PTP4A3 (protein tyrosine phosphatase 4A3)

Gene: PTP4A3 (protein tyrosine phosphatase 4A3) Homo sapiens

Analyze

Symbol:

PTP4A3

Name:

protein tyrosine phosphatase 4A3

RGD ID:

1318604

HGNC Page

HGNC:9636

Description:

Predicted to enable protein tyrosine phosphatase activity. Involved in positive regulation of establishment of protein localization; positive regulation of non-canonical NF-kappaB signal transduction; and regulation of DNA-templated transcription. Acts upstream of or within endothelial cell migration. Located in cytoplasm and nucleus.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

phosphatase of regenerating liver 3; potentially prenylated protein tyrosine phosphatase; PRL-3; PRL-R; PRL3; protein tyrosine phosphatase type IVA 3; protein-tyrosine phosphatase 4a3; protein-tyrosine phosphatase of regenerating liver 3

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):	Ptp4a3 (protein tyrosine phosphatase 4a3)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Ptp4a3 (protein tyrosine phosphatase 4A3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ptp4a3 (protein tyrosine phosphatase 4A3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	PTP4A3 (protein tyrosine phosphatase 4A3)	NCBI	Ortholog
Canis lupus familiaris (dog):	PTP4A3 (protein tyrosine phosphatase 4A3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ptp4a3 (protein tyrosine phosphatase 4A3)	NCBI	Ortholog
Sus scrofa (pig):	PTP4A3 (protein tyrosine phosphatase 4A3)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	PTP4A3 (protein tyrosine phosphatase 4A3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ptp4a3 (protein tyrosine phosphatase 4A3)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Ptp4a3 (protein tyrosine phosphatase 4A3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Ptp4a3 (protein tyrosine phosphatase 4a3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ptp4a3a (protein tyrosine phosphatase type IVA, member 3a)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid\|ZFIN)
Danio rerio (zebrafish):	ptp4a3b (protein tyrosine phosphatase type IVA, member 3b)	Alliance	DIOPT (Ensembl Compara\|PANTHER\|ZFIN)
Caenorhabditis elegans (roundworm):	T19D2.2	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	PRL-1	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	ptp4a3	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	ptp4a3.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	ptp4a3.S	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	8	141,392,021 - 141,432,454 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	141,391,995 - 141,432,454 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	142,402,121 - 142,442,554 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	142,501,189 - 142,510,802 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	8	142,501,188 - 142,510,802	NCBI
Celera	8	138,607,734 - 138,608,044 (+)	NCBI		Celera
Cytogenetic Map	8	q24.3	NCBI
HuRef	8	137,748,484 - 137,759,930 (+)	NCBI		HuRef
CHM1_1	8	142,471,719 - 142,482,782 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	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

Colonic Neoplasms (EXP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

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

2-acetamidofluorene (ISO)

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

acrylamide (EXP,ISO)

aflatoxin B1 (EXP,ISO)

all-trans-retinoic acid (ISO)

amphetamine (ISO)

belinostat (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

bisphenol F (ISO)

bortezomib (EXP)

C60 fullerene (ISO)

cadmium atom (EXP)

cantharidin (ISO)

choline (ISO)

cisplatin (ISO)

cycloheximide (EXP)

disodium selenite (EXP)

dorsomorphin (EXP)

doxorubicin (EXP)

endosulfan (EXP)

ethanol (ISO)

fenvalerate (ISO)

folic acid (ISO)

hypochlorous acid (ISO)

indole-3-methanol (ISO)

inulin (ISO)

L-methionine (ISO)

lead diacetate (ISO)

lead(0) (ISO)

lipopolysaccharide (EXP)

mercury dibromide (EXP)

methyl methanesulfonate (EXP)

mono(2-ethylhexyl) phthalate (EXP)

N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal (ISO)

ozone (ISO)

paracetamol (ISO)

perfluorooctane-1-sulfonic acid (ISO)

phenylmercury acetate (EXP)

pirinixic acid (ISO)

potassium dichromate (ISO)

quercetin (EXP)

raloxifene (EXP)

rotenone (ISO)

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

SB 431542 (EXP)

silicon dioxide (EXP,ISO)

sodium arsenite (EXP)

sunitinib (EXP)

tamoxifen (EXP)

thimerosal (EXP)

urethane (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cellular response to leukemia inhibitory factor (IEA,ISO)

endothelial cell migration (IBA,IEA,IMP)

Notch signaling pathway (IEA,ISO)

positive regulation of establishment of protein localization (IMP)

positive regulation of non-canonical NF-kappaB signal transduction (IDA)

positive regulation of vascular permeability (IEA,ISO)

regulation of DNA-templated transcription (IDA)

regulation of vascular endothelial growth factor signaling pathway (IEA,ISO)

Cellular Component

cytoplasm (IBA,IMP)

early endosome (IEA)

endosome (IEA)

nucleus (IBA,IMP)

plasma membrane (IEA)

Molecular Function

phosphoprotein phosphatase activity (IEA)

prenylated protein tyrosine phosphatase activity (TAS)

protein binding (IPI)

protein tyrosine phosphatase activity (IBA,IEA)

References

References - curated

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

Additional References at PubMed

PMID:9514946	PMID:9633825	PMID:10747914	PMID:11355880	PMID:11598267	PMID:12107411	PMID:12235145	PMID:12477932	PMID:12516958	PMID:12782572	PMID:14654542	PMID:14704153
PMID:15135076	PMID:15161639	PMID:15489334	PMID:15534108	PMID:15788667	PMID:16203771	PMID:16472776	PMID:16505094	PMID:16832410	PMID:16873432	PMID:17018620	PMID:17235563
PMID:17353931	PMID:17440740	PMID:17545014	PMID:17545077	PMID:17717498	PMID:17934070	PMID:18021371	PMID:18078820	PMID:18268019	PMID:18561324	PMID:18636172	PMID:18684031
PMID:18803057	PMID:18813812	PMID:19002188	PMID:19009246	PMID:19040419	PMID:19087692	PMID:19101992	PMID:19115206	PMID:19132388	PMID:19152186	PMID:19187591	PMID:19214221
PMID:19236507	PMID:19322201	PMID:19322925	PMID:19424625	PMID:19440036	PMID:19586538	PMID:19757198	PMID:19846928	PMID:19930715	PMID:19945467	PMID:20045518	PMID:20140626
PMID:20364335	PMID:20516731	PMID:20609352	PMID:20806969	PMID:20860603	PMID:21084277	PMID:21135111	PMID:21159255	PMID:21291404	PMID:21320469	PMID:21466710	PMID:21478108
PMID:21589872	PMID:21725609	PMID:21790231	PMID:21806020	PMID:21873635	PMID:21914394	PMID:22028901	PMID:22073279	PMID:22131018	PMID:22137788	PMID:22261620	PMID:22331511
PMID:22340241	PMID:22345654	PMID:22413991	PMID:22440248	PMID:22469786	PMID:22595524	PMID:22677902	PMID:22825514	PMID:22855168	PMID:22995644	PMID:23036709	PMID:23092334
PMID:23178297	PMID:23362275	PMID:23364316	PMID:23418787	PMID:23462371	PMID:23572150	PMID:23691193	PMID:23729584	PMID:23867504	PMID:23929599	PMID:23989302	PMID:24030100
PMID:24204707	PMID:24403062	PMID:24632616	PMID:24686170	PMID:24696260	PMID:24737397	PMID:24885636	PMID:25136802	PMID:25139404	PMID:25475733	PMID:25687758	PMID:26041460
PMID:26070892	PMID:26433386	PMID:26548949	PMID:26563151	PMID:26597054	PMID:26669864	PMID:26846972	PMID:26874360	PMID:26967563	PMID:26975394	PMID:27036022	PMID:27096756
PMID:27229929	PMID:27328425	PMID:27432908	PMID:27452906	PMID:27572739	PMID:27656108	PMID:27698077	PMID:27880917	PMID:27911713	PMID:28063378	PMID:28068414	PMID:28246390
PMID:28284838	PMID:28319085	PMID:28330616	PMID:28482095	PMID:28514442	PMID:28675297	PMID:28791350	PMID:28980126	PMID:29190795	PMID:29207031	PMID:29556339	PMID:30305722
PMID:30418964	PMID:30498084	PMID:30816227	PMID:31171773	PMID:31298325	PMID:31337650	PMID:31546234	PMID:32413665	PMID:32571875	PMID:32606318	PMID:32616539	PMID:32652076
PMID:32918875	PMID:32929353	PMID:33179291	PMID:33566385	PMID:33961781	PMID:34092011	PMID:34129057	PMID:34209460	PMID:34237211	PMID:34482023	PMID:34630392	PMID:35098869
PMID:35817112	PMID:36336860

Genomics

Comparative Map Data

PTP4A3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	141,391,995 - 141,432,454 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	142,402,121 - 142,442,554 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	142,501,189 - 142,510,802 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	8	142,501,188 - 142,510,802	NCBI
Celera	8	138,607,734 - 138,608,044 (+)	NCBI		Celera
Cytogenetic Map	8	q24.3	NCBI
HuRef	8	137,748,484 - 137,759,930 (+)	NCBI		HuRef
CHM1_1	8	142,471,719 - 142,482,782 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI		T2T-CHM13v2.0

Ptp4a3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	15	73,594,991 - 73,629,075 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	15	73,594,994 - 73,630,615 (+)	Ensembl		GRCm39 Ensembl
GRCm38	15	73,723,145 - 73,758,766 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	15	73,723,145 - 73,758,766 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	15	73,553,575 - 73,589,196 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	15	73,575,667 - 73,586,021 (+)	NCBI		MGSCv36	mm8
Celera	15	75,228,105 - 75,263,862 (+)	NCBI		Celera
Cytogenetic Map	15	D3	NCBI
cM Map	15	34.05	NCBI

Ptp4a3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	7	107,518,220 - 107,549,949 (+)	NCBI		GRCr8
mRatBN7.2	7	105,650,640 - 105,660,921 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	7	105,628,029 - 105,660,919 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	7	107,413,296 - 107,419,095 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	7	109,634,779 - 109,640,578 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	7	109,582,889 - 109,588,687 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	7	114,969,699 - 115,002,902 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	7	114,997,103 - 115,002,902 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	7	114,892,674 - 114,924,154 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	7	111,462,191 - 111,468,045 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	7	111,467,866 - 111,502,275 (+)	NCBI
Celera	7	102,062,262 - 102,068,065 (+)	NCBI		Celera
Cytogenetic Map	7	q34	NCBI

Ptp4a3
(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_004955454	429,792 - 441,268 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955454	429,051 - 440,328 (+)	NCBI	ChiLan1.0	ChiLan1.0

PTP4A3
(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	7	158,783,895 - 158,830,201 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	8	134,314,474 - 134,360,646 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	8	138,062,418 - 138,108,281 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	8	141,166,898 - 141,187,383 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	8	141,166,898 - 141,188,314 (+)	Ensembl	panpan1.1		panPan2

PTP4A3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	13	35,875,467 - 35,886,330 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	13	35,880,005 - 35,886,324 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	13	35,734,643 - 35,745,436 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	13	36,261,162 - 36,271,948 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	13	36,262,778 - 36,273,628 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	13	35,981,264 - 35,992,052 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	13	36,071,127 - 36,081,934 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	13	36,491,590 - 36,502,389 (+)	NCBI		UU_Cfam_GSD_1.0

Ptp4a3
(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_024405303	2,616,806 - 2,626,450 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936470	10,042,906 - 10,052,480 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936470	10,042,903 - 10,052,475 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

PTP4A3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	4	2,345,118 - 2,364,672 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	4	2,345,119 - 2,376,765 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

PTP4A3
(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	8	135,663,128 - 135,672,523 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	8	135,663,149 - 135,671,300 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666039	4,456,641 - 4,500,393 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ptp4a3
(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_004624735	14,964,014 - 15,000,477 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624735	14,964,403 - 14,977,441 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in PTP4A3
13 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 8q24.21-24.3(chr8:128220912-145049449)x3	copy number gain	See cases [RCV000050830]	Chr8:128220912..145049449 [GRCh38] Chr8:129233158..146274835 [GRCh37] Chr8:129302340..146245639 [NCBI36] Chr8:8q24.21-24.3	pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3	copy number gain	See cases [RCV000050638]	Chr8:113580402..145054634 [GRCh38] Chr8:114592631..146280020 [GRCh37] Chr8:114661807..146250824 [NCBI36] Chr8:8q23.3-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	copy number gain	See cases [RCV000051206]	Chr8:241530..145049449 [GRCh38] Chr8:191530..146274835 [GRCh37] Chr8:181530..146245639 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q24.3(chr8:141131265-142117372)x3	copy number gain	See cases [RCV000052186]	Chr8:141131265..142117372 [GRCh38] Chr8:142141364..143198733 [GRCh37] Chr8:142210546..143196640 [NCBI36] Chr8:8q24.3	uncertain significance
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]\|See cases [RCV000053677]	Chr8:95606052..145054775 [GRCh38] Chr8:96618280..146280161 [GRCh37] Chr8:96687456..146250965 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3	copy number gain	See cases [RCV000053678]	Chr8:124514090..145054634 [GRCh38] Chr8:125526331..146280020 [GRCh37] Chr8:125595512..146250824 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh38/hg38 8q24.3(chr8:139447227-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]\|See cases [RCV000053701]	Chr8:139447227..145054775 [GRCh38] Chr8:140459470..146280161 [GRCh37] Chr8:140528652..146250965 [NCBI36] Chr8:8q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|See cases [RCV000053604]	Chr8:244417..145054775 [GRCh38] Chr8:194417..146280161 [GRCh37] Chr8:184417..146250965 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000053602]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
NM_007079.3(PTP4A3):c.99C>T (p.Phe33=)	single nucleotide variant	Malignant melanoma [RCV000068186]	Chr8:141422339 [GRCh38] Chr8:142432439 [GRCh37] Chr8:142501621 [NCBI36] Chr8:8q24.3	not provided
NC_000008.11:g.141405741A>G	single nucleotide variant	Lung cancer [RCV000107204]	Chr8:141405741 [GRCh38] Chr8:142415841 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	copy number gain	not provided [RCV000848192]	Chr8:31936551..146295771 [GRCh37] Chr8:8p12-q24.3	pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3	copy number gain	See cases [RCV000134353]	Chr8:94682154..145068656 [GRCh38] Chr8:95694382..146294042 [GRCh37] Chr8:95763558..146264846 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q24.3(chr8:139236824-145068712)x3	copy number gain	See cases [RCV000137466]	Chr8:139236824..145068712 [GRCh38] Chr8:140249067..146294098 [GRCh37] Chr8:140318249..146264902 [NCBI36] Chr8:8q24.3	likely pathogenic
GRCh38/hg38 8q24.22-24.3(chr8:130639182-145068712)x3	copy number gain	See cases [RCV000137644]	Chr8:130639182..145068712 [GRCh38] Chr8:131651428..146294098 [GRCh37] Chr8:131720610..146264902 [NCBI36] Chr8:8q24.22-24.3	pathogenic\|conflicting data from submitters
GRCh38/hg38 8q24.3(chr8:139004218-145049449)x3	copy number gain	See cases [RCV000137340]	Chr8:139004218..145049449 [GRCh38] Chr8:140016461..146274835 [GRCh37] Chr8:140085643..146245639 [NCBI36] Chr8:8q24.3	likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3	copy number gain	See cases [RCV000137346]	Chr8:124498498..145068712 [GRCh38] Chr8:125510739..146294098 [GRCh37] Chr8:125579920..146264902 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	copy number gain	See cases [RCV000138643]	Chr8:241605..145054781 [GRCh38] Chr8:191605..146280167 [GRCh37] Chr8:181605..146250971 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3	copy number gain	See cases [RCV000138551]	Chr8:87931152..145068712 [GRCh38] Chr8:88943380..146294098 [GRCh37] Chr8:89012496..146264902 [NCBI36] Chr8:8q21.3-24.3	pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3	copy number gain	See cases [RCV000139036]	Chr8:77480050..145068712 [GRCh38] Chr8:78392286..146294098 [GRCh37] Chr8:78554841..146264902 [NCBI36] Chr8:8q21.13-24.3	pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3	copy number gain	See cases [RCV000140447]	Chr8:97382873..145070385 [GRCh38] Chr8:98395101..146295771 [GRCh37] Chr8:98464277..146266575 [NCBI36] Chr8:8q22.1-24.3	pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3	copy number gain	See cases [RCV000141694]	Chr8:100867343..145070385 [GRCh38] Chr8:101879571..146295771 [GRCh37] Chr8:101948747..146266575 [NCBI36] Chr8:8q22.3-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	copy number gain	See cases [RCV000141808]	Chr8:208048..145070385 [GRCh38] Chr8:158048..146295771 [GRCh37] Chr8:148048..146266575 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	copy number gain	See cases [RCV000142021]	Chr8:21291522..145070385 [GRCh38] Chr8:21149033..146295771 [GRCh37] Chr8:21193313..146266575 [NCBI36] Chr8:8p21.3-q24.3	pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3	copy number gain	See cases [RCV000142810]	Chr8:103306336..145068712 [GRCh38] Chr8:104318564..146294098 [GRCh37] Chr8:104387740..146264902 [NCBI36] Chr8:8q22.3-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	copy number gain	See cases [RCV000142858]	Chr8:226452..145068712 [GRCh38] Chr8:176452..146294098 [GRCh37] Chr8:166452..146264902 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3	copy number gain	See cases [RCV000142597]	Chr8:78614077..145054634 [GRCh38] Chr8:79526312..146280020 [GRCh37] Chr8:79688867..146250824 [NCBI36] Chr8:8q21.13-24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000148092]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3	copy number gain	See cases [RCV000143659]	Chr8:85765999..145070385 [GRCh38] Chr8:86778228..146295771 [GRCh37] Chr8:86863079..146266575 [NCBI36] Chr8:8q21.2-24.3	pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3	copy number gain	See cases [RCV000148117]	Chr8:124514090..145054634 [GRCh38] Chr8:125526331..146280020 [GRCh37] Chr8:125595512..146250824 [NCBI36] Chr8:8q24.13-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not provided [RCV000848478]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	copy number gain	See cases [RCV000447507]	Chr8:158991..146280828 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.3(chr8:142438569-142482615)	copy number gain	Abnormal esophagus morphology [RCV000416898]	Chr8:142438569..142482615 [GRCh37] Chr8:8q24.3	benign
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4	copy number gain	See cases [RCV000448954]	Chr8:98432250..146222672 [GRCh37] Chr8:8q22.1-24.3	pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:134825277-146280828)x3	copy number gain	See cases [RCV000448348]	Chr8:134825277..146280828 [GRCh37] Chr8:8q24.22-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	copy number gain	See cases [RCV000510234]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:136378789-146295771)x3	copy number gain	See cases [RCV000512003]	Chr8:136378789..146295771 [GRCh37] Chr8:8q24.22-24.3	likely pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	copy number gain	See cases [RCV000511095]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3	copy number gain	See cases [RCV000511002]	Chr8:86841154..146295771 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3	copy number gain	See cases [RCV000510854]	Chr8:86841228..142689874 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3	copy number gain	See cases [RCV000512401]	Chr8:114853126..146295771 [GRCh37] Chr8:8q23.3-24.3	pathogenic
GRCh37/hg19 8q24.3(chr8:141850516-143511413)x3	copy number gain	See cases [RCV000512275]	Chr8:141850516..143511413 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	copy number gain	See cases [RCV000512169]	Chr8:12490999..146295771 [GRCh37] Chr8:8p23.1-q24.3	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3	copy number gain	not provided [RCV000683044]	Chr8:121694649..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3	copy number gain	not provided [RCV000747254]	Chr8:164984..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3	copy number gain	not provided [RCV000747248]	Chr8:10213..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:126892814-143750028)x1	copy number loss	not provided [RCV001006144]	Chr8:126892814..143750028 [GRCh37] Chr8:8q24.13-24.3	pathogenic
GRCh37/hg19 8q24.3(chr8:142132678-145569441)x1	copy number loss	not provided [RCV001006150]	Chr8:142132678..145569441 [GRCh37] Chr8:8q24.3	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3	copy number gain	not provided [RCV000849762]	Chr8:122193546..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:136059859-146295771)x3	copy number gain	not provided [RCV000847171]	Chr8:136059859..146295771 [GRCh37] Chr8:8q24.22-24.3	pathogenic
GRCh37/hg19 8q24.23-24.3(chr8:139188797-146295771)x3	copy number gain	not provided [RCV000846814]	Chr8:139188797..146295771 [GRCh37] Chr8:8q24.23-24.3	pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3	copy number gain	not provided [RCV001006140]	Chr8:121042467..146295771 [GRCh37] Chr8:8q24.12-24.3	pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3	copy number gain	not provided [RCV000845705]	Chr8:125496223..146295771 [GRCh37] Chr8:8q24.13-24.3	pathogenic
NM_032611.3(PTP4A3):c.199-5C>T	single nucleotide variant	not provided [RCV000948810]	Chr8:141426934 [GRCh38] Chr8:142437034 [GRCh37] Chr8:8q24.3	benign
GRCh37/hg19 8q24.21-24.3(chr8:131138343-143473913)	copy number gain	Distal trisomy 8q [RCV003325441]	Chr8:131138343..143473913 [GRCh37] Chr8:8q24.21-24.3	pathogenic
GRCh37/hg19 8q24.3(chr8:142309348-143247742)x3	copy number gain	not provided [RCV002472745]	Chr8:142309348..143247742 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8q24.21-24.3(chr8:128877995-146295771)x3	copy number gain	not provided [RCV001006146]	Chr8:128877995..146295771 [GRCh37] Chr8:8q24.21-24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	copy number gain	Polydactyly [RCV002280629]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:84712253-146295771)x3	copy number gain	See cases [RCV002285066]	Chr8:84712253..146295771 [GRCh37] Chr8:8q21.2-24.3	pathogenic
GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771)	copy number gain	not specified [RCV002053772]	Chr8:70382990..146295771 [GRCh37] Chr8:8q13.2-24.3	pathogenic
GRCh37/hg19 8q24.21-24.3(chr8:130863093-146295771)	copy number gain	not specified [RCV002053797]	Chr8:130863093..146295771 [GRCh37] Chr8:8q24.21-24.3	pathogenic
GRCh37/hg19 8q24.3(chr8:142326501-143237710)	copy number gain	not specified [RCV002053803]	Chr8:142326501..143237710 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8q22.1-24.3(chr8:96496503-146295711)	copy number gain	not provided [RCV002221452]	Chr8:96496503..146295711 [GRCh37] Chr8:8q22.1-24.3	pathogenic
GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2	copy number gain	See cases [RCV002292707]	Chr8:68912432..146295771 [GRCh37] Chr8:8q13.2-24.3	pathogenic
NM_032611.3(PTP4A3):c.512G>T (p.Cys171Phe)	single nucleotide variant	Inborn genetic diseases [RCV002865818]	Chr8:141431034 [GRCh38] Chr8:142441134 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.412C>T (p.Arg138Cys)	single nucleotide variant	Inborn genetic diseases [RCV002704214]	Chr8:141430934 [GRCh38] Chr8:142441034 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.493A>C (p.Thr165Pro)	single nucleotide variant	Inborn genetic diseases [RCV002798413]	Chr8:141431015 [GRCh38] Chr8:142441115 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.385G>A (p.Ala129Thr)	single nucleotide variant	Inborn genetic diseases [RCV002984026]	Chr8:141427805 [GRCh38] Chr8:142437905 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.487C>T (p.Pro163Ser)	single nucleotide variant	Inborn genetic diseases [RCV002767393]	Chr8:141431009 [GRCh38] Chr8:142441109 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.307C>T (p.His103Tyr)	single nucleotide variant	Inborn genetic diseases [RCV003203698]	Chr8:141427047 [GRCh38] Chr8:142437147 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.236A>G (p.Lys79Arg)	single nucleotide variant	Inborn genetic diseases [RCV003198446]	Chr8:141426976 [GRCh38] Chr8:142437076 [GRCh37] Chr8:8q24.3	uncertain significance
NM_032611.3(PTP4A3):c.476G>A (p.Arg159Gln)	single nucleotide variant	Inborn genetic diseases [RCV003347598]	Chr8:141430998 [GRCh38] Chr8:142441098 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8q24.3(chr8:141825923-142558013)x4	copy number gain	not provided [RCV003485353]	Chr8:141825923..142558013 [GRCh37] Chr8:8q24.3	uncertain significance
GRCh37/hg19 8q24.3(chr8:141419599-146295771)x3	copy number gain	not provided [RCV003484752]	Chr8:141419599..146295771 [GRCh37] Chr8:8q24.3	pathogenic
NM_032611.3(PTP4A3):c.-3G>T	single nucleotide variant	not provided [RCV003440700]	Chr8:141422238 [GRCh38] Chr8:142432338 [GRCh37] Chr8:8q24.3	likely benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not specified [RCV003986742]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	copy number gain	not provided [RCV003885521]	Chr8:113392581..146364022 [GRCh37] Chr8:8q23.3-24.3	pathogenic

miRNA Target Status

Confirmed Target Of

miRNA Gene	Mature miRNA	Method Name	Result Type	Data Type	Support Type	PMID
MIR551A	hsa-miR-551a	OncomiRDB	external_info	NA	NA	22469786
MIR495	hsa-miR-495-3p	OncomiRDB	external_info	NA	NA	22469786

Predicted Target Of

	Summary Value
Count of predictions:	2478
Count of miRNA genes:	579
Interacting mature miRNAs:	654
Transcripts:	ENST00000329397, ENST00000349124, ENST00000520105, ENST00000521578, ENST00000523147, ENST00000524028
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

RH41881

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	142,441,347 - 142,441,486	UniSTS	GRCh37
Build 36	8	142,510,529 - 142,510,668	RGD	NCBI36
Celera	8	138,607,771 - 138,607,910	RGD
Cytogenetic Map	8	q24.3	UniSTS
HuRef	8	137,758,723 - 137,758,862	UniSTS
GeneMap99-GB4 RH Map	8	566.1	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			3		1		1	1	3		11					1
Medium	2219	2687	1294	279	1467	137	4204	2157	2829	334	1350	1529	150	1	1199	2740	2	1
Low	215	303	423	341	440	323	147	32	884	77	93	73	25		5	47	2	1
Below cutoff	5	1	3	1	28	2	5	5	15	7	6	11					2

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_007079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_032611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005250764	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006716500	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011516803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011516805	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012998	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012999	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024447057	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421287	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421288	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421290	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421291	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421293	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421294	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421298	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421305	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328786	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328787	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328788	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328789	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328790	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328791	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328792	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328794	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328797	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328798	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328804	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328805	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328806	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328808	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328809	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054328821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333054	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333056	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333057	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333062	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333066	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333067	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333068	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333069	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333071	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333074	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333075	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054333081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359641	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359644	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359648	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359651	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359653	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359655	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359658	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359659	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359660	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359661	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359662	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359663	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359664	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359665	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359666	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359667	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359668	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359670	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359675	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359676	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC100803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC241442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF041434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI742376	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ276554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311257	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC003105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BE778111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
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	CH471060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U87168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000329397 ⟹ ENSP00000332274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,413,418 - 141,432,415 (+)	Ensembl

RefSeq Acc Id:

ENST00000349124 ⟹ ENSP00000331730

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,416,078 - 141,432,415 (+)	Ensembl

RefSeq Acc Id:

ENST00000520105 ⟹ ENSP00000428758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,391,995 - 141,431,520 (+)	Ensembl

RefSeq Acc Id:

ENST00000521578 ⟹ ENSP00000428976

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,392,021 - 141,432,454 (+)	Ensembl

RefSeq Acc Id:

ENST00000523147 ⟹ ENSP00000428725

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,392,021 - 141,426,951 (+)	Ensembl

RefSeq Acc Id:

ENST00000524028 ⟹ ENSP00000430332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,422,018 - 141,431,520 (+)	Ensembl

RefSeq Acc Id:

ENST00000680615 ⟹ ENSP00000505068

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,416,142 - 141,432,415 (+)	Ensembl

RefSeq Acc Id:

ENST00000681443 ⟹ ENSP00000506615

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	141,417,909 - 141,431,520 (+)	Ensembl

RefSeq Acc Id:

NM_007079 ⟹ NP_009010

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,421,388 - 141,432,454 (+)	NCBI
GRCh37	8	142,402,093 - 142,442,554 (+)	NCBI
Build 36	8	142,501,189 - 142,510,802 (+)	NCBI Archive
HuRef	8	137,748,484 - 137,759,930 (+)	NCBI
CHM1_1	8	142,471,719 - 142,482,782 (+)	NCBI
T2T-CHM13v2.0	8	142,548,745 - 142,559,812 (+)	NCBI

Sequence:

show sequence

ATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGTGGGCCACGGGGCCCAGCCCTAAGCAC
TGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTCCCCGTGCCACTGGCTCTCACCATTG
CCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGCCAGCTCTACCGCCTGAGCCCCCTGC
CCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGTGACACAGGCCCCACACGTCAGAGGCC
GCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAAGGCAGCTGGAGTTGGTTCAGTTCAAG
TTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCACCTCTGAGTGAAGGGGGCTGTCTGCCC
ATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTCCAGCTCTGGACACTGCTTGGCGGCCG
GGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTTTTTTGGTTGTTCTTTTTATTTTTTGC
CTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTGGAGTTGCCCGCTTTACTTTGGTTGGG
TTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTTTTAAGAGTTGGGTTTTCTTTTTTAAT
TATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAGTATTTGCACAATATTTGTGCGGGGTA
TGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAGCACAGGGATCTCGTTCTCCTCATTTT
TTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAGCCTTCTCTGCAGTCCCTTCTGCCCTG
CCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCGCCCGGCCCCGGTGGAGGTGAGCTACA
AACACATGCGCTTCCTCATCACCCACAACCCCACCAACGCCACGCTCAGCACCTTCATTGAGGA
CCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTGACCTATGACAAAACGCCG
CTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATGGGGCGCCCCCGCCCGGCA
AGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGAGGCCCCCGGCAGCTGCGT
GGCTGTGCACTGCGTGGCGGGCCTGGGCCGGAAGCGCCGCGGAGCCATCAACAGCAAGCAGCTC
ACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAGACCCACACACGCACAAGA
CCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCGTCATGTAGGTCAGGACCT
TGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAGCAGGGGCTCCAGGCCTTG
GCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTGTGTCCGAGGAGCGAGGAG
CCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGCCACTCCCTCTGGCGGCGC
TGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCCGCCCCCTCCCACACCAGC
CAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATTTTGTAACCACTGGGCCCC
CAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCTTAAATTATTAGACCCCGG
GGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCGTGGCCGTGTGTGTGGAGT
GGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAGAGGCTGCTGTCTGGATCC
TGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCCTCTGGTGGCCGCTCTGGG
TCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGATACCGAGGTGGGAGCCCT
GCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACATTGGAAGGCGAGGCAGGTC
ACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCTTCTCAGGGCCTGTGTCCG
GCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGGCTCCGAGGCGCAGAGAAG
GGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCCAGGGAGGGAGGGTGCCAC
CTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCCGGAGGGCGTGGACCAGAT
GCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCACCCTGGGCCGGGGTGCAT
GGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCTCCAGGGTGTGGAGAGCCT
GGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGCGACTGGGGCAGGTGCTGG
AGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCCCCTTCTCAGGCAGCCCTG
CCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCCCCAGCTCCTGTGTGGAGA
AAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAACACATTTGGAACTCAAGTA
AATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

NM_032611 ⟹ NP_116000

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI
GRCh37	8	142,402,093 - 142,442,554 (+)	NCBI
Build 36	8	142,501,189 - 142,510,802 (+)	NCBI Archive
HuRef	8	137,748,484 - 137,759,930 (+)	NCBI
CHM1_1	8	142,471,719 - 142,482,782 (+)	NCBI
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI

Sequence:

show sequence

GTGCGCGAGGGCGCGCGCGTCCCGAGCCCTCCACCCGTCGTGCCGGCGCCGCCCGGACCGCCAG
ATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGTGGGCCACGGGGCCCAGCCCTAAGCAC
TGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTCCCCGTGCCACTGGCTCTCACCATTG
CCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGCCAGCTCTACCGCCTGAGCCCCCTGC
CCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGTGACACAGGCCCCACACGTCAGAGGCC
GCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAAGGCAGCTGGAGTTGGTTCAGTTCAAG
TTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCACCTCTGAGTGAAGGGGGCTGTCTGCCC
ATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTCCAGCTCTGGACACTGCTTGGCGGCCG
GGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTTTTTTGGTTGTTCTTTTTATTTTTTGC
CTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTGGAGTTGCCCGCTTTACTTTGGTTGGG
TTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTTTTAAGAGTTGGGTTTTCTTTTTTAAT
TATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAGTATTTGCACAATATTTGTGCGGGGTA
TGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAGCACAGGGATCTCGTTCTCCTCATTTT
TTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAGCCTTCTCTGCAGTCCCTTCTGCCCTG
CCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCGCCCGGCCCCGGTGGAGGTGAGCTACA
AACACATGCGCTTCCTCATCACCCACAACCCCACCAACGCCACGCTCAGCACCTTCATTGAGGA
CCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTGACCTATGACAAAACGCCG
CTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATGGGGCGCCCCCGCCCGGCA
AGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGAGGCCCCCGGCAGCTGCGT
GGCTGTGCACTGCGTGGCGGGCCTGGGCCGGGCTCCAGTCCTTGTGGCGCTGGCCCTTATTGAG
AGCGGGATGAAGTACGAGGACGCCATCCAGTTCATCCGCCAGAAGCGCCGCGGAGCCATCAACA
GCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAGACCCACA
CACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCGTCATGTA
GGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAGCAGGGGC
TCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTGTGTCCGA
GGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGCCACTCCC
TCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCCGCCCCCT
CCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATTTTGTAAC
CACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCTTAAATTA
TTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCGTGGCCGT
GTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAGAGGCTGC
TGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCCTCTGGTG
GCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGATACCGAG
GTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACATTGGAAGG
CGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCTTCTCAGG
GCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGGCTCCGAG
GCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCCAGGGAGG
GAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCCGGAGGGC
GTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCACCCTGGG
CCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCTCCAGGGT
GTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGCGACTGGG
GCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCCCCTTCTC
AGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCCCCAGCTC
CTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAACACATTTG
GAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_005250764 ⟹ XP_005250821

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

Sequence:

show sequence

ACTTTTGTAGCGCCAGAGGCGACGGGCTCTGTCTGGTTGTAGCATCACAGAGCTTGATGGGAAC
TTTCACTCTGAGACCCCTTTTATGGATAAGAAAACTGAGGCTGGGGGGCAGGAGCAGCTTACCC
CAGAGGTCCTCTCTCCCAGAGGGCTAGGGTGGGGATAAGCAGGGTCTCGGGGGCAGCAAGACCC
AGCTCCAAATGTGGTTTTTCTGCCTTCTGGCTGTGTGACTCAGAAGGGTTGCTCAGCTTCTCTG
TGCTGTTATGGTTTGTCAGTGCAGTGTGGCAGTGCCTCAGTTTCCTCACCAGTACGCTAGGAGA
GACCAGCGTAGCCAGCCACAGCGGGGTCGTGAGGATTAAGTGAGGGGACAGCAGTGTCTGGCAC
GATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGTGGGCCACGGGGCCCAGCCCTAAGCA
CTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTCCCCGTGCCACTGGCTCTCACCATT
GCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGCCAGCTCTACCGCCTGAGCCCCCTG
CCCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGTGACACAGGCCCCACACGTCAGAGGC
CGCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAAGGCAGCTGGAGTTGGTTCAGTTCAA
GTTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCACCTCTGAGTGAAGGGGGCTGTCTGCC
CATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTCCAGCTCTGGACACTGCTTGGCGGCC
GGGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTTTTTTGGTTGTTCTTTTTATTTTTTG
CCTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTGGAGTTGCCCGCTTTACTTTGGTTGG
GTTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTTTTAAGAGTTGGGTTTTCTTTTTTAA
TTATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAGTATTTGCACAATATTTGTGCGGGGT
ATGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAGCACAGGGATCTCGTTCTCCTCATTT
TTTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAGCCTTCTCTGCAGTCCCTTCTGCCCT
GCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCGCCCGGCCCCGGTGGAGGTGAGCTAC
AAACACATGCGCTTCCTCATCACCCACAACCCCACCAACGCCACGCTCAGCACCTTCATTGAGG
ACCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTGACCTATGACAAAACGCC
GCTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATGGGGCGCCCCCGCCCGGC
AAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGAGGCCCCCGGCAGCTGCG
TGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGGCTCCAGTCCTTGTGGCGCTGGCCCTTATTGA
GAGCGGGATGAAGTACGAGGACGCCATCCAGTTCATCCGCCAGAAGCGCCGCGGAGCCATCAAC
AGCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAGACCCAC
ACACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCGTCATGT
AGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAGCAGGGG
CTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTGTGTCCG
AGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGCCACTCC
CTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCCGCCCCC
TCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATTTTGTAA
CCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCTTAAATT
ATTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCGTGGCCG
TGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAGAGGCTG
CTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCCTCTGGT
GGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGATACCGA
GGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACATTGGAAG
GCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCTTCTCAG
GGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGGCTCCGA
GGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCCAGGGAG
GGAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCCGGAGGG
CGTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCACCCTGG
GCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCTCCAGGG
TGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGCGACTGG
GGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCCCCTTCT
CAGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCCCCAGCT
CCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAACACATTT
GGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_006716500 ⟹ XP_006716563

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI

Sequence:

show sequence

AAGCCGGTGGAGCCGCGGCCGCGCCTGTGCGCGAGGGCGCGCGCGTCCCGAGCCCTCCACCCGT
CGTGCCGGCGCCGCCCGGACCGCCAGATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGT
GGGCCACGGGGCCCAGCCCTAAGCACTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGT
CCCCGTGCCACTGGCTCTCACCATTGCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGG
CCAGCTCTACCGCCTGAGCCCCCTGCCCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGT
GACACAGGCCCCACACGTCAGAGGCCGCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAA
GGCAGCTGGAGTTGGTTCAGTTCAAGTTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCAC
CTCTGAGTGAAGGGGGCTGTCTGCCCATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTC
CAGCTCTGGACACTGCTTGGCGGCCGGGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTT
TTTTGGTTGTTCTTTTTATTTTTTGCCTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTG
GAGTTGCCCGCTTTACTTTGGTTGGGTTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTT
TTAAGAGTTGGGTTTTCTTTTTTAATTATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAG
TATTTGCACAATATTTGTGCGGGGTATGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAG
CACAGGGATCTCGTTCTCCTCATTTTTTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAG
CCTTCTCTGCAGTCCCTTCTGCCCTGCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCG
CCCGGCCCCGGTGGAGGACCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTG
ACCTATGACAAAACGCCGCTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATG
GGGCGCCCCCGCCCGGCAAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGA
GGCCCCCGGCAGCTGCGTGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGGCTCCAGTCCTTGTG
GCGCTGGCCCTTATTGAGAGCGGGATGAAGTACGAGGACGCCATCCAGTTCATCCGCCAGAAGC
GCCGCGGAGCCATCAACAGCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCT
GCGGTTCAAAGACCCACACACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCT
GGGCCTGGTCGTCATGTAGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCT
GCCCAGCCCAGCAGGGGCTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCT
CCGTGCACTTGTGTCCGAGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCT
CCTGTCTCCGCCACTCCCTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGC
GCCCTCTGCCCGCCCCCTCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGT
GGGGGTATATTTTGTAACCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGT
TCTCGGCACCTTAAATTATTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAA
AACAGGAGCCGTGGCCGTGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCT
GGGGGCCCCAGAGGCTGCTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTC
TTGCGCTGCCCTCTGGTGGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTG
TCCTGTCCTGATACCGAGGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGG
GACTGTGACATTGGAAGGCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTC
ATTTGGCAGCTTCTCAGGGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTC
CACATTTCCGGCTCCGAGGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCA
TCCATCAGCCCAGGGAGGGAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGAC
CAGGGCCCGCCGGAGGGCGTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGG
GGCTGGCCCCACCCTGGGCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCC
TAGGGCTGGCTCCAGGGTGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTC
CCGCAAGGAGCGACTGGGGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAA
CCCCAAAAGCCCCTTCTCAGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAG
ACCTGGCTCCCCCAGCTCCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCC
TTTCCTCAAACACATTTGGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_011516803 ⟹ XP_011515105

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,400,571 - 141,432,454 (+)	NCBI

Sequence:

show sequence

GAATGAAACTCCATGCCCTCCGGGACACCATGCCCACTTCTGGGTACTGGCCTTCAGGGGCCTT
GGATGTGGGTGGCATGGCACTGGCTAAATGGGGCCCAGGAGGAAGGCAGCAGGACCGTGGGCAT
GCAGGCCTAATGCCAGGGCCAGGGCAGGCTTCATGTGGGCTTCCTCCTGTCTGGAATCCTGGAG
CCGCACAATTTCCGACCCAACACCCCGTACTCCAGAGCGACTGGCTCTTAACGGAAGCTGCTGC
TGGCAGATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGTGGGCCACGGGGCCCAGCCCT
AAGCACTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTCCCCGTGCCACTGGCTCTCA
CCATTGCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGCCAGCTCTACCGCCTGAGCC
CCCTGCCCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGTGACACAGGCCCCACACGTCA
GAGGCCGCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAAGGCAGCTGGAGTTGGTTCAG
TTCAAGTTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCACCTCTGAGTGAAGGGGGCTGT
CTGCCCATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTCCAGCTCTGGACACTGCTTGG
CGGCCGGGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTTTTTTGGTTGTTCTTTTTATT
TTTTGCCTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTGGAGTTGCCCGCTTTACTTTG
GTTGGGTTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTTTTAAGAGTTGGGTTTTCTTT
TTTAATTATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAGTATTTGCACAATATTTGTGC
GGGGTATGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAGCACAGGGATCTCGTTCTCCT
CATTTTTTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAGCCTTCTCTGCAGTCCCTTCT
GCCCTGCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCGCCCGGCCCCGGTGGAGGTGA
GCTACAAACACATGCGCTTCCTCATCACCCACAACCCCACCAACGCCACGCTCAGCACCTTCAT
TGAGGACCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTGACCTATGACAAA
ACGCCGCTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATGGGGCGCCCCCGC
CCGGCAAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGAGGCCCCCGGCAG
CTGCGTGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGGCTCCAGTCCTTGTGGCGCTGGCCCTT
ATTGAGAGCGGGATGAAGTACGAGGACGCCATCCAGTTCATCCGCCAGAAGCGCCGCGGAGCCA
TCAACAGCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAGA
CCCACACACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCGT
CATGTAGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAGC
AGGGGCTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTGT
GTCCGAGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGCC
ACTCCCTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCCG
CCCCCTCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATTT
TGTAACCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCTT
AAATTATTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCGT
GGCCGTGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAGA
GGCTGCTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCCT
CTGGTGGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGAT
ACCGAGGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACATT
GGAAGGCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCTT
CTCAGGGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGGC
TCCGAGGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCCA
GGGAGGGAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCCG
GAGGGCGTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCAC
CCTGGGCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCTC
CAGGGTGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGCG
ACTGGGGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCCC
CTTCTCAGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCCC
CAGCTCCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAACA
CATTTGGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_011516805 ⟹ XP_011515107

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI

Sequence:

show sequence

AGCCGGTGGAGCCGCGGCCGCGCCTGTGCGCGAGGGCGCGCGCGTCCCGAGCCCTCCACCCGTC
GTGCCGGCGCCGCCCGGACCGCCAGATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGTG
GGCCACGGGGCCCAGCCCTAAGCACTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTC
CCCGTGCCACTGGCTCTCACCATTGCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGC
CAGCTCTACCGCCTGAGCCCCCTGCCCCACTCCAGGACTCACCGTACCCCGATGGGGTCGTGTC
CCCAGCCTTCTCTGCAGTCCCTTCTGCCCTGCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATG
AACCGCCCGGCCCCGGTGGAGGTGAGCTACAAACACATGCGCTTCCTCATCACCCACAACCCCA
CCAACGCCACGCTCAGCACCTTCATTGAGGACCTGAAGAAGTACGGGGCTACCACTGTGGTGCG
TGTGTGTGAAGTGACCTATGACAAAACGCCGCTGGAGAAGGATGGCATCACCGTTGTGGACTGG
CCGTTTGACGATGGGGCGCCCCCGCCCGGCAAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGG
CCAAGTTCTGTGAGGCCCCCGGCAGCTGCGTGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGGC
TCCAGTCCTTGTGGCGCTGGCCCTTATTGAGAGCGGGATGAAGTACGAGGACGCCATCCAGTTC
ATCCGCCAGAAGCGCCGCGGAGCCATCAACAGCAAGCAGCTCACCTACCTGGAGAAATACCGGC
CCAAACAGAGGCTGCGGTTCAAAGACCCACACACGCACAAGACCCGGTGCTGCGTTATGTAGCT
CAGGACCTTGGCTGGGCCTGGTCGTCATGTAGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGC
CCAGCCCTGCTCTGCCCAGCCCAGCAGGGGCTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTC
CTCCCCGACACCTCCGTGCACTTGTGTCCGAGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCT
CTGGGCCCTTTCTCCTGTCTCCGCCACTCCCTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTG
AGGTGGGTCGGGCGCCCTCTGCCCGCCCCCTCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTG
TTTGTTGTGGGGTGGGGGTATATTTTGTAACCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCT
TGTCCTGACCTGTTCTCGGCACCTTAAATTATTAGACCCCGGGGCAGTCAGGTGCTCCGGACAC
CCGAAGGCAATAAAACAGGAGCCGTGGCCGTGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGC
GGGCTGGTGGCCTGGGGGCCCCAGAGGCTGCTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGG
CTCCCGCGTGCTCTTGCGCTGCCCTCTGGTGGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGG
CCAGCCTGCCCTGTCCTGTCCTGATACCGAGGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGT
TGACGGTTCTTGGGACTGTGACATTGGAAGGCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGA
TGGGCTGGGATTCATTTGGCAGCTTCTCAGGGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCC
CAAACCAGGTGTCCACATTTCCGGCTCCGAGGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTG
GAGGAAGTCACCATCCATCAGCCCAGGGAGGGAGGGTGCCACCTGGGCACCTGGGGCTGGATGT
GAGAGGCCTGGACCAGGGCCCGCCGGAGGGCGTGGACCAGATGCTCATGTGTTCCTGGGTGCAG
TGTCTGTGTTGGGGGCTGGCCCCACCCTGGGCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGG
AGGAAGGTGGGCCTAGGGCTGGCTCCAGGGTGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGG
CCCCAGGAGGTTCCCGCAAGGAGCGACTGGGGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGG
GGAGATGTGGAAACCCCAAAAGCCCCTTCTCAGGCAGCCCTGCCCCCAAGACCGACAGATGGCT
AAGGGGGCCGCAGACCTGGCTCCCCCAGCTCCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGAT
GGTTATTCTCTCCTTTCCTCAAACACATTTGGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_017012998 ⟹ XP_016868487

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI

Sequence:

show sequence

AAGCCGGTGGAGCCGCGGCCGCGCCTGTGCGCGAGGGCGCGCGCGTCCCGAGCCCTCCACCCGT
CGTGCCGGCGCCGCCCGGACCGCCAGATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGT
GGGCCACGGGGCCCAGCCCTAAGCACTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGT
CCCCGTGCCACTGGCTCTCACCATTGCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGG
CCAGCTCTACCGCCTGAGCCCCCTGCCCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGT
GACACAGGCCCCACACGTCAGAGGCCGCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAA
GGCAGCTGGAGTTGGTTCAGTTCAAGTTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCAC
CTCTGAGTGAAGGGGGCTGTCTGCCCATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTC
CAGCTCTGGACACTGCTTGGCGGCCGGGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTT
TTTTGGTTGTTCTTTTTATTTTTTGCCTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTG
GAGTTGCCCGCTTTACTTTGGTTGGGTTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTT
TTAAGAGTTGGGTTTTCTTTTTTAATTATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAG
TATTTGCACAATATTTGTGCGGGGTATGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAG
CACAGGGATCTCGTTCTCCTCATTTTTTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAG
CCTTCTCTGCAGTCCCTTCTGCCCTGCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCG
CCCGGCCCCGGTGGAGGTGAGCTACAAACACATGCGCTTCCTCATCACCCACAACCCCACCAAC
GCCACGCTCAGCACCTTCATTGAGGACCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGT
GTGAAGTGACCTATGACAAAACGCCGCTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTT
TGACGATGGGGCGCCCCCGCCCGGCAAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAG
TTCTGTGAGGCCCCCGGCAGCTGCGTGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGAAGCGCC
GCGGAGCCATCAACAGCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCG
GTTCAAAGACCCACACACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGG
CCTGGTCGTCATGTAGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCC
CAGCCCAGCAGGGGCTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCG
TGCACTTGTGTCCGAGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCT
GTCTCCGCCACTCCCTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCC
CTCTGCCCGCCCCCTCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGG
GGTATATTTTGTAACCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCT
CGGCACCTTAAATTATTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAAC
AGGAGCCGTGGCCGTGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGG
GGCCCCAGAGGCTGCTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTG
CGCTGCCCTCTGGTGGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCC
TGTCCTGATACCGAGGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGAC
TGTGACATTGGAAGGCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATT
TGGCAGCTTCTCAGGGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCAC
ATTTCCGGCTCCGAGGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCC
ATCAGCCCAGGGAGGGAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAG
GGCCCGCCGGAGGGCGTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGC
TGGCCCCACCCTGGGCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAG
GGCTGGCTCCAGGGTGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCG
CAAGGAGCGACTGGGGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCC
CAAAAGCCCCTTCTCAGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACC
TGGCTCCCCCAGCTCCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTT
CCTCAAACACATTTGGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_017012999 ⟹ XP_016868488

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,392,021 - 141,432,454 (+)	NCBI

Sequence:

show sequence

AAGCCGGTGGAGCCGCGGCCGCGCCTGTGCGCGAGGGCGCGCGCGTCCCGAGCCCTCCACCCGT
CGTGCCGGCGCCGCCCGGACCGCCAGATGCTGTGTGCTGTGGACCCACCTGGGGTTCATGGAGT
GGGCCACGGGGCCCAGCCCTAAGCACTGCTGCGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGT
CCCCGTGCCACTGGCTCTCACCATTGCCCTCGCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGG
CCAGCTCTACCGCCTGAGCCCCCTGCCCCACTCCAGGACTCACCGTACCCCGATGGGGTAACGT
GACACAGGCCCCACACGTCAGAGGCCGCTGTCCCCACGGCCACTGCCCGTGACCCCTGGCCCAA
GGCAGCTGGAGTTGGTTCAGTTCAAGTTCATTCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCAC
CTCTGAGTGAAGGGGGCTGTCTGCCCATCCACCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTC
CAGCTCTGGACACTGCTTGGCGGCCGGGTTCACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTT
TTTTGGTTGTTCTTTTTATTTTTTGCCTCTTTATGACTATCCAGCTCTGAGAGACGGGAGTTTG
GAGTTGCCCGCTTTACTTTGGTTGGGTTGGGGGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTT
TTAAGAGTTGGGTTTTCTTTTTTAATTATCCAAACAGTGGGCAGCTTCCTCCCCCACACCCAAG
TATTTGCACAATATTTGTGCGGGGTATGGGGGTGGGTTTTTAAATCTCGTTTCTCTTGGACAAG
CACAGGGATCTCGTTCTCCTCATTTTTTGGGGGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAG
CCTTCTCTGCAGTCCCTTCTGCCCTGCCGGGCCCGTCGGGAGGCGCCATGGCTCGGATGAACCG
CCCGGCCCCGGTGGAGGACCTGAAGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTG
ACCTATGACAAAACGCCGCTGGAGAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATG
GGGCGCCCCCGCCCGGCAAGGTAGTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGA
GGCCCCCGGCAGCTGCGTGGCTGTGCACTGCGTGGCGGGCCTGGGCCGGAAGCGCCGCGGAGCC
ATCAACAGCAAGCAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAG
ACCCACACACGCACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCG
TCATGTAGGTCAGGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAG
CAGGGGCTCCAGGCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTG
TGTCCGAGGAGCGAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGC
CACTCCCTCTGGCGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCC
GCCCCCTCCCACACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATT
TTGTAACCACTGGGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCT
TAAATTATTAGACCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCG
TGGCCGTGTGTGTGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAG
AGGCTGCTGTCTGGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCC
TCTGGTGGCCGCTCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGA
TACCGAGGTGGGAGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACAT
TGGAAGGCGAGGCAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCT
TCTCAGGGCCTGTGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGG
CTCCGAGGCGCAGAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCC
AGGGAGGGAGGGTGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCC
GGAGGGCGTGGACCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCA
CCCTGGGCCGGGGTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCT
CCAGGGTGTGGAGAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGC
GACTGGGGCAGGTGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCC
CCTTCTCAGGCAGCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCC
CCAGCTCCTGTGTGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAAC
ACATTTGGAACTCAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_024447057 ⟹ XP_024302825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

Sequence:

show sequence

AGCACCGTGGGCACCGCCAGGCCGGCGCGTATGGAGGCGGTGGGACGCCTGCGGCGCGGATGCT
GTGTGCTGTGGACCCACCTGGGGTTCATGGAGTGGGCCACGGGGCCCAGCCCTAAGCACTGCTG
CGCCCAGGGTCGCCGCGCCTCCTGCTGAGGGGTCCCCGTGCCACTGGCTCTCACCATTGCCCTC
GCCTGCCGATGGCCTCTGCTGCCCAGCCTGGGGCCAGCTCTACCGCCTGAGCCCCCTGCCCCAC
TCCAGGACTCACCGTACCCCGATGGGGTAACGTGACACAGGCCCCACACGTCAGAGGCCGCTGT
CCCCACGGCCACTGCCCGTGACCCCTGGCCCAAGGCAGCTGGAGTTGGTTCAGTTCAAGTTCAT
TCTTCCTCTGGCCCTTGGGGGCTTGGGGCCCACCTCTGAGTGAAGGGGGCTGTCTGCCCATCCA
CCAATGTGGAGAGGGCGCCCCCGGTGTGGGGTCCAGCTCTGGACACTGCTTGGCGGCCGGGTTC
ACTTTGAGTTTTTAAGTTTTCTTTGCTGAGCTTTTTTGGTTGTTCTTTTTATTTTTTGCCTCTT
TATGACTATCCAGCTCTGAGAGACGGGAGTTTGGAGTTGCCCGCTTTACTTTGGTTGGGTTGGG
GGGGGCGGCGGGCTGTTTTGTTCCTTTTCTTTTTTAAGAGTTGGGTTTTCTTTTTTAATTATCC
AAACAGTGGGCAGCTTCCTCCCCCACACCCAAGTATTTGCACAATATTTGTGCGGGGTATGGGG
GTGGGTTTTTAAATCTCGTTTCTCTTGGACAAGCACAGGGATCTCGTTCTCCTCATTTTTTGGG
GGTGTGTGGGGACTTCTCAGGTCGTGTCCCCAGCCTTCTCTGCAGTCCCTTCTGCCCTGCCGGG
CCCGTCGGGAGGCGCCATGGCTCGGATGAACCGCCCGGCCCCGGTGGAGGTGAGCTACAAACAC
ATGCGCTTCCTCATCACCCACAACCCCACCAACGCCACGCTCAGCACCTTCATTGAGGACCTGA
AGAAGTACGGGGCTACCACTGTGGTGCGTGTGTGTGAAGTGACCTATGACAAAACGCCGCTGGA
GAAGGATGGCATCACCGTTGTGGACTGGCCGTTTGACGATGGGGCGCCCCCGCCCGGCAAGGTA
GTGGAAGACTGGCTGAGCCTGGTGAAGGCCAAGTTCTGTGAGGCCCCCGGCAGCTGCGTGGCTG
TGCACTGCGTGGCGGGCCTGGGCCGGGCTCCAGTCCTTGTGGCGCTGGCCCTTATTGAGAGCGG
GATGAAGTACGAGGACGCCATCCAGTTCATCCGCCAGAAGCGCCGCGGAGCCATCAACAGCAAG
CAGCTCACCTACCTGGAGAAATACCGGCCCAAACAGAGGCTGCGGTTCAAAGACCCACACACGC
ACAAGACCCGGTGCTGCGTTATGTAGCTCAGGACCTTGGCTGGGCCTGGTCGTCATGTAGGTCA
GGACCTTGGCTGGACCTGGAGGCCCTGCCCAGCCCTGCTCTGCCCAGCCCAGCAGGGGCTCCAG
GCCTTGGCTGGCCCCACATCGCCTTTTCCTCCCCGACACCTCCGTGCACTTGTGTCCGAGGAGC
GAGGAGCCCCTCGGGCCCTGGGTGGCCTCTGGGCCCTTTCTCCTGTCTCCGCCACTCCCTCTGG
CGGCGCTGGCCGTGGCTCTGTCTCTCTGAGGTGGGTCGGGCGCCCTCTGCCCGCCCCCTCCCAC
ACCAGCCAGGCTGGTCTCCTCTAGCCTGTTTGTTGTGGGGTGGGGGTATATTTTGTAACCACTG
GGCCCCCAGCCCCTCTTTTGCGACCCCTTGTCCTGACCTGTTCTCGGCACCTTAAATTATTAGA
CCCCGGGGCAGTCAGGTGCTCCGGACACCCGAAGGCAATAAAACAGGAGCCGTGGCCGTGTGTG
TGGAGTGGGCTACAGCGTCAGGCGGGGCGGGCTGGTGGCCTGGGGGCCCCAGAGGCTGCTGTCT
GGATCCTGGGCTGGTGCCCAGGATGGGGCTCCCGCGTGCTCTTGCGCTGCCCTCTGGTGGCCGC
TCTGGGTCCTTGCACCCCGACCCAGGGGCCAGCCTGCCCTGTCCTGTCCTGATACCGAGGTGGG
AGCCCTGCCTTGGCCAGGGTGGCCGTGTTGACGGTTCTTGGGACTGTGACATTGGAAGGCGAGG
CAGGTCACCAGCACTGTCCTCTGCAGGATGGGCTGGGATTCATTTGGCAGCTTCTCAGGGCCTG
TGTCCGGCTGGTTGGTCCCTGTGCTGCCCAAACCAGGTGTCCACATTTCCGGCTCCGAGGCGCA
GAGAAGGGGGCAGGTGGTGGCTTGGGTGGAGGAAGTCACCATCCATCAGCCCAGGGAGGGAGGG
TGCCACCTGGGCACCTGGGGCTGGATGTGAGAGGCCTGGACCAGGGCCCGCCGGAGGGCGTGGA
CCAGATGCTCATGTGTTCCTGGGTGCAGTGTCTGTGTTGGGGGCTGGCCCCACCCTGGGCCGGG
GTGCATGGAGGGCATGGCCCCAGCGGGGAGGAAGGTGGGCCTAGGGCTGGCTCCAGGGTGTGGA
GAGCCTGGGAGTGGTCTCCGTCCTGGGGCCCCAGGAGGTTCCCGCAAGGAGCGACTGGGGCAGG
TGCTGGAGGAGGTCAGTGGACAAGATGGGGAGATGTGGAAACCCCAAAAGCCCCTTCTCAGGCA
GCCCTGCCCCCAAGACCGACAGATGGCTAAGGGGGCCGCAGACCTGGCTCCCCCAGCTCCTGTG
TGGAGAAAGGGCAACAGCTGTCCCGGATGGTTATTCTCTCCTTTCCTCAAACACATTTGGAACT
CAAGTAAATCCAATGCATGTTGGGTGAA

hide sequence

RefSeq Acc Id:

XM_047421287 ⟹ XP_047277243

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421288 ⟹ XP_047277244

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421289 ⟹ XP_047277245

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421290 ⟹ XP_047277246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,415,401 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421291 ⟹ XP_047277247

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421292 ⟹ XP_047277248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421293 ⟹ XP_047277249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421294 ⟹ XP_047277250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421295 ⟹ XP_047277251

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421296 ⟹ XP_047277252

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,400,571 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421297 ⟹ XP_047277253

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421298 ⟹ XP_047277254

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421299 ⟹ XP_047277255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421300 ⟹ XP_047277256

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,400,571 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421301 ⟹ XP_047277257

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421302 ⟹ XP_047277258

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421303 ⟹ XP_047277259

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421304 ⟹ XP_047277260

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,416,126 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421305 ⟹ XP_047277261

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,415,413 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_047421306 ⟹ XP_047277262

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	141,417,909 - 141,432,454 (+)	NCBI

RefSeq Acc Id:

XM_054359641 ⟹ XP_054215616

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,271 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359642 ⟹ XP_054215617

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,259 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359643 ⟹ XP_054215618

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,477 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359644 ⟹ XP_054215619

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,534,741 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359645 ⟹ XP_054215620

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,369 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359646 ⟹ XP_054215621

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,271 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359647 ⟹ XP_054215622

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,471 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359648 ⟹ XP_054215623

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,536,670 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359649 ⟹ XP_054215624

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,537,617 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359650 ⟹ XP_054215625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,440 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359651 ⟹ XP_054215626

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,238 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359652 ⟹ XP_054215627

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,271 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359653 ⟹ XP_054215628

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359654 ⟹ XP_054215629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,537,353 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359655 ⟹ XP_054215630

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,281 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359656 ⟹ XP_054215631

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,238 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359657 ⟹ XP_054215632

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359658 ⟹ XP_054215633

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,537,383 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359659 ⟹ XP_054215634

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,534,789 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359660 ⟹ XP_054215635

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,544,047 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359661 ⟹ XP_054215636

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,491 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359662 ⟹ XP_054215637

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,265 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359663 ⟹ XP_054215638

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,238 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359664 ⟹ XP_054215639

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,537,383 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359665 ⟹ XP_054215640

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359666 ⟹ XP_054215641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,488 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359667 ⟹ XP_054215642

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,245 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359668 ⟹ XP_054215643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,534,779 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359669 ⟹ XP_054215644

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,488 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359670 ⟹ XP_054215645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,471 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359671 ⟹ XP_054215646

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,543,666 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359672 ⟹ XP_054215647

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,536,632 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359673 ⟹ XP_054215648

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,238 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359674 ⟹ XP_054215649

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,513,520 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359675 ⟹ XP_054215650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,537,370 - 142,559,812 (+)	NCBI

RefSeq Acc Id:

XM_054359676 ⟹ XP_054215651

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	142,545,284 - 142,559,812 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_009010	(Get FASTA)	NCBI Sequence Viewer
	NP_116000	(Get FASTA)	NCBI Sequence Viewer
	XP_005250821	(Get FASTA)	NCBI Sequence Viewer
	XP_006716563	(Get FASTA)	NCBI Sequence Viewer
	XP_011515105	(Get FASTA)	NCBI Sequence Viewer
	XP_011515107	(Get FASTA)	NCBI Sequence Viewer
	XP_016868487	(Get FASTA)	NCBI Sequence Viewer
	XP_016868488	(Get FASTA)	NCBI Sequence Viewer
	XP_024302825	(Get FASTA)	NCBI Sequence Viewer
	XP_047277243	(Get FASTA)	NCBI Sequence Viewer
	XP_047277244	(Get FASTA)	NCBI Sequence Viewer
	XP_047277245	(Get FASTA)	NCBI Sequence Viewer
	XP_047277246	(Get FASTA)	NCBI Sequence Viewer
	XP_047277247	(Get FASTA)	NCBI Sequence Viewer
	XP_047277248	(Get FASTA)	NCBI Sequence Viewer
	XP_047277249	(Get FASTA)	NCBI Sequence Viewer
	XP_047277250	(Get FASTA)	NCBI Sequence Viewer
	XP_047277251	(Get FASTA)	NCBI Sequence Viewer
	XP_047277252	(Get FASTA)	NCBI Sequence Viewer
	XP_047277253	(Get FASTA)	NCBI Sequence Viewer
	XP_047277254	(Get FASTA)	NCBI Sequence Viewer
	XP_047277255	(Get FASTA)	NCBI Sequence Viewer
	XP_047277256	(Get FASTA)	NCBI Sequence Viewer
	XP_047277257	(Get FASTA)	NCBI Sequence Viewer
	XP_047277258	(Get FASTA)	NCBI Sequence Viewer
	XP_047277259	(Get FASTA)	NCBI Sequence Viewer
	XP_047277260	(Get FASTA)	NCBI Sequence Viewer
	XP_047277261	(Get FASTA)	NCBI Sequence Viewer
	XP_047277262	(Get FASTA)	NCBI Sequence Viewer
	XP_054184761	(Get FASTA)	NCBI Sequence Viewer
	XP_054184762	(Get FASTA)	NCBI Sequence Viewer
	XP_054184763	(Get FASTA)	NCBI Sequence Viewer
	XP_054184764	(Get FASTA)	NCBI Sequence Viewer
	XP_054184765	(Get FASTA)	NCBI Sequence Viewer
	XP_054184766	(Get FASTA)	NCBI Sequence Viewer
	XP_054184767	(Get FASTA)	NCBI Sequence Viewer
	XP_054184768	(Get FASTA)	NCBI Sequence Viewer
	XP_054184769	(Get FASTA)	NCBI Sequence Viewer
	XP_054184770	(Get FASTA)	NCBI Sequence Viewer
	XP_054184771	(Get FASTA)	NCBI Sequence Viewer
	XP_054184772	(Get FASTA)	NCBI Sequence Viewer
	XP_054184773	(Get FASTA)	NCBI Sequence Viewer
	XP_054184774	(Get FASTA)	NCBI Sequence Viewer
	XP_054184775	(Get FASTA)	NCBI Sequence Viewer
	XP_054184776	(Get FASTA)	NCBI Sequence Viewer
	XP_054184777	(Get FASTA)	NCBI Sequence Viewer
	XP_054184778	(Get FASTA)	NCBI Sequence Viewer
	XP_054184779	(Get FASTA)	NCBI Sequence Viewer
	XP_054184780	(Get FASTA)	NCBI Sequence Viewer
	XP_054184781	(Get FASTA)	NCBI Sequence Viewer
	XP_054184782	(Get FASTA)	NCBI Sequence Viewer
	XP_054184783	(Get FASTA)	NCBI Sequence Viewer
	XP_054184784	(Get FASTA)	NCBI Sequence Viewer
	XP_054184785	(Get FASTA)	NCBI Sequence Viewer
	XP_054184786	(Get FASTA)	NCBI Sequence Viewer
	XP_054184787	(Get FASTA)	NCBI Sequence Viewer
	XP_054184788	(Get FASTA)	NCBI Sequence Viewer
	XP_054184789	(Get FASTA)	NCBI Sequence Viewer
	XP_054184790	(Get FASTA)	NCBI Sequence Viewer
	XP_054184791	(Get FASTA)	NCBI Sequence Viewer
	XP_054184792	(Get FASTA)	NCBI Sequence Viewer
	XP_054184793	(Get FASTA)	NCBI Sequence Viewer
	XP_054184794	(Get FASTA)	NCBI Sequence Viewer
	XP_054184795	(Get FASTA)	NCBI Sequence Viewer
	XP_054184796	(Get FASTA)	NCBI Sequence Viewer
	XP_054189029	(Get FASTA)	NCBI Sequence Viewer
	XP_054189030	(Get FASTA)	NCBI Sequence Viewer
	XP_054189031	(Get FASTA)	NCBI Sequence Viewer
	XP_054189032	(Get FASTA)	NCBI Sequence Viewer
	XP_054189033	(Get FASTA)	NCBI Sequence Viewer
	XP_054189034	(Get FASTA)	NCBI Sequence Viewer
	XP_054189035	(Get FASTA)	NCBI Sequence Viewer
	XP_054189036	(Get FASTA)	NCBI Sequence Viewer
	XP_054189037	(Get FASTA)	NCBI Sequence Viewer
	XP_054189038	(Get FASTA)	NCBI Sequence Viewer
	XP_054189039	(Get FASTA)	NCBI Sequence Viewer
	XP_054189040	(Get FASTA)	NCBI Sequence Viewer
	XP_054189041	(Get FASTA)	NCBI Sequence Viewer
	XP_054189042	(Get FASTA)	NCBI Sequence Viewer
	XP_054189043	(Get FASTA)	NCBI Sequence Viewer
	XP_054189044	(Get FASTA)	NCBI Sequence Viewer
	XP_054189045	(Get FASTA)	NCBI Sequence Viewer
	XP_054189046	(Get FASTA)	NCBI Sequence Viewer
	XP_054189047	(Get FASTA)	NCBI Sequence Viewer
	XP_054189048	(Get FASTA)	NCBI Sequence Viewer
	XP_054189049	(Get FASTA)	NCBI Sequence Viewer
	XP_054189050	(Get FASTA)	NCBI Sequence Viewer
	XP_054189051	(Get FASTA)	NCBI Sequence Viewer
	XP_054189052	(Get FASTA)	NCBI Sequence Viewer
	XP_054189053	(Get FASTA)	NCBI Sequence Viewer
	XP_054189054	(Get FASTA)	NCBI Sequence Viewer
	XP_054189055	(Get FASTA)	NCBI Sequence Viewer
	XP_054189056	(Get FASTA)	NCBI Sequence Viewer
	XP_054215616	(Get FASTA)	NCBI Sequence Viewer
	XP_054215617	(Get FASTA)	NCBI Sequence Viewer
	XP_054215618	(Get FASTA)	NCBI Sequence Viewer
	XP_054215619	(Get FASTA)	NCBI Sequence Viewer
	XP_054215620	(Get FASTA)	NCBI Sequence Viewer
	XP_054215621	(Get FASTA)	NCBI Sequence Viewer
	XP_054215622	(Get FASTA)	NCBI Sequence Viewer
	XP_054215623	(Get FASTA)	NCBI Sequence Viewer
	XP_054215624	(Get FASTA)	NCBI Sequence Viewer
	XP_054215625	(Get FASTA)	NCBI Sequence Viewer
	XP_054215626	(Get FASTA)	NCBI Sequence Viewer
	XP_054215627	(Get FASTA)	NCBI Sequence Viewer
	XP_054215628	(Get FASTA)	NCBI Sequence Viewer
	XP_054215629	(Get FASTA)	NCBI Sequence Viewer
	XP_054215630	(Get FASTA)	NCBI Sequence Viewer
	XP_054215631	(Get FASTA)	NCBI Sequence Viewer
	XP_054215632	(Get FASTA)	NCBI Sequence Viewer
	XP_054215633	(Get FASTA)	NCBI Sequence Viewer
	XP_054215634	(Get FASTA)	NCBI Sequence Viewer
	XP_054215635	(Get FASTA)	NCBI Sequence Viewer
	XP_054215636	(Get FASTA)	NCBI Sequence Viewer
	XP_054215637	(Get FASTA)	NCBI Sequence Viewer
	XP_054215638	(Get FASTA)	NCBI Sequence Viewer
	XP_054215639	(Get FASTA)	NCBI Sequence Viewer
	XP_054215640	(Get FASTA)	NCBI Sequence Viewer
	XP_054215641	(Get FASTA)	NCBI Sequence Viewer
	XP_054215642	(Get FASTA)	NCBI Sequence Viewer
	XP_054215643	(Get FASTA)	NCBI Sequence Viewer
	XP_054215644	(Get FASTA)	NCBI Sequence Viewer
	XP_054215645	(Get FASTA)	NCBI Sequence Viewer
	XP_054215646	(Get FASTA)	NCBI Sequence Viewer
	XP_054215647	(Get FASTA)	NCBI Sequence Viewer
	XP_054215648	(Get FASTA)	NCBI Sequence Viewer
	XP_054215649	(Get FASTA)	NCBI Sequence Viewer
	XP_054215650	(Get FASTA)	NCBI Sequence Viewer
	XP_054215651	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB47560	(Get FASTA)	NCBI Sequence Viewer
	AAC29314	(Get FASTA)	NCBI Sequence Viewer
	AAH03105	(Get FASTA)	NCBI Sequence Viewer
	AAP35967	(Get FASTA)	NCBI Sequence Viewer
	CAC81757	(Get FASTA)	NCBI Sequence Viewer
	EAW92231	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000331730
	ENSP00000331730.2
	ENSP00000332274
	ENSP00000332274.1
	ENSP00000428725.1
	ENSP00000428758
	ENSP00000428758.1
	ENSP00000428976
	ENSP00000428976.1
	ENSP00000430332.1
	ENSP00000481205.1
	ENSP00000484500.1
	ENSP00000487595.1
	ENSP00000487610.1
	ENSP00000487861.1
	ENSP00000505068
	ENSP00000505068.1
	ENSP00000506615
	ENSP00000506615.1
	ENSP00000516925.1
	ENSP00000516927.1
	ENSP00000516928.1
	ENSP00000516929.1
	ENSP00000516930.1
	ENSP00000516931.1
GenBank Protein	O75365	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_116000 ⟸ NM_032611
- Peptide Label:	isoform 1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYED AIQFIRQKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	NP_009010 ⟸ NM_007079
- Peptide Label:	isoform 2
- UniProtKB:	O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRKRRGAINSKQLTYLEKYR PKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_005250821 ⟸ XM_005250764
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYED AIQFIRQKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_006716563 ⟸ XM_006716500
- Peptide Label:	isoform X2
- Sequence:	show sequence MARMNRPAPVEDLKKYGATTVVRVCEVTYDKTPLEKDGITVVDWPFDDGAPPPGKVVEDWLSLV KAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYEDAIQFIRQKRRGAINSKQLTYLEKY RPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_011515107 ⟸ XM_011516805
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYED AIQFIRQKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_011515105 ⟸ XM_011516803
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYED AIQFIRQKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_016868487 ⟸ XM_017012998
- Peptide Label:	isoform X3
- UniProtKB:	O75365 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRKRRGAINSKQLTYLEKYR PKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_016868488 ⟸ XM_017012999
- Peptide Label:	isoform X4
- Sequence:	show sequence MARMNRPAPVEDLKKYGATTVVRVCEVTYDKTPLEKDGITVVDWPFDDGAPPPGKVVEDWLSLV KAKFCEAPGSCVAVHCVAGLGRKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:	XP_024302825 ⟸ XM_024447057
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARMNRPAPVEVSYKHMRFLITHNPTNATLSTFIEDLKKYGATTVVRVCEVTYDKTPLEKDGIT VVDWPFDDGAPPPGKVVEDWLSLVKAKFCEAPGSCVAVHCVAGLGRAPVLVALALIESGMKYED AIQFIRQKRRGAINSKQLTYLEKYRPKQRLRFKDPHTHKTRCCVM hide sequence

RefSeq Acc Id:

ENSP00000331730 ⟸ ENST00000349124

RefSeq Acc Id:

ENSP00000428758 ⟸ ENST00000520105

RefSeq Acc Id:

ENSP00000428976 ⟸ ENST00000521578

RefSeq Acc Id:

ENSP00000428725 ⟸ ENST00000523147

RefSeq Acc Id:

ENSP00000430332 ⟸ ENST00000524028

RefSeq Acc Id:

ENSP00000332274 ⟸ ENST00000329397

RefSeq Acc Id:

ENSP00000506615 ⟸ ENST00000681443

RefSeq Acc Id:

ENSP00000505068 ⟸ ENST00000680615

RefSeq Acc Id:	XP_047277256 ⟸ XM_047421300
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277252 ⟸ XM_047421296
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047277246 ⟸ XM_047421290
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277261 ⟸ XM_047421305
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277254 ⟸ XM_047421298
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277244 ⟸ XM_047421288
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277257 ⟸ XM_047421301
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277253 ⟸ XM_047421297
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047277247 ⟸ XM_047421291
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277260 ⟸ XM_047421304
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277259 ⟸ XM_047421303
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277248 ⟸ XM_047421292
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277250 ⟸ XM_047421294
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277245 ⟸ XM_047421289
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277258 ⟸ XM_047421302
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277243 ⟸ XM_047421287
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277249 ⟸ XM_047421293
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047277255 ⟸ XM_047421299
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047277251 ⟸ XM_047421295
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047277262 ⟸ XM_047421306
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054215640 ⟸ XM_054359665
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215632 ⟸ XM_054359657
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215649 ⟸ XM_054359674
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054215628 ⟸ XM_054359653
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215619 ⟸ XM_054359644
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215643 ⟸ XM_054359668
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215634 ⟸ XM_054359659
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215647 ⟸ XM_054359672
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215623 ⟸ XM_054359648
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215629 ⟸ XM_054359654
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215650 ⟸ XM_054359675
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054215639 ⟸ XM_054359664
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215633 ⟸ XM_054359658
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215624 ⟸ XM_054359649
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215620 ⟸ XM_054359645
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215625 ⟸ XM_054359650
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215622 ⟸ XM_054359647
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215645 ⟸ XM_054359670
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215618 ⟸ XM_054359643
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215641 ⟸ XM_054359666
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215644 ⟸ XM_054359669
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215636 ⟸ XM_054359661
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215646 ⟸ XM_054359671
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215635 ⟸ XM_054359660
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215638 ⟸ XM_054359663
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215631 ⟸ XM_054359656
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215648 ⟸ XM_054359673
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054215626 ⟸ XM_054359651
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215642 ⟸ XM_054359667
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215617 ⟸ XM_054359642
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215637 ⟸ XM_054359662
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215621 ⟸ XM_054359646
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215616 ⟸ XM_054359641
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215627 ⟸ XM_054359652
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215630 ⟸ XM_054359655
- Peptide Label:	isoform X1
- UniProtKB:	Q99849 (UniProtKB/Swiss-Prot), Q8IVN5 (UniProtKB/Swiss-Prot), O75365 (UniProtKB/Swiss-Prot), Q9BTW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054215651 ⟸ XM_054359676
- Peptide Label:	isoform X4

Protein Domains

Tyrosine-protein phosphatase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O75365-F1-model_v2	AlphaFold	O75365	1-173	view protein structure

Promoters

RGD ID:

7214271

Promoter ID:

EPDNEW_H12882

Type:

initiation region

Name:

PTP4A3_1

Description:

protein tyrosine phosphatase type IVA, member 3

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	8	141,421,447 - 141,421,507	EPDNEW

RGD ID:

6813492

Promoter ID:

HG_ACW:79244

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

PTP4A3.IAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	142,493,831 - 142,494,331 (+)	MPROMDB

RGD ID:

6813488

Promoter ID:

HG_ACW:79246

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

PTP4A3.HAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	142,496,131 - 142,496,631 (+)	MPROMDB

RGD ID:

6813487

Promoter ID:

HG_ACW:79247

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, Jurkat, K562, Lymphoblastoid

Transcripts:

PTP4A3.DAPR07, PTP4A3.FAPR07, PTP4A3.KAPR07, PTP4A3.MAPR07, PTP4A3.QAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	142,497,029 - 142,497,529 (+)	MPROMDB

RGD ID:

6806820

Promoter ID:

HG_KWN:62213

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

ENST00000327627, NM_007079, NM_032611, UC010MET.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	142,500,179 - 142,500,679 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:9636	AgrOrtholog
COSMIC	PTP4A3	COSMIC
Ensembl Genes	ENSG00000184489	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENSG00000275575	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENSG00000291470	UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000329397	ENTREZGENE
	ENST00000329397.6	UniProtKB/Swiss-Prot
	ENST00000349124	ENTREZGENE
	ENST00000349124.3	UniProtKB/Swiss-Prot
	ENST00000520105	ENTREZGENE
	ENST00000520105.5	UniProtKB/Swiss-Prot
	ENST00000521578	ENTREZGENE
	ENST00000521578.6	UniProtKB/Swiss-Prot
	ENST00000523147.5	UniProtKB/TrEMBL
	ENST00000524028.1	UniProtKB/TrEMBL
	ENST00000614325.2	UniProtKB/Swiss-Prot
	ENST00000622569.3	UniProtKB/Swiss-Prot
	ENST00000633262.1	UniProtKB/TrEMBL
	ENST00000633518.1	UniProtKB/Swiss-Prot
	ENST00000633621.1	UniProtKB/Swiss-Prot
	ENST00000680615	ENTREZGENE
	ENST00000680615.1	UniProtKB/Swiss-Prot
	ENST00000681443	ENTREZGENE
	ENST00000681443.1	UniProtKB/Swiss-Prot
	ENST00000707614.1	UniProtKB/Swiss-Prot
	ENST00000707616.1	UniProtKB/Swiss-Prot
	ENST00000707617.1	UniProtKB/Swiss-Prot
	ENST00000707618.1	UniProtKB/Swiss-Prot
	ENST00000707619.1	UniProtKB/Swiss-Prot
	ENST00000707620.1	UniProtKB/Swiss-Prot
Gene3D-CATH	3.90.190.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000184489	GTEx
	ENSG00000275575	GTEx
	ENSG00000291470	GTEx
HGNC ID	HGNC:9636	ENTREZGENE
Human Proteome Map	PTP4A3	Human Proteome Map
InterPro	Prot-tyrosine_phosphatase-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTP_cat	UniProtKB/Swiss-Prot
	Tyr_Pase_cat	UniProtKB/Swiss-Prot
	TYR_PHOSPHATASE_dom	UniProtKB/Swiss-Prot
	TYR_PHOSPHATASE_DUAL_dom	UniProtKB/Swiss-Prot
KEGG Report	hsa:11156	UniProtKB/Swiss-Prot
NCBI Gene	11156	ENTREZGENE
OMIM	606449	OMIM
PANTHER	PROTEIN TYROSINE PHOSPHATASE TYPE IVA 3	UniProtKB/Swiss-Prot
	TYROSINE SPECIFIC PROTEIN PHOSPHATASE AND DUAL SPECIFICITY PROTEIN PHOSPHATASE	UniProtKB/Swiss-Prot
Pfam	Y_phosphatase	UniProtKB/Swiss-Prot
PharmGKB	PA33979	PharmGKB
PROSITE	TYR_PHOSPHATASE_2	UniProtKB/Swiss-Prot
	TYR_PHOSPHATASE_DUAL	UniProtKB/Swiss-Prot
SMART	PTPc_motif	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF52799	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	E5RFQ4_HUMAN	UniProtKB/TrEMBL
	E5RGR3_HUMAN	UniProtKB/TrEMBL
	O75365	ENTREZGENE
	Q8IVN5	ENTREZGENE
	Q99849	ENTREZGENE
	Q9BTW5	ENTREZGENE
	TP4A3_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q8IVN5	UniProtKB/Swiss-Prot
	Q99849	UniProtKB/Swiss-Prot
	Q9BTW5	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2019-02-19	PTP4A3	protein tyrosine phosphatase 4A3	PTP4A3	protein tyrosine phosphatase type IVA, member 3	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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Imported Disease Annotations - CTD

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD