases [RCV000510263]	Chr17:5871307..6472074 [GRCh37] Chr17:17p13.2	uncertain significance
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3	copy number gain	See cases [RCV000511786]	Chr17:525..15027737 [GRCh37] Chr17:17p13.3-12	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
NM_015253.2(WSCD1):c.731G>A (p.Arg244Gln)	single nucleotide variant	not specified [RCV004281683]	Chr17:6095105 [GRCh38] Chr17:5998425 [GRCh37] Chr17:17p13.2	uncertain significance
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 17p13.3-12(chr17:525-11186432)x3	copy number gain	not provided [RCV000683866]	Chr17:525..11186432 [GRCh37] Chr17:17p13.3-12	pathogenic
GRCh37/hg19 17p13.2(chr17:5725112-6145658)x3	copy number gain	not provided [RCV000683884]	Chr17:5725112..6145658 [GRCh37] Chr17:17p13.2	likely benign
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 17p13.2-13.1(chr17:5892651-6850368)x3	copy number gain	not provided [RCV000751911]	Chr17:5892651..6850368 [GRCh37] Chr17:17p13.2-13.1	uncertain significance
GRCh37/hg19 17p13.2(chr17:5973448-5974332)x1	copy number loss	not provided [RCV000751912]	Chr17:5973448..5974332 [GRCh37] Chr17:17p13.2	benign
GRCh37/hg19 17p13.2(chr17:5973710-5974192)x4	copy number gain	not provided [RCV000751913]	Chr17:5973710..5974192 [GRCh37] Chr17:17p13.2	benign
GRCh37/hg19 17p13.3-13.2(chr17:47546-6287620)	copy number gain	Chromosome 17P13.3, telomeric, duplication syndrome [RCV000767586]	Chr17:47546..6287620 [GRCh37] Chr17:17p13.3-13.2	pathogenic
GRCh37/hg19 17p13.2(chr17:3759126-6128911)x1	copy number loss	not provided [RCV000849625]	Chr17:3759126..6128911 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1022C>T (p.Thr341Ile)	single nucleotide variant	not specified [RCV004685615]	Chr17:6110783 [GRCh38] Chr17:6014103 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.905C>G (p.Pro302Arg)	single nucleotide variant	not specified [RCV004685613]	Chr17:6109662 [GRCh38] Chr17:6012982 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.463G>A (p.Glu155Lys)	single nucleotide variant	not specified [RCV004685614]	Chr17:6088025 [GRCh38] Chr17:5991345 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1660C>T (p.Arg554Trp)	single nucleotide variant	not specified [RCV004292727]	Chr17:6120593 [GRCh38] Chr17:6023913 [GRCh37] Chr17:17p13.2	uncertain significance
GRCh37/hg19 17p13.2(chr17:5783282-6054342)x1	copy number loss	not provided [RCV001829185]	Chr17:5783282..6054342 [GRCh37] Chr17:17p13.2	uncertain significance
NC_000017.10:g.(?_5289526)_(6616652_?)dup	duplication	Developmental and epileptic encephalopathy, 25 [RCV003113887]	Chr17:5289526..6616652 [GRCh37] Chr17:17p13.2-13.1	uncertain significance
NM_015253.2(WSCD1):c.140G>C (p.Arg47Pro)	single nucleotide variant	not specified [RCV004327680]	Chr17:6080798 [GRCh38] Chr17:5984118 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.853T>C (p.Phe285Leu)	single nucleotide variant	not specified [RCV004312241]	Chr17:6109610 [GRCh38] Chr17:6012930 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.312C>A (p.Ser104Arg)	single nucleotide variant	not specified [RCV004318638]	Chr17:6080970 [GRCh38] Chr17:5984290 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1505G>A (p.Arg502Gln)	single nucleotide variant	not specified [RCV004204759]	Chr17:6120438 [GRCh38] Chr17:6023758 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.88G>A (p.Gly30Ser)	single nucleotide variant	not specified [RCV004191509]	Chr17:6080746 [GRCh38] Chr17:5984066 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.307C>T (p.Arg103Trp)	single nucleotide variant	not specified [RCV004144240]	Chr17:6080965 [GRCh38] Chr17:5984285 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1406C>T (p.Ser469Leu)	single nucleotide variant	not specified [RCV004091344]	Chr17:6120339 [GRCh38] Chr17:6023659 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.713C>T (p.Pro238Leu)	single nucleotide variant	not specified [RCV004231268]	Chr17:6090491 [GRCh38] Chr17:5993811 [GRCh37] Chr17:17p13.2	likely benign
NM_015253.2(WSCD1):c.190G>A (p.Val64Met)	single nucleotide variant	not specified [RCV004232257]	Chr17:6080848 [GRCh38] Chr17:5984168 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1600C>T (p.Arg534Cys)	single nucleotide variant	not specified [RCV004157631]	Chr17:6120533 [GRCh38] Chr17:6023853 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.809A>G (p.Asn270Ser)	single nucleotide variant	not specified [RCV004212300]	Chr17:6095183 [GRCh38] Chr17:5998503 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.116G>A (p.Arg39His)	single nucleotide variant	not specified [RCV004141684]	Chr17:6080774 [GRCh38] Chr17:5984094 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1030A>G (p.Arg344Gly)	single nucleotide variant	not specified [RCV004199616]	Chr17:6110791 [GRCh38] Chr17:6014111 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.4G>A (p.Ala2Thr)	single nucleotide variant	not specified [RCV004130211]	Chr17:6080662 [GRCh38] Chr17:5983982 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.5C>A (p.Ala2Asp)	single nucleotide variant	not specified [RCV004130212]	Chr17:6080663 [GRCh38] Chr17:5983983 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1594G>A (p.Gly532Ser)	single nucleotide variant	not specified [RCV004184374]	Chr17:6120527 [GRCh38] Chr17:6023847 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1721C>T (p.Pro574Leu)	single nucleotide variant	not specified [RCV004125401]	Chr17:6120654 [GRCh38] Chr17:6023974 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1639G>A (p.Asp547Asn)	single nucleotide variant	not specified [RCV004086112]	Chr17:6120572 [GRCh38] Chr17:6023892 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1151T>C (p.Phe384Ser)	single nucleotide variant	not specified [RCV004218081]	Chr17:6110912 [GRCh38] Chr17:6014232 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.329G>A (p.Arg110His)	single nucleotide variant	not specified [RCV004149123]	Chr17:6080987 [GRCh38] Chr17:5984307 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1471G>A (p.Glu491Lys)	single nucleotide variant	not specified [RCV004165364]	Chr17:6120404 [GRCh38] Chr17:6023724 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.830C>T (p.Ser277Leu)	single nucleotide variant	not specified [RCV004140749]	Chr17:6095204 [GRCh38] Chr17:5998524 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.182C>T (p.Ala61Val)	single nucleotide variant	not specified [RCV004244052]	Chr17:6080840 [GRCh38] Chr17:5984160 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.356A>G (p.His119Arg)	single nucleotide variant	not specified [RCV004107116]	Chr17:6081014 [GRCh38] Chr17:5984334 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.425G>A (p.Arg142Gln)	single nucleotide variant	not specified [RCV004197040]	Chr17:6081083 [GRCh38] Chr17:5984403 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1601G>A (p.Arg534His)	single nucleotide variant	not specified [RCV004185858]	Chr17:6120534 [GRCh38] Chr17:6023854 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.502A>G (p.Lys168Glu)	single nucleotide variant	not specified [RCV004097908]	Chr17:6088064 [GRCh38] Chr17:5991384 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.919C>T (p.Arg307Trp)	single nucleotide variant	not specified [RCV004197740]	Chr17:6109676 [GRCh38] Chr17:6012996 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1273A>G (p.Ile425Val)	single nucleotide variant	not specified [RCV004170025]	Chr17:6118086 [GRCh38] Chr17:6021406 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1682G>A (p.Arg561His)	single nucleotide variant	not specified [RCV004081458]	Chr17:6120615 [GRCh38] Chr17:6023935 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.298C>T (p.Arg100Cys)	single nucleotide variant	not specified [RCV004284991]	Chr17:6080956 [GRCh38] Chr17:5984276 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1358G>A (p.Arg453His)	single nucleotide variant	not specified [RCV004272774]	Chr17:6118171 [GRCh38] Chr17:6021491 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1211G>A (p.Arg404His)	single nucleotide variant	not specified [RCV004262541]	Chr17:6118024 [GRCh38] Chr17:6021344 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1286G>A (p.Arg429Gln)	single nucleotide variant	not specified [RCV004273882]	Chr17:6118099 [GRCh38] Chr17:6021419 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1634T>C (p.Met545Thr)	single nucleotide variant	not specified [RCV004280702]	Chr17:6120567 [GRCh38] Chr17:6023887 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1481G>A (p.Arg494Gln)	single nucleotide variant	not specified [RCV004259474]	Chr17:6120414 [GRCh38] Chr17:6023734 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.953A>G (p.Asp318Gly)	single nucleotide variant	not specified [RCV004259045]	Chr17:6109710 [GRCh38] Chr17:6013030 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1216A>G (p.Ile406Val)	single nucleotide variant	not specified [RCV004287415]	Chr17:6118029 [GRCh38] Chr17:6021349 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.331C>A (p.Gln111Lys)	single nucleotide variant	not specified [RCV004260043]	Chr17:6080989 [GRCh38] Chr17:5984309 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.887A>T (p.Tyr296Phe)	single nucleotide variant	not specified [RCV004268642]	Chr17:6109644 [GRCh38] Chr17:6012964 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1576G>A (p.Gly526Ser)	single nucleotide variant	not specified [RCV004685612]	Chr17:6120509 [GRCh38] Chr17:6023829 [GRCh37] Chr17:17p13.2	uncertain significance
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3	copy number gain	Chromosome 17p13.3 duplication syndrome [RCV003327726]	Chr17:165730..11404096 [GRCh38] Chr17:17p13.3-12	pathogenic
NM_015253.2(WSCD1):c.1201C>T (p.Arg401Trp)	single nucleotide variant	not specified [RCV004350477]	Chr17:6118014 [GRCh38] Chr17:6021334 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.922G>A (p.Asp308Asn)	single nucleotide variant	not specified [RCV004359235]	Chr17:6109679 [GRCh38] Chr17:6012999 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.908G>A (p.Arg303Gln)	single nucleotide variant	not specified [RCV004341993]	Chr17:6109665 [GRCh38] Chr17:6012985 [GRCh37] Chr17:17p13.2	likely benign
NM_015253.2(WSCD1):c.588C>T (p.Cys196=)	single nucleotide variant	not provided [RCV003419595]	Chr17:6090366 [GRCh38] Chr17:5993686 [GRCh37] Chr17:17p13.2	likely benign
GRCh37/hg19 17p13.2(chr17:5692922-6101185)x3	copy number gain	not provided [RCV003485143]	Chr17:5692922..6101185 [GRCh37] Chr17:17p13.2	uncertain significance
NM_001388405.1(WSCD1):c.-289+64G>A	single nucleotide variant	not provided [RCV003428085]	Chr17:6069271 [GRCh38] Chr17:5972591 [GRCh37] Chr17:17p13.2	likely benign
NM_015253.2(WSCD1):c.558C>T (p.Ala186=)	single nucleotide variant	not provided [RCV003419594]	Chr17:6090336 [GRCh38] Chr17:5993656 [GRCh37] Chr17:17p13.2	likely benign
GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1	copy number loss	not specified [RCV003987214]	Chr17:9474..6017500 [GRCh37] Chr17:17p13.3-13.2	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
NM_015253.2(WSCD1):c.1100C>T (p.Ala367Val)	single nucleotide variant	not specified [RCV004483223]	Chr17:6110861 [GRCh38] Chr17:6014181 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1357C>T (p.Arg453Cys)	single nucleotide variant	not specified [RCV004483224]	Chr17:6118170 [GRCh38] Chr17:6021490 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1586G>A (p.Arg529Gln)	single nucleotide variant	not specified [RCV004483225]	Chr17:6120519 [GRCh38] Chr17:6023839 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.169G>A (p.Val57Met)	single nucleotide variant	not specified [RCV004483226]	Chr17:6080827 [GRCh38] Chr17:5984147 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.259A>G (p.Met87Val)	single nucleotide variant	not specified [RCV004483228]	Chr17:6080917 [GRCh38] Chr17:5984237 [GRCh37] Chr17:17p13.2	likely benign
NM_015253.2(WSCD1):c.308G>A (p.Arg103Gln)	single nucleotide variant	not specified [RCV004483229]	Chr17:6080966 [GRCh38] Chr17:5984286 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.397G>A (p.Glu133Lys)	single nucleotide variant	not specified [RCV004483230]	Chr17:6081055 [GRCh38] Chr17:5984375 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.41G>A (p.Arg14Gln)	single nucleotide variant	not specified [RCV004483231]	Chr17:6080699 [GRCh38] Chr17:5984019 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.694C>T (p.Arg232Cys)	single nucleotide variant	not specified [RCV004483232]	Chr17:6090472 [GRCh38] Chr17:5993792 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.736G>A (p.Ala246Thr)	single nucleotide variant	not specified [RCV004483233]	Chr17:6095110 [GRCh38] Chr17:5998430 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.740C>T (p.Thr247Ile)	single nucleotide variant	not specified [RCV004483234]	Chr17:6095114 [GRCh38] Chr17:5998434 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.761T>C (p.Leu254Pro)	single nucleotide variant	not specified [RCV004483235]	Chr17:6095135 [GRCh38] Chr17:5998455 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.907C>T (p.Arg303Trp)	single nucleotide variant	not specified [RCV004483236]	Chr17:6109664 [GRCh38] Chr17:6012984 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.157C>A (p.Gln53Lys)	single nucleotide variant	not specified [RCV004685609]	Chr17:6080815 [GRCh38] Chr17:5984135 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1592G>A (p.Arg531His)	single nucleotide variant	not specified [RCV004685610]	Chr17:6120525 [GRCh38] Chr17:6023845 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1588C>T (p.Arg530Trp)	single nucleotide variant	not specified [RCV004688795]	Chr17:6120521 [GRCh38] Chr17:6023841 [GRCh37] Chr17:17p13.2	uncertain significance
NC_000017.10:g.(?_422368)_(8285628_?)dup	duplication	not provided [RCV004581443]	Chr17:422368..8285628 [GRCh37] Chr17:17p13.3-13.1	uncertain significance
NM_015253.2(WSCD1):c.611G>A (p.Ser204Asn)	single nucleotide variant	not specified [RCV004685611]	Chr17:6090389 [GRCh38] Chr17:5993709 [GRCh37] Chr17:17p13.2	uncertain significance
GRCh37/hg19 17p13.2-12(chr17:4678235-14745263)x3	copy number gain	not provided [RCV004819316]	Chr17:4678235..14745263 [GRCh37] Chr17:17p13.2-12	pathogenic
NM_015253.2(WSCD1):c.1591C>T (p.Arg531Cys)	single nucleotide variant	not specified [RCV004890690]	Chr17:6120524 [GRCh38] Chr17:6023844 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.556G>A (p.Ala186Thr)	single nucleotide variant	not specified [RCV004890691]	Chr17:6090334 [GRCh38] Chr17:5993654 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1495C>T (p.Pro499Ser)	single nucleotide variant	not specified [RCV004890692]	Chr17:6120428 [GRCh38] Chr17:6023748 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.188G>T (p.Gly63Val)	single nucleotide variant	not specified [RCV004890693]	Chr17:6080846 [GRCh38] Chr17:5984166 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1423G>T (p.Val475Phe)	single nucleotide variant	not specified [RCV004890694]	Chr17:6120356 [GRCh38] Chr17:6023676 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.148G>A (p.Gly50Ser)	single nucleotide variant	not specified [RCV004880043]	Chr17:6080806 [GRCh38] Chr17:5984126 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.817G>A (p.Val273Met)	single nucleotide variant	not specified [RCV004880044]	Chr17:6095191 [GRCh38] Chr17:5998511 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1528G>A (p.Val510Met)	single nucleotide variant	not specified [RCV004880045]	Chr17:6120461 [GRCh38] Chr17:6023781 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1451G>A (p.Arg484Gln)	single nucleotide variant	not specified [RCV004880046]	Chr17:6120384 [GRCh38] Chr17:6023704 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1540G>A (p.Glu514Lys)	single nucleotide variant	not specified [RCV004880047]	Chr17:6120473 [GRCh38] Chr17:6023793 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.658T>C (p.Ser220Pro)	single nucleotide variant	not specified [RCV004880048]	Chr17:6090436 [GRCh38] Chr17:5993756 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.527A>T (p.Asp176Val)	single nucleotide variant	not specified [RCV004880049]	Chr17:6088089 [GRCh38] Chr17:5991409 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1415C>T (p.Ser472Phe)	single nucleotide variant	not specified [RCV004880050]	Chr17:6120348 [GRCh38] Chr17:6023668 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.904C>G (p.Pro302Ala)	single nucleotide variant	not specified [RCV004880051]	Chr17:6109661 [GRCh38] Chr17:6012981 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.1195C>T (p.His399Tyr)	single nucleotide variant	not specified [RCV004880052]	Chr17:6118008 [GRCh38] Chr17:6021328 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.832G>A (p.Gly278Ser)	single nucleotide variant	not specified [RCV004890689]	Chr17:6095206 [GRCh38] Chr17:5998526 [GRCh37] Chr17:17p13.2	uncertain significance
NM_015253.2(WSCD1):c.343C>A (p.Arg115Ser)	single nucleotide variant	not specified [RCV004890688]	Chr17:6081001 [GRCh38] Chr17:5984321 [GRCh37] Chr17:17p13.2	uncertain significance
GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3	copy number gain	See cases [RCV000134970]	Chr17:198748..7491129 [GRCh38] Chr17:50690..7394448 [GRCh37] Chr17:48539..7335172 [NCBI36] Chr17:17p13.3-13.1	pathogenic
NM_015253.2(WSCD1):c.286C>T (p.Arg96Trp)	single nucleotide variant	not specified [RCV004337632]	Chr17:6080944 [GRCh38] Chr17:5984264 [GRCh37] Chr17:17p13.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	7566
Count of miRNA genes:	1322
Interacting mature miRNAs:	1740
Transcripts:	ENST00000317744, ENST00000539421, ENST00000563763, ENST00000571494, ENST00000571973, ENST00000572764, ENST00000573619, ENST00000573634, ENST00000574232, ENST00000574946, ENST00000576083, ENST00000576233, ENST00000576947
Prediction methods:	Microtar, Miranda, Pita, Rnahybrid, Targetscan
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597434028	GWAS1530102_H	protein measurement QTL GWAS1530102 (human)		1e-17	protein measurement		17	6070542	6070543	Human

D17S1832

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	5,972,677 - 5,972,867	UniSTS	GRCh37
Build 36	17	5,913,401 - 5,913,591	RGD	NCBI36
Celera	17	5,988,550 - 5,988,738	RGD
Cytogenetic Map	17	p13.2	UniSTS
HuRef	17	5,863,800 - 5,863,988	UniSTS
Marshfield Genetic Map	17	13.07	UniSTS
Marshfield Genetic Map	17	13.07	RGD
Genethon Genetic Map	17	13.0	UniSTS
Whitehead-YAC Contig Map	17		UniSTS
GeneMap99-G3 RH Map	17	349.0	UniSTS

SHGC-150915

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	5,972,629 - 5,972,909	UniSTS	GRCh37
Build 36	17	5,913,353 - 5,913,633	RGD	NCBI36
Celera	17	5,988,502 - 5,988,780	RGD
Cytogenetic Map	17	p13.2	UniSTS
HuRef	17	5,863,752 - 5,864,030	UniSTS
TNG Radiation Hybrid Map	17	3167.0	UniSTS
TNG Radiation Hybrid Map	14	12682.0	UniSTS

D17S1414E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	6,027,526 - 6,027,635	UniSTS	GRCh37
Build 36	17	5,968,250 - 5,968,359	RGD	NCBI36
Celera	17	6,043,382 - 6,043,491	RGD
Cytogenetic Map	17	p13.2	UniSTS
HuRef	17	5,918,885 - 5,918,994	UniSTS
GeneMap99-GB4 RH Map	17	46.33	UniSTS
NCBI RH Map	17	102.8	UniSTS

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2403	2788	2234	4926	1719	2317	4	618	1503	459	2241	6825	6024	40	3709	843	1718	1587	172	1


RefSeq Transcripts	NM_001388405	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388407	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388408	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388409	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001388411	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_015253	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005256572	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435702	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB011095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC001231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104770	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK000243	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289603	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL833730	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC009975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BE504506	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471108	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000317744 ⟹ ENSP00000323087

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,070,379 - 6,124,427 (+)	Ensembl

Ensembl Acc Id:

ENST00000539421 ⟹ ENSP00000446032

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,071,108 - 6,121,300 (+)	Ensembl

Ensembl Acc Id:

ENST00000571494 ⟹ ENSP00000458339

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,080,659 - 6,121,301 (+)	Ensembl

Ensembl Acc Id:

ENST00000571973 ⟹ ENSP00000458527

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,077,950 - 6,124,427 (+)	Ensembl

Ensembl Acc Id:

ENST00000572764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,057,807 - 6,080,649 (+)	Ensembl

Ensembl Acc Id:

ENST00000573634 ⟹ ENSP00000460396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,069,117 - 6,120,738 (+)	Ensembl

Ensembl Acc Id:

ENST00000574232 ⟹ ENSP00000458374

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,071,108 - 6,120,710 (+)	Ensembl

Ensembl Acc Id:

ENST00000574946 ⟹ ENSP00000460825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,069,106 - 6,124,427 (+)	Ensembl

Ensembl Acc Id:

ENST00000576083 ⟹ ENSP00000460041

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,070,424 - 6,088,104 (+)	Ensembl

Ensembl Acc Id:

ENST00000576233 ⟹ ENSP00000461642

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,080,147 - 6,124,427 (+)	Ensembl

Ensembl Acc Id:

ENST00000576947 ⟹ ENSP00000460428

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,081,882 - 6,090,361 (+)	Ensembl

Ensembl Acc Id:

ENST00000714059 ⟹ ENSP00000519349

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,069,115 - 6,123,265 (+)	Ensembl

Ensembl Acc Id:

ENST00000714060 ⟹ ENSP00000519350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	6,070,912 - 6,124,426 (+)	Ensembl

RefSeq Acc Id:

NM_001388405 ⟹ NP_001375334

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,069,116 - 6,124,427 (+)	NCBI
T2T-CHM13v2.0	17	5,963,314 - 6,018,611 (+)	NCBI

Sequence:

show sequence

CTTTTAGGAAGACGGAGTAAGAGGCACCACCACCTGCTCCTGCTGCCTCTGCTGTCCTCAGCTTCTGGGAGCATCTTAGCAGCCAGCTCCGGATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCCT
GGAATGGAGATGTCCTTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGGC
GAGCACAGGCAGGTGCCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATGG
CCAAACCTTTCTTCCGACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACAG
GGCCCCCGGGCACCCGGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACAT
GCTGCAGAGCCCCCTGACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCCC
TGGGCCCCGAGGCTGCCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCC
CACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAA
AGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACA
TCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCAGGGGCTGGGAATGCTACTGTGCTTACCCT
ACCCCCCGGTTCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACACCTGTGCAAGACACTCGTTGTACAGACAG
GAGGTTCCTGCCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGGCTTCTATACAGGGAGCTACTACTTTGATG
GAACCCTCTACAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTGAGATGTTTGATTCAGCCATCCTGCTAATC
CGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCGGACTTTGTCAACAGCTACGCCTCGTGGTG
GTCCTCGCACGTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGATGGTGGCCTTCCTCAACGTGTCTGTGAGCG
AGGAGCGGCTGCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAGACTTGATCAATGGCTACATCCGGACGGTG
GACCAAGCCCTGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCAATCGCACCACGGGGCTGCGCTCCCCACTC
TGATGCTCAGGCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACACATCACAAGGCGAACACAAATGGACACACA
TACCTGGCCACGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCAGGCACCCCCAGATACAAATGCAGCCACGC
ACAGACGTAACACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCCCTGGGCTTCCTGTGTGTAGCCCTGGCATA
GACTTGCTCGTCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGACTGCTGCTTCCAGGGTGTGCGGCCCTGGCC
GTGTGTCTGACATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCACCATGGGCAGGGTTGAGGACTGCCCCCCAC
CCCGCCCAAGCCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGGGCCTGGGGCCTCCTTGCCTGGCTTCTTCC
TCCAGCTATCCTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGGGGAGCCCAGGACCCCTGGGGACCTGTACA
CTAGCAGGATGGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTCTCTGGGGTCCCACACTGGGGTCATGAGAG
CTAGTTAGTACTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGAGGCCAGGAGGTTCAAGTATGGAGGGTAGG
AGTGCAACCCAGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAAGGTGGGTGGGCCTGAACTCAGGCAGCCCT
TCAGTGGCTTCTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTGCATTGGGAGGAGAAGGCAGGGTGAGGGAT
CTGGGAGAGCAGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAAGGCCCAGTAGAGCTGCCCTTCCCCAGATG
GAAGCTTCCTCCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACACTGATGCGAAGCTGTTCTTGACCCTCCCAT
AGCATCAACTCAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTGATGGAGCTATTTCTTCCTAGTATCAGGAG
CAATTGAGACCCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAGGCGTGGCAGTGGGGAAGCCATGGAGGCTG
GGAAGGGCAAAGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATTCACTGCTGCCAGGTACCCAGAGATGTCAT
CTCTCTCCAGGTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCATCCAGTTTACGCTGAGTCAGTCCATACAG
CAAGACACCTGGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAGGTCTGCCTACGTGGGAGATCTCATCAGAA
ACAGGAACGGGGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATACTCTCCCAACCAGCCAAGGAATAAAAGCTG
ATCTGTATGTAGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAGCCTGTGGAGTTACACAAACCTGTGTTAAA
ACATGTAATTTTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAGTGATGTGTAAATGAGAGAGAAGAATAGAC
AGGCTTCCAAACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTGATAATGTTTGCATATCAGAATGCATTCTC
CCCTTAAAAGTAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACACAGGTTTGTTTTCTGCTGACTTGCTCGGAA
ACCCATTGGAGGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATATTGGGTGAGTTGGTCTGAACAAGGTGGGG
ATAAAGTAGAGTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCCAGTCTCAGTTTCCCATCCATAAAATGGGG
GAAGTGGTAGGTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAGCCTCTCCAGGGGTGGAATACATGTCCTGG
ACTAAGCCAATGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTTATGGGAATGCTGGGTAGAAGCTGTTTTAA
TTCCCCTGTTGAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACACCACTGAAGGGAGAGTTGAGAGGCAGAAA
GAGATCAAGTCCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATTCTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

NM_001388406 ⟹ NP_001375335

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,071,095 - 6,124,427 (+)	NCBI
T2T-CHM13v2.0	17	5,965,296 - 6,018,611 (+)	NCBI

Sequence:

show sequence

AAGAGAGGCTTCCGGTCAGCGGAGGGTTTGCTCCGTCTCTTGGTGAACTTGAACAGAGGCAGAGGCAAAAGCAAAACATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCCTGGAATGGAGATGTCC
TTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGGCGAGCACAGGCAGGTG
CCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATGGCCAAACCTTTCTTCC
GACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACAGGGCCCCCGGGCACCC
GGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACATGCTGCAGAGCCCCCT
GACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCCCTGGGCCCCGAGGCTG
CCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGGATGCG
TGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTC
TGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGCCTTCC
CCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCAGGGGCTGGGAATGCTACTGTGCTTACCCTACCCCCCGGTTCAAC
CTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACACCTGTGCAAGACACTCGTTGTACAGACAGGAGGTTCCTGCCTAA
CAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGGCTTCTATACAGGGAGCTACTACTTTGATGGAACCCTCTACAACA
AAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTGAGATGTTTGATTCAGCCATCCTGCTAATCCGGAACCCATACAGG
TCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCGGACTTTGTCAACAGCTACGCCTCGTGGTGGTCCTCGCACGTCCT
GGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGATGGTGGCCTTCCTCAACGTGTCTGTGAGCGAGGAGCGGCTGCTCT
GCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAGACTTGATCAATGGCTACATCCGGACGGTGGACCAAGCCCTGCGT
GACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCAATCGCACCACGGGGCTGCGCTCCCCACTCTGATGCTCAGGCCCG
TGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACACATCACAAGGCGAACACAAATGGACACACATACCTGGCCACGAAC
CCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCAGGCACCCCCAGATACAAATGCAGCCACGCACAGACGTAACACAC
AGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCCCTGGGCTTCCTGTGTGTAGCCCTGGCATAGACTTGCTCGTCAGG
GTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGACTGCTGCTTCCAGGGTGTGCGGCCCTGGCCGTGTGTCTGACATCC
CATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCACCATGGGCAGGGTTGAGGACTGCCCCCCACCCCGCCCAAGCCAAT
GCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGGGCCTGGGGCCTCCTTGCCTGGCTTCTTCCTCCAGCTATCCTCAG
GGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGGGGAGCCCAGGACCCCTGGGGACCTGTACACTAGCAGGATGGGTC
TTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTCTCTGGGGTCCCACACTGGGGTCATGAGAGCTAGTTAGTACTCAG
CCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGAGGCCAGGAGGTTCAAGTATGGAGGGTAGGAGTGCAACCCAGGAG
CAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAAGGTGGGTGGGCCTGAACTCAGGCAGCCCTTCAGTGGCTTCTTCA
GGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTGCATTGGGAGGAGAAGGCAGGGTGAGGGATCTGGGAGAGCAGGAC
GTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAAGGCCCAGTAGAGCTGCCCTTCCCCAGATGGAAGCTTCCTCCAAC
CTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACACTGATGCGAAGCTGTTCTTGACCCTCCCATAGCATCAACTCAGTT
CAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTGATGGAGCTATTTCTTCCTAGTATCAGGAGCAATTGAGACCCCTC
AGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAGGCGTGGCAGTGGGGAAGCCATGGAGGCTGGGAAGGGCAAAGTGT
GGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATTCACTGCTGCCAGGTACCCAGAGATGTCATCTCTCTCCAGGTAGA
GCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCATCCAGTTTACGCTGAGTCAGTCCATACAGCAAGACACCTGGCAC
TTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAGGTCTGCCTACGTGGGAGATCTCATCAGAAACAGGAACGGGGATC
TGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATACTCTCCCAACCAGCCAAGGAATAAAAGCTGATCTGTATGTAGGGC
AGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAGCCTGTGGAGTTACACAAACCTGTGTTAAAACATGTAATTTTTAT
GGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAGTGATGTGTAAATGAGAGAGAAGAATAGACAGGCTTCCAAACCCT
GGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTGATAATGTTTGCATATCAGAATGCATTCTCCCCTTAAAAGTAGCA
GTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACACAGGTTTGTTTTCTGCTGACTTGCTCGGAAACCCATTGGAGGTAT
CTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATATTGGGTGAGTTGGTCTGAACAAGGTGGGGATAAAGTAGAGTGGA
AATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCCAGTCTCAGTTTCCCATCCATAAAATGGGGGAAGTGGTAGGTCTT
GCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAGCCTCTCCAGGGGTGGAATACATGTCCTGGACTAAGCCAATGACA
CCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTTATGGGAATGCTGGGTAGAAGCTGTTTTAATTCCCCTGTTGAATG
TGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACACCACTGAAGGGAGAGTTGAGAGGCAGAAAGAGATCAAGTCCTTG
GTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATTCTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

NM_001388407 ⟹ NP_001375336

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,379 - 6,124,427 (+)	NCBI
T2T-CHM13v2.0	17	5,964,580 - 6,018,611 (+)	NCBI

Sequence:

show sequence

GCAGAGCCCGGCGCCCGCTCGCCCGCCCGCTGCCCGCCCCGGCTCCGCGCCCGCCCGCCCGCCCCGCCGTTCAGCCCGGACGCCAGCAGCCCCGGGGAGCCAGGCGGCGGCGCCCTGTGCCCGGGCGC
GTGGGTCCGCTTGCCGCGGGCGGCCGGAGACGTGCGGGCGCCGGGGCTTCTGGGCTCCGGGCACTGCGGGGGGCTGCGGGCTCGGCGCCCGGGGAAGGCGGGCCATGGGCGCGGGTGCGGGCGCCCCA
GCCGGCCGCGATCGCGGGGTGAGTCCTGTCTCTCGGCGCTCCAGCCGGACCCCCGCGCGGGCTGCGAGCAGGGTGTTCCCCTTGCCGCGGGCAAACAAGTTTGTGCAGACGCGGTTGGGAGCGCGGCG
GGGCTGCACCTGCTCCGGCTGCAGGGCGGGCTTGCCGGGGGCACCTTCCCGGGGGCCCGGGGCGGCTCGGCCGGGGCAGGGGAGAGTGAGCGGATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCC
TGGAATGGAGATGTCCTTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGG
CGAGCACAGGCAGGTGCCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATG
GCCAAACCTTTCTTCCGACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACA
GGGCCCCCGGGCACCCGGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACA
TGCTGCAGAGCCCCCTGACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCC
CTGGGCCCCGAGGCTGCCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTC
CCACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCA
AAGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAAC
ATCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCAGGGGCTGGGAATGCTACTGTGCTTACCC
TACCCCCCGGTTCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACACCTGTGCAAGACACTCGTTGTACAGACA
GGAGGTTCCTGCCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGGCTTCTATACAGGGAGCTACTACTTTGAT
GGAACCCTCTACAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTGAGATGTTTGATTCAGCCATCCTGCTAAT
CCGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCGGACTTTGTCAACAGCTACGCCTCGTGGT
GGTCCTCGCACGTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGATGGTGGCCTTCCTCAACGTGTCTGTGAGC
GAGGAGCGGCTGCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAGACTTGATCAATGGCTACATCCGGACGGT
GGACCAAGCCCTGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCAATCGCACCACGGGGCTGCGCTCCCCACT
CTGATGCTCAGGCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACACATCACAAGGCGAACACAAATGGACACAC
ATACCTGGCCACGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCAGGCACCCCCAGATACAAATGCAGCCACG
CACAGACGTAACACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCCCTGGGCTTCCTGTGTGTAGCCCTGGCAT
AGACTTGCTCGTCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGACTGCTGCTTCCAGGGTGTGCGGCCCTGGC
CGTGTGTCTGACATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCACCATGGGCAGGGTTGAGGACTGCCCCCCA
CCCCGCCCAAGCCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGGGCCTGGGGCCTCCTTGCCTGGCTTCTTC
CTCCAGCTATCCTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGGGGAGCCCAGGACCCCTGGGGACCTGTAC
ACTAGCAGGATGGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTCTCTGGGGTCCCACACTGGGGTCATGAGA
GCTAGTTAGTACTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGAGGCCAGGAGGTTCAAGTATGGAGGGTAG
GAGTGCAACCCAGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAAGGTGGGTGGGCCTGAACTCAGGCAGCCC
TTCAGTGGCTTCTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTGCATTGGGAGGAGAAGGCAGGGTGAGGGA
TCTGGGAGAGCAGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAAGGCCCAGTAGAGCTGCCCTTCCCCAGAT
GGAAGCTTCCTCCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACACTGATGCGAAGCTGTTCTTGACCCTCCCA
TAGCATCAACTCAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTGATGGAGCTATTTCTTCCTAGTATCAGGA
GCAATTGAGACCCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAGGCGTGGCAGTGGGGAAGCCATGGAGGCT
GGGAAGGGCAAAGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATTCACTGCTGCCAGGTACCCAGAGATGTCA
TCTCTCTCCAGGTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCATCCAGTTTACGCTGAGTCAGTCCATACA
GCAAGACACCTGGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAGGTCTGCCTACGTGGGAGATCTCATCAGA
AACAGGAACGGGGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATACTCTCCCAACCAGCCAAGGAATAAAAGCT
GATCTGTATGTAGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAGCCTGTGGAGTTACACAAACCTGTGTTAA
AACATGTAATTTTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAGTGATGTGTAAATGAGAGAGAAGAATAGA
CAGGCTTCCAAACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTGATAATGTTTGCATATCAGAATGCATTCT
CCCCTTAAAAGTAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACACAGGTTTGTTTTCTGCTGACTTGCTCGGA
AACCCATTGGAGGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATATTGGGTGAGTTGGTCTGAACAAGGTGGG
GATAAAGTAGAGTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCCAGTCTCAGTTTCCCATCCATAAAATGGG
GGAAGTGGTAGGTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAGCCTCTCCAGGGGTGGAATACATGTCCTG
GACTAAGCCAATGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTTATGGGAATGCTGGGTAGAAGCTGTTTTA
ATTCCCCTGTTGAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACACCACTGAAGGGAGAGTTGAGAGGCAGAA
AGAGATCAAGTCCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATTCTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

NM_001388408 ⟹ NP_001375337

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,069,116 - 6,124,427 (+)	NCBI
T2T-CHM13v2.0	17	5,963,314 - 6,018,611 (+)	NCBI

Sequence:

show sequence

CTTTTAGGAAGACGGAGTAAGAGGCACCACCACCTGCTCCTGCTGCCTCTGCTGTCCTCAGCTTCTGGGAGCATCTTAGCAGCCAGCTCCGGGTGAGGACAGGGTCCACCGGTGCACATGGCAGAGCA
GGGCAGATGCTGTGACTTGGCGGCTTTGGGGGAACAGGGTGGGGCTCCTCCCTGGGAAAAATCTTTAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGT
TTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTG
GGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTA
CCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCA
GGGGCTGGGAATGCTACTGTGCTTACCCTACCCCCCGGTTCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACA
CCTGTGCAAGACACTCGTTGTACAGACAGGAGGTTCCTGCCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGG
CTTCTATACAGGGAGCTACTACTTTGATGGAACCCTCTACAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTG
AGATGTTTGATTCAGCCATCCTGCTAATCCGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCG
GACTTTGTCAACAGCTACGCCTCGTGGTGGTCCTCGCACGTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGAT
GGTGGCCTTCCTCAACGTGTCTGTGAGCGAGGAGCGGCTGCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAG
ACTTGATCAATGGCTACATCCGGACGGTGGACCAAGCCCTGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCA
ATCGCACCACGGGGCTGCGCTCCCCACTCTGATGCTCAGGCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACAC
ATCACAAGGCGAACACAAATGGACACACATACCTGGCCACGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCA
GGCACCCCCAGATACAAATGCAGCCACGCACAGACGTAACACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCC
CTGGGCTTCCTGTGTGTAGCCCTGGCATAGACTTGCTCGTCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGAC
TGCTGCTTCCAGGGTGTGCGGCCCTGGCCGTGTGTCTGACATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCAC
CATGGGCAGGGTTGAGGACTGCCCCCCACCCCGCCCAAGCCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGG
GCCTGGGGCCTCCTTGCCTGGCTTCTTCCTCCAGCTATCCTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGG
GGAGCCCAGGACCCCTGGGGACCTGTACACTAGCAGGATGGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTC
TCTGGGGTCCCACACTGGGGTCATGAGAGCTAGTTAGTACTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGA
GGCCAGGAGGTTCAAGTATGGAGGGTAGGAGTGCAACCCAGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAA
GGTGGGTGGGCCTGAACTCAGGCAGCCCTTCAGTGGCTTCTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTG
CATTGGGAGGAGAAGGCAGGGTGAGGGATCTGGGAGAGCAGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAA
GGCCCAGTAGAGCTGCCCTTCCCCAGATGGAAGCTTCCTCCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACAC
TGATGCGAAGCTGTTCTTGACCCTCCCATAGCATCAACTCAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTG
ATGGAGCTATTTCTTCCTAGTATCAGGAGCAATTGAGACCCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAG
GCGTGGCAGTGGGGAAGCCATGGAGGCTGGGAAGGGCAAAGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATT
CACTGCTGCCAGGTACCCAGAGATGTCATCTCTCTCCAGGTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCA
TCCAGTTTACGCTGAGTCAGTCCATACAGCAAGACACCTGGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAG
GTCTGCCTACGTGGGAGATCTCATCAGAAACAGGAACGGGGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATAC
TCTCCCAACCAGCCAAGGAATAAAAGCTGATCTGTATGTAGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAG
CCTGTGGAGTTACACAAACCTGTGTTAAAACATGTAATTTTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAG
TGATGTGTAAATGAGAGAGAAGAATAGACAGGCTTCCAAACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTG
ATAATGTTTGCATATCAGAATGCATTCTCCCCTTAAAAGTAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACAC
AGGTTTGTTTTCTGCTGACTTGCTCGGAAACCCATTGGAGGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATA
TTGGGTGAGTTGGTCTGAACAAGGTGGGGATAAAGTAGAGTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCC
AGTCTCAGTTTCCCATCCATAAAATGGGGGAAGTGGTAGGTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAG
CCTCTCCAGGGGTGGAATACATGTCCTGGACTAAGCCAATGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTT
ATGGGAATGCTGGGTAGAAGCTGTTTTAATTCCCCTGTTGAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACA
CCACTGAAGGGAGAGTTGAGAGGCAGAAAGAGATCAAGTCCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATT
CTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

NM_001388409 ⟹ NP_001375338

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,379 - 6,124,427 (+)	NCBI
T2T-CHM13v2.0	17	5,964,580 - 6,018,611 (+)	NCBI

Sequence:

show sequence

GCAGAGCCCGGCGCCCGCTCGCCCGCCCGCTGCCCGCCCCGGCTCCGCGCCCGCCCGCCCGCCC
CGCCGTTCAGCCCGGACGCCAGCAGCCCCGGGGAGCCAGGCGGCGGCGCCCTGTGCCCGGGCGCGTGGGTCCGCTTGCCGCGGGCGGCCGGAGACGTGCGGGCGCCGGGGCTTCTGGGCTCCGGGCAC
TGCGGGGGGCTGCGGGCTCGGCGCCCGGGGAAGGCGGGCCATGGGCGCGGGTGCGGGCGCCCCAGCCGGCCGCGATCGCGGGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCT
GAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGC
CAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGG
CGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCC
CTTGGCCATTCTCAGGGGCTGGGAATGCTACTGTGCTTACCCTACCCCCCGGTTCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTG
AGGTCTACCAGACACCTGTGCAAGACACTCGTTGTACAGACAGGAGGTTCCTGCCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATT
GAGCATGCCACTGGCTTCTATACAGGGAGCTACTACTTTGATGGAACCCTCTACAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGG
CAGGAGGGAGATTGAGATGTTTGATTCAGCCATCCTGCTAATCCGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGA
GCAAAGAGTGGCCGGACTTTGTCAACAGCTACGCCTCGTGGTGGTCCTCGCACGTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCC
ACGTTACGGGAGATGGTGGCCTTCCTCAACGTGTCTGTGAGCGAGGAGCGGCTGCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCAC
CCCGGAGATGAAAGACTTGATCAATGGCTACATCCGGACGGTGGACCAAGCCCTGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCC
CGCTGAGTGACGCAATCGCACCACGGGGCTGCGCTCCCCACTCTGATGCTCAGGCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGA
CACAACAGACACACATCACAAGGCGAACACAAATGGACACACATACCTGGCCACGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCA
CGTGGGGTGTGCCAGGCACCCCCAGATACAAATGCAGCCACGCACAGACGTAACACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTG
GGATCCGGGAGGCCCTGGGCTTCCTGTGTGTAGCCCTGGCATAGACTTGCTCGTCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAG
GTGGGCACAAAGACTGCTGCTTCCAGGGTGTGCGGCCCTGGCCGTGTGTCTGACATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGC
TGGGCTGGCTGCACCATGGGCAGGGTTGAGGACTGCCCCCCACCCCGCCCAAGCCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTA
CACCATGCTCCGGGGCCTGGGGCCTCCTTGCCTGGCTTCTTCCTCCAGCTATCCTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGA
GCTGAAGTTCCAGGGGAGCCCAGGACCCCTGGGGACCTGTACACTAGCAGGATGGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATA
GGGGCCCTGTTCTCTCTGGGGTCCCACACTGGGGTCATGAGAGCTAGTTAGTACTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACA
AGTGAGGCTGTGGAGGCCAGGAGGTTCAAGTATGGAGGGTAGGAGTGCAACCCAGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGT
CAGGGAGGTGGGAAGGTGGGTGGGCCTGAACTCAGGCAGCCCTTCAGTGGCTTCTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAG
CCTGAGCCAAGCTGCATTGGGAGGAGAAGGCAGGGTGAGGGATCTGGGAGAGCAGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACA
GGCCGGGGGTGGAAGGCCCAGTAGAGCTGCCCTTCCCCAGATGGAAGCTTCCTCCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTC
CCCCAAACCCACACTGATGCGAAGCTGTTCTTGACCCTCCCATAGCATCAACTCAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATC
TGCGAAGGCCCCTGATGGAGCTATTTCTTCCTAGTATCAGGAGCAATTGAGACCCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTT
GAAAGCAATGTCAGGCGTGGCAGTGGGGAAGCCATGGAGGCTGGGAAGGGCAAAGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGT
TGGATTGGTACATTCACTGCTGCCAGGTACCCAGAGATGTCATCTCTCTCCAGGTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGAT
GGGGTCAGTGTCCATCCAGTTTACGCTGAGTCAGTCCATACAGCAAGACACCTGGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCAC
AGCCTTCATCCCAGGTCTGCCTACGTGGGAGATCTCATCAGAAACAGGAACGGGGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTC
AGTAAAGAGGATACTCTCCCAACCAGCCAAGGAATAAAAGCTGATCTGTATGTAGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCA
ACTTTAATAGCAAGCCTGTGGAGTTACACAAACCTGTGTTAAAACATGTAATTTTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACAT
CCTGGTAGTCCCAGTGATGTGTAAATGAGAGAGAAGAATAGACAGGCTTCCAAACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAG
TGCATGAATCTGTGATAATGTTTGCATATCAGAATGCATTCTCCCCTTAAAAGTAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAG
AATTCTTGGGACACAGGTTTGTTTTCTGCTGACTTGCTCGGAAACCCATTGGAGGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTT
ATCACCACTCAATATTGGGTGAGTTGGTCTGAACAAGGTGGGGATAAAGTAGAGTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAG
CTTTTCCCATCTCCAGTCTCAGTTTCCCATCCATAAAATGGGGGAAGTGGTAGGTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCAT
ATGATCTGCCAGAGCCTCTCCAGGGGTGGAATACATGTCCTGGACTAAGCCAATGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGG
GAATTTCAAGACTTATGGGAATGCTGGGTAGAAGCTGTTTTAATTCCCCTGTTGAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATC
ACGTGAAGCTGACACCACTGAAGGGAGAGTTGAGAGGCAGAAAGAGATCAAGTCCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATA
TGAGCTAATAAATTCTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

NM_001388410 ⟹ NP_001375339

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,077,959 - 6,102,623 (+)	NCBI
T2T-CHM13v2.0	17	5,972,160 - 5,996,818 (+)	NCBI

Sequence:

show sequence

AACTCCATGCGTCTGAAAGCCCTCAGCTCCGTTAAGCTGTGTTCCTGGACCGCCTGGGGGCCTG
TGCCTATGCACTGCTCCATCTCTCCCATGTTTCAGGCTTCATCCATGGCTCTGGATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCCTGGAATGGAGATGTCCTTGACGCCTGGGCAGAGGCTGCA
GCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGGCGAGCACAGGCAGGTGCCAGGAGCCAGGATGCAAGGATG
ACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATGGCCAAACCTTTCTTCCGACTCCAGAAGTTTCTCCGCCGA
ACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACAGGGCCCCCGGGCACCCGGCCCCCTGCAGACCTTGCCAGT
GGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACATGCTGCAGAGCCCCCTGACCCGGCCCCGGCCCGGCCCCC
GCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCCCTGGGCCCCGAGGCTGCCAGGCCCGCCATCCACAGCCGA
GGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTA
CGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGC
TCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAAT
GTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGTGTACCGAGTGTCATGGCCACCTCCAGATAACACCATGTGTTCAGAACATCATGATGACCTGCATTTGCATATTAAAGGACTAAGGTG
GGAGGGCCAGGTTTTTCAAGGGCTACGTAAATGACACACCTGGTCAAACCAATCCCCTGGGCCTTATGGAACGCAGACACCGCTTCCTCCAGCATCCCAATATAAGCAGCCACTTTTCCGCTGCACAC
GGGGTTTTCTCTTTGTTCAAATCCCCCCTCCCTCTGTCTCTGTACGGGGAGCTGTTTTCTTCTTCCTTCCTTCTTTCTTGCCTGTTAAACTTTTCACTCCTTAAAATCACCCCACATGTGTCCATGTC
TAAACCGGCACGAGACCAAGAACCCTGGTGTCCCTCCAGTCATCAGAGCCATATAGCTTGAATGCCTGCCTCAAGGTTGAGACTTTTTTCAGTGGGTGGGAGGGGCTGGTATGGCTTGTGTGGCACTT
TATAGCTGCAGGTAGGATGTTCTGGAGCACGGAGAGGATGAGAGCTAATAAAGAAGGGAGTAGGTCTAAGAGACACCACAGGGTTGGAATCCACAAGAGAGGATGTGGGGGCATGAAAGAAGGAGTGG
GAACCCCCAGGGAGGAGGATGAGGCATGGATGGGTTTGTGGGTGAGCGGGGCAGCTGACCTGTCCAATGTGGGAGGGAAGTTCTCCTTGGATCCTTCTGGGATACAGCATTTCTCAGGGGTACCCTCA
GAGATGCCTTGGCAAAGCTGCCACAGAAGTCGACCTGTGACCTGGTTCTGGAGTTAGGGATTTCAGGTAGGGCAAGAACAGTGCCCTGGATGTCATGCCTTTAAGTCAAACCGCCATCTGCCCAACGG
AGCGAGCCTTTGGCTCCCAGATTGTCCATCCATTCTCGCTTGTCTCGCCCGTGGATGTGGGTGTAACTTGAACTCAAACCGTCTGTACTGTTAGCCCCTCAGCTCTGAGCTCTGCAGATGCCTGGCAG
GGGTTTTGCTGGAATTCTGACTTCACTCTAGAGCAGGGGTTCACAGCCTTGGATCTGTTGGCATTTGGGGTTGGATATTACTCATGTTGGGATCTGTCTGTGCATTGTAGGATATCTAGCAGCATCCC
TAGCCTCTACCCACTAGATGCCAACAGCCCATATTCCCTCAGTTGTGACACACAGTCCCCACACATTGCCGTATGTCCTCTGGAGGGTAAAATCACCCCTGGTTGAGAACCACAGCCCTGGAGAGCCA
CCTGAAGATGCCAGGCAGCCATGCCCAGTCATGGCCCATATCCCCGTGGGGCTGAATCCTGGGGAGCAATGGTCTCTTCCAACCATTGTGAGGATGGAGAAGCAAATTCTCCCTCTAGTATTGAGGTC
TGATGGATGTGAAATTGTTTGGAAGTTGATCTGACCCAGACCTGCAGAGGCCAGAGAACTCTTTGCAGGGAATGGTATCCTCTCTTCCCTCCTGAATGTTGAGGGTGGCGAGAGAGGTGAATCTGGGG
ATGTCTGGCCGTATTTGCCTGCTCTGAAGTGCCAAGCACGTCCTCTCTGGAAAGGCCAGTGGTGTGGAGGCTGCCTGGCAGTCCCGGTGGCAGCTTTATCTCATCCTAATTTGGCCGAAAAACAAGCT
CAAATGTCCTATGATGTGGGAATGGTTAAATTATGCCACGGCCATACAGTGGACTATAATACAACCATTGAAAATGTTTTCAAAGACTTTGATGATGGAAAATGCTCACAGTAGAATGTTAAATGGGG
CAGAGCTGAGCCTGGGGGTAGGAAGCTAGGGGCTTAATTAGAGCTGGCCGGGCAGTGGGGCTGGGAGCAGCAGATGTGAGAGGTGGGGCTTGGAAACAGGAAAAGAGGAGGGGGTTCCTTGTAGTGCC
CCCACCTTTGAGCACCATCTGAGGCTTATTTGTGGCCCCAGATAAAATGTCTACTGTTTTTGCTAGTTCGCGAAAATGGATTTGGGGAGATCCAAGAGTGTAGTTTGACAGAAAAAGAACATTCCAGG
TGATATCTGCATCTTAATGATCTGACTCTCTGCCAGCAAGAGGGAATTGACCAATGTAATGTGTTTTTAAAGCCCAGTGAAATGATCTTGTCTAATTTCCTGTGATCGTATGGAGATGGAAAGAGACC
TGCTCATTCTCAGTCCCCTTCAGGATCCTATCGGCTCCTTTGTTTCAACGCAAGGCAAGAGTGAGCAGGGGGCAGCTTCGATATTTGCATTGCTACCAATTCAGATCTGGGGTAATTAGTTTTGTCGC
CTGATATTTGTGCTCAAGTAGATAGGCCATTTGTGGGGGTGCTCCGAAAGGAGGCTGATGAGCGAAATCTAACACCATCTGCAAATAGGTTACTAATGTGAGACACTCCACCGGCGATTATACCTTGT
GATGTGAGGTTTGTTCTCCCAGCTGCTGTTAGTGATTCTACTGATAAAGGAATCGCAGGGAGAGGAGGAAGAAAGGTGTTGAGCTTTCTTTTTCCCCTCTTTTAGCCTCTTTTGGGCGTCTAAATTCT
TTACGCATTAATCACCTGGATGTTTTCCCATTGACATTTCTTCTAAGTTTTTTTGCTTGTTTGGCCATTTAATGGTGGTGCTCATCTAGCCACCTTTCAAATGGAAAAGCATGCATTAATATGGAACC
TGTTTGTTCTCAGCTGGGCAGCTGCTCTTGCAAAATCCACTTGGATTCCAATAGATTCGGTCTATCCAAGGTAGCCTTATGGTCTCCATGGGGCACCCAAGTTCATGTCTTTGCCAATGGTTGGGTCT
GTAAGAGTCTGGGTTTTGTGAGCCTTGAGAATAAGAATTTTCTCTTTGACAAAATGCTGTAGTCATTCCAAGAGCTATTGGATATGCTTTGAATTGCTTATAAAAAGTCTGTGGTAAACCTGTTGATA
CTGTACTCTCTGCATATTTTGAAAAACACGTATTGTTTGTTTTTCTGGGGGGTTAACACATATCTATTTTAGAGAATTTGAAAATTTTCCAAGTGCAGAAATAAAAATAGAATGCACCTGTAACAACT
AA

hide sequence

RefSeq Acc Id:

NM_001388411 ⟹ NP_001375340

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,379 - 6,102,623 (+)	NCBI
T2T-CHM13v2.0	17	5,964,580 - 5,996,818 (+)	NCBI

Sequence:

show sequence

GCAGAGCCCGGCGCCCGCTCGCCCGCCCGCTGCCCGCCCCGGCTCCGCGCCCGCCCGCCCGCCC
CGCCGTTCAGCCCGGACGCCAGCAGCCCCGGGGAGCCAGGCGGCGGCGCCCTGTGCCCGGGCGCGTGGGTCCGCTTGCCGCGGGCGGCCGGAGACGTGCGGGCGCCGGGGCTTCTGGGCTCCGGGCAC
TGCGGGGGGCTGCGGGCTCGGCGCCCGGGGAAGGCGGGCCATGGGCGCGGGTGCGGGCGCCCCAGCCGGCCGCGATCGCGGGATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCCTGGAATGGAGA
TGTCCTTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGGCGAGCACAGGC
AGGTGCCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATGGCCAAACCTTT
CTTCCGACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACAGGGCCCCCGGG
CACCCGGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACATGCTGCAGAGC
CCCCTGACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCCCTGGGCCCCGA
GGCTGCCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGG
ATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAG
GGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGC
CTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGTGTACCGAGTGTCATGGCCACCTCCAGATAACACCATGTGTTCAGAACATCATGATGACC
TGCATTTGCATATTAAAGGACTAAGGTGGGAGGGCCAGGTTTTTCAAGGGCTACGTAAATGACACACCTGGTCAAACCAATCCCCTGGGCCTTATGGAACGCAGACACCGCTTCCTCCAGCATCCCAA
TATAAGCAGCCACTTTTCCGCTGCACACGGGGTTTTCTCTTTGTTCAAATCCCCCCTCCCTCTGTCTCTGTACGGGGAGCTGTTTTCTTCTTCCTTCCTTCTTTCTTGCCTGTTAAACTTTTCACTCC
TTAAAATCACCCCACATGTGTCCATGTCTAAACCGGCACGAGACCAAGAACCCTGGTGTCCCTCCAGTCATCAGAGCCATATAGCTTGAATGCCTGCCTCAAGGTTGAGACTTTTTTCAGTGGGTGGG
AGGGGCTGGTATGGCTTGTGTGGCACTTTATAGCTGCAGGTAGGATGTTCTGGAGCACGGAGAGGATGAGAGCTAATAAAGAAGGGAGTAGGTCTAAGAGACACCACAGGGTTGGAATCCACAAGAGA
GGATGTGGGGGCATGAAAGAAGGAGTGGGAACCCCCAGGGAGGAGGATGAGGCATGGATGGGTTTGTGGGTGAGCGGGGCAGCTGACCTGTCCAATGTGGGAGGGAAGTTCTCCTTGGATCCTTCTGG
GATACAGCATTTCTCAGGGGTACCCTCAGAGATGCCTTGGCAAAGCTGCCACAGAAGTCGACCTGTGACCTGGTTCTGGAGTTAGGGATTTCAGGTAGGGCAAGAACAGTGCCCTGGATGTCATGCCT
TTAAGTCAAACCGCCATCTGCCCAACGGAGCGAGCCTTTGGCTCCCAGATTGTCCATCCATTCTCGCTTGTCTCGCCCGTGGATGTGGGTGTAACTTGAACTCAAACCGTCTGTACTGTTAGCCCCTC
AGCTCTGAGCTCTGCAGATGCCTGGCAGGGGTTTTGCTGGAATTCTGACTTCACTCTAGAGCAGGGGTTCACAGCCTTGGATCTGTTGGCATTTGGGGTTGGATATTACTCATGTTGGGATCTGTCTG
TGCATTGTAGGATATCTAGCAGCATCCCTAGCCTCTACCCACTAGATGCCAACAGCCCATATTCCCTCAGTTGTGACACACAGTCCCCACACATTGCCGTATGTCCTCTGGAGGGTAAAATCACCCCT
GGTTGAGAACCACAGCCCTGGAGAGCCACCTGAAGATGCCAGGCAGCCATGCCCAGTCATGGCCCATATCCCCGTGGGGCTGAATCCTGGGGAGCAATGGTCTCTTCCAACCATTGTGAGGATGGAGA
AGCAAATTCTCCCTCTAGTATTGAGGTCTGATGGATGTGAAATTGTTTGGAAGTTGATCTGACCCAGACCTGCAGAGGCCAGAGAACTCTTTGCAGGGAATGGTATCCTCTCTTCCCTCCTGAATGTT
GAGGGTGGCGAGAGAGGTGAATCTGGGGATGTCTGGCCGTATTTGCCTGCTCTGAAGTGCCAAGCACGTCCTCTCTGGAAAGGCCAGTGGTGTGGAGGCTGCCTGGCAGTCCCGGTGGCAGCTTTATC
TCATCCTAATTTGGCCGAAAAACAAGCTCAAATGTCCTATGATGTGGGAATGGTTAAATTATGCCACGGCCATACAGTGGACTATAATACAACCATTGAAAATGTTTTCAAAGACTTTGATGATGGAA
AATGCTCACAGTAGAATGTTAAATGGGGCAGAGCTGAGCCTGGGGGTAGGAAGCTAGGGGCTTAATTAGAGCTGGCCGGGCAGTGGGGCTGGGAGCAGCAGATGTGAGAGGTGGGGCTTGGAAACAGG
AAAAGAGGAGGGGGTTCCTTGTAGTGCCCCCACCTTTGAGCACCATCTGAGGCTTATTTGTGGCCCCAGATAAAATGTCTACTGTTTTTGCTAGTTCGCGAAAATGGATTTGGGGAGATCCAAGAGTG
TAGTTTGACAGAAAAAGAACATTCCAGGTGATATCTGCATCTTAATGATCTGACTCTCTGCCAGCAAGAGGGAATTGACCAATGTAATGTGTTTTTAAAGCCCAGTGAAATGATCTTGTCTAATTTCC
TGTGATCGTATGGAGATGGAAAGAGACCTGCTCATTCTCAGTCCCCTTCAGGATCCTATCGGCTCCTTTGTTTCAACGCAAGGCAAGAGTGAGCAGGGGGCAGCTTCGATATTTGCATTGCTACCAAT
TCAGATCTGGGGTAATTAGTTTTGTCGCCTGATATTTGTGCTCAAGTAGATAGGCCATTTGTGGGGGTGCTCCGAAAGGAGGCTGATGAGCGAAATCTAACACCATCTGCAAATAGGTTACTAATGTG
AGACACTCCACCGGCGATTATACCTTGTGATGTGAGGTTTGTTCTCCCAGCTGCTGTTAGTGATTCTACTGATAAAGGAATCGCAGGGAGAGGAGGAAGAAAGGTGTTGAGCTTTCTTTTTCCCCTCT
TTTAGCCTCTTTTGGGCGTCTAAATTCTTTACGCATTAATCACCTGGATGTTTTCCCATTGACATTTCTTCTAAGTTTTTTTGCTTGTTTGGCCATTTAATGGTGGTGCTCATCTAGCCACCTTTCAA
ATGGAAAAGCATGCATTAATATGGAACCTGTTTGTTCTCAGCTGGGCAGCTGCTCTTGCAAAATCCACTTGGATTCCAATAGATTCGGTCTATCCAAGGTAGCCTTATGGTCTCCATGGGGCACCCAA
GTTCATGTCTTTGCCAATGGTTGGGTCTGTAAGAGTCTGGGTTTTGTGAGCCTTGAGAATAAGAATTTTCTCTTTGACAAAATGCTGTAGTCATTCCAAGAGCTATTGGATATGCTTTGAATTGCTTA
TAAAAAGTCTGTGGTAAACCTGTTGATACTGTACTCTCTGCATATTTTGAAAAACACGTATTGTTTGTTTTTCTGGGGGGTTAACACATATCTATTTTAGAGAATTTGAAAATTTTCCAAGTGCAGAA
ATAAAAATAGAATGCACCTGTAACAACTAA

hide sequence

RefSeq Acc Id:

NM_015253 ⟹ NP_056068

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,379 - 6,124,427 (+)	NCBI
GRCh37	17	5,972,426 - 6,027,747 (+)	NCBI
Build 36	17	5,914,658 - 5,968,471 (+)	NCBI Archive
Celera	17	5,989,799 - 6,043,603 (+)	RGD
HuRef	17	5,875,040 - 5,919,106 (+)	RGD
CHM1_1	17	5,983,259 - 6,037,060 (+)	NCBI
T2T-CHM13v2.0	17	5,964,580 - 6,018,611 (+)	NCBI

Sequence:

show sequence

GCAGAGCCCGGCGCCCGCTCGCCCGCCCGCTGCCCGCCCCGGCTCCGCGCCCGCCCGCCCGCCC
CGCCGTTCAGCCCGGACGCCAGCAGCCCCGGGGAGCCAGGCGGCGGCGCCCTGTGCCCGGGCGCGTGGGTCCGCTTGCCGCGGGCGGCCGGAGACGTGCGGGCGCCGGGGCTTCTGGGCTCCGGGCAC
TGCGGGGGGCTGCGGGCTCGGCGCCCGGGGAAGGCGGGCCATGGGCGCGGGTGCGGGCGCCCCAGCCGGCCGCGATCGCGGGATTTCTGCGCCAGGAGATGAGGGGCGGTAGAGCCCTGGAATGGAGA
TGTCCTTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGGGGCAGGAACAGTGAGTGACCCCAGGCGAGCACAGGC
AGGTGCCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCCAGGAGCCCTGCTGCCCAGGGGCATGGCCAAACCTTT
CTTCCGACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGCAGCGGGTCCGCGTGGCTCTCCCACAGGGCCCCCGGG
CACCCGGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGCCCAGAGCTGCTGCTGGGTGTGGACATGCTGCAGAGC
CCCCTGACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCATGAGTGACTCCCAGGGACCGCCCGCCCTGGGCCCCGA
GGCTGCCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTTATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGG
ATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAG
GGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCGCGGATGCTTCCGACTGCCAGAGAACATCACACATGC
CTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCAGGGGCTGGGAATGCTACTGTGCTTACCCTACCCCCCGGT
TCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACACCTGTGCAAGACACTCGTTGTACAGACAGGAGGTTCCTG
CCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGGCTTCTATACAGGGAGCTACTACTTTGATGGAACCCTCTA
CAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTGAGATGTTTGATTCAGCCATCCTGCTAATCCGGAACCCAT
ACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCGGACTTTGTCAACAGCTACGCCTCGTGGTGGTCCTCGCAC
GTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGATGGTGGCCTTCCTCAACGTGTCTGTGAGCGAGGAGCGGCT
GCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAGACTTGATCAATGGCTACATCCGGACGGTGGACCAAGCCC
TGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCAATCGCACCACGGGGCTGCGCTCCCCACTCTGATGCTCAG
GCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACACATCACAAGGCGAACACAAATGGACACACATACCTGGCCA
CGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCAGGCACCCCCAGATACAAATGCAGCCACGCACAGACGTAA
CACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCCCTGGGCTTCCTGTGTGTAGCCCTGGCATAGACTTGCTCG
TCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGACTGCTGCTTCCAGGGTGTGCGGCCCTGGCCGTGTGTCTGA
CATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCACCATGGGCAGGGTTGAGGACTGCCCCCCACCCCGCCCAAG
CCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGGGCCTGGGGCCTCCTTGCCTGGCTTCTTCCTCCAGCTATC
CTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGGGGAGCCCAGGACCCCTGGGGACCTGTACACTAGCAGGAT
GGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTCTCTGGGGTCCCACACTGGGGTCATGAGAGCTAGTTAGTA
CTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGAGGCCAGGAGGTTCAAGTATGGAGGGTAGGAGTGCAACCC
AGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAAGGTGGGTGGGCCTGAACTCAGGCAGCCCTTCAGTGGCTT
CTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTGCATTGGGAGGAGAAGGCAGGGTGAGGGATCTGGGAGAGC
AGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAAGGCCCAGTAGAGCTGCCCTTCCCCAGATGGAAGCTTCCT
CCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACACTGATGCGAAGCTGTTCTTGACCCTCCCATAGCATCAACT
CAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTGATGGAGCTATTTCTTCCTAGTATCAGGAGCAATTGAGAC
CCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAGGCGTGGCAGTGGGGAAGCCATGGAGGCTGGGAAGGGCAA
AGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATTCACTGCTGCCAGGTACCCAGAGATGTCATCTCTCTCCAG
GTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCATCCAGTTTACGCTGAGTCAGTCCATACAGCAAGACACCT
GGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAGGTCTGCCTACGTGGGAGATCTCATCAGAAACAGGAACGG
GGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATACTCTCCCAACCAGCCAAGGAATAAAAGCTGATCTGTATGT
AGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAGCCTGTGGAGTTACACAAACCTGTGTTAAAACATGTAATT
TTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAGTGATGTGTAAATGAGAGAGAAGAATAGACAGGCTTCCAA
ACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTGATAATGTTTGCATATCAGAATGCATTCTCCCCTTAAAAG
TAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACACAGGTTTGTTTTCTGCTGACTTGCTCGGAAACCCATTGGA
GGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATATTGGGTGAGTTGGTCTGAACAAGGTGGGGATAAAGTAGA
GTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCCAGTCTCAGTTTCCCATCCATAAAATGGGGGAAGTGGTAG
GTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAGCCTCTCCAGGGGTGGAATACATGTCCTGGACTAAGCCAA
TGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTTATGGGAATGCTGGGTAGAAGCTGTTTTAATTCCCCTGTT
GAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACACCACTGAAGGGAGAGTTGAGAGGCAGAAAGAGATCAAGT
CCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATTCTGTTTATTGTTTAA

hide sequence

RefSeq Acc Id:

XM_005256572 ⟹ XP_005256629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,077,959 - 6,124,427 (+)	NCBI
GRCh37	17	5,972,426 - 6,027,747 (+)	NCBI

Sequence:

show sequence

AACTCCATGCGTCTGAAAGCCCTCAGCTCCGTTAAGCTGTGTTCCTGGACCGCCTGGGGGCCTGTGCCTATGCACTGCTCCATCTCTCCCATGTTTCAGGCTTCATCCATGGCTCTGGATTTCTGCGC
CAGGAGATGAGGGGCGGTAGAGCCCTGGAATGGAGATGTCCTTGACGCCTGGGCAGAGGCTGCAGCTGCAGGACCCTGTGGCCACTGGAGATAAGTAATGGTGCCATTTGAACACCTACTGGAAACGG
GGCAGGAACAGTGAGTGACCCCAGGCGAGCACAGGCAGGTGCCAGGAGCCAGGATGCAAGGATGACGCCTCCGGAGGCCCTGGCCTCACTCCCACCTGGGCGCTAGGAGCCATCCCGGGGCTCCAGCC
AGGAGCCCTGCTGCCCAGGGGCATGGCCAAACCTTTCTTCCGACTCCAGAAGTTTCTCCGCCGAACACAGTTCCTGCTGTTCTTCCTCACGGCTGCCTACCTGATGACCGGCAGCCTGCTGCTGCTGC
AGCGGGTCCGCGTGGCTCTCCCACAGGGCCCCCGGGCACCCGGCCCCCTGCAGACCTTGCCAGTGGCCGCCGTGGCGCTGGGCGTGGGCTTGCTGGACAGCAGAGCCCTGCACGACCCTCGAGTCAGC
CCAGAGCTGCTGCTGGGTGTGGACATGCTGCAGAGCCCCCTGACCCGGCCCCGGCCCGGCCCCCGCTGGCTCCGGAGCCGCAACTCGGAGCTGCGTCAGTTGCGTCGCCGCTGGTTCCACCACTTCAT
GAGTGACTCCCAGGGACCGCCCGCCCTGGGCCCCGAGGCTGCCAGGCCCGCCATCCACAGCCGAGGCACCTACATTGGATGCTTCAGTGACGATGGCCACGAGAGGACTCTGAAAGGAGCTGTGTTTT
ATGACTTGAGAAAGATGACTGTCTCCCACTGCCAGGATGCGTGTGCTGAGCGGTCCTATGTCTACGCCGGCTTGGAGGCCGGGGCGGAGTGTTACTGCGGGAACCGGCTGCCAGCGGTGAGCGTGGGG
CTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGGCTGTGGACCGGCTCTCCGTGTACCGTGTGGACGAGCTGCAGCCGGGCTCCAGGAAGCGGCGGACCGCCACCTACCG
CGGATGCTTCCGACTGCCAGAGAACATCACACATGCCTTCCCCAGCTCCCTGATACAGGCCAATGTGACCGTGGGGACTTGCTCGGGCTTTTGTTCCCAGAAAGAGTTCCCCTTGGCCATTCTCAGGG
GCTGGGAATGCTACTGTGCTTACCCTACCCCCCGGTTCAACCTGCGGGATGCCATGGACAGCTCAGTATGTGGCCAGGACCCTGAGGCACAGAGGCTGGCAGAATACTGTGAGGTCTACCAGACACCT
GTGCAAGACACTCGTTGTACAGACAGGAGGTTCCTGCCTAACAAATCCAAAGTGTTTGTGGCTTTGTCAAGCTTCCCAGGAGCCGGGAACACATGGGCACGGCACCTCATTGAGCATGCCACTGGCTT
CTATACAGGGAGCTACTACTTTGATGGAACCCTCTACAACAAAGGGTTCAAGGGCGAAAAGGACCACTGGCGGAGCCGACGCACCATCTGTGTCAAAACCCACGAGAGTGGCAGGAGGGAGATTGAGA
TGTTTGATTCAGCCATCCTGCTAATCCGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACAGAAAATGTGCCGGGCACCTGGGATATGCAGCTGACCGCAACTGGAAGAGCAAAGAGTGGCCGGAC
TTTGTCAACAGCTACGCCTCGTGGTGGTCCTCGCACGTCCTGGACTGGCTCAAGTACGGGAAGCGGCTGCTGGTGGTGCACTACGAGGAGCTGCGGCGCAGCCTGGTGCCCACGTTACGGGAGATGGT
GGCCTTCCTCAACGTGTCTGTGAGCGAGGAGCGGCTGCTCTGCGTGGAGAACAACAAGGAGGGCAGCTTCCGGCGGCGCGGCCGGCGCTCCCACGACCCTGAGCCCTTCACCCCGGAGATGAAAGACT
TGATCAATGGCTACATCCGGACGGTGGACCAAGCCCTGCGTGACCACAACTGGACGGGGCTGCCCAGGGAGTATGTGCCCAGATGATAGGCCTGGCCCACGCCGCCGCCCCCGCTGAGTGACGCAATC
GCACCACGGGGCTGCGCTCCCCACTCTGATGCTCAGGCCCGTGGCCTCACTGGGACGAACGGTGGGTGGGGGGCTCACCCTGGTGCTGCCTCCCGCACAAGGAGACCTGGACACAACAGACACACATC
ACAAGGCGAACACAAATGGACACACATACCTGGCCACGAACCCACACCTCCTCAGACACTCAGACACCACTCCAGGCTCATAGCCCCGTCTTGATGCAGAGAAGCCACCCACGTGGGGTGTGCCAGGC
ACCCCCAGATACAAATGCAGCCACGCACAGACGTAACACACAGGTGCCAGGCCGTGTGCTCCTGGAGGCTGGCTGGCTGTCTCTCTCACACAGATACACGTGCGCTCCCTGGGATCCGGGAGGCCCTG
GGCTTCCTGTGTGTAGCCCTGGCATAGACTTGCTCGTCAGGGTGTTCGACTCTGGGATGCTGGGCCGGGCAGACATTTATGCTCTGAGCAGCAAGGACCATTGGGATGGAGGTGGGCACAAAGACTGC
TGCTTCCAGGGTGTGCGGCCCTGGCCGTGTGTCTGACATCCCATAAATGTGTGTGTGGTGTGACTACGGGCACCACAAACTCCGCAGCCTTGCCTCTCTTTTCTCTGTGGCTGGGCTGGCTGCACCAT
GGGCAGGGTTGAGGACTGCCCCCCACCCCGCCCAAGCCAATGCAGACACTGACCTCAAGACCAGCCACACCAAGTCTGTGCACTGCCCACCACCCCCTTCAACCCCTCCTACACCATGCTCCGGGGCC
TGGGGCCTCCTTGCCTGGCTTCTTCCTCCAGCTATCCTCAGGGAAGCTGGAGATTCAAGTCATGCCCCAGAAGCAAGGTGTAAGCATGGGGGCGTGGGGAAGAGGGCAGGAGCTGAAGTTCCAGGGGA
GCCCAGGACCCCTGGGGACCTGTACACTAGCAGGATGGGTCTTGGGAGTTGGCATGGGGAGATTGTAAGGGCTGTATCTCCGCGATTACTGGTACTGGTGCTCCACCCATAGGGGCCCTGTTCTCTCT
GGGGTCCCACACTGGGGTCATGAGAGCTAGTTAGTACTCAGCCTGACCCCTAGGTCTGGTCCTGCCAGCCTGGGATGGGGGTCAATGTATGCTACACATCTTGGGCTCACAAGTGAGGCTGTGGAGGC
CAGGAGGTTCAAGTATGGAGGGTAGGAGTGCAACCCAGGAGCAACGCTCAAGGTGGCCGAGATGCAGGGAGGATTGTGGCGATCCGGTTGCACACTGGCCTCTGTGGAGGTCAGGGAGGTGGGAAGGT
GGGTGGGCCTGAACTCAGGCAGCCCTTCAGTGGCTTCTTCAGGCCTAGGATAACCCTGGCCAGGCCCCATGGTCCTGCTCTGGGTCAGCTGTCAGGGAGACCTCCCTTCAGCCTGAGCCAAGCTGCAT
TGGGAGGAGAAGGCAGGGTGAGGGATCTGGGAGAGCAGGACGTTGAGATATCCTGACCCTCTGCTTCCTAGCCTGATGATGGGGAACCCAGAGCCACCCGCTATGAGCACAGGCCGGGGGTGGAAGGC
CCAGTAGAGCTGCCCTTCCCCAGATGGAAGCTTCCTCCAACCTTCAGTTTGGCCAGTGGGTGGGTTTGGGCATCTGTGCCCCTGGTGGCCTCCAAATCCTTCCTGGGATTCCCCCAAACCCACACTGA
TGCGAAGCTGTTCTTGACCCTCCCATAGCATCAACTCAGTTCAGCTCAAAGCTAGAAACACCAAGGTCTTTGAAAATGTTTATTGGCTCAGGATAGCTTCGGCATCCAATCTGCGAAGGCCCCTGATG
GAGCTATTTCTTCCTAGTATCAGGAGCAATTGAGACCCCTCAGGAGTTTCCACACTGCTGTGGACGGGATAGCCAGGGCAGACCTGCATCCCAGAGCAAGCCTAGATCCTTGAAAGCAATGTCAGGCG
TGGCAGTGGGGAAGCCATGGAGGCTGGGAAGGGCAAAGTGTGGAGAGAGGAGTGACCGGGACTGGAGCCAGGGTCTGGGGAGAGCAACAGCACCAGGCTTTTCCTGGTAGTTGGATTGGTACATTCAC
TGCTGCCAGGTACCCAGAGATGTCATCTCTCTCCAGGTAGAGCATCACCAGCTCCTGTGGCCTTGTAGATGACTCTGTACCTCAGTGAAGAGTGCAGGCAAGTAGAGTGATGGGGTCAGTGTCCATCC
AGTTTACGCTGAGTCAGTCCATACAGCAAGACACCTGGCACTTGGCAGGTACTCCTGGATGTTGATGAGCAAGGAAGAGCAACGGCCCTGTCAGCTGGCAGTGGTCCTCACAGCCTTCATCCCAGGTC
TGCCTACGTGGGAGATCTCATCAGAAACAGGAACGGGGATCTGTCTGTGCTTGCAGGAAAGTCCATTTGTTTTTCTCCAAGTTAGGTCTCATCTACAGCTCTTAGCTTCTCAGTAAAGAGGATACTCT
CCCAACCAGCCAAGGAATAAAAGCTGATCTGTATGTAGGGCAGAAGTGTGGCAAATGCATCAGGAACCGGTTAGAACAGAACAGAGAAACCCTGACTGTCTACAGATTCCAACTTTAATAGCAAGCCT
GTGGAGTTACACAAACCTGTGTTAAAACATGTAATTTTTATGGATTTCATCTCCCGTTGTGGATCAATTTGGAAAAACCAAAATATGTAATTTTAAAAAACTAAAACACATCCTGGTAGTCCCAGTGA
TGTGTAAATGAGAGAGAAGAATAGACAGGCTTCCAAACCCTGGGAAGAAAGCTGCTTAATTATGTGAACATCTTATAATGAAGTCTCTTGCAGCTAAAATTAGATTTTGAGTGCATGAATCTGTGATA
ATGTTTGCATATCAGAATGCATTCTCCCCTTAAAAGTAGCAGTAGCCACTTGGTTCTTAGGGGGCCCCAAGAGGAGAGGAGAAGTGCTGAGGTTGATGTTACGACTGCAAGAATTCTTGGGACACAGG
TTTGTTTTCTGCTGACTTGCTCGGAAACCCATTGGAGGTATCTGAAATGTGATGACTCCAAAGGGGTTCATTTCACTATAGGGAGAAATTGATTCGTCTGACTTCCTATTTATCACCACTCAATATTG
GGTGAGTTGGTCTGAACAAGGTGGGGATAAAGTAGAGTGGAAATAATGTAGAGTCGTCAGACTGAAAGGCCAGGTTGTAGTCCCAGCTCTTATCTGCCATCTTGGACAAAGCTTTTCCCATCTCCAGT
CTCAGTTTCCCATCCATAAAATGGGGGAAGTGGTAGGTCTTGCTGATTGCATCCACATTCATTCCTCCATTTCCTTTCCCAGCAACCCCCCATTTCTGTTTGGGAATTCATATGATCTGCCAGAGCCT
CTCCAGGGGTGGAATACATGTCCTGGACTAAGCCAATGACACCTTCCATCTTTCCAGCTATGGTGACTGGGTTAGGTATGATCTTGTGAGTTAAGACAATGAAGCCAGAGGGAATTTCAAGACTTATG
GGAATGCTGGGTAGAAGCTGTTTTAATTCCCCTGTTGAATGTGAAAAAGGTAGTAGTATTCCTGGGTCTTTATGATGACCACCTTGGGCCTTGGGATCATGACCAGGAATCACGTGAAGCTGACACCA
CTGAAGGGAGAGTTGAGAGGCAGAAAGAGATCAAGTCCTTGGTGAAATTGTTTAAGTACAGGATCAAGCCTTGCTTGAGATTGGCCTTACCTCTGGACTTTTTTTGTTATATGAGCTAATAAATTCTG
TTTATTGTTTAA

hide sequence

RefSeq Acc Id:

XM_047435701 ⟹ XP_047291657

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,379 - 6,124,427 (+)	NCBI

RefSeq Acc Id:

XM_047435702 ⟹ XP_047291658

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,071,095 - 6,124,427 (+)	NCBI

RefSeq Acc Id:

XM_054315620 ⟹ XP_054171595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	5,972,160 - 6,018,611 (+)	NCBI

RefSeq Acc Id:

XM_054315621 ⟹ XP_054171596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	5,964,580 - 6,018,611 (+)	NCBI

RefSeq Acc Id:

XM_054315622 ⟹ XP_054171597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	5,965,296 - 6,018,611 (+)	NCBI


Protein RefSeqs	NP_001375334	(Get FASTA)	NCBI Sequence Viewer
	NP_001375335	(Get FASTA)	NCBI Sequence Viewer
	NP_001375336	(Get FASTA)	NCBI Sequence Viewer
	NP_001375337	(Get FASTA)	NCBI Sequence Viewer
	NP_001375338	(Get FASTA)	NCBI Sequence Viewer
	NP_001375339	(Get FASTA)	NCBI Sequence Viewer
	NP_001375340	(Get FASTA)	NCBI Sequence Viewer
	NP_056068	(Get FASTA)	NCBI Sequence Viewer
	XP_005256629	(Get FASTA)	NCBI Sequence Viewer
	XP_047291657	(Get FASTA)	NCBI Sequence Viewer
	XP_047291658	(Get FASTA)	NCBI Sequence Viewer
	XP_054171595	(Get FASTA)	NCBI Sequence Viewer
	XP_054171596	(Get FASTA)	NCBI Sequence Viewer
	XP_054171597	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH09975	(Get FASTA)	NCBI Sequence Viewer
	BAA25449	(Get FASTA)	NCBI Sequence Viewer
	BAF82292	(Get FASTA)	NCBI Sequence Viewer
	CAH56249	(Get FASTA)	NCBI Sequence Viewer
	EAW90316	(Get FASTA)	NCBI Sequence Viewer
	EAW90317	(Get FASTA)	NCBI Sequence Viewer
	EAW90318	(Get FASTA)	NCBI Sequence Viewer
	EAW90319	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000323087
	ENSP00000323087.5
	ENSP00000458374
	ENSP00000458374.1
	ENSP00000458527
	ENSP00000458527.2
	ENSP00000460396
	ENSP00000460825
	ENSP00000460825.1
	ENSP00000461642.2
	ENSP00000519350
	ENSP00000519350.1
GenBank Protein	Q658N2	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_056068 ⟸ NM_015253
- Peptide Label:	isoform 1
- UniProtKB:	O60276 (UniProtKB/Swiss-Prot), D3DTM3 (UniProtKB/Swiss-Prot), A8K0N8 (UniProtKB/Swiss-Prot), Q96G45 (UniProtKB/Swiss-Prot), Q658N2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAKPFFRLQKFLRRTQFLLFFLTAAYLMTGSLLLLQRVRVALPQGPRAPGPLQTLPVAAVALGVGLLDSRALHDPRVSPELLLGVDMLQSPLTRPRPGPRWLRSRNSELRQLRRRWFHHFMSDSQGPP ALGPEAARPAIHSRGTYIGCFSDDGHERTLKGAVFYDLRKMTVSHCQDACAERSYVYAGLEAGAECYCGNRLPAVSVGLEECNHECKGEKGSVCGAVDRLSVYRVDELQPGSRKRRTATYRGCFRLPE NITHAFPSSLIQANVTVGTCSGFCSQKEFPLAILRGWECYCAYPTPRFNLRDAMDSSVCGQDPEAQRLAEYCEVYQTPVQDTRCTDRRFLPNKSKVFVALSSFPGAGNTWARHLIEHATGFYTGSYYF DGTLYNKGFKGEKDHWRSRRTICVKTHESGRREIEMFDSAILLIRNPYRSLVAEFNRKCAGHLGYAADRNWKSKEWPDFVNSYASWWSSHVLDWLKYGKRLLVVHYEELRRSLVPTLREMVAFLNVSV SEERLLCVENNKEGSFRRRGRRSHDPEPFTPEMKDLINGYIRTVDQALRDHNWTGLPREYVPR hide sequence

RefSeq Acc Id:	XP_005256629 ⟸ XM_005256572
- Peptide Label:	isoform X1
- UniProtKB:	O60276 (UniProtKB/Swiss-Prot), D3DTM3 (UniProtKB/Swiss-Prot), A8K0N8 (UniProtKB/Swiss-Prot), Q96G45 (UniProtKB/Swiss-Prot), Q658N2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAKPFFRLQKFLRRTQFLLFFLTAAYLMTGSLLLLQRVRVALPQGPRAPGPLQTLPVAAVALGV GLLDSRALHDPRVSPELLLGVDMLQSPLTRPRPGPRWLRSRNSELRQLRRRWFHHFMSDSQGPPALGPEAARPAIHSRGTYIGCFSDDGHERTLKGAVFYDLRKMTVSHCQDACAERSYVYAGLEAGA ECYCGNRLPAVSVGLEECNHECKGEKGSVCGAVDRLSVYRVDELQPGSRKRRTATYRGCFRLPENITHAFPSSLIQANVTVGTCSGFCSQKEFPLAILRGWECYCAYPTPRFNLRDAMDSSVCGQDPE AQRLAEYCEVYQTPVQDTRCTDRRFLPNKSKVFVALSSFPGAGNTWARHLIEHATGFYTGSYYFDGTLYNKGFKGEKDHWRSRRTICVKTHESGRREIEMFDSAILLIRNPYRSLVAEFNRKCAGHLG YAADRNWKSKEWPDFVNSYASWWSSHVLDWLKYGKRLLVVHYEELRRSLVPTLREMVAFLNVSVSEERLLCVENNKEGSFRRRGRRSHDPEPFTPEMKDLINGYIRTVDQALRDHNWTGLPREYVPR hide sequence

Ensembl Acc Id:

ENSP00000458339 ⟸ ENST00000571494

Ensembl Acc Id:

ENSP00000458527 ⟸ ENST00000571973

Ensembl Acc Id:

ENSP00000460396 ⟸ ENST00000573634

Protein Domains

WSC

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q658N2-F1-model_v2	AlphaFold	Q658N2	1-575	view protein structure

RGD ID:

7233567

Promoter ID:

EPDNEW_H22529

Type:

initiation region

Name:

WSCD1_2

Description:

WSC domain containing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22530 EPDNEW_H22531 EPDNEW_H22532 EPDNEW_H22533

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,069,116 - 6,069,176	EPDNEW

RGD ID:

7233569

Promoter ID:

EPDNEW_H22530

Type:

initiation region

Name:

WSCD1_4

Description:

WSC domain containing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22529 EPDNEW_H22531 EPDNEW_H22532 EPDNEW_H22533

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,070,552 - 6,070,612	EPDNEW

RGD ID:

7233571

Promoter ID:

EPDNEW_H22531

Type:

initiation region

Name:

WSCD1_1

Description:

WSC domain containing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22529 EPDNEW_H22530 EPDNEW_H22532 EPDNEW_H22533

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,071,095 - 6,071,155	EPDNEW

RGD ID:

7233573

Promoter ID:

EPDNEW_H22532

Type:

initiation region

Name:

WSCD1_3

Description:

WSC domain containing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22529 EPDNEW_H22530 EPDNEW_H22531 EPDNEW_H22533

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,077,959 - 6,078,019	EPDNEW

RGD ID:

7233575

Promoter ID:

EPDNEW_H22533

Type:

initiation region

Name:

WSCD1_5

Description:

WSC domain containing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H22529 EPDNEW_H22530 EPDNEW_H22531 EPDNEW_H22532

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	6,080,748 - 6,080,808	EPDNEW

Database	Acc Id	Source(s)
COSMIC	WSCD1	COSMIC
Ensembl Genes	ENSG00000179314	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000317744	ENTREZGENE
	ENST00000317744.10	UniProtKB/Swiss-Prot
	ENST00000571973	ENTREZGENE
	ENST00000571973.2	UniProtKB/Swiss-Prot
	ENST00000573634	ENTREZGENE
	ENST00000574232	ENTREZGENE
	ENST00000574232.5	UniProtKB/Swiss-Prot
	ENST00000574946	ENTREZGENE
	ENST00000574946.5	UniProtKB/Swiss-Prot
	ENST00000576233.2	UniProtKB/Swiss-Prot
	ENST00000714060	ENTREZGENE
	ENST00000714060.1	UniProtKB/Swiss-Prot
Gene3D-CATH	3.40.50.300	UniProtKB/Swiss-Prot
GTEx	ENSG00000179314	GTEx
HGNC ID	HGNC:29060	ENTREZGENE
Human Proteome Map	WSCD1	Human Proteome Map
InterPro	P-loop_NTPase	UniProtKB/Swiss-Prot
	Sialate-O-sulfotransferase	UniProtKB/Swiss-Prot
	Sulfotransferase_dom	UniProtKB/Swiss-Prot
	WSC_carb-bd	UniProtKB/Swiss-Prot
KEGG Report	hsa:23302	UniProtKB/Swiss-Prot
NCBI Gene	23302	ENTREZGENE
OMIM	619584	OMIM
PANTHER	SIALATE:O-SULFOTRANSFERASE 1	UniProtKB/Swiss-Prot
	WSCD FAMILY MEMBER CG9164	UniProtKB/Swiss-Prot
Pfam	Sulfotransfer_1	UniProtKB/Swiss-Prot
	WSC	UniProtKB/Swiss-Prot
PharmGKB	PA162409253	PharmGKB
PROSITE	WSC	UniProtKB/Swiss-Prot
SMART	WSC	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF52540	UniProtKB/Swiss-Prot
UniProt	A0A1B0GXC0_HUMAN	UniProtKB/TrEMBL
	A0AAQ5BHC8_HUMAN	UniProtKB/TrEMBL
	A8K0N8	ENTREZGENE
	D3DTM3	ENTREZGENE
	I3L0U0_HUMAN	UniProtKB/TrEMBL
	I3L127_HUMAN	UniProtKB/TrEMBL
	I3L3E6	ENTREZGENE, UniProtKB/TrEMBL
	O60276	ENTREZGENE
	Q658N2	ENTREZGENE
	Q96G45	ENTREZGENE
	WSCD1_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A8K0N8	UniProtKB/Swiss-Prot
	D3DTM3	UniProtKB/Swiss-Prot
	O60276	UniProtKB/Swiss-Prot
	Q96G45	UniProtKB/Swiss-Prot

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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