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Gene: STRIP2 (striatin interacting protein 2) Homo sapiens

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Symbol:

STRIP2

Name:

striatin interacting protein 2

RGD ID:

1344527

HGNC Page

HGNC:22209

Description:

Involved in cell migration; cytoskeleton organization; and regulation of cell shape. Located in cytosol. Part of FAR/SIN/STRIPAK complex.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FAM40B; family with sequence similarity 40, member B; FAR11 factor arrest 11 homolog B; FAR11B; homolog of yeast FAR11 protein 2; hypothetical protein LOC57464; striatin-interacting protein 2

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Strip2 (striatin interacting protein 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Strip2 (striatin interacting protein 2)	HGNC	Ensembl, HomoloGene, NCBI
Chinchilla lanigera (long-tailed chinchilla):	Strip2 (striatin interacting protein 2)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	STRIP2 (striatin interacting protein 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	STRIP2 (striatin interacting protein 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Strip2 (striatin interacting protein 2)	NCBI	Ortholog
Sus scrofa (pig):	STRIP2 (striatin interacting protein 2)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	STRIP2 (striatin interacting protein 2)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Strip2 (striatin interacting protein 2)	NCBI	Ortholog
Other homologs ²
Mus musculus (house mouse):	Strip1 (striatin interacting protein 1)	HGNC	OrthoMCL
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Strip2 (striatin interacting protein 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Strip2 (striatin interacting protein 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	strip2 (striatin interacting protein 2)	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	FAR11	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OrthoFinder\|OrthoInspector\|PANTHER)
Drosophila melanogaster (fruit fly):	Strip	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	farl-11	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	strip2.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	129,434,432 - 129,488,399 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	129,434,432 - 129,488,399 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	129,074,273 - 129,128,240 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	128,861,536 - 128,915,473 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	7	123,871,017 - 123,924,972 (+)	NCBI		Celera
Cytogenetic Map	7	q32.1	NCBI
HuRef	7	123,435,594 - 123,489,594 (+)	NCBI		HuRef
CHM1_1	7	129,007,840 - 129,061,781 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	7	130,747,403 - 130,801,465 (+)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	128,458,245 - 128,512,203 (+)	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
STRIP2	Human	pleomorphic xanthoastrocytoma		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Pleomorphic xanthoastrocytoma	ClinVar	PMID:28299358

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
STRIP2	Human	(-)-demecolcine	decreases expression	EXP		6480464	Demecolcine results in decreased expression of STRIP2 mRNA	CTD	PMID:23649840
STRIP2	Human	(S)-nicotine	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Nicotine results in decreased expression of STRIP2 mRNA	CTD	PMID:21955143
STRIP2	Human	1,2-dimethylhydrazine	decreases expression	ISO	Strip2 (Mus musculus)	6480464	1 and 2-Dimethylhydrazine results in decreased expression of STRIP2 mRNA	CTD	PMID:22206623
STRIP2	Human	17beta-estradiol	affects expression	EXP		6480464	Estradiol affects the expression of STRIP2 mRNA	CTD	PMID:22574217
STRIP2	Human	17beta-estradiol	multiple interactions	ISO	Strip2 (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of STRIP2 mRNA	CTD	PMID:32741896
STRIP2	Human	17beta-estradiol 3-benzoate	multiple interactions	ISO	Strip2 (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of STRIP2 mRNA	CTD	PMID:32741896
STRIP2	Human	2,2',4,4',5,5'-hexachlorobiphenyl	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
STRIP2	Human	2,2',5,5'-tetrachlorobiphenyl	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
STRIP2	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	EXP		6480464	Tetrachlorodibenzodioxin results in decreased expression of STRIP2 mRNA	CTD	PMID:20106945
STRIP2	Human	2,4-dibromophenyl 2,4,5-tribromophenyl ether	affects expression	ISO	Strip2 (Mus musculus)	6480464	2 more ...	CTD	PMID:38648751
STRIP2	Human	2-hydroxypropanoic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of STRIP2 mRNA	CTD	PMID:30851411
STRIP2	Human	3,4-methylenedioxymethamphetamine	increases expression	ISO	Strip2 (Mus musculus)	6480464	N-Methyl-3 and 4-methylenedioxyamphetamine results in increased expression of STRIP2 mRNA	CTD	PMID:20188158
STRIP2	Human	aflatoxin B1	increases expression	EXP		6480464	Aflatoxin B1 results in increased expression of STRIP2 mRNA	CTD	PMID:22100608
STRIP2	Human	aldehydo-D-glucose	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	fucoxanthin inhibits the reaction [Glucose results in increased expression of STRIP2 mRNA]	CTD	PMID:33448797
STRIP2	Human	aldehydo-D-glucose	increases expression	ISO	Strip2 (Mus musculus)	6480464	Glucose results in increased expression of STRIP2 mRNA	CTD	PMID:33448797
STRIP2	Human	all-trans-retinoic acid	decreases expression	EXP		6480464	Tretinoin results in decreased expression of STRIP2 mRNA	CTD	PMID:21934132 and PMID:33167477
STRIP2	Human	all-trans-retinoic acid	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Tretinoin results in decreased expression of STRIP2 mRNA	CTD	PMID:36189433
STRIP2	Human	all-trans-retinoic acid	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[mono-(2-ethylhexyl)phthalate co-treated with Tretinoin] results in decreased expression of STRIP2 mRNA	CTD	PMID:36189433
STRIP2	Human	amphetamine	increases expression	ISO	Strip2 (Rattus norvegicus)	6480464	Amphetamine results in increased expression of STRIP2 mRNA	CTD	PMID:30779732
STRIP2	Human	arsane	affects methylation	EXP		6480464	Arsenic affects the methylation of STRIP2 gene	CTD	PMID:25304211
STRIP2	Human	arsenic atom	affects methylation	EXP		6480464	Arsenic affects the methylation of STRIP2 gene	CTD	PMID:25304211
STRIP2	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of STRIP2 mRNA	CTD	PMID:20106945
STRIP2	Human	benzo[a]pyrene	increases expression	EXP		6480464	Benzo(a)pyrene results in increased expression of STRIP2 mRNA	CTD	PMID:32234424
STRIP2	Human	benzo[a]pyrene	increases expression	ISO	Strip2 (Mus musculus)	6480464	Benzo(a)pyrene results in increased expression of STRIP2 mRNA	CTD	PMID:27195522
STRIP2	Human	bis(2-ethylhexyl) phthalate	decreases expression	EXP		6480464	Diethylhexyl Phthalate results in decreased expression of STRIP2 mRNA	CTD	PMID:31163220
STRIP2	Human	bisphenol A	increases expression	ISO	Strip2 (Mus musculus)	6480464	bisphenol A results in increased expression of STRIP2 mRNA	CTD	PMID:20739668 and PMID:35598803
STRIP2	Human	bisphenol A	decreases methylation	EXP		6480464	bisphenol A results in decreased methylation of STRIP2 gene	CTD	PMID:31601247
STRIP2	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of STRIP2 mRNA	CTD	PMID:33670352
STRIP2	Human	cantharidin	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Cantharidin results in decreased expression of STRIP2 mRNA	CTD	PMID:36907384
STRIP2	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to STRIP2 gene]	CTD	PMID:28238834
STRIP2	Human	chlorpyrifos	increases expression	ISO	Strip2 (Mus musculus)	6480464	Chlorpyrifos results in increased expression of STRIP2 mRNA	CTD	PMID:37019170
STRIP2	Human	cocaine	increases expression	ISO	Strip2 (Mus musculus)	6480464	Cocaine deficiency results in increased expression of STRIP2 mRNA	CTD	PMID:27126842
STRIP2	Human	crocidolite asbestos	decreases expression	EXP		6480464	Asbestos and Crocidolite results in decreased expression of STRIP2 mRNA	CTD	PMID:29523930
STRIP2	Human	cyclosporin A	decreases expression	EXP		6480464	Cyclosporine results in decreased expression of STRIP2 mRNA	CTD	PMID:20106945
STRIP2	Human	D-glucose	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	fucoxanthin inhibits the reaction [Glucose results in increased expression of STRIP2 mRNA]	CTD	PMID:33448797
STRIP2	Human	D-glucose	increases expression	ISO	Strip2 (Mus musculus)	6480464	Glucose results in increased expression of STRIP2 mRNA	CTD	PMID:33448797
STRIP2	Human	dexamethasone	increases expression	ISO	Strip2 (Mus musculus)	6480464	Dexamethasone results in increased expression of STRIP2 mRNA	CTD	PMID:22733784
STRIP2	Human	dibutyl phthalate	increases expression	ISO	Strip2 (Mus musculus)	6480464	Dibutyl Phthalate results in increased expression of STRIP2 mRNA	CTD	PMID:21266533
STRIP2	Human	dioxygen	decreases expression	EXP		6480464	Oxygen deficiency results in decreased expression of STRIP2 mRNA	CTD	PMID:26516004
STRIP2	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
STRIP2	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of STRIP2 mRNA	CTD	PMID:29803840
STRIP2	Human	ethanol	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Ethanol results in decreased expression of STRIP2 mRNA	CTD	PMID:21955143
STRIP2	Human	ethanol	affects splicing	ISO	Strip2 (Mus musculus)	6480464	Ethanol affects the splicing of STRIP2 mRNA	CTD	PMID:30319688
STRIP2	Human	FR900359	increases phosphorylation	EXP		6480464	FR900359 results in increased phosphorylation of STRIP2 protein	CTD	PMID:37730182
STRIP2	Human	fucoxanthin	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	fucoxanthin inhibits the reaction [Glucose results in increased expression of STRIP2 mRNA]	CTD	PMID:33448797
STRIP2	Human	glucose	increases expression	ISO	Strip2 (Mus musculus)	6480464	Glucose results in increased expression of STRIP2 mRNA	CTD	PMID:33448797
STRIP2	Human	glucose	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	fucoxanthin inhibits the reaction [Glucose results in increased expression of STRIP2 mRNA]	CTD	PMID:33448797
STRIP2	Human	hydrogen peroxide	affects expression	EXP		6480464	Hydrogen Peroxide affects the expression of STRIP2 mRNA	CTD	PMID:21179406
STRIP2	Human	lead diacetate	increases expression	ISO	Strip2 (Mus musculus)	6480464	lead acetate results in increased expression of STRIP2 mRNA	CTD	PMID:20542052
STRIP2	Human	methyl methanesulfonate	increases expression	EXP		6480464	Methyl Methanesulfonate results in increased expression of STRIP2 mRNA	CTD	PMID:23649840
STRIP2	Human	mono(2-ethylhexyl) phthalate	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[mono-(2-ethylhexyl)phthalate co-treated with Tretinoin] results in decreased expression of STRIP2 mRNA	CTD	PMID:36189433
STRIP2	Human	morphine	increases expression	ISO	Strip2 (Mus musculus)	6480464	Morphine results in increased expression of STRIP2 mRNA	CTD	PMID:21955143
STRIP2	Human	morphine	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Morphine deficiency results in decreased expression of STRIP2 mRNA	CTD	PMID:27126842
STRIP2	Human	N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal	decreases expression	ISO	Strip2 (Mus musculus)	6480464	benzyloxycarbonylleucyl-leucyl-leucine aldehyde results in decreased expression of STRIP2 mRNA	CTD	PMID:25566086
STRIP2	Human	nicotine	decreases expression	ISO	Strip2 (Mus musculus)	6480464	Nicotine results in decreased expression of STRIP2 mRNA	CTD	PMID:21955143
STRIP2	Human	paracetamol	increases expression	EXP		6480464	Acetaminophen results in increased expression of STRIP2 mRNA	CTD	PMID:22230336
STRIP2	Human	PCB138	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
STRIP2	Human	perfluorooctanoic acid	increases expression	ISO	Strip2 (Rattus norvegicus)	6480464	perfluorooctanoic acid results in increased expression of STRIP2 mRNA	CTD	PMID:35163327
STRIP2	Human	pirinixic acid	multiple interactions	ISO	Strip2 (Mus musculus)	6480464	[pirinixic acid co-treated with PPARA] results in increased expression of STRIP2 mRNA	CTD	PMID:20813756
STRIP2	Human	pirinixic acid	increases expression	ISO	Strip2 (Mus musculus)	6480464	pirinixic acid results in increased expression of STRIP2 mRNA	CTD	PMID:20813756
STRIP2	Human	rac-lactic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of STRIP2 mRNA	CTD	PMID:30851411
STRIP2	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
STRIP2	Human	silicon dioxide	increases expression	EXP		6480464	Silicon Dioxide analog results in increased expression of STRIP2 mRNA	CTD	PMID:25895662
STRIP2	Human	sulforaphane	increases expression	ISO	Strip2 (Mus musculus)	6480464	sulforaphane results in increased expression of STRIP2 mRNA	CTD	PMID:30529165
STRIP2	Human	sunitinib	decreases expression	EXP		6480464	Sunitinib results in decreased expression of STRIP2 mRNA	CTD	PMID:31533062
STRIP2	Human	testosterone	multiple interactions	ISO	Strip2 (Rattus norvegicus)	6480464	[estradiol 3-benzoate co-treated with [Testosterone co-treated with Estradiol]] results in increased expression of STRIP2 mRNA	CTD	PMID:32741896
STRIP2	Human	titanium dioxide	increases methylation	ISO	Strip2 (Mus musculus)	6480464	titanium dioxide results in increased methylation of STRIP2 promoter	CTD	PMID:35295148
STRIP2	Human	trichostatin A	decreases expression	EXP		6480464	trichostatin A results in decreased expression of STRIP2 mRNA	CTD	PMID:24935251 and PMID:26272509
STRIP2	Human	trichostatin A	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of STRIP2 mRNA	CTD	PMID:27188386
STRIP2	Human	triclosan	decreases expression	EXP		6480464	Triclosan results in decreased expression of STRIP2 mRNA	CTD	PMID:30510588
STRIP2	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of STRIP2 mRNA	CTD	PMID:37042841
STRIP2	Human	triptonide	increases expression	ISO	Strip2 (Mus musculus)	6480464	triptonide results in increased expression of STRIP2 mRNA	CTD	PMID:33045310
STRIP2	Human	urethane	increases expression	EXP		6480464	Urethane results in increased expression of STRIP2 mRNA	CTD	PMID:28818685
STRIP2	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of STRIP2 mRNA	CTD	PMID:23179753 and PMID:26272509
STRIP2	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of STRIP2 mRNA	CTD	PMID:27188386
STRIP2	Human	vinclozolin	affects expression	ISO	Strip2 (Rattus norvegicus)	6480464	vinclozolin affects the expression of STRIP2 mRNA	CTD	PMID:23869203
STRIP2	Human	vincristine	decreases expression	EXP		6480464	Vincristine results in decreased expression of STRIP2 mRNA	CTD	PMID:23649840

Biological Process

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
STRIP2	Human	cell migration	involved_in	IMP		150520179	PMID:21834987	UniProt	PMID:21834987
STRIP2	Human	cytoskeleton organization	involved_in	IMP		150520179	PMID:21834987	UniProt	PMID:21834987
STRIP2	Human	cytoskeleton organization	involved_in	IBA	FB:FBgn0035437 more ...	150520179		GO_Central	GO_REF:0000033
STRIP2	Human	regulation of cell shape	involved_in	IMP		150520179	PMID:21834987	UniProt	PMID:21834987

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
STRIP2	Human	cytoplasm	located_in	IEA	UniProtKB-SubCell:SL-0086	150520179		UniProt	GO_REF:0000044
STRIP2	Human	cytoplasm	located_in	IEA	UniProtKB-KW:KW-0963	150520179		UniProt	GO_REF:0000043
STRIP2	Human	cytoplasm	located_in	IDA		150520179	PMID:21834987	UniProt	PMID:21834987
STRIP2	Human	cytosol	located_in	IDA		150520179		HPA	GO_REF:0000052
STRIP2	Human	cytosol	is_active_in	IBA	PANTHER:PTN000326293 more ...	150520179		GO_Central	GO_REF:0000033
STRIP2	Human	FAR/SIN/STRIPAK complex	part_of	IDA		150520179	PMID:18782753	UniProt	PMID:18782753

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
STRIP2	Human	Pleomorphic xanthoastrocytoma		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Pleomorphic xanthoastrocytoma	ClinVar	PMID:28299358

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

PMID:10574461	PMID:11076863	PMID:12477932	PMID:12588993	PMID:15489334	PMID:15489336	PMID:16344560	PMID:16381901	PMID:18782753	PMID:19615732	PMID:21832049	PMID:21834987
PMID:21873635	PMID:22298706	PMID:22782902	PMID:23455922	PMID:24366813	PMID:25531779	PMID:25798074	PMID:26186194	PMID:26496610	PMID:27122098	PMID:28330616	PMID:28514442
PMID:30509168	PMID:31901223	PMID:32640226	PMID:32707033	PMID:33853758	PMID:33961781	PMID:34079125	PMID:34672954	PMID:35271311	PMID:36639675	PMID:36724073	PMID:36897256
PMID:37219487	PMID:39191354

STRIP2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	129,434,432 - 129,488,399 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	129,434,432 - 129,488,399 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	129,074,273 - 129,128,240 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	128,861,536 - 128,915,473 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	7	123,871,017 - 123,924,972 (+)	NCBI		Celera
Cytogenetic Map	7	q32.1	NCBI
HuRef	7	123,435,594 - 123,489,594 (+)	NCBI		HuRef
CHM1_1	7	129,007,840 - 129,061,781 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	7	130,747,403 - 130,801,465 (+)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	128,458,245 - 128,512,203 (+)	NCBI

Strip2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	29,916,975 - 29,959,680 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	29,917,011 - 29,959,680 (+)	Ensembl		GRCm39 Ensembl
GRCm38	6	29,916,976 - 29,959,681 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	29,917,012 - 29,959,681 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	29,867,013 - 29,909,681 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	29,867,023 - 29,909,691 (+)	NCBI		MGSCv36	mm8
Celera	6	29,927,990 - 29,969,287 (+)	NCBI		Celera
Cytogenetic Map	6	A3.3	NCBI
cM Map	6	12.36	NCBI

Strip2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	4	59,503,478 - 59,545,745 (+)	NCBI		GRCr8
mRatBN7.2	4	58,536,034 - 58,578,279 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	58,536,055 - 58,578,291 (+)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	4	57,204,850 - 57,248,912 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	57,204,944 - 57,246,675 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	56,972,022 - 57,011,392 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	56,810,184 - 56,860,306 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	4	53,637,351 - 53,679,028 (+)	NCBI		Celera
Cytogenetic Map	4	q22	NCBI

Strip2
(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_004955479	10,217,782 - 10,267,897 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955479	10,218,648 - 10,267,897 (+)	NCBI	ChiLan1.0	ChiLan1.0

STRIP2
(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	6	166,247,164 - 166,305,342 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	7	18,257,409 - 18,315,587 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	7	121,391,919 - 121,450,204 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	7	133,914,060 - 133,971,515 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	7	133,917,544 - 133,971,515 (+)	Ensembl	panpan1.1		panPan2

STRIP2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	14	7,291,995 - 7,341,528 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	14	7,294,330 - 7,341,567 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	14	6,978,676 - 7,027,694 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	14	7,056,790 - 7,105,827 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	14	6,970,763 - 7,105,818 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	14	7,261,989 - 7,311,030 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	14	7,004,097 - 7,053,099 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	14	7,148,709 - 7,197,749 (-)	NCBI		UU_Cfam_GSD_1.0

Strip2
(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_024405118	25,514,531 - 25,560,488 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936579	5,646,658 - 5,693,136 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936579	5,648,944 - 5,693,076 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

STRIP2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	18	19,209,051 - 19,255,676 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	18	19,209,047 - 19,255,671 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	18	20,279,736 - 20,326,447 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

STRIP2
(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	21	98,037,893 - 98,093,145 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	21	98,037,961 - 98,094,883 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666042	5,311,022 - 5,366,356 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Strip2
(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_004624783	6,740,818 - 6,788,236 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624783	6,740,253 - 6,787,966 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in STRIP2
47 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3	copy number gain	See cases [RCV000050876]	Chr7:129310166..159282390 [GRCh38] Chr7:128950007..159075079 [GRCh37] Chr7:128737243..158767840 [NCBI36] Chr7:7q32.1-36.3	pathogenic
GRCh38/hg38 7q32.1-33(chr7:128747478-134018250)x3	copy number gain	See cases [RCV000051072]	Chr7:128747478..134018250 [GRCh38] Chr7:128387532..133703003 [GRCh37] Chr7:128174768..133353543 [NCBI36] Chr7:7q32.1-33	pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1	copy number loss	See cases [RCV000052250]	Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
GRCh38/hg38 7q31.33-32.3(chr7:126859732-132750936)x1	copy number loss	See cases [RCV000054171]	Chr7:126859732..132750936 [GRCh38] Chr7:126499786..132435696 [GRCh37] Chr7:126287022..132086236 [NCBI36] Chr7:7q31.33-32.3	pathogenic
NM_020704.2(STRIP2):c.2306C>T (p.Ala769Val)	single nucleotide variant	Malignant melanoma [RCV000067633]	Chr7:129485630 [GRCh38] Chr7:129125471 [GRCh37] Chr7:128912707 [NCBI36] Chr7:7q32.1	not provided
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	copy number loss	See cases [RCV000135401]	Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3	copy number gain	See cases [RCV000136717]	Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3	pathogenic
GRCh38/hg38 7q31.2-33(chr7:117326805-134790689)x1	copy number loss	See cases [RCV000138226]	Chr7:117326805..134790689 [GRCh38] Chr7:116966859..134475440 [GRCh37] Chr7:116754095..134125980 [NCBI36] Chr7:7q31.2-33	pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3	copy number gain	See cases [RCV000138847]	Chr7:121863759..159335865 [GRCh38] Chr7:121503813..159128555 [GRCh37] Chr7:121291049..158821316 [NCBI36] Chr7:7q31.32-36.3	pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3	copy number gain	See cases [RCV000141413]	Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3	pathogenic
GRCh38/hg38 7q31.33-33(chr7:124170657-134163594)x1	copy number loss	See cases [RCV000142552]	Chr7:124170657..134163594 [GRCh38] Chr7:123810711..133848346 [GRCh37] Chr7:123597947..133498886 [NCBI36] Chr7:7q31.33-33	pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220)	copy number gain	not provided [RCV000767558]	Chr7:128312450..159119220 [GRCh37] Chr7:7q32.1-36.3	pathogenic
TMEM106B-BRAF fusion	deletion	Pleomorphic xanthoastrocytoma [RCV000454357]	Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1	copy number loss	See cases [RCV000446044]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7q32.1(chr7:128837666-129131364)x1	copy number loss	See cases [RCV000448798]	Chr7:128837666..129131364 [GRCh37] Chr7:7q32.1	uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3	copy number gain	See cases [RCV000447709]	Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3	pathogenic
GRCh37/hg19 7q32.1-34(chr7:127295698-139524358)x1	copy number loss	See cases [RCV000447722]	Chr7:127295698..139524358 [GRCh37] Chr7:7q32.1-34	pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3	copy number gain	See cases [RCV000447956]	Chr7:128276078..159119707 [GRCh37] Chr7:7q32.1-36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)	copy number gain	See cases [RCV000510686]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3	copy number gain	See cases [RCV000511549]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
NM_020704.3(STRIP2):c.1901G>C (p.Cys634Ser)	single nucleotide variant	not specified [RCV004296942]	Chr7:129470672 [GRCh38] Chr7:129110513 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2056G>A (p.Val686Ile)	single nucleotide variant	not specified [RCV004297805]	Chr7:129482848 [GRCh38] Chr7:129122689 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2086C>T (p.Arg696Trp)	single nucleotide variant	not specified [RCV004326833]	Chr7:129482878 [GRCh38] Chr7:129122719 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1934C>G (p.Thr645Ser)	single nucleotide variant	not specified [RCV004298899]	Chr7:129470705 [GRCh38] Chr7:129110546 [GRCh37] Chr7:7q32.1	uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3	copy number gain	not provided [RCV000682911]	Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3	copy number gain	not provided [RCV000746278]	Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3	copy number gain	not provided [RCV000746280]	Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3	copy number gain	not provided [RCV000848126]	Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7q31.32-32.2(chr7:121480906-129389003)x1	copy number loss	not provided [RCV000847911]	Chr7:121480906..129389003 [GRCh37] Chr7:7q31.32-32.2	pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3	copy number gain	not provided [RCV001005994]	Chr7:109251060..159119707 [GRCh37] Chr7:7q31.1-36.3	pathogenic
Single allele	complex	Ring chromosome 7 [RCV002280646]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7q31.33-33(chr7:124103982-134693590)	copy number loss	not specified [RCV002053726]	Chr7:124103982..134693590 [GRCh37] Chr7:7q31.33-33	pathogenic
GRCh37/hg19 7q32.1(chr7:128837666-129131364)	copy number loss	not specified [RCV002053730]	Chr7:128837666..129131364 [GRCh37] Chr7:7q32.1	uncertain significance
GRCh37/hg19 7q32.1-34(chr7:127295698-139524358)	copy number loss	not specified [RCV002053727]	Chr7:127295698..139524358 [GRCh37] Chr7:7q32.1-34	pathogenic
GRCh37/hg19 7q31.33-33(chr7:123967475-132729981)	copy number loss	not specified [RCV002053723]	Chr7:123967475..132729981 [GRCh37] Chr7:7q31.33-33	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	copy number loss	See cases [RCV002287832]	Chr7:56604613..96692931 [GRCh37] Chr7:7p22.3-q36.3	uncertain significance
NM_020704.3(STRIP2):c.1025G>C (p.Arg342Pro)	single nucleotide variant	not specified [RCV004306402]	Chr7:129456629 [GRCh38] Chr7:129096470 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1687G>A (p.Val563Met)	single nucleotide variant	not specified [RCV004295450]	Chr7:129464649 [GRCh38] Chr7:129104490 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.992T>G (p.Leu331Arg)	single nucleotide variant	not specified [RCV004197068]	Chr7:129456596 [GRCh38] Chr7:129096437 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1435A>C (p.Ile479Leu)	single nucleotide variant	not specified [RCV004162336]	Chr7:129460331 [GRCh38] Chr7:129100172 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2225G>A (p.Arg742His)	single nucleotide variant	not specified [RCV004195242]	Chr7:129483017 [GRCh38] Chr7:129122858 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.185C>A (p.Ala62Glu)	single nucleotide variant	not specified [RCV004113624]	Chr7:129440077 [GRCh38] Chr7:129079918 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1576G>A (p.Ala526Thr)	single nucleotide variant	not specified [RCV004078321]	Chr7:129464068 [GRCh38] Chr7:129103909 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1667G>A (p.Ser556Asn)	single nucleotide variant	not specified [RCV004231679]	Chr7:129464629 [GRCh38] Chr7:129104470 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2125G>A (p.Val709Ile)	single nucleotide variant	not specified [RCV004157295]	Chr7:129482917 [GRCh38] Chr7:129122758 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1801G>C (p.Val601Leu)	single nucleotide variant	not specified [RCV004115713]	Chr7:129467374 [GRCh38] Chr7:129107215 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2108C>A (p.Ala703Asp)	single nucleotide variant	not specified [RCV004214471]	Chr7:129482900 [GRCh38] Chr7:129122741 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1714A>G (p.Lys572Glu)	single nucleotide variant	not specified [RCV004273480]	Chr7:129464676 [GRCh38] Chr7:129104517 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2425C>T (p.His809Tyr)	single nucleotide variant	not specified [RCV004251405]	Chr7:129485749 [GRCh38] Chr7:129125590 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2177A>G (p.Lys726Arg)	single nucleotide variant	not specified [RCV004260083]	Chr7:129482969 [GRCh38] Chr7:129122810 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.164A>G (p.Tyr55Cys)	single nucleotide variant	not specified [RCV004337779]	Chr7:129440056 [GRCh38] Chr7:129079897 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.956C>T (p.Pro319Leu)	single nucleotide variant	not specified [RCV004348847]	Chr7:129456560 [GRCh38] Chr7:129096401 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1927C>A (p.Leu643Ile)	single nucleotide variant	not specified [RCV004359228]	Chr7:129470698 [GRCh38] Chr7:129110539 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.727G>A (p.Glu243Lys)	single nucleotide variant	not specified [RCV004360770]	Chr7:129455264 [GRCh38] Chr7:129095105 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.386G>A (p.Arg129Gln)	single nucleotide variant	not specified [RCV004351349]	Chr7:129451724 [GRCh38] Chr7:129091565 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1139A>T (p.Asp380Val)	single nucleotide variant	not specified [RCV004339770]	Chr7:129458315 [GRCh38] Chr7:129098156 [GRCh37] Chr7:7q32.1	uncertain significance
GRCh37/hg19 7q31.33-32.2(chr7:127076892-129405807)x1	copy number loss	not provided [RCV003482986]	Chr7:127076892..129405807 [GRCh37] Chr7:7q31.33-32.2	pathogenic
GRCh37/hg19 7q31.31-33(chr7:120582003-137699953)x1	copy number loss	not specified [RCV003986721]	Chr7:120582003..137699953 [GRCh37] Chr7:7q31.31-33	pathogenic
NM_020704.3(STRIP2):c.1601A>G (p.Lys534Arg)	single nucleotide variant	not specified [RCV004458499]	Chr7:129464093 [GRCh38] Chr7:129103934 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2041C>T (p.Arg681Trp)	single nucleotide variant	not specified [RCV004458502]	Chr7:129480881 [GRCh38] Chr7:129120722 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2312T>C (p.Ile771Thr)	single nucleotide variant	not specified [RCV004458503]	Chr7:129485636 [GRCh38] Chr7:129125477 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.344G>A (p.Arg115Gln)	single nucleotide variant	not specified [RCV004458505]	Chr7:129451682 [GRCh38] Chr7:129091523 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.410G>A (p.Gly137Asp)	single nucleotide variant	not specified [RCV004458506]	Chr7:129453227 [GRCh38] Chr7:129093068 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.281G>T (p.Gly94Val)	single nucleotide variant	not specified [RCV004458504]	Chr7:129451619 [GRCh38] Chr7:129091460 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1751A>G (p.His584Arg)	single nucleotide variant	not specified [RCV004458500]	Chr7:129464713 [GRCh38] Chr7:129104554 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1786G>T (p.Val596Leu)	single nucleotide variant	not specified [RCV004458501]	Chr7:129467359 [GRCh38] Chr7:129107200 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.796A>G (p.Ile266Val)	single nucleotide variant	not specified [RCV004458507]	Chr7:129455333 [GRCh38] Chr7:129095174 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2257A>G (p.Ile753Val)	single nucleotide variant	not specified [RCV004668206]	Chr7:129485581 [GRCh38] Chr7:129125422 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.688A>T (p.Thr230Ser)	single nucleotide variant	not specified [RCV004668205]	Chr7:129454509 [GRCh38] Chr7:129094350 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1933A>G (p.Thr645Ala)	single nucleotide variant	not specified [RCV004668207]	Chr7:129470704 [GRCh38] Chr7:129110545 [GRCh37] Chr7:7q32.1	uncertain significance
GRCh37/hg19 7q31.32-36.1(chr7:122190535-149944340)x1	copy number loss	not provided [RCV004819354]	Chr7:122190535..149944340 [GRCh37] Chr7:7q31.32-36.1	pathogenic
NM_020704.3(STRIP2):c.2108C>G (p.Ala703Gly)	single nucleotide variant	not specified [RCV004868778]	Chr7:129482900 [GRCh38] Chr7:129122741 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1423G>A (p.Ala475Thr)	single nucleotide variant	not specified [RCV004868779]	Chr7:129460319 [GRCh38] Chr7:129100160 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.188C>T (p.Ala63Val)	single nucleotide variant	not specified [RCV004868780]	Chr7:129440080 [GRCh38] Chr7:129079921 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2233G>A (p.Asp745Asn)	single nucleotide variant	not specified [RCV004877872]	Chr7:129483025 [GRCh38] Chr7:129122866 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1285A>C (p.Ile429Leu)	single nucleotide variant	not specified [RCV004868781]	Chr7:129458722 [GRCh38] Chr7:129098563 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.2426A>G (p.His809Arg)	single nucleotide variant	not specified [RCV004868782]	Chr7:129485750 [GRCh38] Chr7:129125591 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1330A>G (p.Thr444Ala)	single nucleotide variant	not specified [RCV004868783]	Chr7:129458767 [GRCh38] Chr7:129098608 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1461G>C (p.Lys487Asn)	single nucleotide variant	not specified [RCV004868784]	Chr7:129460357 [GRCh38] Chr7:129100198 [GRCh37] Chr7:7q32.1	uncertain significance
NM_020704.3(STRIP2):c.1420A>G (p.Ile474Val)	single nucleotide variant	not specified [RCV004868785]	Chr7:129460316 [GRCh38] Chr7:129100157 [GRCh37] Chr7:7q32.1	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	1277
Count of miRNA genes:	767
Interacting mature miRNAs:	875
Transcripts:	ENST00000249344, ENST00000435494, ENST00000465033
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597181788	GWAS1277862_H	hemoglobin measurement QTL GWAS1277862 (human)		0.0000002	hemoglobin measurement	hemoglobin measurement (CMO:0000508)	7	129484907	129484908	Human

STS-AA011441

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,128,072 - 129,128,206	UniSTS	GRCh37
Build 36	7	128,915,308 - 128,915,442	RGD	NCBI36
Celera	7	123,924,804 - 123,924,938	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,489,426 - 123,489,560	UniSTS
CRA_TCAGchr7v2	7	128,512,035 - 128,512,169	UniSTS
GeneMap99-GB4 RH Map	7	588.28	UniSTS
NCBI RH Map	7	1192.6	UniSTS

SHGC-32481

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,114,783 - 129,114,912	UniSTS	GRCh37
Build 36	7	128,902,019 - 128,902,148	RGD	NCBI36
Celera	7	123,911,519 - 123,911,648	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,476,091 - 123,476,220	UniSTS
CRA_TCAGchr7v2	7	128,498,747 - 128,498,876	UniSTS
Whitehead-RH Map	7	554.8	UniSTS

RH93307

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,127,977 - 129,128,099	UniSTS	GRCh37
Build 36	7	128,915,213 - 128,915,335	RGD	NCBI36
Celera	7	123,924,709 - 123,924,831	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,489,331 - 123,489,453	UniSTS
CRA_TCAGchr7v2	7	128,511,940 - 128,512,062	UniSTS
GeneMap99-GB4 RH Map	7	589.99	UniSTS

SHGC-84574

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,073,443 - 129,073,752	UniSTS	GRCh37
Build 36	7	128,860,679 - 128,860,988	RGD	NCBI36
Celera	7	123,870,186 - 123,870,495	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,434,763 - 123,435,072	UniSTS
CRA_TCAGchr7v2	7	128,457,414 - 128,457,723	UniSTS
TNG Radiation Hybrid Map	7	58245.0	UniSTS

GDB:4585005

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,110,616 - 129,110,757	UniSTS	GRCh37
Build 36	7	128,897,852 - 128,897,993	RGD	NCBI36
Celera	7	123,907,352 - 123,907,493	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,471,928 - 123,472,069	UniSTS
CRA_TCAGchr7v2	7	128,494,580 - 128,494,721	UniSTS

GDB:4585689

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	129,090,190 - 129,090,272	UniSTS	GRCh37
Build 36	7	128,877,426 - 128,877,508	RGD	NCBI36
Celera	7	123,886,934 - 123,887,016	RGD
Cytogenetic Map	7	q32.1	UniSTS
HuRef	7	123,451,511 - 123,451,593	UniSTS
CRA_TCAGchr7v2	7	128,474,162 - 128,474,244	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2438	2788	2253	4973	1723	2348	6	621	1947	462	2269	7294	6465	53	3734	1	848	1741	1617	174	1


RefSeq Transcripts	NM_001134336	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_020704	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006716069	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011516432	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011516435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012470	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012471	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047420656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047420657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054358713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001744839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001744840	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001744841	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008487707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008487708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008487709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_927493	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB032996	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC009244	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK290165	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC019064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH236950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA409007	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000249344 ⟹ ENSP00000249344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	129,434,432 - 129,488,399 (+)	Ensembl

Ensembl Acc Id:

ENST00000435494 ⟹ ENSP00000392393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	129,434,446 - 129,483,631 (+)	Ensembl

Ensembl Acc Id:

ENST00000465033

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	129,458,242 - 129,460,548 (+)	Ensembl

RefSeq Acc Id:

NM_001134336 ⟹ NP_001127808

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,483,631 (+)	NCBI
GRCh37	7	129,074,274 - 129,128,240 (+)	RGD
Celera	7	123,871,017 - 123,924,972 (+)	RGD
HuRef	7	123,435,594 - 123,489,594 (+)	ENTREZGENE
CHM1_1	7	129,007,840 - 129,057,038 (+)	NCBI
T2T-CHM13v2.0	7	130,747,403 - 130,796,702 (+)	NCBI
CRA_TCAGchr7v2	7	128,458,245 - 128,512,203 (+)	ENTREZGENE

Sequence:

show sequence

CAAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGGACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCC
AAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCTGGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACAC
TGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGGGCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACC
GGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAAGGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTC
CTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAGCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAG
GGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCTGTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGG
AGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTCCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAG
CATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAGTATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGA
GTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCACTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCA
CAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTAGAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCT
TTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGATGAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACC
CAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGCAGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGGGGAAGAGGTGGTACCAG
AGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCTGCTTAAGATTCTGCTGGCTGCAGCTCCCACCTCTAAGGCTAAGACAGACTCTATCAATATCCTG
GCAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATGTGAACAGGCACAAGGAGATTATTGTAAAGAGTATCTCTACCCTGCTTCTGCTACTCCTCAAACA
CTTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGCATCCCCTTGATCCTGAAGTTCTTCAATCAAAATATCTTGTCATACATCACTGCCAAAAACAGCA
TCTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCTGGAAGCTGGAGACAACAGCCAGTTCTGCTGGAGGAACCTCTTTTCCTGCATCAACCTCCTGAGG
CTGCTCAATAAACTGACCAAATGGAAACATTCCCGGACCATGATGCTGGTAGTGTTTAAATCGGCACCAATCTTAAAGCGGGCCCTCAAGGTCAAACAGGCCATGCTGCAACTTTATGTCCTAAAGCT
ACTAAAGTTACAGACCAAGTACCTGGGGCGCCAATGGAGGAAAAGCAACATGAAAACCATGTCAGCCATTTACCAGAAAGTGCGTCACCGCATGAACGATGACTGGGCTTACGGGAATGGTGAGTCTT
CCCAAAGCTCTTGACTTCCTGGAGTTTCCTGGGGTTTAGACAAAACTAAATAAATATTTATCACTCCTCTTTTGGCATGAATTGTTACATATTTTAGATGAAAAAATATGTGATTATAGGTCAGGCGC
TGATACACCAAACTTTAAGGTTATGCCTCAAATTCTAGTATGTACCCTTGTCCTATGTAAACTATGAAAATCCGTTTTATAAAACAAGTAAATTGAGAGATAATTAATTGCCTTTCCAAAACATTCTT
TTAAATGACAGCTTTCTCCAAAAGATTTAAATTAAAACAACTTTTTATTATTACAAAGCAGTTAGAAAAAAAGATAGAAAATACAAGTAAACAAACATTTTACTATATTATATTTATGCCATATTTGT
ACTATGCAGAAATTGCCACCATTAACATCTTATTGTATATTCCTCCAGATCTTTTTCTATGCATATACATGCATATTTTATCAAAATGAAAGCAAGTTATGTATGCTATTTTGTAATTTTCTCTTTTA
ACATTATCTCTACCTTTTCATGTCAGTACATTTTCATTTCATCTAATAAAGTTCATATTCACAA

hide sequence

RefSeq Acc Id:

NM_020704 ⟹ NP_065755

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,488,399 (+)	NCBI
GRCh37	7	129,074,274 - 129,128,240 (+)	RGD
Build 36	7	128,861,536 - 128,915,473 (+)	NCBI Archive
Celera	7	123,871,017 - 123,924,972 (+)	RGD
HuRef	7	123,435,594 - 123,489,594 (+)	ENTREZGENE
CHM1_1	7	129,007,840 - 129,061,781 (+)	NCBI
T2T-CHM13v2.0	7	130,747,403 - 130,801,465 (+)	NCBI
CRA_TCAGchr7v2	7	128,458,245 - 128,512,203 (+)	ENTREZGENE

Sequence:

show sequence

CAAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGG
GACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCAAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTC
TGGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACTGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAG
GGCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCGGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCA
AGGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACA
GCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCC
TGTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTT
CCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACA
GTATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTC
ACTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCT
AGAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGA
TGAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTG
CAGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGGGGAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCT
GCTTAAGATTCTGCTGGCTGCAGCTCCCACCTCTAAGGCTAAGACAGACTCTATCAATATCCTGGCAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATG
TGAACAGGCACAAGGAGATTATTGTAAAGAGTATCTCTACCCTGCTTCTGCTACTCCTCAAACACTTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGC
ATCCCCTTGATCCTGAAGTTCTTCAATCAAAATATCTTGTCATACATCACTGCCAAAAACAGCATCTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCT
GGAAGCTGGAGACAACAGCCAGTTCTGCTGGAGGAACCTCTTTTCCTGCATCAACCTCCTGAGGCTGCTCAATAAACTGACCAAATGGAAACATTCCCGGACCATGATGCTGGTAGTGTTTAAATCGG
CACCAATCTTAAAGCGGGCCCTCAAGGTCAAACAGGCCATGCTGCAACTTTATGTCCTAAAGCTACTAAAGTTACAGACCAAGTACCTGGGGCGCCAATGGAGGAAAAGCAACATGAAAACCATGTCA
GCCATTTACCAGAAAGTGCGTCACCGCATGAACGATGACTGGGCTTACGGGAATGACATCGATGCCAGACCATGGGACTTCCAAGCAGAAGAATGTACCTTGAGGGCCAACATTGAGGCTTTTAACAG
CCGTCGCTATGACAGACCCCAGGACTCTGAGTTTTCACCTGTGGATAACTGCTTGCAGAGCGTACTGGGGCAGAGGTTGGATCTGCCTGAAGATTTCCACTATTCATATGAGCTCTGGCTCGAGAGAG
AGGTGTTTTCACAGCCCATCTGTTGGGAGGAGCTGCTCCAGAATCACTGACTAAGTTCTTGTCAACAAGCATCAATAGATAGAGGTCAGCTCCAATAAACTGTGCTCTGCCTACCCTGTCCATACAGG
CGCTGTTACCAGTTCAGGGCTCTTCTGGGGGCTCTTGGGCCTAAAGATGGTGCAAGGGTGGGATCCTGAATCACAATAAAATGATCAACTTGCCCTGGGGTCAGTTGGGTGCCCAGTTGGCCTTGGAA
ATCTTTTGGTGGATCAATTCTAGACAAGCTCTTTGGTAGGACCTTTTCCTGCTTTAGTCTTGGCTACAACCAGGCTAGACTTTGCTGGCTCTAAAAGAGGAAATTTGTTATGGCATTTGACCCATGGC
ATTCATCACAGATAGTGGGAGGTACAAGTCATAAAATAGGGAGAAAGTTTTCTTCTTGCTCACACTGGATTCCTAGGACTTATCAGAGATTTGGAAAAACCAACTTTGAAATTAAGTTTGCATTTTAA
ATTTCAAATTTGGAAGCCTCTTTCTGAAATCATTAGCTCTAAGATTATTTTAGAGCACCTGCACCTTCTTTGTGAAGGATGATGATTTACTATTCCCTCAATACTGCATGTTATCGAAAAGTGTGTTG
TGTAAAGTGTTTTTTTCCTCATTCTGTAAGAGATCTATATTCAATGTGAAAATTATTTCCTTGTGTACTCTGTATAGGGCATGGAATGCTCTGCCATTTTTAAAGAGCCACAACCAATATGAAATAAT
TAGGTCCTCTCTAAGGATGTTTCATGTTTTTCTTAAATGACTCCAGTCTTCAAATGGCTGAGCATACTGCAGAAAATTATCCTTTTCATCTAATTCATTTTTTAAATGACAAGTTAACTACAGGAGGC
TTTATTTATTCAGATGGTATGTCCACTTGTGGTCGTGATCAATATATTTTTCTAATTGAAAAGTAAAAGCATCACAGCTTACCATTTTTCTTTTTCTGCAGTGTTGATTAATGATTTTTTTCCCGTTT
ATTGCTAGCAGTTTCAAAGTGTCATGTGGAGATTTAGCAATACTGTCTCTACTTAAAAGTATTGCACATTTCATTGAAAATGTGAGAGTTGATATACCAGCCTCTTTATATTTCTCTTTTACAGCAGA
ATCACATACTTCTCAAGATAAACAAGGTTTTTAAAAAAGTTTCTGATTTAGTTAGGATCATATGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAAG
CTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGGAGCTGGGATTACAGGCACGCACCACCATGCCTGGCTAATTTTTTG
TATTTTTAGTAGAAACAGGGTTTCACCATGTTAGCCAGGCTGACCTCAAACTCCTGACCTCAGGTGATCCGCCCGCCTCCACCTCCCAGGGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCT
CTTCAAGCTTTTTTACTATACATGTTGCCCCTCTCCCCCAACTTAGGCACTACTGAATTTTTTATGATGGCACCAGGTCACTTTATGCTGGGTGATATAGTCAAAATTTGCTTATTTACTCTGCCCCT
CGTCAACCACAGTATCATTTCAAGGACATGAATAAAATACTTGACAGTATCCAAAGGAGCTATACCAAAATCTAACAAGTAAATTTTGGATTTTGCCTCTTTGTGCTTTAAAGTACCAGGATTTCTGT
CTCTATGGATAGGTCTTGGAGAATGTTAAGTAATGGATGAAACTTTTTAAAATAATTTGTAAATTTTACCTAAGTAGGACAGTAGTCCTTACTGCAATCAAAATAATTTACTGAGCACAACTCCTGTA
AATTAATCTACAGTCAGGCTAGTATGATTTTAATATGATTTGAGTAAAAAGATAATTTTCAAGGAAAGAGTAATCATCCATCAATTTATTATAAAGCCAGATAGTATTCAATTTATGTCAAGAACAAA
GAAATTGCCCTTTTAAAAGCATGTACGTGAATGCTTTTTGAGGCACAGAAGTATGCTAAGCTTTAACATTTTGTATTTATTTACAACCCTTTTCTAAGGGAAGGTTACTTCTCAGTGCAGATGGAGAA
ACTGAAGCACTAAGGATAAATGATTAGTTTCCAATCACATCATTTTTTTCCACAGACTTGCTGGGACTAGCTTTCAGGTATTGACAGCCAGCCCCATATATTAAGGTAACCAGGTTGAATCTTCCAAT
TTGAGAACCCATGTATGGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCATCCTGGGCAACAAGAACGAAACTCCGTCTCAAAAACAAAGAAGGATATAATAAAGTTAATATATAAACCATGTAT
GTGGTTAGGAATAAATTCAAATTCACCAGTCTCCAATGGTGATTACTTTTACTACATAGAAAAACATTTTAGTGACTTACAGAGGATTTTTATTTGTGAATATTTCAGTAAAGTTTGTGTTGATTGTT
GATAACACTGTTCATCTACTGAAGCACTTTAATAAAAATAAAATGAGCTGGAATTAGAAA

hide sequence

RefSeq Acc Id:

XM_006716069 ⟹ XP_006716132

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,488,399 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGG
ACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCAAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCT
GGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACTGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGG
GCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCGGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAA
GGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAG
CCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCT
GTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTC
CCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAG
TATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCA
CTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTA
GAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGAT
GAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGC
AGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGGGGAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCTG
CTTAAGATTCTGCTGGCTGCAGCTCCCACCTCTAAGGCTAAGACAGACTCTATCAATATCCTGGCAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATGT
GAACAGGCACAAGGAGATTATTGTAAAGAGTATCTCTACCCTGCTTCTGCTACTCCTCAAACACTTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGCA
TCCCCTTGATCCTGAAGTTCTTCAATCAAAATATCTTGTCATACATCACTGCCAAAAACAGCATCTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCTG
GAAGCTGGAGACAACAGCCAGTTCTGCTGGAGGAACCTCTTTTCCTGCATCAACCTCCTGAGGCTGCTCAATAAACTGACCAAATGGAAACATTCCCGGACCATGACATCGATGCCAGACCATGGGAC
TTCCAAGCAGAAGAATGTACCTTGAGGGCCAACATTGAGGCTTTTAACAGCCGTCGCTATGACAGACCCCAGGACTCTGAGTTTTCACCTGTGGATAACTGCTTGCAGAGCGTACTGGGGCAGAGGTT
GGATCTGCCTGAAGATTTCCACTATTCATATGAGCTCTGGCTCGAGAGAGAGGTGTTTTCACAGCCCATCTGTTGGGAGGAGCTGCTCCAGAATCACTGACTAAGTTCTTGTCAACAAGCATCAATAG
ATAGAGGTCAGCTCCAATAAACTGTGCTCTGCCTACCCTGTCCATACAGGCGCTGTTACCAGTTCAGGGCTCTTCTGGGGGCTCTTGGGCCTAAAGATGGTGCAAGGGTGGGATCCTGAATCACAATA
AAATGATCAACTTGCCCTGGGGTCAGTTGGGTGCCCAGTTGGCCTTGGAAATCTTTTGGTGGATCAATTCTAGACAAGCTCTTTGGTAGGACCTTTTCCTGCTTTAGTCTTGGCTACAACCAGGCTAG
ACTTTGCTGGCTCTAAAAGAGGAAATTTGTTATGGCATTTGACCCATGGCATTCATCACAGATAGTGGGAGGTACAAGTCATAAAATAGGGAGAAAGTTTTCTTCTTGCTCACACTGGATTCCTAGGA
CTTATCAGAGATTTGGAAAAACCAACTTTGAAATTAAGTTTGCATTTTAAATTTCAAATTTGGAAGCCTCTTTCTGAAATCATTAGCTCTAAGATTATTTTAGAGCACCTGCACCTTCTTTGTGAAGG
ATGATGATTTACTATTCCCTCAATACTGCATGTTATCGAAAAGTGTGTTGTGTAAAGTGTTTTTTTCCTCATTCTGTAAGAGATCTATATTCAATGTGAAAATTATTTCCTTGTGTACTCTGTATAGG
GCATGGAATGCTCTGCCATTTTTAAAGAGCCACAACCAATATGAAATAATTAGGTCCTCTCTAAGGATGTTTCATGTTTTTCTTAAATGACTCCAGTCTTCAAATGGCTGAGCATACTGCAGAAAATT
ATCCTTTTCATCTAATTCATTTTTTAAATGACAAGTTAACTACAGGAGGCTTTATTTATTCAGATGGTATGTCCACTTGTGGTCGTGATCAATATATTTTTCTAATTGAAAAGTAAAAGCATCACAGC
TTACCATTTTTCTTTTTCTGCAGTGTTGATTAATGATTTTTTTCCCGTTTATTGCTAGCAGTTTCAAAGTGTCATGTGGAGATTTAGCAATACTGTCTCTACTTAAAAGTATTGCACATTTCATTGAA
AATGTGAGAGTTGATATACCAGCCTCTTTATATTTCTCTTTTACAGCAGAATCACATACTTCTCAAGATAAACAAGGTTTTTAAAAAAGTTTCTGATTTAGTTAGGATCATATGCTTTTTTTTTTTTT
TTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAAGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCC
CAAGGAGCTGGGATTACAGGCACGCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTAGCCAGGCTGACCTCAAACTCCTGACCTCAGGTGATCCGCCCGCCT
CCACCTCCCAGGGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCTCTTCAAGCTTTTTTACTATACATGTTGCCCCTCTCCCCCAACTTAGGCACTACTGAATTTTTTATGATGGCACCAGGT
CACTTTATGCTGGGTGATATAGTCAAAATTTGCTTATTTACTCTGCCCCTCGTCAACCACAGTATCATTTCAAGGACATGAATAAAATACTTGACAGTATCCAAAGGAGCTATACCAAAATCTAACAA
GTAAATTTTGGATTTTGCCTCTTTGTGCTTTAAAGTACCAGGATTTCTGTCTCTATGGATAGGTCTTGGAGAATGTTAAGTAATGGATGAAACTTTTTAAAATAATTTGTAAATTTTACCTAAGTAGG
ACAGTAGTCCTTACTGCAATCAAAATAATTTACTGAGCACAACTCCTGTAAATTAATCTACAGTCAGGCTAGTATGATTTTAATATGATTTGAGTAAAAAGATAATTTTCAAGGAAAGAGTAATCATC
CATCAATTTATTATAAAGCCAGATAGTATTCAATTTATGTCAAGAACAAAGAAATTGCCCTTTTAAAAGCATGTACGTGAATGCTTTTTGAGGCACAGAAGTATGCTAAGCTTTAACATTTTGTATTT
ATTTACAACCCTTTTCTAAGGGAAGGTTACTTCTCAGTGCAGATGGAGAAACTGAAGCACTAAGGATAAATGATTAGTTTCCAATCACATCATTTTTTTCCACAGACTTGCTGGGACTAGCTTTCAGG
TATTGACAGCCAGCCCCATATATTAAGGTAACCAGGTTGAATCTTCCAATTTGAGAACCCATGTATGGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCATCCTGGGCAACAAGAACGAAACTCC
GTCTCAAAAACAAAGAAGGATATAATAAAGTTAATATATAAACCATGTATGTGGTTAGGAATAAATTCAAATTCACCAGTCTCCAATGGTGATTACTTTTACTACATAGAAAAACATTTTAGTGACTT
ACAGAGGATTTTTATTTGTGAATATTTCAGTAAAGTTTGTGTTGATTGTTGATAACACTGTTCATCTACTGAAGCACTTTAATAAAAATAAAATGAGCTGGAATTAGAAA

hide sequence

RefSeq Acc Id:

XM_011516432 ⟹ XP_011514734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,452,120 - 129,488,399 (+)	NCBI

Sequence:

show sequence

GAAATAGGAGAGTGTCACAGATACACATGGACCCCTTGCATTGTTTCTCATTGGCATTTTGAAAGTTCAAGCCAACATAACTGCGGGAGTGGATGCTGTACTTTTGGGGAATGTGATTCAGAGGTCGA
TGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAGCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAG
CTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCTGTGGGTGGAGAACAGCCCGGGAGACCTTCCGC
ACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTCCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAA
GGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAGTATCCAGGTGGTGAAGAGCATGCGTGCTGCCT
CCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCACTAAGCAGGACAGCCTGGACATCTACAATGAA
AGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTAGAGCAGGACCCTCTGGTGCCACCTCCACCCTC
ACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGATGAGCAGGAACAAGTTCATCGGATTCACCCTGG
GGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGCAGATCAAGAATGAAGAGGAGCTGGAGAAGTGC
CCTATGTCTTTGGGGGAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCTGCTTAAGATTCTGCTGGCTGCAGCTCCCACCTC
TAAGGCTAAGACAGACTCTATCAATATCCTGGCAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATGTGAACAGGCACAAGGAGATTATTGTAAAGAGTA
TCTCTACCCTGCTTCTGCTACTCCTCAAACACTTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGCATCCCCTTGATCCTGAAGTTCTTCAATCAAAAT
ATCTTGTCATACATCACTGCCAAAAACAGCATCTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCTGGAAGCTGGAGACAACAGCCAGTTCTGCTGGAG
GAACCTCTTTTCCTGCATCAACCTCCTGAGGCTGCTCAATAAACTGACCAAATGGAAACATTCCCGGACCATGATGCTGGTAGTGTTTAAATCGGCACCAATCTTAAAGCGGGCCCTCAAGGTCAAAC
AGGCCATGCTGCAACTTTATGTCCTAAAGCTACTAAAGTTACAGACCAAGTACCTGGGGCGCCAATGGAGGAAAAGCAACATGAAAACCATGTCAGCCATTTACCAGAAAGTGCGTCACCGCATGAAC
GATGACTGGGCTTACGGGAATGACATCGATGCCAGACCATGGGACTTCCAAGCAGAAGAATGTACCTTGAGGGCCAACATTGAGGCTTTTAACAGCCGTCGCTATGACAGACCCCAGGACTCTGAGTT
TTCACCTGTGGATAACTGCTTGCAGAGCGTACTGGGGCAGAGGTTGGATCTGCCTGAAGATTTCCACTATTCATATGAGCTCTGGCTCGAGAGAGAGGTGTTTTCACAGCCCATCTGTTGGGAGGAGC
TGCTCCAGAATCACTGACTAAGTTCTTGTCAACAAGCATCAATAGATAGAGGTCAGCTCCAATAAACTGTGCTCTGCCTACCCTGTCCATACAGGCGCTGTTACCAGTTCAGGGCTCTTCTGGGGGCT
CTTGGGCCTAAAGATGGTGCAAGGGTGGGATCCTGAATCACAATAAAATGATCAACTTGCCCTGGGGTCAGTTGGGTGCCCAGTTGGCCTTGGAAATCTTTTGGTGGATCAATTCTAGACAAGCTCTT
TGGTAGGACCTTTTCCTGCTTTAGTCTTGGCTACAACCAGGCTAGACTTTGCTGGCTCTAAAAGAGGAAATTTGTTATGGCATTTGACCCATGGCATTCATCACAGATAGTGGGAGGTACAAGTCATA
AAATAGGGAGAAAGTTTTCTTCTTGCTCACACTGGATTCCTAGGACTTATCAGAGATTTGGAAAAACCAACTTTGAAATTAAGTTTGCATTTTAAATTTCAAATTTGGAAGCCTCTTTCTGAAATCAT
TAGCTCTAAGATTATTTTAGAGCACCTGCACCTTCTTTGTGAAGGATGATGATTTACTATTCCCTCAATACTGCATGTTATCGAAAAGTGTGTTGTGTAAAGTGTTTTTTTCCTCATTCTGTAAGAGA
TCTATATTCAATGTGAAAATTATTTCCTTGTGTACTCTGTATAGGGCATGGAATGCTCTGCCATTTTTAAAGAGCCACAACCAATATGAAATAATTAGGTCCTCTCTAAGGATGTTTCATGTTTTTCT
TAAATGACTCCAGTCTTCAAATGGCTGAGCATACTGCAGAAAATTATCCTTTTCATCTAATTCATTTTTTAAATGACAAGTTAACTACAGGAGGCTTTATTTATTCAGATGGTATGTCCACTTGTGGT
CGTGATCAATATATTTTTCTAATTGAAAAGTAAAAGCATCACAGCTTACCATTTTTCTTTTTCTGCAGTGTTGATTAATGATTTTTTTCCCGTTTATTGCTAGCAGTTTCAAAGTGTCATGTGGAGAT
TTAGCAATACTGTCTCTACTTAAAAGTATTGCACATTTCATTGAAAATGTGAGAGTTGATATACCAGCCTCTTTATATTTCTCTTTTACAGCAGAATCACATACTTCTCAAGATAAACAAGGTTTTTA
AAAAAGTTTCTGATTTAGTTAGGATCATATGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAAGCTGGAGTGCAATGGCACGATCTCGGCTCACTGC
AACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGGAGCTGGGATTACAGGCACGCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTA
GCCAGGCTGACCTCAAACTCCTGACCTCAGGTGATCCGCCCGCCTCCACCTCCCAGGGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCTCTTCAAGCTTTTTTACTATACATGTTGCCCCTC
TCCCCCAACTTAGGCACTACTGAATTTTTTATGATGGCACCAGGTCACTTTATGCTGGGTGATATAGTCAAAATTTGCTTATTTACTCTGCCCCTCGTCAACCACAGTATCATTTCAAGGACATGAAT
AAAATACTTGACAGTATCCAAAGGAGCTATACCAAAATCTAACAAGTAAATTTTGGATTTTGCCTCTTTGTGCTTTAAAGTACCAGGATTTCTGTCTCTATGGATAGGTCTTGGAGAATGTTAAGTAA
TGGATGAAACTTTTTAAAATAATTTGTAAATTTTACCTAAGTAGGACAGTAGTCCTTACTGCAATCAAAATAATTTACTGAGCACAACTCCTGTAAATTAATCTACAGTCAGGCTAGTATGATTTTAA
TATGATTTGAGTAAAAAGATAATTTTCAAGGAAAGAGTAATCATCCATCAATTTATTATAAAGCCAGATAGTATTCAATTTATGTCAAGAACAAAGAAATTGCCCTTTTAAAAGCATGTACGTGAATG
CTTTTTGAGGCACAGAAGTATGCTAAGCTTTAACATTTTGTATTTATTTACAACCCTTTTCTAAGGGAAGGTTACTTCTCAGTGCAGATGGAGAAACTGAAGCACTAAGGATAAATGATTAGTTTCCA
ATCACATCATTTTTTTCCACAGACTTGCTGGGACTAGCTTTCAGGTATTGACAGCCAGCCCCATATATTAAGGTAACCAGGTTGAATCTTCCAATTTGAGAACCCATGTATGGGTTGCAGTGAGCCGA
GATCATGCCACTGCACTCCATCCTGGGCAACAAGAACGAAACTCCGTCTCAAAAACAAAGAAGGATATAATAAAGTTAATATATAAACCATGTATGTGGTTAGGAATAAATTCAAATTCACCAGTCTC
CAATGGTGATTACTTTTACTACATAGAAAAACATTTTAGTGACTTACAGAGGATTTTTATTTGTGAATATTTCAGTAAAGTTTGTGTTGATTGTTGATAACACTGTTCATCTACTGAAGCACTTTAAT
AAAAATAAAATGAGCTGGAATTAGAAA

hide sequence

RefSeq Acc Id:

XM_011516435 ⟹ XP_011514737

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,463,040 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGG
ACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCAAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCT
GGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACTGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGG
GCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCGGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAA
GGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAG
CCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCT
GTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTC
CCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAG
TATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCA
CTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTA
GAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGAT
GAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGC
AGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGTGAGCCAAGGAAGCCCTACACAGGAGGAGAGTAGAAGAAAACCTGTCTTCAGTGTTGTCACAGAGCATGTGTGCATGCATTCA
TTCAGCATATTAGGCTGTAACTGTGTTCCAGGCAAGACAAGGCTTACAGAACGTTCTAGAGTTTTCAGCCTCAGATCCACACCATAGGAAGTGCTTCTGTAGCATCTGTTCCAGTATCCCAGGGGGAA
GAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATG

hide sequence

RefSeq Acc Id:

XM_017012470 ⟹ XP_016867959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,480,878 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGGACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCA
AGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCTGGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACT
GAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGGGCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCG
GCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAAGGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCC
TGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAGCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGG
GTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCTGTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGA
GCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTCCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGC
ATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAGTATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAG
TCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCACTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCAC
AGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTAGAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTT
TTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGATGAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCC
AGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGCAGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGGGGAAGAGGTGGTACCAGA
GACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCTGCTTAAGATTCTGCTGGCTGCAGCTCCCACCTCTAAGGCTAAGACAGACTCTATCAATATCCTGG
CAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATGTGAACAGGCACAAGGAGATTATTGTAAAGAGTATCTCTACCCTGCTTCTGCTACTCCTCAAACAC
TTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGCATCCCCTTGATCCTGAAGTTCTTCAATCAAAATATCTTGTCATACATCACTGCCAAAAACAGCAT
CTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCTGAGCAATAAGCTACACAAGAAAACTTGCCTGAATCAGGTTCCTGTGCTCATGTATCATCTTTCTA
ACCAACACATGCTGTAGGTAGAGTCTTCCAGGATTGGCAGCTGAGGGGGTTTTTAAACCATGGGCTTTGGAGACTTCAGTGTGTTAAGAAACAGGAAGGTGAGGAGGTATTATTTCATACAGGAAGGC
CTCACCTAAACTGACCAACATTGACTTCCAGGCTTCTGTGGGAATTAAAGCCTTGTA

hide sequence

RefSeq Acc Id:

XM_017012471 ⟹ XP_016867960

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,454,142 - 129,488,399 (+)	NCBI

Sequence:

show sequence

CAACAGCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAG
CTCAGGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTCCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGG
TCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAGTATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCG
CCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCACTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGA
TCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTAGAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGG
CACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGATGAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAG
GACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGCAGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTAT
GTCTTTGGGGGAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATGATCGCTCTGCTTAAGATTCTGCTGGCTGCAGCTCCCACCTCTAAGG
CTAAGACAGACTCTATCAATATCCTGGCAGATGTCCTACCTGAGGAGATGCCCATCACTGTTCTCCAGAGCATGAAGCTGGGCATCGATGTGAACAGGCACAAGGAGATTATTGTAAAGAGTATCTCT
ACCCTGCTTCTGCTACTCCTCAAACACTTCAAACTCAACCATATCTACCAGTTTGAATATGTATCGCAACATTTGGTATTTGCCAACTGCATCCCCTTGATCCTGAAGTTCTTCAATCAAAATATCTT
GTCATACATCACTGCCAAAAACAGCATCTCAGTCCTGGATTATCCTTGCTGTACCATCCAGGATTTGCCGGAGCTTACTACTGAAAGTCTGGAAGCTGGAGACAACAGCCAGTTCTGCTGGAGGAACC
TCTTTTCCTGCATCAACCTCCTGAGGCTGCTCAATAAACTGACCAAATGGAAACATTCCCGGACCATGATGCTGGTAGTGTTTAAATCGGCACCAATCTTAAAGCGGGCCCTCAAGGTCAAACAGGCC
ATGCTGCAACTTTATGTCCTAAAGCTACTAAAGTTACAGACCAAGTACCTGGGGCGCCAATGGAGGAAAAGCAACATGAAAACCATGTCAGCCATTTACCAGAAAGTGCGTCACCGCATGAACGATGA
CTGGGCTTACGGGAATGACATCGATGCCAGACCATGGGACTTCCAAGCAGAAGAATGTACCTTGAGGGCCAACATTGAGGCTTTTAACAGCCGTCGCTATGACAGACCCCAGGACTCTGAGTTTTCAC
CTGTGGATAACTGCTTGCAGAGCGTACTGGGGCAGAGGTTGGATCTGCCTGAAGATTTCCACTATTCATATGAGCTCTGGCTCGAGAGAGAGGTGTTTTCACAGCCCATCTGTTGGGAGGAGCTGCTC
CAGAATCACTGACTAAGTTCTTGTCAACAAGCATCAATAGATAGAGGTCAGCTCCAATAAACTGTGCTCTGCCTACCCTGTCCATACAGGCGCTGTTACCAGTTCAGGGCTCTTCTGGGGGCTCTTGG
GCCTAAAGATGGTGCAAGGGTGGGATCCTGAATCACAATAAAATGATCAACTTGCCCTGGGGTCAGTTGGGTGCCCAGTTGGCCTTGGAAATCTTTTGGTGGATCAATTCTAGACAAGCTCTTTGGTA
GGACCTTTTCCTGCTTTAGTCTTGGCTACAACCAGGCTAGACTTTGCTGGCTCTAAAAGAGGAAATTTGTTATGGCATTTGACCCATGGCATTCATCACAGATAGTGGGAGGTACAAGTCATAAAATA
GGGAGAAAGTTTTCTTCTTGCTCACACTGGATTCCTAGGACTTATCAGAGATTTGGAAAAACCAACTTTGAAATTAAGTTTGCATTTTAAATTTCAAATTTGGAAGCCTCTTTCTGAAATCATTAGCT
CTAAGATTATTTTAGAGCACCTGCACCTTCTTTGTGAAGGATGATGATTTACTATTCCCTCAATACTGCATGTTATCGAAAAGTGTGTTGTGTAAAGTGTTTTTTTCCTCATTCTGTAAGAGATCTAT
ATTCAATGTGAAAATTATTTCCTTGTGTACTCTGTATAGGGCATGGAATGCTCTGCCATTTTTAAAGAGCCACAACCAATATGAAATAATTAGGTCCTCTCTAAGGATGTTTCATGTTTTTCTTAAAT
GACTCCAGTCTTCAAATGGCTGAGCATACTGCAGAAAATTATCCTTTTCATCTAATTCATTTTTTAAATGACAAGTTAACTACAGGAGGCTTTATTTATTCAGATGGTATGTCCACTTGTGGTCGTGA
TCAATATATTTTTCTAATTGAAAAGTAAAAGCATCACAGCTTACCATTTTTCTTTTTCTGCAGTGTTGATTAATGATTTTTTTCCCGTTTATTGCTAGCAGTTTCAAAGTGTCATGTGGAGATTTAGC
AATACTGTCTCTACTTAAAAGTATTGCACATTTCATTGAAAATGTGAGAGTTGATATACCAGCCTCTTTATATTTCTCTTTTACAGCAGAATCACATACTTCTCAAGATAAACAAGGTTTTTAAAAAA
GTTTCTGATTTAGTTAGGATCATATGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAAGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCT
CCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGGAGCTGGGATTACAGGCACGCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTAGCCAG
GCTGACCTCAAACTCCTGACCTCAGGTGATCCGCCCGCCTCCACCTCCCAGGGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCTCTTCAAGCTTTTTTACTATACATGTTGCCCCTCTCCCC
CAACTTAGGCACTACTGAATTTTTTATGATGGCACCAGGTCACTTTATGCTGGGTGATATAGTCAAAATTTGCTTATTTACTCTGCCCCTCGTCAACCACAGTATCATTTCAAGGACATGAATAAAAT
ACTTGACAGTATCCAAAGGAGCTATACCAAAATCTAACAAGTAAATTTTGGATTTTGCCTCTTTGTGCTTTAAAGTACCAGGATTTCTGTCTCTATGGATAGGTCTTGGAGAATGTTAAGTAATGGAT
GAAACTTTTTAAAATAATTTGTAAATTTTACCTAAGTAGGACAGTAGTCCTTACTGCAATCAAAATAATTTACTGAGCACAACTCCTGTAAATTAATCTACAGTCAGGCTAGTATGATTTTAATATGA
TTTGAGTAAAAAGATAATTTTCAAGGAAAGAGTAATCATCCATCAATTTATTATAAAGCCAGATAGTATTCAATTTATGTCAAGAACAAAGAAATTGCCCTTTTAAAAGCATGTACGTGAATGCTTTT
TGAGGCACAGAAGTATGCTAAGCTTTAACATTTTGTATTTATTTACAACCCTTTTCTAAGGGAAGGTTACTTCTCAGTGCAGATGGAGAAACTGAAGCACTAAGGATAAATGATTAGTTTCCAATCAC
ATCATTTTTTTCCACAGACTTGCTGGGACTAGCTTTCAGGTATTGACAGCCAGCCCCATATATTAAGGTAACCAGGTTGAATCTTCCAATTTGAGAACCCATGTATGGGTTGCAGTGAGCCGAGATCA
TGCCACTGCACTCCATCCTGGGCAACAAGAACGAAACTCCGTCTCAAAAACAAAGAAGGATATAATAAAGTTAATATATAAACCATGTATGTGGTTAGGAATAAATTCAAATTCACCAGTCTCCAATG
GTGATTACTTTTACTACATAGAAAAACATTTTAGTGACTTACAGAGGATTTTTATTTGTGAATATTTCAGTAAAGTTTGTGTTGATTGTTGATAACACTGTTCATCTACTGAAGCACTTTAATAAAAA
TAAAATGAGCTGGAATTAGAAA

hide sequence

RefSeq Acc Id:

XM_047420656 ⟹ XP_047276612

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,464,141 (+)	NCBI

RefSeq Acc Id:

XM_047420657 ⟹ XP_047276613

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,456,700 - 129,488,399 (+)	NCBI

RefSeq Acc Id:

XM_054358707 ⟹ XP_054214682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,801,465 (+)	NCBI

RefSeq Acc Id:

XM_054358708 ⟹ XP_054214683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,793,945 (+)	NCBI

RefSeq Acc Id:

XM_054358709 ⟹ XP_054214684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,765,083 - 130,801,465 (+)	NCBI

RefSeq Acc Id:

XM_054358710 ⟹ XP_054214685

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,767,105 - 130,801,465 (+)	NCBI

RefSeq Acc Id:

XM_054358711 ⟹ XP_054214686

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,777,104 (+)	NCBI

RefSeq Acc Id:

XM_054358712 ⟹ XP_054214687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,776,003 (+)	NCBI

RefSeq Acc Id:

XM_054358713 ⟹ XP_054214688

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,769,663 - 130,801,465 (+)	NCBI

RefSeq Acc Id:

XR_001744840

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,463,004 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGG
ACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCAAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCT
GGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACTGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGG
GCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCGGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAA
GGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAG
CCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCT
GTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTC
CCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAG
TATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCA
CTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTA
GAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGAT
GAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGC
AGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGTGAGCCAAGGAAGCCCTACACAGGAGGAGAGTAGAAGAAAACCTGTCTTCAGTGTTGTCACAGAGCATGTGTGCATGCATTCA
TTCAGCATATTAGGCTGTAACTGTGTTCCAGGCAAGACAAGTCCATAGGTTACCCAACTTCCTTTTAAACCCACACTATTGAGCCACCTACCTCTCCTTCCAGGCTTACAGAACGTTCTAGAGTTTTC
AGCCTCAGATCCACACCATAGGAAGTGCTTCTGTAGCATCTGTTCCAGTATCCCAGGGGGAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTC

hide sequence

RefSeq Acc Id:

XR_001744841

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,463,004 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGGACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCA
AGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCTGGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACT
GAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGGGCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCG
GCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAAGGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCC
TGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAGCCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGG
GTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCTGTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGA
GCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTCCCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGC
ATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAGTATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAG
TCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCACTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCAC
AGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTAGAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTT
TTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGATGAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCC
AGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGCAGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGTCCATAGGTTACCCAACTTC
CTTTTAAACCCACACTATTGAGCCACCTACCTCTCCTTCCAGGCTTACAGAACGTTCTAGAGTTTTCAGCCTCAGATCCACACCATAGGAAGTGCTTCTGTAGCATCTGTTCCAGTATCCCAGGGGGA
AGAGGTGGTACCAGAGACGCCATGTGAAATCCTC

hide sequence

RefSeq Acc Id:

XR_008487707

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,775,967 (+)	NCBI

RefSeq Acc Id:

XR_008487708

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,775,967 (+)	NCBI

RefSeq Acc Id:

XR_008487709

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	7	130,747,403 - 130,776,003 (+)	NCBI

RefSeq Acc Id:

XR_927493

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,432 - 129,463,040 (+)	NCBI

Sequence:

show sequence

AAAGCGAGCTGAACCCTGAGGGGAGCCGCTGACCAGCAGCATGGAGGACCCCGCCGCGCCTGGG
ACCGGGGGCCCGCCCGCAAATGGCAATGGCAACGGCGGCGGCAAAGGGAAGCAGGCGGCGCCCAAGGGCCGCGAAGCGTTCCGAAGCCAGCGGCGGGAGTCAGAGGGCTCTGTGGACTGTCCCACTCT
GGAGTTTGAGTATGGAGATGCAGATGGGCATGCAGCCGAGTTGTCAGAATTGTATAGTTACACTGAGAACCTGGAATTCACCAATAACAGGAGGTGCTTTGAAGAAGATTTCAAGACTCAAGTGCAGG
GCAAGGAATGGCTGGAGTTGGAAGAAGATGCCCAAAAGGCCTATATAATGGGACTCTTGGACCGGCTAGAGGTGGTCAGTAGGGAACGGCGGCTGAAGGTGGCCCGGGCTGTTCTCTACCTGGCCCAA
GGTACTTTTGGGGAATGTGATTCAGAGGTCGATGTGCTACACTGGTCCAGGTACAACTGCTTCCTGCTGTATCAGATGGGGACCTTCTCCACCTTCCTGGAGCTACTCCACATGGAAATTGACAACAG
CCAGGCCTGTAGCAGTGCCCTTCGGAAACCAGCTGTCTCCATAGCTGATAGCACAGAGCTCAGGGTGCTGCTGAGTGTTATGTACCTAATGGTGGAAAATATTCGCCTGGAGCGAGAGACAGACCCCT
GTGGGTGGAGAACAGCCCGGGAGACCTTCCGCACTGAATTAAGCTTCTCCATGCATAATGAGGAGCCTTTTGCCCTTTTACTCTTCTCCATGGTTACCAAGTTCTGCAGTGGCCTGGCTCCTCACTTC
CCCATAAAGAAGGTCCTGCTCCTGCTCTGGAAGGTGGTCATGTTTACCCTCGGTGGATTTGAGCATCTGCAGACTCTCAAAGTACAGAAGCGGGCAGAATTGGGCCTGCCTCCACTGGCTGAAGACAG
TATCCAGGTGGTGAAGAGCATGCGTGCTGCCTCCCCGCCCTCTTACACTCTTGACCTGGGAGAGTCTCAGCTGGCACCCCCACCCTCCAAGCTGCGAGGCCGCCGTGGCTCTCGAAGGCAACTCCTCA
CTAAGCAGGACAGCCTGGACATCTACAATGAAAGGGATCTCTTCAAGACTGAGGAGCCCGCCACAGAGGAGGAAGAGGAGTCTGCTGGTGATGGAGAACGAACCTTGGATGGAGAGCTAGACCTGCTA
GAGCAGGACCCTCTGGTGCCACCTCCACCCTCACAGGCACCCCTCTCTGCTGAGCGGGTGGCTTTTCCCAAGGGCCTGCCCTGGGCCCCAAAGGTCAGACAGAAGGACATTGAGCACTTCTTGGAGAT
GAGCAGGAACAAGTTCATCGGATTCACCCTGGGGCAGGACACAGATACATTGGTTGGATTACCCAGGCCCATCCATGAGAGTGTGAAGACCCTAAAGCAGCACAAGTATATCTCCATCGCAGATGTGC
AGATCAAGAATGAAGAGGAGCTGGAGAAGTGCCCTATGTCTTTGGCTTACAGAACGTTCTAGAGTTTTCAGCCTCAGATCCACACCATAGGAAGTGCTTCTGTAGCATCTGTTCCAGTATCCCAGGGG
GAAGAGGTGGTACCAGAGACGCCATGTGAAATCCTCTACCAGGGAATGCTGTACAGCCTTCCGCAGTATATG

hide sequence


Protein RefSeqs	NP_001127808	(Get FASTA)	NCBI Sequence Viewer
	NP_065755	(Get FASTA)	NCBI Sequence Viewer
	XP_006716132	(Get FASTA)	NCBI Sequence Viewer
	XP_011514734	(Get FASTA)	NCBI Sequence Viewer
	XP_011514737	(Get FASTA)	NCBI Sequence Viewer
	XP_016867959	(Get FASTA)	NCBI Sequence Viewer
	XP_016867960	(Get FASTA)	NCBI Sequence Viewer
	XP_047276612	(Get FASTA)	NCBI Sequence Viewer
	XP_047276613	(Get FASTA)	NCBI Sequence Viewer
	XP_054214682	(Get FASTA)	NCBI Sequence Viewer
	XP_054214683	(Get FASTA)	NCBI Sequence Viewer
	XP_054214684	(Get FASTA)	NCBI Sequence Viewer
	XP_054214685	(Get FASTA)	NCBI Sequence Viewer
	XP_054214686	(Get FASTA)	NCBI Sequence Viewer
	XP_054214687	(Get FASTA)	NCBI Sequence Viewer
	XP_054214688	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH19064	(Get FASTA)	NCBI Sequence Viewer
	BAA86484	(Get FASTA)	NCBI Sequence Viewer
	BAF82854	(Get FASTA)	NCBI Sequence Viewer
	BAH13679	(Get FASTA)	NCBI Sequence Viewer
	EAL24101	(Get FASTA)	NCBI Sequence Viewer
	EAW83719	(Get FASTA)	NCBI Sequence Viewer
	EAW83720	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000249344
	ENSP00000249344.2
	ENSP00000392393
	ENSP00000392393.2
GenBank Protein	Q9ULQ0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_065755 ⟸ NM_020704
- Peptide Label:	isoform a
- UniProtKB:	Q8WUZ4 (UniProtKB/Swiss-Prot), Q9ULQ0 (UniProtKB/Swiss-Prot), A8K2A0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEDPAAPGTGGPPANGNGNGGGKGKQAAPKGREAFRSQRRESEGSVDCPTLEFEYGDADGHAAELSELYSYTENLEFTNNRRCFEEDFKTQVQGKEWLELEEDAQKAYIMGLLDRLEVVSRERRLKVA RAVLYLAQGTFGECDSEVDVLHWSRYNCFLLYQMGTFSTFLELLHMEIDNSQACSSALRKPAVSIADSTELRVLLSVMYLMVENIRLERETDPCGWRTARETFRTELSFSMHNEEPFALLLFSMVTKF CSGLAPHFPIKKVLLLLWKVVMFTLGGFEHLQTLKVQKRAELGLPPLAEDSIQVVKSMRAASPPSYTLDLGESQLAPPPSKLRGRRGSRRQLLTKQDSLDIYNERDLFKTEEPATEEEEESAGDGERT LDGELDLLEQDPLVPPPPSQAPLSAERVAFPKGLPWAPKVRQKDIEHFLEMSRNKFIGFTLGQDTDTLVGLPRPIHESVKTLKQHKYISIADVQIKNEEELEKCPMSLGEEVVPETPCEILYQGMLYS LPQYMIALLKILLAAAPTSKAKTDSINILADVLPEEMPITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYVSQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDL PELTTESLEAGDNSQFCWRNLFSCINLLRLLNKLTKWKHSRTMMLVVFKSAPILKRALKVKQAMLQLYVLKLLKLQTKYLGRQWRKSNMKTMSAIYQKVRHRMNDDWAYGNDIDARPWDFQAEECTLR ANIEAFNSRRYDRPQDSEFSPVDNCLQSVLGQRLDLPEDFHYSYELWLEREVFSQPICWEELLQNH hide sequence

RefSeq Acc Id:	NP_001127808 ⟸ NM_001134336
- Peptide Label:	isoform b
- UniProtKB:	A8K2A0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEDPAAPGTGGPPANGNGNGGGKGKQAAPKGREAFRSQRRESEGSVDCPTLEFEYGDADGHAAELSELYSYTENLEFTNNRRCFEEDFKTQVQGKEWLELEEDAQKAYIMGLLDRLEVVSRERRLKVA RAVLYLAQGTFGECDSEVDVLHWSRYNCFLLYQMGTFSTFLELLHMEIDNSQACSSALRKPAVSIADSTELRVLLSVMYLMVENIRLERETDPCGWRTARETFRTELSFSMHNEEPFALLLFSMVTKF CSGLAPHFPIKKVLLLLWKVVMFTLGGFEHLQTLKVQKRAELGLPPLAEDSIQVVKSMRAASPPSYTLDLGESQLAPPPSKLRGRRGSRRQLLTKQDSLDIYNERDLFKTEEPATEEEEESAGDGERT LDGELDLLEQDPLVPPPPSQAPLSAERVAFPKGLPWAPKVRQKDIEHFLEMSRNKFIGFTLGQDTDTLVGLPRPIHESVKTLKQHKYISIADVQIKNEEELEKCPMSLGEEVVPETPCEILYQGMLYS LPQYMIALLKILLAAAPTSKAKTDSINILADVLPEEMPITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYVSQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDL PELTTESLEAGDNSQFCWRNLFSCINLLRLLNKLTKWKHSRTMMLVVFKSAPILKRALKVKQAMLQLYVLKLLKLQTKYLGRQWRKSNMKTMSAIYQKVRHRMNDDWAYGNGESSQSS hide sequence

RefSeq Acc Id:	XP_006716132 ⟸ XM_006716069
- Peptide Label:	isoform X1
- UniProtKB:	A8K2A0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEDPAAPGTGGPPANGNGNGGGKGKQAAPKGREAFRSQRRESEGSVDCPTLEFEYGDADGHAAELSELYSYTENLEFTNNRRCFEEDFKTQVQGKEWLELEEDAQKAYIMGLLDRLEVVSRERRLKVA RAVLYLAQGTFGECDSEVDVLHWSRYNCFLLYQMGTFSTFLELLHMEIDNSQACSSALRKPAVSIADSTELRVLLSVMYLMVENIRLERETDPCGWRTARETFRTELSFSMHNEEPFALLLFSMVTKF CSGLAPHFPIKKVLLLLWKVVMFTLGGFEHLQTLKVQKRAELGLPPLAEDSIQVVKSMRAASPPSYTLDLGESQLAPPPSKLRGRRGSRRQLLTKQDSLDIYNERDLFKTEEPATEEEEESAGDGERT LDGELDLLEQDPLVPPPPSQAPLSAERVAFPKGLPWAPKVRQKDIEHFLEMSRNKFIGFTLGQDTDTLVGLPRPIHESVKTLKQHKYISIADVQIKNEEELEKCPMSLGEEVVPETPCEILYQGMLYS LPQYMIALLKILLAAAPTSKAKTDSINILADVLPEEMPITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYVSQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDL PELTTESLEAGDNSQFCWRNLFSCINLLRLLNKLTKWKHSRTMTSMPDHGTSKQKNVP hide sequence

RefSeq Acc Id:

XP_011514737 ⟸ XM_011516435

- Peptide Label:

isoform X6

- Sequence:

show sequence

MEDPAAPGTGGPPANGNGNGGGKGKQAAPKGREAFRSQRRESEGSVDCPTLEFEYGDADGHAAE
LSELYSYTENLEFTNNRRCFEEDFKTQVQGKEWLELEEDAQKAYIMGLLDRLEVVSRERRLKVARAVLYLAQGTFGECDSEVDVLHWSRYNCFLLYQMGTFSTFLELLHMEIDNSQACSSALRKPAVS
IADSTELRVLLSVMYLMVENIRLERETDPCGWRTARETFRTELSFSMHNEEPFALLLFSMVTKFCSGLAPHFPIKKVLLLLWKVVMFTLGGFEHLQTLKVQKRAELGLPPLAEDSIQVVKSMRAASPP
SYTLDLGESQLAPPPSKLRGRRGSRRQLLTKQDSLDIYNERDLFKTEEPATEEEEESAGDGERTLDGELDLLEQDPLVPPPPSQAPLSAERVAFPKGLPWAPKVRQKDIEHFLEMSRNKFIGFTLGQD
TDTLVGLPRPIHESVKTLKQHKYISIADVQIKNEEELEKCPMSLVSQGSPTQEESRRKPVFSVVTEHVCMHSFSILGCNCVPGKTRLTERSRVFSLRSTP

hide sequence

RefSeq Acc Id:	XP_011514734 ⟸ XM_011516432
- Peptide Label:	isoform X3
- UniProtKB:	A8K2A0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGTFSTFLELLHMEIDNSQACSSALRKPAVSIADSTELRVLLSVMYLMVENIRLERETDPCGWRTARETFRTELSFSMHNEEPFALLLFSMVTKFCSGLAPHFPIKKVLLLLWKVVMFTLGGFEHLQT LKVQKRAELGLPPLAEDSIQVVKSMRAASPPSYTLDLGESQLAPPPSKLRGRRGSRRQLLTKQDSLDIYNERDLFKTEEPATEEEEESAGDGERTLDGELDLLEQDPLVPPPPSQAPLSAERVAFPKG LPWAPKVRQKDIEHFLEMSRNKFIGFTLGQDTDTLVGLPRPIHESVKTLKQHKYISIADVQIKNEEELEKCPMSLGEEVVPETPCEILYQGMLYSLPQYMIALLKILLAAAPTSKAKTDSINILADVL PEEMPITVLQSMKLGIDVNRHKEIIVKSISTLLLLLLKHFKLNHIYQFEYVSQHLVFANCIPLILKFFNQNILSYITAKNSISVLDYPCCTIQDLPELTTESLEAGDNSQFCWRNLFSCINLLRLLNK LTKWKHSRTMMLVVFKSAPILKRALKVKQAMLQLYVLKLLKLQTKYLGRQWRKSNMKTMSAIYQKVRHRMNDDWAYGNDIDARPWDFQAEECTLRANIEAFNSRRYDRPQDSEFSPVDNCLQSVLGQR LDLPEDFHYSYELWLEREVFSQPICWEELLQNH hide sequence

Protein Domains

Far11/STRP C-terminal Far11/STRP N-terminal

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9ULQ0-F1-model_v2	AlphaFold	Q9ULQ0	1-834	view protein structure

RGD ID:

6805655

Promoter ID:

HG_KWN:59661

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_001134336, NM_020704, UC003VOX.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	7	128,861,121 - 128,861,621 (+)	MPROMDB

RGD ID:

7211901

Promoter ID:

EPDNEW_H11696

Type:

initiation region

Name:

STRIP2_1

Description:

striatin interacting protein 2

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	129,434,433 - 129,434,493	EPDNEW

Database	Acc Id	Source(s)
COSMIC	STRIP2	COSMIC
Ensembl Genes	ENSG00000128578	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000249344	ENTREZGENE
	ENST00000249344.7	UniProtKB/Swiss-Prot
	ENST00000435494	ENTREZGENE
	ENST00000435494.2	UniProtKB/Swiss-Prot
GTEx	ENSG00000128578	GTEx
HGNC ID	HGNC:22209	ENTREZGENE
Human Proteome Map	STRIP2	Human Proteome Map
InterPro	Far11/STRP	UniProtKB/Swiss-Prot
	Far11/STRP_C	UniProtKB/Swiss-Prot
	Far11/STRP_N	UniProtKB/Swiss-Prot
KEGG Report	hsa:57464	UniProtKB/Swiss-Prot
NCBI Gene	57464	ENTREZGENE
OMIM	617919	OMIM
PANTHER	PTHR13239	UniProtKB/Swiss-Prot
	STRIATIN-INTERACTING PROTEIN 2	UniProtKB/Swiss-Prot
Pfam	DUF3402	UniProtKB/Swiss-Prot
	N1221	UniProtKB/Swiss-Prot
PharmGKB	PA134923427	PharmGKB
SMART	DUF3402	UniProtKB/Swiss-Prot
	N1221	UniProtKB/Swiss-Prot
UniProt	A8K2A0	ENTREZGENE, UniProtKB/TrEMBL
	Q8WUZ4	ENTREZGENE
	Q9ULQ0	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	Q8WUZ4	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2012-11-15	STRIP2	striatin interacting protein 2	FAM40B	family with sequence similarity 40, member B	Symbol and/or name change	5135510	APPROVED

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


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


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

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar