CHST10 (carbohydrate sulfotransferase 10)

Gene: CHST10 (carbohydrate sulfotransferase 10) Homo sapiens

Analyze

Symbol:

CHST10

Name:

carbohydrate sulfotransferase 10

RGD ID:

1353236

HGNC Page

HGNC:19650

Description:

Enables sulfotransferase activity. Involved in androgen metabolic process and estrogen metabolic process. Predicted to be located in Golgi membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

HNK-1 sulfotransferase; HNK-1ST; HNK1ST; huHNK-1ST; MGC17148

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Chst10 (carbohydrate sulfotransferase 10)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Chst10 (carbohydrate sulfotransferase 10)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Chst10 (carbohydrate sulfotransferase 10)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CHST10 (carbohydrate sulfotransferase 10)	NCBI	Ortholog
Canis lupus familiaris (dog):	CHST10 (carbohydrate sulfotransferase 10)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Chst10 (carbohydrate sulfotransferase 10)	NCBI	Ortholog
Sus scrofa (pig):	CHST10 (carbohydrate sulfotransferase 10)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CHST10 (carbohydrate sulfotransferase 10)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Chst10 (carbohydrate sulfotransferase 10)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Chst10 (carbohydrate sulfotransferase 10)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Chst10 (carbohydrate sulfotransferase 10)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	chst10 (carbohydrate sulfotransferase 10)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG13937	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER)
Xenopus laevis (African clawed frog):	chst10.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	chst10	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)

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	2	100,391,860 - 100,417,668 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	100,391,860 - 100,417,668 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	101,008,322 - 101,034,130 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	100,374,754 - 100,400,523 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	100,466,839 - 100,492,609	NCBI
Celera	2	95,212,945 - 95,238,710 (-)	NCBI		Celera
Cytogenetic Map	2	q11.2	NCBI
HuRef	2	94,773,099 - 94,798,904 (-)	NCBI		HuRef
CHM1_1	2	101,012,667 - 101,038,475 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

autism spectrum disorder (EXP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (EXP)

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP)

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

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP)

ammonium chloride (ISO)

amphetamine (ISO)

atrazine (ISO)

bisphenol A (ISO)

buta-1,3-diene (ISO)

butanal (EXP)

cannabidiol (ISO)

endosulfan (ISO)

furan (ISO)

gentamycin (ISO)

leflunomide (EXP)

manganese(II) chloride (ISO)

N,N-diethyl-m-toluamide (ISO)

N-methyl-4-phenylpyridinium (ISO)

ozone (ISO)

paracetamol (ISO)

permethrin (ISO)

potassium chromate (EXP)

silicon dioxide (ISO)

sodium arsenite (EXP)

tamoxifen (ISO)

temozolomide (EXP)

triptonide (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

androgen metabolic process (IDA)

carbohydrate biosynthetic process (IEA)

cell adhesion (TAS)

estrogen metabolic process (IDA)

learning (IEA,ISO)

long-term memory (IEA,ISO)

proteoglycan biosynthetic process (IBA,IEA)

steroid metabolic process (IEA)

Cellular Component

Golgi apparatus (IEA,TAS)

Golgi membrane (IEA,ISS,TAS)

membrane (IEA,TAS)

Molecular Function

HNK-1 sulfotransferase activity (ISO,TAS)

sulfotransferase activity (IBA,IDA,IEA,TAS)

transferase activity (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

O-linked glycan biosynthetic pathway (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
3.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1433500	PMID:8419650	PMID:8619474	PMID:9110174	PMID:9478973	PMID:10464296	PMID:12080076	PMID:12477932	PMID:15489334	PMID:16344560	PMID:19470764	PMID:20950796
PMID:21828042	PMID:21873635	PMID:21988832	PMID:22020094	PMID:22268729	PMID:22801424	PMID:22990118	PMID:23269668	PMID:26186194	PMID:28514442	PMID:30021884	PMID:32149355
PMID:33961781

Genomics

Comparative Map Data

CHST10
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	100,391,860 - 100,417,668 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	101,008,322 - 101,034,130 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	100,374,754 - 100,400,523 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	100,466,839 - 100,492,609	NCBI
Celera	2	95,212,945 - 95,238,710 (-)	NCBI		Celera
Cytogenetic Map	2	q11.2	NCBI
HuRef	2	94,773,099 - 94,798,904 (-)	NCBI		HuRef
CHM1_1	2	101,012,667 - 101,038,475 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI		T2T-CHM13v2.0

Chst10
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	38,902,948 - 38,937,256 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	38,902,948 - 38,937,242 (-)	Ensembl		GRCm39 Ensembl
GRCm38	1	38,863,867 - 38,898,177 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	38,863,867 - 38,898,161 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	1	38,920,717 - 38,955,005 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	1	38,808,418 - 38,842,706 (-)	NCBI		MGSCv36	mm8
Celera	1	38,649,369 - 38,684,228 (-)	NCBI		Celera
Cytogenetic Map	1	B	NCBI
cM Map	1	17.24	NCBI

Chst10
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	9	48,588,575 - 48,618,487 (-)	NCBI		GRCr8
mRatBN7.2	9	41,092,805 - 41,122,737 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	9	41,092,808 - 41,122,503 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	9	49,587,281 - 49,617,111 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	9	54,710,040 - 54,739,861 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	9	52,993,583 - 53,023,446 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	9	45,528,928 - 45,559,365 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	9	45,528,928 - 45,559,140 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	9	45,222,140 - 45,252,382 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	9	37,851,796 - 37,881,657 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	9	37,853,210 - 37,883,071 (-)	NCBI
Celera	9	38,843,700 - 38,873,565 (-)	NCBI		Celera
Cytogenetic Map	9	q22	NCBI

Chst10
(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_004955470	6,448,167 - 6,468,386 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955470	6,448,167 - 6,468,386 (-)	NCBI	ChiLan1.0	ChiLan1.0

CHST10
(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	12	27,808,690 - 27,834,580 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2A	27,811,461 - 27,837,341 (+)	NCBI		NHGRI_mPanPan1
PanPan1.1	2A	101,372,705 - 101,398,242 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2A	101,372,705 - 101,397,850 (-)	Ensembl	panpan1.1		panPan2

CHST10
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	10	42,311,166 - 42,340,856 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	10	42,312,903 - 42,339,732 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	10	42,234,013 - 42,264,162 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	10	43,177,124 - 43,209,302 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	10	43,177,402 - 43,209,296 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	10	42,899,764 - 42,930,103 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	10	43,172,135 - 43,203,986 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	10	43,363,262 - 43,393,384 (+)	NCBI		UU_Cfam_GSD_1.0

Chst10
(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_024406292	86,020,788 - 86,046,099 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936661	523,407 - 551,526 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936661	523,440 - 548,718 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CHST10
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	53,862,618 - 53,898,103 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	53,804,502 - 53,899,244 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	56,449,429 - 56,484,860 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CHST10
(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	14	4,114,495 - 4,139,741 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	14	4,114,464 - 4,131,524 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	171,732,801 - 171,758,688 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Chst10
(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_004624749	5,269,849 - 5,293,680 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624749	5,269,849 - 5,293,747 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CHST10
22 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_004854.4(CHST10):c.-33+81A>G	single nucleotide variant	Lung cancer [RCV000091072]	Chr2:100414960 [GRCh38] Chr2:101031422 [GRCh37] Chr2:2q11.2	uncertain significance
GRCh38/hg38 2q11.2-12.3(chr2:100378510-108472871)x3	copy number gain	See cases [RCV000050836]	Chr2:100378510..108472871 [GRCh38] Chr2:100994972..109089327 [GRCh37] Chr2:100361404..108455759 [NCBI36] Chr2:2q11.2-12.3	pathogenic
GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3	copy number gain	See cases [RCV000052946]	Chr2:94817406..103252396 [GRCh38] Chr2:95618109..103868854 [GRCh37] Chr2:94846878..103235286 [NCBI36] Chr2:2q11.1-12.1	pathogenic
GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3	copy number gain	See cases [RCV000052947]	Chr2:97672522..110211318 [GRCh38] Chr2:98288985..110968895 [GRCh37] Chr2:97655417..110326184 [NCBI36] Chr2:2q11.2-13	pathogenic
GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3	copy number gain	See cases [RCV000052945]	Chr2:91443218..102334856 [GRCh38] Chr2:91617683..102951316 [GRCh37] Chr2:90981410..102317748 [NCBI36] Chr2:2p11.2-q11.2	pathogenic
GRCh38/hg38 2q11.2(chr2:98787057-100785053)x1	copy number loss	See cases [RCV000054057]	Chr2:98787057..100785053 [GRCh38] Chr2:99403520..101401515 [GRCh37] Chr2:98769952..100767947 [NCBI36] Chr2:2q11.2	pathogenic
GRCh38/hg38 2q11.2(chr2:99253497-101559639)x3	copy number gain	See cases [RCV000136916]	Chr2:99253497..101559639 [GRCh38] Chr2:99869960..102176101 [GRCh37] Chr2:99236392..101542533 [NCBI36] Chr2:2q11.2	uncertain significance
GRCh38/hg38 2q11.2(chr2:100404604-100908738)x3	copy number gain	See cases [RCV000139353]	Chr2:100404604..100908738 [GRCh38] Chr2:101021066..101525200 [GRCh37] Chr2:100387498..100891632 [NCBI36] Chr2:2q11.2	likely benign
GRCh38/hg38 2q11.2(chr2:98411773-101636907)x1	copy number loss	See cases [RCV000139206]	Chr2:98411773..101636907 [GRCh38] Chr2:99028236..102253369 [GRCh37] Chr2:98394668..101619801 [NCBI36] Chr2:2q11.2	likely pathogenic
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3	copy number gain	See cases [RCV000141075]	Chr2:94678532..110602409 [GRCh38] Chr2:95344257..111359986 [GRCh37] Chr2:94707984..111076455 [NCBI36] Chr2:2q11.1-13	pathogenic
GRCh38/hg38 2q11.2(chr2:100406992-100919730)x3	copy number gain	See cases [RCV000143677]	Chr2:100406992..100919730 [GRCh38] Chr2:101023454..101536192 [GRCh37] Chr2:100389886..100902624 [NCBI36] Chr2:2q11.2	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266)	copy number gain	See cases [RCV000449270]	Chr2:95529039..108518266 [GRCh37] Chr2:2q11.1-12.3	pathogenic
GRCh37/hg19 2q11.1-13(chr2:95327499-111370025)x4	copy number gain	See cases [RCV000446842]	Chr2:95327499..111370025 [GRCh37] Chr2:2q11.1-13	pathogenic
GRCh37/hg19 2q11.2(chr2:100890121-101188008)x3	copy number gain	See cases [RCV000445655]	Chr2:100890121..101188008 [GRCh37] Chr2:2q11.2	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127)	copy number gain	See cases [RCV000511158]	Chr2:95518497..107186127 [GRCh37] Chr2:2q11.1-12.2	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q11.2(chr2:101022472-101536192)x3	copy number gain	not provided [RCV000682080]	Chr2:101022472..101536192 [GRCh37] Chr2:2q11.2	likely benign\|uncertain significance
GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3	copy number gain	not provided [RCV000682168]	Chr2:96353030..114045463 [GRCh37] Chr2:2q11.1-13	pathogenic
Single allele	deletion	not provided [RCV000714264]	Chr2:40608411..146900718 [GRCh37] Chr2:2p22.1-q22.3	likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
NM_004854.5(CHST10):c.483G>C (p.Lys161Asn)	single nucleotide variant	not provided [RCV001355648]	Chr2:100395559 [GRCh38] Chr2:101012021 [GRCh37] Chr2:2q11.2	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	copy number loss	See cases [RCV002287563]	Chr2:11504318..111365996 [GRCh37] Chr2:2p25.1-q13	pathogenic
NM_004854.5(CHST10):c.662T>C (p.Ile221Thr)	single nucleotide variant	Inborn genetic diseases [RCV002728087]	Chr2:100393654 [GRCh38] Chr2:101010116 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.557T>A (p.Phe186Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002682356]	Chr2:100393759 [GRCh38] Chr2:101010221 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.410T>G (p.Val137Gly)	single nucleotide variant	Inborn genetic diseases [RCV002727991]	Chr2:100397925 [GRCh38] Chr2:101014387 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.901C>T (p.His301Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002976843]	Chr2:100393415 [GRCh38] Chr2:101009877 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.106A>G (p.Ser36Gly)	single nucleotide variant	Inborn genetic diseases [RCV002981188]	Chr2:100402650 [GRCh38] Chr2:101019112 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.281A>G (p.Asp94Gly)	single nucleotide variant	Inborn genetic diseases [RCV002661364]	Chr2:100398054 [GRCh38] Chr2:101014516 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.998G>A (p.Arg333Gln)	single nucleotide variant	Inborn genetic diseases [RCV002980441]	Chr2:100393318 [GRCh38] Chr2:101009780 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.457G>A (p.Glu153Lys)	single nucleotide variant	Inborn genetic diseases [RCV002980592]	Chr2:100395585 [GRCh38] Chr2:101012047 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.310C>T (p.Pro104Ser)	single nucleotide variant	Inborn genetic diseases [RCV002787385]	Chr2:100398025 [GRCh38] Chr2:101014487 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.724C>T (p.Arg242Cys)	single nucleotide variant	Inborn genetic diseases [RCV002986338]	Chr2:100393592 [GRCh38] Chr2:101010054 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.298C>G (p.Leu100Val)	single nucleotide variant	Inborn genetic diseases [RCV002708610]	Chr2:100398037 [GRCh38] Chr2:101014499 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.568G>C (p.Asp190His)	single nucleotide variant	Inborn genetic diseases [RCV002984057]	Chr2:100393748 [GRCh38] Chr2:101010210 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.293A>G (p.Lys98Arg)	single nucleotide variant	Inborn genetic diseases [RCV002826291]	Chr2:100398042 [GRCh38] Chr2:101014504 [GRCh37] Chr2:2q11.2	likely benign
NM_004854.5(CHST10):c.908T>C (p.Val303Ala)	single nucleotide variant	Inborn genetic diseases [RCV002984580]	Chr2:100393408 [GRCh38] Chr2:101009870 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.695C>T (p.Thr232Ile)	single nucleotide variant	Inborn genetic diseases [RCV003175879]	Chr2:100393621 [GRCh38] Chr2:101010083 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.134C>A (p.Thr45Lys)	single nucleotide variant	Inborn genetic diseases [RCV003208543]	Chr2:100402622 [GRCh38] Chr2:101019084 [GRCh37] Chr2:2q11.2	uncertain significance
NM_004854.5(CHST10):c.989G>A (p.Arg330Gln)	single nucleotide variant	Inborn genetic diseases [RCV003364629]	Chr2:100393327 [GRCh38] Chr2:101009789 [GRCh37] Chr2:2q11.2	uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95773428-102550061)x3	copy number gain	not provided [RCV003484069]	Chr2:95773428..102550061 [GRCh37] Chr2:2q11.1-11.2	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3032
Count of miRNA genes:	1016
Interacting mature miRNAs:	1232
Transcripts:	ENST00000264249, ENST00000409046, ENST00000409701, ENST00000418201, ENST00000420858, ENST00000421474, ENST00000435960, ENST00000448989, ENST00000466583, ENST00000484382, ENST00000485085, ENST00000487860, ENST00000542617
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

A004V45

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,018,628 - 101,018,903	UniSTS	GRCh37
Build 36	2	100,385,060 - 100,385,335	RGD	NCBI36
Celera	2	95,223,249 - 95,223,524	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,783,402 - 94,783,677	UniSTS
GeneMap99-GB4 RH Map	2	355.47	UniSTS
Whitehead-RH Map	2	511.7	UniSTS

D2S1711E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,018,667 - 101,018,914	UniSTS	GRCh37
Build 36	2	100,385,099 - 100,385,346	RGD	NCBI36
Celera	2	95,223,288 - 95,223,535	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,783,441 - 94,783,688	UniSTS

WI-21792

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,017,845 - 101,018,096	UniSTS	GRCh37
Build 36	2	100,384,277 - 100,384,528	RGD	NCBI36
Celera	2	95,222,466 - 95,222,717	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,782,619 - 94,782,870	UniSTS
GeneMap99-GB4 RH Map	2	356.23	UniSTS
Whitehead-RH Map	2	512.3	UniSTS

WI-19927

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,008,380 - 101,008,644	UniSTS	GRCh37
Build 36	2	100,374,812 - 100,375,076	RGD	NCBI36
Celera	2	95,213,003 - 95,213,267	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,773,157 - 94,773,421	UniSTS
GeneMap99-GB4 RH Map	2	355.14	UniSTS
Whitehead-RH Map	2	507.3	UniSTS

A005U12

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,017,837 - 101,018,056	UniSTS	GRCh37
Build 36	2	100,384,269 - 100,384,488	RGD	NCBI36
Celera	2	95,222,458 - 95,222,677	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,782,611 - 94,782,830	UniSTS
GeneMap99-GB4 RH Map	2	355.3	UniSTS
NCBI RH Map	2	558.7	UniSTS

G20503

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,017,837 - 101,018,056	UniSTS	GRCh37
Build 36	2	100,384,269 - 100,384,488	RGD	NCBI36
Celera	2	95,222,458 - 95,222,677	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,782,611 - 94,782,830	UniSTS

STS-W80636

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	101,008,379 - 101,008,618	UniSTS	GRCh37
Build 36	2	100,374,811 - 100,375,050	RGD	NCBI36
Celera	2	95,213,002 - 95,213,241	RGD
Cytogenetic Map	2	q11.2	UniSTS
HuRef	2	94,773,156 - 94,773,395	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

215

599

361

741

175

2831

643

583

456

Low

2101

2626

880

360

1255

202

3607

2017

903

339

804

1013

168

1203

2331

Below cutoff

313

241

320

241

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_028153	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_004854	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512210	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005380	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005381	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005382	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005383	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024453248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047446433	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047446434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047446436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047446437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047446438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344644	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344648	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344651	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344653	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344655	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054344658	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC012493	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF003827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF033827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF070594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313241	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AU124707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC010441	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU849869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471127	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CS255950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA522916	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA732392	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HI968225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000264249 ⟹ ENSP00000264249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,391,860 - 100,417,668 (-)	Ensembl

RefSeq Acc Id:

ENST00000409046 ⟹ ENSP00000387121

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,397,911 - 100,417,334 (-)	Ensembl

RefSeq Acc Id:

ENST00000409701 ⟹ ENSP00000387309

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,393,245 - 100,417,011 (-)	Ensembl

RefSeq Acc Id:

ENST00000418201 ⟹ ENSP00000416831

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,402,564 - 100,417,351 (-)	Ensembl

RefSeq Acc Id:

ENST00000420858 ⟹ ENSP00000405922

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,397,936 - 100,415,845 (-)	Ensembl

RefSeq Acc Id:

ENST00000421474 ⟹ ENSP00000407525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,398,080 - 100,417,340 (-)	Ensembl

RefSeq Acc Id:

ENST00000435960 ⟹ ENSP00000395643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,406,576 - 100,417,379 (-)	Ensembl

RefSeq Acc Id:

ENST00000448989 ⟹ ENSP00000387977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,398,052 - 100,417,187 (-)	Ensembl

RefSeq Acc Id:

ENST00000466583

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,415,053 - 100,417,255 (-)	Ensembl

RefSeq Acc Id:

ENST00000484382

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,397,908 - 100,417,454 (-)	Ensembl

RefSeq Acc Id:

ENST00000485085

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,407,673 - 100,417,614 (-)	Ensembl

RefSeq Acc Id:

ENST00000487860

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	100,408,174 - 100,417,411 (-)	Ensembl

RefSeq Acc Id:

NM_004854 ⟹ NP_004845

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI
GRCh37	2	101,008,322 - 101,034,130 (-)	ENTREZGENE
Build 36	2	100,374,754 - 100,400,523 (-)	NCBI Archive
Celera	2	95,212,945 - 95,238,710 (-)	RGD
HuRef	2	94,773,099 - 94,798,904 (-)	ENTREZGENE
CHM1_1	2	101,012,667 - 101,038,475 (-)	NCBI
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI

Sequence:

show sequence

AGGCGGCGCGCACGGCCGGATAGGCGCGAGGGGGCCGCGTGAGGCGGTGCCGGCGTTCTGGCCC
CCAAAGCCGGTCTAGCGCGCCGGGCGTCTTCCTTACTTCCGCTGCCGCCGCCGCCACATCCCGG
GACCCGACGGGCCGCGGCGCGGAGGCCTCGGGGCAAGGTGGGGCGGGCCTCCCGAGCTCCCAGG
ACCCCGCGCGCTTCGCCCACAGGCCCGGCGAAGCCCGACCCGCGCGGCGCCCCCAGGGCCAGGG
GAGGAGCCTAAGGACCCGGACGAGCGCCGCTCCAGTAGGTGACAAGAGGAACCAAGAACCTCAG
TTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGGAAGAGTCAGTGAATGGC
TGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGATTTTCAT
GTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAGTGCCAAA
CAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAGCACATTC
CTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCCTGGTCTA
CATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCTCTCGCAC
ACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATTCTTTTCT
GCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATGGAGCATT
TTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCTTCCTCGG
CTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTTTTTATTG
TAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATCCCCGGTT
TGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAACCGGACA
GAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCACAGATGGC
TAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTGCTCCCTG
TGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATACATCTTA
AAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACCGTGTATA
ACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCCTGTATGC
CCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAACTAATGC
ATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATCTGAGCCC
AGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACAGGCCTGT
GAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAAGATGCTC
TGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCTCAGAGGG
GAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAGCGTTAGG
AGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTCAGGGTGG
CTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAGAGAAGCA
AGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGGCACCTCT
GGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTATTTTGTTC
CTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCCAGAATCC
ATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTCATTCAGC
ACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGGGGAGTGT
CTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGAGCTCAGG
CTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTGAATCTCC
ACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTGCCAGCAT
CACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCACTGCCAG
AGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAAGTTCACC
AGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGGTAGGCCC
TGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTGAGAACTG
GGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGGGTGGAGG
AGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGATTGTGTC
AATGTGAAAGTTAAATAAAATTTATGTGCCAAACCTGA

hide sequence

RefSeq Acc Id:

XM_011512207 ⟹ XP_011510509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI

Sequence:

show sequence

AGTAGGGTGAGCTCGGGGACGCGCAGGCGGGTGGGTTTCAGCGCCTGGGCCCCTCTCCCCGCCG
CGGGGCGCACGGAAAAACCGGGGAACCCGCGGGTTTTGTCCTGGCGAGCCACATCCCGTGACAA
GAGGAACCAAGAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAA
GGAAGAGTCAGTGAATGGCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCAT
GCTTTTGGGTGATTTTCATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCC
AGATGTGTACAGTGCCAAACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTG
CCAGAAGAGAAGCACATTCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGC
TCGTTCAGCCCCTGGTCTACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGC
CCTGAAGAATCTCTCGCACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGAC
AAGCACAAGATTCTTTTCTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGA
TTGTTCTAAATGGAGCATTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGA
GAAGAACGGCCTTCCTCGGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACA
TACTTCAAGTTTTTTATTGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAAT
TTGTTCACAATCCCCGGTTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAA
ATACAGGAGGAACCGGACAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGC
GATCCGAACCACAGATGGCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATG
TAGAGCTCTGTGCTCCCTGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGA
CGATGCCCCATACATCTTAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCT
CCGGGCATTACCGTGTATAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAG
ACATCCGACGCCTGTATGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGA
CTTTTTGCTAAACTAATGCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAAC
CAGGTGAAGATCTGAGCCCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCG
GGGTCTCCCACAGGCCTGTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTA
GTTTGGATGTAAGATGCTCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGC
CTTTGCTCACCTCAGAGGGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGA
AGCATCACACAGCGTTAGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTC
TCCTGGCTAGTCAGGGTGGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCT
GAGGAGGGACAGAGAAGCAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGA
GGAGTAAAACGGCACCTCTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCT
TTCTGTGACTATTTTGTTCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGG
GTCCATCTTTCCAGAATCCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCA
AGCGCCTATTTCATTCAGCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTC
TACCTGAGAAGGGGAGTGTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTG
GTTGGGCTTGGAGCTCAGGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGG
TGGACAGCAGTGAATCTCCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGC
AGGGGCAACCTGCCAGCATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCA
GCAAAATGGGCACTGCCAGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAG
GTGGGTAACCAAGTTCACCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTC
CTGGCAACAAGGTAGGCCCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAG
CCAGGACCGCTGAGAACTGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCC
GCCGAGCCCGGGGTGGAGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGA
ATGGTTTCCTGATTGTGTCAATGTGAAAGTTAAATAAAATTTATGTGCCAAACCTGA

hide sequence

RefSeq Acc Id:

XM_011512208 ⟹ XP_011510510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,379 (-)	NCBI

Sequence:

show sequence

GTGACTGGGTTAAAATGAAAAGACACAAAGAGAGAAGTGGTCTTTTCCCTTCCCTCCCCATTAT
AATTAAGAGCTTAGTCCATCTTGGCTCAGAATTGGAATTCAGAATTCAGAATTGCTCTTGACCC
TGAAGAATAGAATCTCAAAGAAATACCTGAGCAGAAAATTCTCTTCTTCGCTGAAATGAAAATT
GGAGTGTTTGCAAAACTGAACAAAGAAAGGAAAGAATTTGTAAACATCACAGGCAACTTGCAGT
TATATTCGGATCATTTTTCAGTGTTTGAGGAGTTCATACAATAAAAAGTGACAAGAGGAACCAA
GAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGGAAGAGTCA
GTGAATGGCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGT
GATTTTCATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTAC
AGTGCCAAACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGA
AGCACATTCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCC
CCTGGTCTACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAAT
CTCTCGCACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGA
TTCTTTTCTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAA
TGGAGCATTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGC
CTTCCTCGGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGT
TTTTTATTGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAA
TCCCCGGTTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGG
AACCGGACAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACC
ACAGATGGCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTG
TGCTCCCTGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCA
TACATCTTAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTA
CCGTGTATAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACG
CCTGTATGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTA
AACTAATGCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGA
TCTGAGCCCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCA
CAGGCCTGTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGT
AAGATGCTCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCAC
CTCAGAGGGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACAC
AGCGTTAGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAG
TCAGGGTGGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGAC
AGAGAAGCAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAAC
GGCACCTCTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACT
ATTTTGTTCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTT
CCAGAATCCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATT
TCATTCAGCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAA
GGGGAGTGTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTG
GAGCTCAGGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAG
TGAATCTCCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACC
TGCCAGCATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGG
CACTGCCAGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACC
AAGTTCACCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAA
GGTAGGCCCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGC
TGAGAACTGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCG
GGGTGGAGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCT
GATTGTGTCAATGTGAAAGTTAAATAAAATTTATGTGCCAAACCTGA

hide sequence

RefSeq Acc Id:

XM_011512210 ⟹ XP_011510512

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI

Sequence:

show sequence

GTTCTGGCCCCCAAAGCCGGTCTAGCGCGCCGGGCGTCTTCCTTACTTCCGCTGCCGCCGCCGC
CACATCCCGGGACCCGACGGGCCGCGGCGCGGAGGCCTCGGGGCAAGGTGGGGCGGGCCTCCCG
AGCTCCCAGGACCCCGCGCGCTTCGCCCACAGGCCCGGCGAAGCCCGACCCGCGCGGCGCCCCC
AGGGCCAGGGGAGGAGCCTAAGGACCCGGACGAGCGCCGCTCCAGTAGGTGACAAGAGGAACCA
AGAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGACCCTACT
GTCGCATTAATTTCTGGCAACCACACTGAGAAAGGTGTAGATTAAGCTGGAAAATCACGAAGAG
TGCCAAGGGATTGGTCAGTTTTTACTGGGGGTCTGCACCAGGCCAGGAAGAGTCAGTGAATGGC
TGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGATTTTCAT
GTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAGTGCCAAA
CAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAGCACATTC
CTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCCTGGTCTA
CATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCTCTCGCAC
ACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATTCTTTTCT
GCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATGGAGCATT
TTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCTTCCTCGG
CTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTTTTTATTG
TAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATCCCCGGTT
TGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAACCGGACA
GAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCACAGATGGC
TAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTGCTCCCTG
TGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATACATCTTA
AAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACCGTGTATA
ACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCCTGTATGC
CCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAACTAATGC
ATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATCTGAGCCC
AGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACAGGCCTGT
GAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAAGATGCTC
TGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCTCAGAGGG
GAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAGCGTTAGG
AGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTCAGGGTGG
CTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAGAGAAGCA
AGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGGCACCTCT
GGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTATTTTGTTC
CTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCCAGAATCC
ATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTCATTCAGC
ACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGGGGAGTGT
CTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGAGCTCAGG
CTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTGAATCTCC
ACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTGCCAGCAT
CACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCACTGCCAG
AGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAAGTTCACC
AGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGGTAGGCCC
TGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTGAGAACTG
GGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGGGTGGAGG
AGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGATTGTGTC
AATGTGAAAGTTAAATAAAATTTATGTGCCAAACCTGA

hide sequence

RefSeq Acc Id:

XM_011512211 ⟹ XP_011510513

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,376 (-)	NCBI

Sequence:

show sequence

AGCGCCTGGGCCCCTCTCCCCGCCGCGGGGCGCACGGAAAAACCGGGGAACCCGCGGGTTTTGT
CCTGGCGAGCCACATCCCGTGACAAGAGGAACCAAGAACCTCAGTTCAGGGGAAACACAGCAAG
GAAATGTGAGCCCCAGGCTGCAGAAGACCCTACTGTCGCATTAATTTCTGGCAACCACACTGAG
AAAGGTGTAGATTAAGCTGGAAAATCACGAAGAGTGCCAAGGGATTGGTCAGTTTTTACTGGGG
GTCTGCACCAGGCCAGGAAGAGTCAGTGAATGGCTGCGGTGTGACAACATGCACCACCAGTGGC
TTCTGCTGGCCGCATGCTTTTGGGTGATTTTCATGTTCATGGTGGCTAGCAAGTTCATCACGTT
GACCTTTAAAGACCCAGATGTGTACAGTGCCAAACAGGAGTTTCTGTTCCTGACAACCATGCCG
GAAGTGAGGAAGTTGCCAGAAGAGAAGCACATTCCTGAGGAACTGAAGCCAACTGGGAAGGAGC
TTCCAGACAGCCAGCTCGTTCAGCCCCTGGTCTACATGGAGCGCCTGGAACTCATCAGAAACGT
CTGCAGGGATGATGCCCTGAAGAATCTCTCGCACACTCCTGTCTCCAAGTTTGTCCTGGACCGA
ATATTTGTCTGTGACAAGCACAAGATTCTTTTCTGCCAGACTCCCAAAGTGGGCAACACCCAGT
GGAAGAAAGTGCTGATTGTTCTAAATGGAGCATTTTCTTCCATTGAGGAGATCCCCGAAAACGT
GGTGCACGACCACGAGAAGAACGGCCTTCCTCGGCTCTCTTCCTTCAGTGATGCAGAAATTCAG
AAGCGATTGAAAACATACTTCAAGTTTTTTATTGTAAGAGATCCCTTCGAAAGACTTATTTCTG
CATTTAAGGATAAATTTGTTCACAATCCCCGGTTTGAGCCTTGGTACAGGCATGAGATTGCTCC
TGGCATCATCAGAAAATACAGGAGGAACCGGACAGAGACCCGGGGGATCCAGTTTGAAGATTTC
GTGCGCTACCTCGGCGATCCGAACCACAGATGGCTAGACCTTCAGTTTGGGGACCACATCATTC
ACTGGGTGACGTATGTAGAGCTCTGTGCTCCCTGTGAGATAATGTACAGTGTGATTGGACACCA
CGAGACCCTGGAGGACGATGCCCCATACATCTTAAAAGAGGCTGGCATTGACCACCTGGTGTCA
TACCCGACTATCCCTCCGGGCATTACCGTGTATAACAGAACCAAGGTGGAGCACTATTTCCTGG
GCATCAGCAAACGAGACATCCGACGCCTGTATGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGG
GTACCAGAAACCAGACTTTTTGCTAAACTAATGCATAAGACCTATGAATTCAAATATCTTTATT
AGACCTGGGGCTAACCAGGTGAAGATCTGAGCCCAGAAATGACCCTTCCTCCACCACACCCCTC
CTTTGAGGACGCCCGGGGTCTCCCACAGGCCTGTGAGTTGCCTCGGCATATGACGCAGAACCCC
AACTGTTACAACTTAGTTTGGATGTAAGATGCTCTGAGGACCCTGCCCACACCCCTGCGTGCAT
TAGGATGTCGCTGGCCTTTGCTCACCTCAGAGGGGAGAAAAGGCTAAAGATTTGCAGTTTGACA
GCCCAGCAGGGAGGAAGCATCACACAGCGTTAGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGG
ATGCCCCTGAGGTTCTCCTGGCTAGTCAGGGTGGCTTCACCCATCACTGGTGGGTTGCAGGAAC
AGCACCCAGGACTCTGAGGAGGGACAGAGAAGCAAGGGGGCTGCTGAAATCGCAGAGACTTTTG
CAGCATCAGATCTGAGGAGTAAAACGGCACCTCTGGCCTTCATCTTGGTGCTGCGACAATTGTG
GAGGCAAAGCATTCTTTCTGTGACTATTTTGTTCCTGTAGACAGTCAGCGATGGCCAGAGGGTG
GTGTGGTGTCCAGGGGTCCATCTTTCCAGAATCCATGCCTGTGTAATGCTGGTCCATGCTTCTG
AACCTGTGTCTGCCAAGCGCCTATTTCATTCAGCACAAGACATACGATTTTAGAAGGTGAGGGG
AGGGGAGGCTTTTTCTACCTGAGAAGGGGAGTGTCTTTGAGGGCCTTAAAAGGACCATGGCCCA
GGAATGGGGGCGCTGGTTGGGCTTGGAGCTCAGGCTGCTGTGGATCCCGGCGCATCAGTTCTGA
CTTGCCTTACCTGGGTGGACAGCAGTGAATCTCCACCTGTCTTCTCCAGGGAGCTCCCATGTTG
GGGCTGAAGACGAGCAGGGGCAACCTGCCAGCATCACAGAATTCAGTGTAGTTTATACATTTCG
ATTCCTTTCATCTCAGCAAAATGGGCACTGCCAGAGCCATTTCTGATCACACCACCATCCTGGA
CCATGTGACTGGAAGGTGGGTAACCAAGTTCACCAGCAATAAAACCCAGCGCCCAGGTAGCCTC
CAGCAGTGCGGCTTCCTGGCAACAAGGTAGGCCCTGGTGCAGGGCAAGCCGCAGCGACCATTTC
AGATACCGTCCACAGCCAGGACCGCTGAGAACTGGGACAGTTTCCTGGGATGAGTGCCAGCCTG
AGCCTGCATGGTGCCGCCGAGCCCGGGGTGGAGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCT
CTACCTTTTCTCAGAATGGTTTCCTGATTGTGTCAATGTGAAAGTTAAATAAAATTTATGTGCC
AAACCTGA

hide sequence

RefSeq Acc Id:

XM_017005380 ⟹ XP_016860869

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI

Sequence:

show sequence

GTTCTGGCCCCCAAAGCCGGTCTAGCGCGCCGGGCGTCTTCCTTACTTCCGCTGCCGCCGCCGC
CACATCCCGGGACCCGACGGGCCGCGGCGCGGAGGCCTCGGGGCAAGGTGGGGCGGGCCTCCCG
AGCTCCCAGGACCCCGCGCGCTTCGCCCACAGGCCCGGCGAAGCCCGACCCGCGCGGCGCCCCC
AGGGCCAGGGGAGGAGCCTAAGGACCCGGACGAGCGCCGCTCCAGTAGGTGACAAGAGGAACCA
AGAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGACCCTACT
GTCGCATTAATTTCTGGCAACCACACTGAGAAAGGTGTAGATTAAGCTGGAAAATCACGAAGAG
TGCCAAGGGATTGGTCAGTTTTTACTGGGGGTCTGCACCAGGCCAGGCAACCCTATTGGTGACC
CCAGGAAACACACGAAGCCTTATACACGGGCACCTGAGGGTGGTTTGCGAGCCATCCGGAGAAA
ACCCAGGCAGCTTGGCAGGTGGTGAGCTCCCCACTGCAGGCTGTATTCAGGTGTGGCCGGATAA
CTACGTGGTGGGTGTGTCATGGATCCTATTTGCATTCCAGATGCCTGGTTCCTGTGAGATTCTA
GGATGTAAATGTTGAGACAAGGAGAGTGATTCACCTGGGTCTTCATGGAGCTCTGACCCACCCA
GGGTTAGGAGGCTCTCTCTGAAATTATTTGCCATCAGCACTGTGTTGAGGGGACCACTTCTCCC
TGCCATGCAGAAGTGATGGATGGCCTCAGTCAGTCGGTGGAAGCCAGCTCAGCCCAGGGTCTTG
TCTGTACGTGGAGAGCTTTGGCTTGAAGAAGCACTGTGTTAAAGGAAGAGTCAGTGAATGGCTG
CGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGATTTTCATGT
TCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAGTGCCAAACA
GGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAGCACATTCCT
GAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCCTGGTCTACA
TGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCTCTCGCACAC
TCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATTCTTTTCTGC
CAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATGGAGCATTTT
CTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCTTCCTCGGCT
CTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTTTTTATTGTA
AGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATCCCCGGTTTG
AGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAACCGGACAGA
GACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCACAGATGGCTA
GACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTGCTCCCTGTG
AGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATACATCTTAAA
AGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACCGTGTATAAC
AGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCCTGTATGCCC
GTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAACTAATGCAT
AAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATCTGAGCCCAG
AAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACAGGCCTGTGA
GTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAAGATGCTCTG
AGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCTCAGAGGGGA
GAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAGCGTTAGGAG
CCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTCAGGGTGGCT
TCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAGAGAAGCAAG
GGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGGCACCTCTGG
CCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTATTTTGTTCCT
GTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCCAGAATCCAT
GCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTCATTCAGCAC
AAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGGGGAGTGTCT
TTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGAGCTCAGGCT
GCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTGAATCTCCAC
CTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTGCCAGCATCA
CAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCACTGCCAGAG
CCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAAGTTCACCAG
CAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGGTAGGCCCTG
GTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTGAGAACTGGG
ACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGGGTGGAGGAG
GGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGATTGTGTCA

hide sequence

RefSeq Acc Id:

XM_017005381 ⟹ XP_016860870

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI

Sequence:

show sequence

ACATCCCGGGACCCGACGGGCCGCGGCGCGGAGGCCTCGGGGCAAGGTGGGGCGGGCCTCCCGA
GCTCCCAGGACCCCGCGCGCTTCGCCCACAGGCCCGGCGAAGCCCGACCCGCGCGGCGCCCCCA
GGGCCAGGGGAGGAGCCTAAGGACCCGGACGAGCGCCGCTCCAGTAGGTGACAAGAGGAACCAA
GAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGACCCTACTG
TCGCATTAATTTCTGGCAACCACACTGAGAAAGGTGTAGATTAAGCTGGAAAATCACGAAGAGT
GCCAAGGGATTGGTCAGTTTTTACTGGGGGTCTGCACCAGGCCAGATGCCTGGTTCCTGTGAGA
TTCTAGGATGTAAATGTTGAGACAAGGAGAGTGATTCACCTGGGTCTTCATGGAGCTCTGACCC
ACCCAGGGTTAGGAGGCTCTCTCTGAAATTATTTGCCATCAGCACTGTGTTGAGGGGACCACTT
CTCCCTGCCATGCAGAAGTGATGGATGGCCTCAGTCAGTCGGTGGAAGCCAGCTCAGCCCAGGG
TCTTGTCTGTACGTGGAGAGCTTTGGCTTGAAGAAGCACTGTGTTAAAGGAAGAGTCAGTGAAT
GGCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGATTTT
CATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAGTGCC
AAACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAGCACA
TTCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCCTGGT
CTACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCTCTCG
CACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATTCTTT
TCTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATGGAGC
ATTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCTTCCT
CGGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTTTTTA
TTGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATCCCCG
GTTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAACCGG
ACAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCACAGAT
GGCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTGCTCC
CTGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATACATC
TTAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACCGTGT
ATAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCCTGTA
TGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAACTAA
TGCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATCTGAG
CCCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACAGGCC
TGTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAAGATG
CTCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCTCAGA
GGGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAGCGTT
AGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTCAGGG
TGGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAGAGAA
GCAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGGCACC
TCTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTATTTTG
TTCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCCAGAA
TCCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTCATTC
AGCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGGGGAG
TGTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGAGCTC
AGGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTGAATC
TCCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTGCCAG
CATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCACTGC
CAGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAAGTTC
ACCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGGTAGG
CCCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTGAGAA
CTGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGGGTGG
AGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGATTGT
GTCA

hide sequence

RefSeq Acc Id:

XM_017005382 ⟹ XP_016860871

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,365 (-)	NCBI

Sequence:

show sequence

TGACTGGGTTAAAATGAAAAGACACAAAGAGAGAAGTGGTCTTTTCCCTTCCCTCCCCATTATA
ATTAAGAGCTTAGTCCATCTTGGCTCAGAATTGGAATTCAGAATTCAGAATTGCTCTTGACCCT
GAAGAATAGAATCTCAAAGAAATACCTGAGCAGAAAATTCTCTTCTTCGCTGAAATGAAAATTG
GAGTGTTTGCAAAACTGAACAAAGAAAGGAAAGAATTTGTAAACATCACAGGCAACTTGCAGTT
ATATTCGGATCATTTTTCAGTGTTTGAGGAGTTCATACAATAAAAAGTGACAAGAGGAACCAAG
AACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGACCCTACTGT
CGCATTAATTTCTGGCAACCACACTGAGAAAGGTGTAGATTAAGCTGGAAAATCACGAAGAGTG
CCAAGGGATTGGTCAGTTTTTACTGGGGGTCTGCACCAGGCCAGATGCCTGGTTCCTGTGAGAT
TCTAGGATGTAAATGTTGAGACAAGGAGAGTGATTCACCTGGGTCTTCATGGAGCTCTGACCCA
CCCAGGGTTAGGAGGCTCTCTCTGAAATTATTTGCCATCAGCACTGTGTTGAGGGGACCACTTC
TCCCTGCCATGCAGAAGTGATGGATGGCCTCAGTCAGTCGGTGGAAGCCAGCTCAGCCCAGGGT
CTTGTCTGTACGTGGAGAGCTTTGGCTTGAAGAAGCACTGTGTTAAAGGAAGAGTCAGTGAATG
GCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGATTTTC
ATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAGTGCCA
AACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAGCACAT
TCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCCTGGTC
TACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCTCTCGC
ACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATTCTTTT
CTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATGGAGCA
TTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCTTCCTC
GGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTTTTTAT
TGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATCCCCGG
TTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAACCGGA
CAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCACAGATG
GCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTGCTCCC
TGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATACATCT
TAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACCGTGTA
TAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCCTGTAT
GCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAACTAAT
GCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATCTGAGC
CCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACAGGCCT
GTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAAGATGC
TCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCTCAGAG
GGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAGCGTTA
GGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTCAGGGT
GGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAGAGAAG
CAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGGCACCT
CTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTATTTTGT
TCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCCAGAAT
CCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTCATTCA
GCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGGGGAGT
GTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGAGCTCA
GGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTGAATCT
CCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTGCCAGC
ATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCACTGCC
AGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAAGTTCA
CCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGGTAGGC
CCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTGAGAAC
TGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGGGTGGA
GGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGATTGTG
TCA

hide sequence

RefSeq Acc Id:

XM_017005383 ⟹ XP_016860872

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,376 (-)	NCBI

Sequence:

show sequence

GGTGAGCTCGGGGACGCGCAGGCGGGTGGGTTTCAGCGCCTGGGCCCCTCTCCCCGCCGCGGGG
CGCACGGAAAAACCGGGGAACCCGCGGGTTTTGTCCTGGCGAGCCACATCCCGGTGTGTTTTGG
CGACTTGAAGACCTCCCTAGTTCGCGGGAGTAGCGGGAAGAGCCTTCCTCGCGTTAATTATGCA
ATAAGAAGGCGTCCTTGTGCGGGATGCTGTGACCCGCGGAATTATTGATATTTGACAAGAGGAA
CCAAGAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGACCCT
ACTGTCGCATTAATTTCTGGCAACCACACTGAGAAAGGTGTAGATTAAGCTGGAAAATCACGAA
GAGTGCCAAGGGATTGGTCAGTTTTTACTGGGGGTCTGCACCAGGCCAGATGCCTGGTTCCTGT
GAGATTCTAGGATGTAAATGTTGAGACAAGGAGAGTGATTCACCTGGGTCTTCATGGAGCTCTG
ACCCACCCAGGGTTAGGAGGCTCTCTCTGAAATTATTTGCCATCAGCACTGTGTTGAGGGGACC
ACTTCTCCCTGCCATGCAGAAGTGATGGATGGCCTCAGTCAGTCGGTGGAAGCCAGCTCAGCCC
AGGGTCTTGTCTGTACGTGGAGAGCTTTGGCTTGAAGAAGCACTGTGTTAAAGGAAGAGTCAGT
GAATGGCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTTGGGTGA
TTTTCATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGTGTACAG
TGCCAAACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAAGAGAAG
CACATTCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTCAGCCCC
TGGTCTACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAAGAATCT
CTCGCACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCACAAGATT
CTTTTCTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTCTAAATG
GAGCATTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAACGGCCT
TCCTCGGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTCAAGTTT
TTTATTGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTCACAATC
CCCGGTTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAGGAGGAA
CCGGACAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCGAACCAC
AGATGGCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGCTCTGTG
CTCCCTGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGCCCCATA
CATCTTAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGCATTACC
GTGTATAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCCGACGCC
TGTATGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTTGCTAAA
CTAATGCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTGAAGATC
TGAGCCCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCTCCCACA
GGCCTGTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGGATGTAA
GATGCTCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGCTCACCT
CAGAGGGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATCACACAG
CGTTAGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGGCTAGTC
AGGGTGGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAGGGACAG
AGAAGCAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTAAAACGG
CACCTCTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGTGACTAT
TTTGTTCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCATCTTTCC
AGAATCCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCCTATTTC
ATTCAGCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTGAGAAGG
GGAGTGTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGGCTTGGA
GCTCAGGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACAGCAGTG
AATCTCCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGCAACCTG
CCAGCATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAATGGGCA
CTGCCAGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGTAACCAA
GTTCACCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCAACAAGG
TAGGCCCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGACCGCTG
AGAACTGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAGCCCGGG
GTGGAGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTTTCCTGA
TTGTGTCA

hide sequence

RefSeq Acc Id:

XM_024453248 ⟹ XP_024309016

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,376 (-)	NCBI

Sequence:

show sequence

GGTGAGCTCGGGGACGCGCAGGCGGGTGGGTTTCAGCGCCTGGGCCCCTCTCCCCGCCGCGGGG
CGCACGGAAAAACCGGGGAACCCGCGGGTTTTGTCCTGGCGAGCCACATCCCGGTGTGTTTTGG
CGACTTGAAGACCTCCCTAGTTCGCGGGAGTAGCGGGAAGAGCCTTCCTCGCGTTAATTATGCA
ATAAGAAGGCGTCCTTGTGCGGGATGCTGTGACCCGCGGAATTATTGATATTTGACAAGAGGAA
CCAAGAACCTCAGTTCAGGGGAAACACAGCAAGGAAATGTGAGCCCCAGGCTGCAGAAGGAAGA
GTCAGTGAATGGCTGCGGTGTGACAACATGCACCACCAGTGGCTTCTGCTGGCCGCATGCTTTT
GGGTGATTTTCATGTTCATGGTGGCTAGCAAGTTCATCACGTTGACCTTTAAAGACCCAGATGT
GTACAGTGCCAAACAGGAGTTTCTGTTCCTGACAACCATGCCGGAAGTGAGGAAGTTGCCAGAA
GAGAAGCACATTCCTGAGGAACTGAAGCCAACTGGGAAGGAGCTTCCAGACAGCCAGCTCGTTC
AGCCCCTGGTCTACATGGAGCGCCTGGAACTCATCAGAAACGTCTGCAGGGATGATGCCCTGAA
GAATCTCTCGCACACTCCTGTCTCCAAGTTTGTCCTGGACCGAATATTTGTCTGTGACAAGCAC
AAGATTCTTTTCTGCCAGACTCCCAAAGTGGGCAACACCCAGTGGAAGAAAGTGCTGATTGTTC
TAAATGGAGCATTTTCTTCCATTGAGGAGATCCCCGAAAACGTGGTGCACGACCACGAGAAGAA
CGGCCTTCCTCGGCTCTCTTCCTTCAGTGATGCAGAAATTCAGAAGCGATTGAAAACATACTTC
AAGTTTTTTATTGTAAGAGATCCCTTCGAAAGACTTATTTCTGCATTTAAGGATAAATTTGTTC
ACAATCCCCGGTTTGAGCCTTGGTACAGGCATGAGATTGCTCCTGGCATCATCAGAAAATACAG
GAGGAACCGGACAGAGACCCGGGGGATCCAGTTTGAAGATTTCGTGCGCTACCTCGGCGATCCG
AACCACAGATGGCTAGACCTTCAGTTTGGGGACCACATCATTCACTGGGTGACGTATGTAGAGC
TCTGTGCTCCCTGTGAGATAATGTACAGTGTGATTGGACACCACGAGACCCTGGAGGACGATGC
CCCATACATCTTAAAAGAGGCTGGCATTGACCACCTGGTGTCATACCCGACTATCCCTCCGGGC
ATTACCGTGTATAACAGAACCAAGGTGGAGCACTATTTCCTGGGCATCAGCAAACGAGACATCC
GACGCCTGTATGCCCGTTTCGAAGGGGACTTTAAGCTCTTTGGGTACCAGAAACCAGACTTTTT
GCTAAACTAATGCATAAGACCTATGAATTCAAATATCTTTATTAGACCTGGGGCTAACCAGGTG
AAGATCTGAGCCCAGAAATGACCCTTCCTCCACCACACCCCTCCTTTGAGGACGCCCGGGGTCT
CCCACAGGCCTGTGAGTTGCCTCGGCATATGACGCAGAACCCCAACTGTTACAACTTAGTTTGG
ATGTAAGATGCTCTGAGGACCCTGCCCACACCCCTGCGTGCATTAGGATGTCGCTGGCCTTTGC
TCACCTCAGAGGGGAGAAAAGGCTAAAGATTTGCAGTTTGACAGCCCAGCAGGGAGGAAGCATC
ACACAGCGTTAGGAGCCGTTTCCTTCAGGTGTTAAGGAAGGGGATGCCCCTGAGGTTCTCCTGG
CTAGTCAGGGTGGCTTCACCCATCACTGGTGGGTTGCAGGAACAGCACCCAGGACTCTGAGGAG
GGACAGAGAAGCAAGGGGGCTGCTGAAATCGCAGAGACTTTTGCAGCATCAGATCTGAGGAGTA
AAACGGCACCTCTGGCCTTCATCTTGGTGCTGCGACAATTGTGGAGGCAAAGCATTCTTTCTGT
GACTATTTTGTTCCTGTAGACAGTCAGCGATGGCCAGAGGGTGGTGTGGTGTCCAGGGGTCCAT
CTTTCCAGAATCCATGCCTGTGTAATGCTGGTCCATGCTTCTGAACCTGTGTCTGCCAAGCGCC
TATTTCATTCAGCACAAGACATACGATTTTAGAAGGTGAGGGGAGGGGAGGCTTTTTCTACCTG
AGAAGGGGAGTGTCTTTGAGGGCCTTAAAAGGACCATGGCCCAGGAATGGGGGCGCTGGTTGGG
CTTGGAGCTCAGGCTGCTGTGGATCCCGGCGCATCAGTTCTGACTTGCCTTACCTGGGTGGACA
GCAGTGAATCTCCACCTGTCTTCTCCAGGGAGCTCCCATGTTGGGGCTGAAGACGAGCAGGGGC
AACCTGCCAGCATCACAGAATTCAGTGTAGTTTATACATTTCGATTCCTTTCATCTCAGCAAAA
TGGGCACTGCCAGAGCCATTTCTGATCACACCACCATCCTGGACCATGTGACTGGAAGGTGGGT
AACCAAGTTCACCAGCAATAAAACCCAGCGCCCAGGTAGCCTCCAGCAGTGCGGCTTCCTGGCA
ACAAGGTAGGCCCTGGTGCAGGGCAAGCCGCAGCGACCATTTCAGATACCGTCCACAGCCAGGA
CCGCTGAGAACTGGGACAGTTTCCTGGGATGAGTGCCAGCCTGAGCCTGCATGGTGCCGCCGAG
CCCGGGGTGGAGGAGGGAGCCAGGCTTCGCTTCAAGGCGGCCTCTACCTTTTCTCAGAATGGTT
TCCTGATTGTGTCAATGTGAAAGTTAAATAAAATTTATGTGCCAAACCTGA

hide sequence

RefSeq Acc Id:

XM_047446433 ⟹ XP_047302389

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,668 (-)	NCBI

RefSeq Acc Id:

XM_047446434 ⟹ XP_047302390

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,369 (-)	NCBI

RefSeq Acc Id:

XM_047446436 ⟹ XP_047302392

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,354 (-)	NCBI

RefSeq Acc Id:

XM_047446437 ⟹ XP_047302393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,376 (-)	NCBI

RefSeq Acc Id:

XM_047446438 ⟹ XP_047302394

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,391,860 - 100,417,376 (-)	NCBI

RefSeq Acc Id:

XM_054344644 ⟹ XP_054200619

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,472 (-)	NCBI

RefSeq Acc Id:

XM_054344645 ⟹ XP_054200620

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,482 (-)	NCBI

RefSeq Acc Id:

XM_054344646 ⟹ XP_054200621

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI

RefSeq Acc Id:

XM_054344647 ⟹ XP_054200622

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI

RefSeq Acc Id:

XM_054344648 ⟹ XP_054200623

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,212 (-)	NCBI

RefSeq Acc Id:

XM_054344649 ⟹ XP_054200624

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,205 (-)	NCBI

RefSeq Acc Id:

XM_054344650 ⟹ XP_054200625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,215 (-)	NCBI

RefSeq Acc Id:

XM_054344651 ⟹ XP_054200626

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,212 (-)	NCBI

RefSeq Acc Id:

XM_054344652 ⟹ XP_054200627

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,504 (-)	NCBI

RefSeq Acc Id:

XM_054344653 ⟹ XP_054200628

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,190 (-)	NCBI

RefSeq Acc Id:

XM_054344654 ⟹ XP_054200629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,212 (-)	NCBI

RefSeq Acc Id:

XM_054344655 ⟹ XP_054200630

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,201 (-)	NCBI

RefSeq Acc Id:

XM_054344656 ⟹ XP_054200631

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,212 (-)	NCBI

RefSeq Acc Id:

XM_054344657 ⟹ XP_054200632

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,876,212 (-)	NCBI

RefSeq Acc Id:

XM_054344658 ⟹ XP_054200633

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	100,850,699 - 100,866,950 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_004845	(Get FASTA)	NCBI Sequence Viewer
	XP_011510509	(Get FASTA)	NCBI Sequence Viewer
	XP_011510510	(Get FASTA)	NCBI Sequence Viewer
	XP_011510512	(Get FASTA)	NCBI Sequence Viewer
	XP_011510513	(Get FASTA)	NCBI Sequence Viewer
	XP_016860869	(Get FASTA)	NCBI Sequence Viewer
	XP_016860870	(Get FASTA)	NCBI Sequence Viewer
	XP_016860871	(Get FASTA)	NCBI Sequence Viewer
	XP_016860872	(Get FASTA)	NCBI Sequence Viewer
	XP_024309016	(Get FASTA)	NCBI Sequence Viewer
	XP_047302389	(Get FASTA)	NCBI Sequence Viewer
	XP_047302390	(Get FASTA)	NCBI Sequence Viewer
	XP_047302392	(Get FASTA)	NCBI Sequence Viewer
	XP_047302393	(Get FASTA)	NCBI Sequence Viewer
	XP_047302394	(Get FASTA)	NCBI Sequence Viewer
	XP_054200619	(Get FASTA)	NCBI Sequence Viewer
	XP_054200620	(Get FASTA)	NCBI Sequence Viewer
	XP_054200621	(Get FASTA)	NCBI Sequence Viewer
	XP_054200622	(Get FASTA)	NCBI Sequence Viewer
	XP_054200623	(Get FASTA)	NCBI Sequence Viewer
	XP_054200624	(Get FASTA)	NCBI Sequence Viewer
	XP_054200625	(Get FASTA)	NCBI Sequence Viewer
	XP_054200626	(Get FASTA)	NCBI Sequence Viewer
	XP_054200627	(Get FASTA)	NCBI Sequence Viewer
	XP_054200628	(Get FASTA)	NCBI Sequence Viewer
	XP_054200629	(Get FASTA)	NCBI Sequence Viewer
	XP_054200630	(Get FASTA)	NCBI Sequence Viewer
	XP_054200631	(Get FASTA)	NCBI Sequence Viewer
	XP_054200632	(Get FASTA)	NCBI Sequence Viewer
	XP_054200633	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAC04707	(Get FASTA)	NCBI Sequence Viewer
	AAC28651	(Get FASTA)	NCBI Sequence Viewer
	AAH10441	(Get FASTA)	NCBI Sequence Viewer
	AAX93044	(Get FASTA)	NCBI Sequence Viewer
	BAG36052	(Get FASTA)	NCBI Sequence Viewer
	BAH12534	(Get FASTA)	NCBI Sequence Viewer
	CAJ75915	(Get FASTA)	NCBI Sequence Viewer
	CBY88424	(Get FASTA)	NCBI Sequence Viewer
	EAX01841	(Get FASTA)	NCBI Sequence Viewer
	EAX01842	(Get FASTA)	NCBI Sequence Viewer
	EAX01843	(Get FASTA)	NCBI Sequence Viewer
	EAX01844	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000264249
	ENSP00000264249.3
	ENSP00000387121.1
	ENSP00000387309
	ENSP00000387309.1
	ENSP00000387977.1
	ENSP00000395643.1
	ENSP00000405922.1
	ENSP00000407525.1
	ENSP00000416831.1
GenBank Protein	O43529	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_004845 ⟸ NM_004854
- Peptide Label:	precursor
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_011510512 ⟸ XM_011512210
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_011510509 ⟸ XM_011512207
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_011510513 ⟸ XM_011512211
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_011510510 ⟸ XM_011512208
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_016860870 ⟸ XM_017005381
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_016860869 ⟸ XM_017005380
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_016860872 ⟸ XM_017005383
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_016860871 ⟸ XM_017005382
- Peptide Label:	isoform X1
- UniProtKB:	Q53T18 (UniProtKB/Swiss-Prot), O43529 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:	XP_024309016 ⟸ XM_024453248
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot), B7Z4E8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MHHQWLLLAACFWVIFMFMVASKFITLTFKDPDVYSAKQEFLFLTTMPEVRKLPEEKHIPEELK PTGKELPDSQLVQPLVYMERLELIRNVCRDDALKNLSHTPVSKFVLDRIFVCDKHKILFCQTPK VGNTQWKKVLIVLNGAFSSIEEIPENVVHDHEKNGLPRLSSFSDAEIQKRLKTYFKFFIVRDPF ERLISAFKDKFVHNPRFEPWYRHEIAPGIIRKYRRNRTETRGIQFEDFVRYLGDPNHRWLDLQF GDHIIHWVTYVELCAPCEIMYSVIGHHETLEDDAPYILKEAGIDHLVSYPTIPPGITVYNRTKV EHYFLGISKRDIRRLYARFEGDFKLFGYQKPDFLLN hide sequence

RefSeq Acc Id:

ENSP00000416831 ⟸ ENST00000418201

RefSeq Acc Id:

ENSP00000387309 ⟸ ENST00000409701

RefSeq Acc Id:

ENSP00000387121 ⟸ ENST00000409046

RefSeq Acc Id:

ENSP00000387977 ⟸ ENST00000448989

RefSeq Acc Id:

ENSP00000405922 ⟸ ENST00000420858

RefSeq Acc Id:

ENSP00000407525 ⟸ ENST00000421474

RefSeq Acc Id:

ENSP00000264249 ⟸ ENST00000264249

RefSeq Acc Id:

ENSP00000395643 ⟸ ENST00000435960

RefSeq Acc Id:	XP_047302389 ⟸ XM_047446433
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047302393 ⟸ XM_047446437
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047302394 ⟸ XM_047446438
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047302390 ⟸ XM_047446434
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047302392 ⟸ XM_047446436
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200621 ⟸ XM_054344646
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200622 ⟸ XM_054344647
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200627 ⟸ XM_054344652
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200620 ⟸ XM_054344645
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200619 ⟸ XM_054344644
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200625 ⟸ XM_054344650
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200623 ⟸ XM_054344648
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200629 ⟸ XM_054344654
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200626 ⟸ XM_054344651
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200631 ⟸ XM_054344656
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200632 ⟸ XM_054344657
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200624 ⟸ XM_054344649
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200630 ⟸ XM_054344655
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200628 ⟸ XM_054344653
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054200633 ⟸ XM_054344658
- Peptide Label:	isoform X1
- UniProtKB:	O43529 (UniProtKB/Swiss-Prot), Q53T18 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O43529-F1-model_v2	AlphaFold	O43529	1-356	view protein structure

Promoters

RGD ID:

6797197

Promoter ID:

HG_KWN:34124

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000264249, ENST00000409046, ENST00000409701, OTTHUMT00000329695, OTTHUMT00000329739, OTTHUMT00000329740, OTTHUMT00000329742, OTTHUMT00000329743, OTTHUMT00000329744, OTTHUMT00000329811, OTTHUMT00000329812

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	100,400,169 - 100,400,669 (-)	MPROMDB

RGD ID:

6861166

Promoter ID:

EPDNEW_H3748

Type:

initiation region

Name:

CHST10_1

Description:

carbohydrate sulfotransferase 10

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	100,417,573 - 100,417,633	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:19650	AgrOrtholog
COSMIC	CHST10	COSMIC
Ensembl Genes	ENSG00000115526	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000264249	ENTREZGENE
	ENST00000264249.8	UniProtKB/Swiss-Prot
	ENST00000409046.5	UniProtKB/TrEMBL
	ENST00000409701	ENTREZGENE
	ENST00000409701.5	UniProtKB/Swiss-Prot
	ENST00000418201.5	UniProtKB/TrEMBL
	ENST00000420858.5	UniProtKB/TrEMBL
	ENST00000421474.5	UniProtKB/TrEMBL
	ENST00000435960.5	UniProtKB/TrEMBL
	ENST00000448989.5	UniProtKB/TrEMBL
GTEx	ENSG00000115526	GTEx
HGNC ID	HGNC:19650	ENTREZGENE
Human Proteome Map	CHST10	Human Proteome Map
InterPro	Carb_sulfotrans_8-10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Sulfotransferase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:9486	UniProtKB/Swiss-Prot
NCBI Gene	9486	ENTREZGENE
OMIM	606376	OMIM
PANTHER	CARBOHYDRATE SULFOTRANSFERASE 10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR12137	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Sulfotransfer_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134920179	PharmGKB
UniProt	B7Z4E8	ENTREZGENE, UniProtKB/TrEMBL
	B8ZZ48_HUMAN	UniProtKB/TrEMBL
	C9J5X0_HUMAN	UniProtKB/TrEMBL
	C9JCK7_HUMAN	UniProtKB/TrEMBL
	C9JI33_HUMAN	UniProtKB/TrEMBL
	C9JUE4_HUMAN	UniProtKB/TrEMBL
	C9JWY0_HUMAN	UniProtKB/TrEMBL
	CHSTA_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q53T18	ENTREZGENE
UniProt Secondary	Q53T18	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)