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Gene: CELF5 (CUGBP Elav-like family member 5) Homo sapiens

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Symbol:

CELF5

Name:

CUGBP Elav-like family member 5

RGD ID:

1345217

HGNC Page

HGNC:14058

Description:

Predicted to enable mRNA binding activity. Involved in regulation of alternative mRNA splicing, via spliceosome. Predicted to be part of ribonucleoprotein complex. Predicted to be active in cytoplasm and nucleus.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

bruno-like 5 RNA binding protein; bruno-like protein 5; BRUNOL-5; BRUNOL5; CELF-5; CUG-BP and ETR-3 like factor 5; CUG-BP- and ETR-3-like factor 5; CUGBP, Elav-like family member 5; RNA-binding protein BRUNOL-5

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):	Celf5 (CUGBP, Elav-like family member 5)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Treefam
Rattus norvegicus (Norway rat):	Celf5 (CUGBP, Elav-like family member 5)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Celf5 (CUGBP Elav-like family member 5)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CELF5 (CUGBP Elav-like family member 5)	NCBI	Ortholog
Canis lupus familiaris (dog):	CELF5 (CUGBP Elav-like family member 5)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Celf5 (CUGBP Elav-like family member 5)	NCBI	Ortholog
Sus scrofa (pig):	CELF5 (CUGBP Elav-like family member 5)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CELF5 (CUGBP Elav-like family member 5)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Celf5 (CUGBP Elav-like family member 5)	NCBI	Ortholog
Alliance orthologs ³
Mus musculus (house mouse):	Celf5 (CUGBP, Elav-like family member 5)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Celf5 (CUGBP, Elav-like family member 5)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	celf5a (cugbp, Elav-like family member 5a)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Danio rerio (zebrafish):	celf5b (cugbp, Elav-like family member 5b)	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Caenorhabditis elegans (roundworm):	unc-75	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	celf5.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	celf5	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

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	19	3,224,661 - 3,297,076 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	3,224,661 - 3,297,076 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	3,224,659 - 3,297,074 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	3,175,701 - 3,248,074 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	3,175,700 - 3,248,071	NCBI
Celera	19	3,161,110 - 3,233,889 (+)	NCBI		Celera
Cytogenetic Map	19	p13.3	NCBI
HuRef	19	2,992,255 - 3,064,363 (+)	NCBI		HuRef
CHM1_1	19	3,224,288 - 3,296,678 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CELF5	Human	Neurodevelopmental Disorders		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Neurodevelopmental disorder	ClinVar	PMID:25741868
CELF5	Human	RASopathy		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: RASopathy	ClinVar	PMID:23379592 more ...

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CELF5	Human	1,2-dimethylhydrazine	decreases expression	ISO	Celf5 (Mus musculus)	6480464	1 and 2-Dimethylhydrazine results in decreased expression of CELF5 mRNA	CTD	PMID:22206623
CELF5	Human	1-naphthyl isothiocyanate	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	1-Naphthylisothiocyanate results in increased expression of CELF5 mRNA	CTD	PMID:30723492
CELF5	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Celf5 (Mus musculus)	6480464	Tetrachlorodibenzodioxin results in increased expression of CELF5 mRNA	CTD	PMID:16962184
CELF5	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in decreased expression of CELF5 mRNA	CTD	PMID:33387578
CELF5	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of CELF5 mRNA	CTD	PMID:32109520
CELF5	Human	4,4'-sulfonyldiphenol	decreases expression	ISO	Celf5 (Mus musculus)	6480464	bisphenol S results in decreased expression of CELF5 mRNA	CTD	PMID:30951980
CELF5	Human	4,4'-sulfonyldiphenol	affects methylation	ISO	Celf5 (Mus musculus)	6480464	bisphenol S affects the methylation of CELF5 gene	CTD	PMID:31683443
CELF5	Human	6-propyl-2-thiouracil	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Propylthiouracil results in increased expression of CELF5 mRNA	CTD	PMID:36843608
CELF5	Human	6-propyl-2-thiouracil	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Propylthiouracil results in decreased expression of CELF5 mRNA	CTD	PMID:30047161
CELF5	Human	7,12-dimethyltetraphene	increases expression	ISO	Celf5 (Mus musculus)	6480464	9 more ...	CTD	PMID:32553695
CELF5	Human	acetamide	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	acetamide results in increased expression of CELF5 mRNA	CTD	PMID:31881176
CELF5	Human	aflatoxin B1	increases methylation	EXP		6480464	Aflatoxin B1 results in increased methylation of CELF5 3' UTR and Aflatoxin B1 results in increased methylation of CELF5 intron	CTD	PMID:30157460
CELF5	Human	Aflatoxin B2 alpha	increases methylation	EXP		6480464	aflatoxin B2 results in increased methylation of CELF5 intron	CTD	PMID:30157460
CELF5	Human	all-trans-retinoic acid	decreases expression	EXP		6480464	Tretinoin results in decreased expression of CELF5 mRNA	CTD	PMID:21934132
CELF5	Human	alpha-Zearalanol	multiple interactions	ISO	Celf5 (Rattus norvegicus)	6480464	[Zeranol co-treated with perfluorooctanoic acid] results in decreased expression of CELF5 mRNA	CTD	PMID:35163327
CELF5	Human	amitrole	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Amitrole results in decreased expression of CELF5 mRNA	CTD	PMID:30047161 and PMID:38685447
CELF5	Human	benzo[a]pyrene	increases mutagenesis	EXP		6480464	Benzo(a)pyrene results in increased mutagenesis of CELF5 gene	CTD	PMID:25435355
CELF5	Human	benzo[a]pyrene	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of CELF5 mRNA	CTD	PMID:27858113
CELF5	Human	benzo[a]pyrene	increases expression	ISO	Celf5 (Mus musculus)	6480464	Benzo(a)pyrene metabolite results in increased expression of CELF5 mRNA and Benzo(a)pyrene results in increased expression of CELF5 mRNA	CTD	PMID:23735875 and PMID:32553695
CELF5	Human	benzo[b]fluoranthene	increases expression	ISO	Celf5 (Mus musculus)	6480464	benzo(b)fluoranthene results in increased expression of CELF5 mRNA	CTD	PMID:26377693
CELF5	Human	benzo[b]fluoranthene	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of CELF5 mRNA	CTD	PMID:27858113
CELF5	Human	benzo[e]pyrene	decreases methylation	EXP		6480464	benzo(e)pyrene results in decreased methylation of CELF5 intron	CTD	PMID:30157460
CELF5	Human	Benzo[ghi]perylene	decreases expression	ISO	Celf5 (Mus musculus)	6480464	1 and 12-benzoperylene results in decreased expression of CELF5 mRNA	CTD	PMID:26377693
CELF5	Human	bisphenol A	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of CELF5 mRNA	CTD	PMID:25181051 and PMID:30816183
CELF5	Human	bisphenol A	decreases expression	ISO	Celf5 (Mus musculus)	6480464	bisphenol A results in decreased expression of CELF5 mRNA	CTD	PMID:32156529
CELF5	Human	bisphenol A	increases methylation	EXP		6480464	bisphenol A results in increased methylation of CELF5 gene	CTD	PMID:31601247
CELF5	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of CELF5 gene	CTD	PMID:31601247
CELF5	Human	bisphenol A	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	bisphenol A results in increased expression of CELF5 mRNA	CTD	PMID:34947998
CELF5	Human	bisphenol F	decreases expression	ISO	Celf5 (Mus musculus)	6480464	bisphenol F results in decreased expression of CELF5 mRNA	CTD	PMID:30951980
CELF5	Human	butanal	increases expression	EXP		6480464	butyraldehyde results in increased expression of CELF5 mRNA	CTD	PMID:26079696
CELF5	Human	Butylparaben	increases expression	EXP		6480464	butylparaben results in increased expression of CELF5 mRNA	CTD	PMID:17121429
CELF5	Human	C60 fullerene	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	fullerene C60 results in decreased expression of CELF5 mRNA	CTD	PMID:19167457
CELF5	Human	cadmium dichloride	increases methylation	ISO	Celf5 (Rattus norvegicus)	6480464	Cadmium Chloride results in increased methylation of CELF5 promoter	CTD	PMID:22457795
CELF5	Human	chlorpyrifos	decreases expression	ISO	Celf5 (Mus musculus)	6480464	Chlorpyrifos results in decreased expression of CELF5 mRNA	CTD	PMID:37019170
CELF5	Human	chrysene	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of CELF5 mRNA	CTD	PMID:27858113
CELF5	Human	cobalt dichloride	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	cobaltous chloride results in decreased expression of CELF5 mRNA	CTD	PMID:24386269
CELF5	Human	copper atom	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of CELF5 mRNA	CTD	PMID:26033743
CELF5	Human	copper atom	multiple interactions	ISO	Celf5 (Rattus norvegicus)	6480464	[Copper co-treated with Dietary Sucrose] results in increased expression of CELF5 mRNA	CTD	PMID:26033743
CELF5	Human	copper(0)	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of CELF5 mRNA	CTD	PMID:26033743
CELF5	Human	copper(0)	multiple interactions	ISO	Celf5 (Rattus norvegicus)	6480464	[Copper co-treated with Dietary Sucrose] results in increased expression of CELF5 mRNA	CTD	PMID:26033743
CELF5	Human	DDE	decreases expression	EXP		6480464	Dichlorodiphenyl Dichloroethylene results in decreased expression of CELF5 mRNA	CTD	PMID:38568856
CELF5	Human	dibenz[a,h]anthracene	increases expression	ISO	Celf5 (Mus musculus)	6480464	1 more ...	CTD	PMID:26377693
CELF5	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with mercuric bromide co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
CELF5	Human	ethanol	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	Ethanol affects the expression of and affects the splicing of CELF5 mRNA	CTD	PMID:30319688
CELF5	Human	fenvalerate	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	fenvalerate results in increased expression of CELF5 mRNA	CTD	PMID:30307764
CELF5	Human	folic acid	decreases expression	ISO	Celf5 (Mus musculus)	6480464	Folic Acid results in decreased expression of CELF5 mRNA	CTD	PMID:25629700
CELF5	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of CELF5 gene	CTD	PMID:31601247
CELF5	Human	gentamycin	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Gentamicins results in decreased expression of CELF5 mRNA	CTD	PMID:33387578
CELF5	Human	Licochalcone B	increases expression	EXP		6480464	licochalcone B results in increased expression of CELF5 mRNA	CTD	PMID:33647349
CELF5	Human	mercury dibromide	decreases expression	EXP		6480464	mercuric bromide results in decreased expression of CELF5 mRNA	CTD	PMID:26272509
CELF5	Human	mercury dibromide	multiple interactions	EXP		6480464	[NOG protein co-treated with mercuric bromide 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 CELF5 mRNA	CTD	PMID:27188386
CELF5	Human	methapyrilene	decreases methylation	EXP		6480464	Methapyrilene results in decreased methylation of CELF5 intron	CTD	PMID:30157460
CELF5	Human	methylmercury chloride	decreases expression	EXP		6480464	methylmercuric chloride results in decreased expression of CELF5 mRNA	CTD	PMID:28001369
CELF5	Human	methylparaben	increases expression	EXP		6480464	methylparaben results in increased expression of CELF5 mRNA	CTD	PMID:17121429
CELF5	Human	ozone	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	[Air Pollutants results in increased abundance of Ozone] which results in increased expression of CELF5 mRNA	CTD	PMID:27106289 and PMID:34911549
CELF5	Human	p-chloromercuribenzoic acid	decreases expression	EXP		6480464	p-Chloromercuribenzoic Acid results in decreased expression of CELF5 mRNA	CTD	PMID:26272509
CELF5	Human	p-chloromercuribenzoic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with p-Chloromercuribenzoic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of CELF5 mRNA	CTD	PMID:27188386
CELF5	Human	panobinostat	decreases expression	EXP		6480464	panobinostat results in decreased expression of CELF5 mRNA	CTD	PMID:26272509
CELF5	Human	panobinostat	multiple interactions	EXP		6480464	[NOG protein co-treated with Panobinostat 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 CELF5 mRNA	CTD	PMID:27188386
CELF5	Human	paracetamol	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Acetaminophen results in increased expression of CELF5 mRNA	CTD	PMID:33387578
CELF5	Human	perfluorooctanoic acid	multiple interactions	ISO	Celf5 (Rattus norvegicus)	6480464	[Zeranol co-treated with perfluorooctanoic acid] results in decreased expression of CELF5 mRNA	CTD	PMID:35163327
CELF5	Human	perfluorooctanoic acid	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	perfluorooctanoic acid results in decreased expression of CELF5 mRNA	CTD	PMID:35163327
CELF5	Human	phenylmercury acetate	decreases expression	EXP		6480464	Phenylmercuric Acetate results in decreased expression of CELF5 mRNA	CTD	PMID:26272509
CELF5	Human	phenylmercury acetate	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of CELF5 mRNA	CTD	PMID:27188386
CELF5	Human	propanal	increases expression	EXP		6480464	propionaldehyde results in increased expression of CELF5 mRNA	CTD	PMID:26079696
CELF5	Human	resveratrol	multiple interactions	EXP		6480464	[Plant Extracts co-treated with Resveratrol] results in decreased expression of CELF5 mRNA	CTD	PMID:23557933
CELF5	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with mercuric bromide co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
CELF5	Human	silicon dioxide	decreases expression	EXP		6480464	Silicon Dioxide analog results in decreased expression of CELF5 mRNA	CTD	PMID:25895662
CELF5	Human	tetraphene	multiple interactions	ISO	Celf5 (Mus musculus)	6480464	[Benzo(a)pyrene co-treated with benz(a)anthracene co-treated with benzo(b)fluoranthene co-treated with chrysene] results in increased expression of CELF5 mRNA	CTD	PMID:27858113
CELF5	Human	thioacetamide	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Thioacetamide results in decreased expression of CELF5 mRNA	CTD	PMID:23411599
CELF5	Human	thioacetamide	increases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Thioacetamide results in increased expression of CELF5 mRNA	CTD	PMID:34492290
CELF5	Human	titanium dioxide	increases methylation	ISO	Celf5 (Mus musculus)	6480464	titanium dioxide results in increased methylation of CELF5 gene	CTD	PMID:35295148
CELF5	Human	trichloroethene	decreases expression	ISO	Celf5 (Rattus norvegicus)	6480464	Trichloroethylene results in decreased expression of CELF5 mRNA	CTD	PMID:33387578
CELF5	Human	trichostatin A	increases expression	EXP		6480464	trichostatin A results in increased expression of CELF5 mRNA	CTD	PMID:24935251
CELF5	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 CELF5 mRNA	CTD	PMID:27188386
CELF5	Human	trichostatin A	decreases expression	EXP		6480464	trichostatin A results in decreased expression of CELF5 mRNA	CTD	PMID:24935251 and PMID:26272509
CELF5	Human	triptonide	increases expression	ISO	Celf5 (Mus musculus)	6480464	triptonide results in increased expression of CELF5 mRNA	CTD	PMID:33045310
CELF5	Human	tris(2-butoxyethyl) phosphate	affects expression	EXP		6480464	tris(2-butoxyethyl) phosphate affects the expression of CELF5 mRNA	CTD	PMID:29024780
CELF5	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of CELF5 mRNA	CTD	PMID:25979313
CELF5	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of CELF5 mRNA	CTD	PMID:19101580 more ...
CELF5	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of CELF5 mRNA	CTD	PMID:28001369
CELF5	Human	valproic acid	affects splicing	ISO	Celf5 (Rattus norvegicus)	6480464	Valproic Acid affects the splicing of CELF5 mRNA	CTD	PMID:29427782

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)
CELF5	Human	mRNA processing	involved_in	IEA	UniProtKB-KW:KW-0507	150520179		UniProt	GO_REF:0000043
CELF5	Human	mRNA splice site recognition	involved_in	IBA	MGI:1338822 more ...	150520179		GO_Central	GO_REF:0000033
CELF5	Human	regulation of alternative mRNA splicing, via spliceosome	involved_in	IDA		150520179	PMID:11158314	UniProt	PMID:11158314
CELF5	Human	regulation of alternative mRNA splicing, via spliceosome	involved_in	IBA	FB:FBgn0000114 more ...	150520179		GO_Central	GO_REF:0000033

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)
CELF5	Human	cytoplasm	located_in	IEA	UniProtKB-SubCell:SL-0086	150520179		UniProt	GO_REF:0000044
CELF5	Human	cytoplasm	is_active_in	IBA	FB:FBgn0000114 more ...	150520179		GO_Central	GO_REF:0000033
CELF5	Human	cytoplasm	located_in	IEA	UniProtKB-KW:KW-0963	150520179		UniProt	GO_REF:0000043
CELF5	Human	nucleus	located_in	ISS	UniProtKB:Q9BZC1	150520179	PMID:11158314	UniProt	PMID:11158314
CELF5	Human	nucleus	is_active_in	IBA	FB:FBgn0000114 more ...	150520179		GO_Central	GO_REF:0000033
CELF5	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043
CELF5	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
CELF5	Human	ribonucleoprotein complex	part_of	IBA	FB:FBgn0265297 more ...	150520179		GO_Central	GO_REF:0000033

Molecular Function

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CELF5	Human	mRNA binding	enables	IBA	FB:FBgn0000114 more ...	150520179		GO_Central	GO_REF:0000033
CELF5	Human	nucleic acid binding	enables	IEA	InterPro:IPR035979	150520179		InterPro	GO_REF:0000002
CELF5	Human	pre-mRNA binding	enables	NAS		150520179	PMID:11158314	UniProt	PMID:11158314
CELF5	Human	protein binding	enables	IPI	UniProtKB:A0AV96 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
CELF5	Human	RNA binding	enables	IEA	UniProtKB-KW:KW-0694	150520179		UniProt	GO_REF:0000043
CELF5	Human	RNA binding	enables	IEA	UniRule:UR000414619	150520179		UniProt	GO_REF:0000104
CELF5	Human	RNA binding	enables	IEA	InterPro:IPR000504 and InterPro:IPR034648	150520179		InterPro	GO_REF:0000002

#	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

PMID:10893231	PMID:11158314	PMID:12477932	PMID:19757395	PMID:20889312	PMID:21873635	PMID:28514442	PMID:32296183	PMID:33961781	PMID:36774506

CELF5
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	3,224,661 - 3,297,076 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	3,224,659 - 3,297,074 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	3,175,701 - 3,248,074 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	3,175,700 - 3,248,071	NCBI
Celera	19	3,161,110 - 3,233,889 (+)	NCBI		Celera
Cytogenetic Map	19	p13.3	NCBI
HuRef	19	2,992,255 - 3,064,363 (+)	NCBI		HuRef
CHM1_1	19	3,224,288 - 3,296,678 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI		T2T-CHM13v2.0

Celf5
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	10	81,295,061 - 81,318,564 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	10	81,295,061 - 81,318,543 (-)	Ensembl		GRCm39 Ensembl
GRCm38	10	81,459,227 - 81,482,730 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	10	81,459,227 - 81,482,709 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	10	80,921,973 - 80,945,454 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	10	80,865,343 - 80,885,807 (-)	NCBI		MGSCv36	mm8
Celera	10	82,482,165 - 82,506,092 (-)	NCBI		Celera
Cytogenetic Map	10	C1	NCBI
cM Map	10	39.72	NCBI

Celf5
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	7	8,876,551 - 8,901,078 (+)	NCBI		GRCr8
mRatBN7.2	7	8,225,787 - 8,250,322 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	7	8,225,825 - 8,250,322 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	7	11,111,860 - 11,136,274 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	7	12,987,344 - 13,011,759 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	7	10,854,468 - 10,879,038 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	7	11,095,449 - 11,119,941 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	7	11,095,468 - 11,119,941 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	7	11,262,391 - 11,287,130 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	7	9,709,875 - 9,735,811 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	7	6,416,360 - 6,439,598 (+)	NCBI		Celera
Cytogenetic Map	7	q11	NCBI

Celf5
(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_004955495	5,185,126 - 5,214,718 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955495	5,182,758 - 5,214,724 (-)	NCBI	ChiLan1.0	ChiLan1.0

CELF5
(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	20	7,620,674 - 7,693,777 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	6,853,922 - 6,928,845 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	2,250,694 - 2,278,961 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	3,230,999 - 3,274,900 (+)	NCBI	panpan1.1	PanPan1.1	panPan2

CELF5
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	56,027,245 - 56,075,579 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	56,029,575 - 56,075,948 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	55,751,352 - 55,799,556 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	56,686,152 - 56,734,387 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	56,686,738 - 56,734,681 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	55,741,712 - 55,789,866 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	56,225,332 - 56,273,852 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	56,424,157 - 56,472,338 (-)	NCBI		UU_Cfam_GSD_1.0

Celf5
(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	215,947,705 - 215,982,648 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936588	1,852,126 - 1,887,240 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936588	1,864,793 - 1,887,082 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CELF5
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	75,314,834 - 75,364,103 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	75,314,808 - 75,364,189 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	75,956,800 - 75,987,394 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CELF5
(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	6	2,988,764 - 3,065,099 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666081	5,518,308 - 5,594,527 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Celf5
(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_004624828	5,982,552 - 6,005,839 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624828	5,980,299 - 6,015,202 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in CELF5
29 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3	copy number gain	See cases [RCV000052878]	Chr19:1565575..4108128 [GRCh38] Chr19:1565574..4108126 [GRCh37] Chr19:1516574..4059126 [NCBI36] Chr19:19p13.3	pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	copy number gain	See cases [RCV000052879]	Chr19:1972245..9648879 [GRCh38] Chr19:1972244..9759555 [GRCh37] Chr19:1923244..9620555 [NCBI36] Chr19:19p13.3-13.2	pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]\|See cases [RCV000052876]	Chr19:265917..8564134 [GRCh38] Chr19:265917..8629018 [GRCh37] Chr19:216917..8535018 [NCBI36] Chr19:19p13.3-13.2	pathogenic
GRCh38/hg38 19p13.3(chr19:233565-4699472)x3	copy number gain	See cases [RCV000052575]	Chr19:233565..4699472 [GRCh38] Chr19:233565..4699484 [GRCh37] Chr19:184565..4650484 [NCBI36] Chr19:19p13.3	pathogenic
GRCh38/hg38 19p13.3(chr19:2926238-4051635)x1	copy number loss	See cases [RCV000053942]	Chr19:2926238..4051635 [GRCh38] Chr19:2926236..4051633 [GRCh37] Chr19:2877236..4002633 [NCBI36] Chr19:19p13.3	pathogenic
NM_001172673.1(CELF5):c.604-604C>A	single nucleotide variant	Lung cancer [RCV000101226]	Chr19:3280595 [GRCh38] Chr19:3280593 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh38/hg38 19p13.3(chr19:1549144-4288720)x1	copy number loss	See cases [RCV000134795]	Chr19:1549144..4288720 [GRCh38] Chr19:1549143..4288717 [GRCh37] Chr19:1500143..4239717 [NCBI36] Chr19:19p13.3	pathogenic
GRCh38/hg38 19p13.3(chr19:3080621-4912622)x3	copy number gain	See cases [RCV000137713]	Chr19:3080621..4912622 [GRCh38] Chr19:3080619..4912634 [GRCh37] Chr19:3031619..4863634 [NCBI36] Chr19:19p13.3	likely pathogenic
GRCh38/hg38 19p13.3(chr19:3080621-3730716)x3	copy number gain	See cases [RCV000054107]	Chr19:3080621..3730716 [GRCh38] Chr19:3080619..3730714 [GRCh37] Chr19:3031619..3681714 [NCBI36] Chr19:19p13.3	uncertain significance
GRCh38/hg38 19p13.3(chr19:3223852-3306533)x3	copy number gain	See cases [RCV000135138]	Chr19:3223852..3306533 [GRCh38] Chr19:3223850..3306531 [GRCh37] Chr19:3174850..3257531 [NCBI36] Chr19:19p13.3	likely benign
GRCh38/hg38 19p13.3(chr19:3020573-3482611)x3	copy number gain	See cases [RCV000139774]	Chr19:3020573..3482611 [GRCh38] Chr19:3020571..3482609 [GRCh37] Chr19:2971571..3433609 [NCBI36] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1091A>C (p.Gln364Pro)	single nucleotide variant	not specified [RCV000414485]	Chr19:3284953 [GRCh38] Chr19:3284951 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.661_664dup (p.Arg222fs)	duplication	not specified [RCV000413090]	Chr19:3281254..3281255 [GRCh38] Chr19:3281252..3281253 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh38/hg38 19p13.3(chr19:2884401-3451078)x3	copy number gain	See cases [RCV000143086]	Chr19:2884401..3451078 [GRCh38] Chr19:2884399..3451076 [GRCh37] Chr19:2835399..3402076 [NCBI36] Chr19:19p13.3	uncertain significance
GRCh38/hg38 19p13.3(chr19:259395-6795611)x3	copy number gain	See cases [RCV000142627]	Chr19:259395..6795611 [GRCh38] Chr19:259395..6795622 [GRCh37] Chr19:210395..6746622 [NCBI36] Chr19:19p13.3	pathogenic
GRCh37/hg19 19p13.3(chr19:2652901-4342179)x3	copy number gain	See cases [RCV000448078]	Chr19:2652901..4342179 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NC_000019.9:g.1406030_3597207dup	duplication	Neurodevelopmental disorder [RCV000787423]	Chr19:1406030..3597207 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3(chr19:3076808-4796782)	copy number loss	not provided [RCV000767742]	Chr19:3076808..4796782 [GRCh37] Chr19:19p13.3	pathogenic
GRCh37/hg19 19p13.3(chr19:3134686-3501127)x3	copy number gain	not provided [RCV000847642]	Chr19:3134686..3501127 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3(chr19:260911-4788357)x3	copy number gain	not provided [RCV000846988]	Chr19:260911..4788357 [GRCh37] Chr19:19p13.3	pathogenic
GRCh37/hg19 19p13.3(chr19:3132909-3907470)x3	copy number gain	not provided [RCV000847631]	Chr19:3132909..3907470 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3(chr19:260911-3501271)x3	copy number gain	not provided [RCV001007025]	Chr19:260911..3501271 [GRCh37] Chr19:19p13.3	pathogenic
GRCh37/hg19 19p13.3(chr19:260912-4384674)x3	copy number gain	See cases [RCV001007443]	Chr19:260912..4384674 [GRCh37] Chr19:19p13.3	pathogenic
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3	copy number gain	not provided [RCV000684096]	Chr19:3120160..9732820 [GRCh37] Chr19:19p13.3-13.2	pathogenic
GRCh37/hg19 19p13.3(chr19:3015481-3543109)x3	copy number gain	not provided [RCV000740000]	Chr19:3015481..3543109 [GRCh37] Chr19:19p13.3	benign
GRCh37/hg19 19p13.3(chr19:3278206-3294279)x3	copy number gain	not provided [RCV000740001]	Chr19:3278206..3294279 [GRCh37] Chr19:19p13.3	benign
Single allele	deletion	Internal malformations [RCV000787421]	Chr19:2229488..4004142 [GRCh37] Chr19:19p13.3	uncertain significance
NC_000019.9:g.(?_589946)_(5696788_?)dup	duplication	not provided [RCV003113597]	Chr19:589946..5696788 [GRCh37] Chr19:19p13.3	uncertain significance
NC_000019.9:g.(?_589946)_(4818389_?)dup	duplication	not provided [RCV003105391]	Chr19:589946..4818389 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.940G>A (p.Val314Met)	single nucleotide variant	not specified [RCV004199241]	Chr19:3282399 [GRCh38] Chr19:3282397 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1084G>A (p.Gly362Arg)	single nucleotide variant	not specified [RCV004179242]	Chr19:3284946 [GRCh38] Chr19:3284944 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1105A>C (p.Met369Leu)	single nucleotide variant	not specified [RCV004121859]	Chr19:3285944 [GRCh38] Chr19:3285942 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.47T>C (p.Leu16Pro)	single nucleotide variant	not specified [RCV004095697]	Chr19:3224786 [GRCh38] Chr19:3224784 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.992A>G (p.His331Arg)	single nucleotide variant	not specified [RCV004077563]	Chr19:3282451 [GRCh38] Chr19:3282449 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.349C>T (p.Arg117Trp)	single nucleotide variant	not specified [RCV004297282]	Chr19:3273878 [GRCh38] Chr19:3273876 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1060G>C (p.Glu354Gln)	single nucleotide variant	not specified [RCV004896519]	Chr19:3284922 [GRCh38] Chr19:3284920 [GRCh37] Chr19:19p13.3	uncertain significance
NC_000019.9:g.(?_1206913)_(3771740_?)dup	duplication	not provided [RCV003154903]	Chr19:1206913..3771740 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.91C>T (p.Pro31Ser)	single nucleotide variant	not specified [RCV004156653]	Chr19:3224830 [GRCh38] Chr19:3224828 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.98G>C (p.Gly33Ala)	single nucleotide variant	not specified [RCV004108006]	Chr19:3224837 [GRCh38] Chr19:3224835 [GRCh37] Chr19:19p13.3	uncertain significance
GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3	copy number gain	not provided [RCV003485190]	Chr19:260912..7246777 [GRCh37] Chr19:19p13.3-13.2	pathogenic
NM_021938.4(CELF5):c.925G>A (p.Ala309Thr)	single nucleotide variant	not specified [RCV004431291]	Chr19:3282384 [GRCh38] Chr19:3282382 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.35A>G (p.Gln12Arg)	single nucleotide variant	not specified [RCV004431288]	Chr19:3224774 [GRCh38] Chr19:3224772 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1451C>G (p.Pro484Arg)	single nucleotide variant	not specified [RCV004431287]	Chr19:3293439 [GRCh38] Chr19:3293437 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1118C>T (p.Ala373Val)	single nucleotide variant	not specified [RCV004431286]	Chr19:3285957 [GRCh38] Chr19:3285955 [GRCh37] Chr19:19p13.3	uncertain significance
NC_000019.9:g.(?_2430909)_(4171966_?)del	deletion	RASopathy [RCV004581149]	Chr19:2430909..4171966 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1046G>A (p.Ser349Asn)	single nucleotide variant	not specified [RCV004896520]	Chr19:3284908 [GRCh38] Chr19:3284906 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1352C>T (p.Pro451Leu)	single nucleotide variant	not specified [RCV004896513]	Chr19:3293340 [GRCh38] Chr19:3293338 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.904C>T (p.Pro302Ser)	single nucleotide variant	not specified [RCV004896514]	Chr19:3282363 [GRCh38] Chr19:3282361 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.386G>A (p.Arg129His)	single nucleotide variant	not specified [RCV004896515]	Chr19:3273915 [GRCh38] Chr19:3273913 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.1241C>T (p.Thr414Met)	single nucleotide variant	not specified [RCV004896516]	Chr19:3290285 [GRCh38] Chr19:3290283 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.213C>G (p.Ile71Met)	single nucleotide variant	not specified [RCV004896517]	Chr19:3224952 [GRCh38] Chr19:3224950 [GRCh37] Chr19:19p13.3	uncertain significance
NM_021938.4(CELF5):c.653G>T (p.Arg218Leu)	single nucleotide variant	not specified [RCV004896518]	Chr19:3281248 [GRCh38] Chr19:3281246 [GRCh37] Chr19:19p13.3	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	4926
Count of miRNA genes:	1121
Interacting mature miRNAs:	1423
Transcripts:	ENST00000292672, ENST00000334293, ENST00000541430, ENST00000586050, ENST00000588101, ENST00000588350, ENST00000589370, ENST00000591483
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597595070	GWAS1651930_H	eosinophil count QTL GWAS1651930 (human)		2e-19	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	19	3235088	3235089	Human
597108375	GWAS1204449_H	self reported educational attainment QTL GWAS1204449 (human)		2e-08	self reported educational attainment		19	3237491	3237492	Human
1643451	SLIPL6_H	Serum lipid level QTL 6 (human)	2.19	0.0008	Lipid level		19	1	16075902	Human
597237757	GWAS1333831_H	cortical thickness QTL GWAS1333831 (human)		4e-15	cortical thickness		19	3283598	3283599	Human
597593819	GWAS1650679_H	eosinophil count QTL GWAS1650679 (human)		3e-22	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	19	3235088	3235089	Human
1581534	BP76_H	Blood pressure QTL 76 (human)	2	0.001	Blood pressure	pulse pressure	19	1	16075902	Human
1581535	BP65_H	Blood pressure QTL 65 (human)	3.1	0.001	Blood pressure	pulse pressure	19	1	16075902	Human
597585300	GWAS1642160_H	eosinophil count QTL GWAS1642160 (human)		2e-18	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	19	3235088	3235089	Human
407023304	GWAS672280_H	mental or behavioural disorder QTL GWAS672280 (human)		0.000005	mental or behavioural disorder		19	3251221	3251222	Human
597211347	GWAS1307421_H	self reported educational attainment QTL GWAS1307421 (human)		3e-11	self reported educational attainment		19	3274772	3274773	Human
597312405	GWAS1408479_H	cortical thickness QTL GWAS1408479 (human)		1e-14	cortical thickness		19	3285487	3285488	Human
1298499	UAE1_H	Urinary albumin excretion QTL 1 (human)	2.73	0.0009	Urinary albumin excretion	urine albumin:creatinine ratio (ACR)	19	1	16075902	Human
597116998	GWAS1213072_H	self reported educational attainment QTL GWAS1213072 (human)		5e-11	self reported educational attainment		19	3274772	3274773	Human
597161005	GWAS1257079_H	IGA glomerulonephritis QTL GWAS1257079 (human)		0.000009	IGA glomerulonephritis		19	3264001	3264002	Human
2314591	INSUL4_H	Insulin level QTL 4 (human)	3.8	0.000038	Insulin level	fasting	19	1	16075902	Human
597586144	GWAS1643004_H	eosinophil count QTL GWAS1643004 (human)		5e-17	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	19	3235088	3235089	Human
1298476	BP3_H	Blood pressure QTL 3 (human)	2.4		Blood pressure	systolic	19	1	16075902	Human

D19S424

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	3,226,373 - 3,226,513	UniSTS	GRCh37
Build 36	19	3,177,373 - 3,177,513	RGD	NCBI36
Celera	19	3,162,782 - 3,162,922	RGD
Cytogenetic Map	19	p13	UniSTS
HuRef	19	2,993,146 - 2,993,302	UniSTS
Marshfield Genetic Map	19	10.97	UniSTS
Marshfield Genetic Map	19	10.97	RGD
Genethon Genetic Map	19	10.8	UniSTS
deCODE Assembly Map	19	10.97	UniSTS

SHGC-2315

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	3,226,382 - 3,226,498	UniSTS	GRCh37
Build 36	19	3,177,382 - 3,177,498	RGD	NCBI36
Celera	19	3,162,791 - 3,162,907	RGD
Cytogenetic Map	19	p13	UniSTS
HuRef	19	2,993,155 - 2,993,287	UniSTS
TNG Radiation Hybrid Map	19	0.0	UniSTS

A009O27

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	3,296,027 - 3,296,157	UniSTS	GRCh37
Build 36	19	3,247,027 - 3,247,157	RGD	NCBI36
Celera	19	3,232,843 - 3,232,973	RGD
Cytogenetic Map	19	p13	UniSTS
HuRef	19	3,063,319 - 3,063,448	UniSTS
GeneMap99-GB4 RH Map	19	29.69	UniSTS

G32708

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	3,296,027 - 3,296,157	UniSTS	GRCh37
Celera	19	3,232,843 - 3,232,973	UniSTS
Cytogenetic Map	19	p13	UniSTS
HuRef	19	3,063,319 - 3,063,448	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1055	2376	2575	2003	4906	1630	2208	4	569	1428	409	2140	6254	5516	43	3692	757	1692	1527	168	1


RefSeq Transcripts	NG_052949	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001172673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_021938	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_033342	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722832	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722833	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722836	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011528173	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011528174	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321697	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321698	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321699	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321700	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001753733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007066936	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008485175	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008485176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008485177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_430147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA448420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB209067	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC005331	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC006505	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC010649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC123911	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF248649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF329266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294109	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL390161	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC028101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047522	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000292672 ⟹ ENSP00000292672

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,224,661 - 3,297,076 (+)	Ensembl

Ensembl Acc Id:

ENST00000334293 ⟹ ENSP00000335182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,225,485 - 3,297,016 (+)	Ensembl

Ensembl Acc Id:

ENST00000541430 ⟹ ENSP00000443498

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,224,704 - 3,296,336 (+)	Ensembl

Ensembl Acc Id:

ENST00000586050

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,270,614 - 3,290,347 (+)	Ensembl

Ensembl Acc Id:

ENST00000588101

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,282,257 - 3,286,791 (+)	Ensembl

Ensembl Acc Id:

ENST00000588350 ⟹ ENSP00000468503

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,273,905 - 3,297,076 (+)	Ensembl

Ensembl Acc Id:

ENST00000589370

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,270,621 - 3,282,453 (+)	Ensembl

Ensembl Acc Id:

ENST00000591483

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	3,284,762 - 3,293,401 (+)	Ensembl

RefSeq Acc Id:

NM_001172673 ⟹ NP_001166144

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI
GRCh37	19	3,224,701 - 3,297,074 (+)	RGD
Celera	19	3,161,110 - 3,233,889 (+)	RGD
HuRef	19	2,992,255 - 3,064,363 (+)	RGD
CHM1_1	19	3,224,289 - 3,296,678 (+)	NCBI
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

Sequence:

show sequence

GGGAGGCGCGGCCGCCGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTCGGTCCCGCGCCCGCCATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCC
TGCAGCCGCGGCCCTCGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGACGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAG
GACCTCAAGCCGCTCTTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACAAAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGC
TCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGC
AGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCG
CAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCT
GGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCT
CACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAAT
GGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCC
CCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAG
AGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGG
ACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGGTGAGCCGCCAGGCGGCCCCACCCCCGCCCAAGCCCCCCGTCTTGTCTGAAACCCCCTCCCGCGGCCCACTTCAT
GCTCCAAACCCTCCCCAGGTGGGGTGATGCTTCAAGAGGCTACAAGAAACCTCCGGGTTGGGTTGGCGGGGACAGAGCTGGATGTAGACACCCCCGATCCCCCTGTGGTTGGGGCTGGAGCAGAGGGT
GGGAATGGGGTAGGGACTGAGGTGAGCCAGGGCCCAGTGAGGTCGGTTAGGGAATCCTTCCCGGAGAAGGCTTTGAGGGCTGAATAGAAGTTCACCTGAGAGGCCAGGTTTGCTCTGGGGGTGGGGGT
GCGGTGGGGAGGGGGTTCTGTCCTGTCCTATGAGTCTGTTTTCCCTGCTGAAAACCCAACACCAGACGGAAATGCCAAGTGCCCACCCCAGACCCCAAACCCTAAGGTTGGACCCCAACTCGGAACCA
GGAGTGGAGCGTGGAAGGTGGGGACAGTGCTCAGGGCCCAGTCCAGTTGGCACTGACAGCTTCCAGTGTCCCCGCTCCATTTCCACTAGTTCCCCTGGGACAAGCGGCCCCTCACTGGGTGTCATTCC
TACCCAATGAGTTGATGGAAAAGTGGGATTCGTGCCCCACCCACCATCATGCAAGAAAAACAAGCAAAACGAAACCCAGACTGTAGTTTGCCATCAGGGCAAACCACTTTCTCAACATTTTTTTGTGG
GGGGATGAACAGTAAACCTTGTGGGGCCACTGTGGAAACTTAACCGTGGGTCTCAAACCTTGATGAGCCTCATCTGTAAAATGGGTTCAAGAAAGTCATCTCCCCAGAGACGGCGGAAACGGTCCACC
TAGGGAACAGAGTGGGGCATCTTTTCGCAGCCGAGCCCAGAACCCATCACCTAAAGAGTTCTGGATGATTCGTTTTGATTTTTTTTTTTTTTAAATCACCATCGCTGTCGTCATCAGAGTCTCGCCTA
GGGCCTGGCACAGAGTAGACGCTCAGTTAGAAGCTGTCTGGCCTTTTCACCTTCTCCCGGGTCAGCACACACAGATTTGGGAGTATTTACCTGCACAGAACGCACCTTCAGGAACTGCCAACCAGAAG
CAAAATCCAAAGCTGCTCTCTGCGATCCCTTCACTTTTAACTCTCAGTCTGCACTTTTTTTTTTTAACTGAGCATCTATTATGTGCTAGGCACTGTTCCAGTGCTCGGGGACGCAGCTGTGAATGAAC
AGAAACGGGGGATGGAGGACAGGGGAGAAACCCCCTTCACGGGCCTTAGATGGCAGGGGGTAGGGAAGGAGAGACAGAAAATAAACAGAAATATCTGTCCCCAGCTGCCAGAGGAGGAGGAAATGGGC
TTGGTGATGGTGACATTAAGTTCTTTGAAAGCTGGGTTTGTTGGCCTCTGAACTCTGGCCTTTGTGGGATCTGTTCTTTTGGAAAAGATGGGAGCCCCTGTGTTCCTAGATCCCAGCCTGGCCGGGTG
GAGTAGGGTGGGGAGGTGGTGTCCACCTGTGTGGCCCCGTTCTCACTCCCTAACGCCCGTCCCTTCTCCCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACT
TACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGC
GGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATA
TATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGG
GGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGAC
TTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGG
ATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGG
GGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCC
GGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGG
GGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGT
TCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCT
ACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGA
ACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGT
GTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCT
GCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTT
GACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGA
AAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

NM_021938 ⟹ NP_068757

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI
GRCh37	19	3,224,701 - 3,297,074 (+)	RGD
Build 36	19	3,175,701 - 3,248,074 (+)	NCBI Archive
Celera	19	3,161,110 - 3,233,889 (+)	RGD
HuRef	19	2,992,255 - 3,064,363 (+)	RGD
CHM1_1	19	3,224,288 - 3,296,678 (+)	NCBI
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

Sequence:

show sequence

GGGAGGCGCGGCCGCCGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTC
GGTCCCGCGCCCGCCATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCTCGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGG
CATGAAGGACCTGGACGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTCTTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCT
ACACGGGGATGCACAAAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCT
GCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCT
CCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGG
TCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTC
ATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGC
TCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCG
TCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCG
CACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACC
CTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCC
AGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGACCTGCGTGATTTGTACAATGTA
CTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGT
GTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAA
ACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

NR_033342

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,225,278 - 3,297,076 (+)	NCBI
GRCh37	19	3,224,701 - 3,297,074 (+)	RGD
Celera	19	3,161,110 - 3,233,889 (+)	RGD
HuRef	19	2,992,255 - 3,064,363 (+)	RGD
CHM1_1	19	3,225,070 - 3,296,678 (+)	NCBI
T2T-CHM13v2.0	19	3,200,157 - 3,272,447 (+)	NCBI

Sequence:

show sequence

CTCTCTCTCCCTTTCTCTTCTCTCCCATCTCCCTCGACCTCTCATCCTTCCCCCCACAGCACCC
TCTCTCTCCCTCCCTCCCTCCCTCACCCTTCCATCCCCCAGACCCCCACCCCTTCCTCCCTCCCTCACCCCACTCTTTCCTGCCCGTTTGCCAGGGGAGCCTCGGGAACGCCGGCACCCCTCCCTGCC
CCCCCACCCCCATTCATTCAGCCTCCCCAGGCCCCGTCGGGGAAGTTTGCACCTGCGGACTCCATTGCTTTGGTTATTTTCACAAAGCCAGGCCGGCGGGGCAGGTCCGGCCGCGGGGGACACGGATG
CCCAGGACCCCAGGCTAATCGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAG
CCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGT
GCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGG
TGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCT
CTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCAT
CGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAA
CCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATC
GCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATC
GAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGG
CCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAAC
TTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTT
CCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTA
AA

hide sequence

RefSeq Acc Id:

XM_006722832 ⟹ XP_006722895

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI

Sequence:

show sequence

CGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTCGGTCCCGCGCCCGCC
ATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCTCGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGA
CGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTCTTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACA
AAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGC
CGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGG
CAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACA
CGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACA
ACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCT
GCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCC
TTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAG
CCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCAT
TTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGA
GGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTC
CAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCT
GTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAAT
CACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGG
GCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACAC
AACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCC
CTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGG
GGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTA
GCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGA
GAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCA
AAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGC
ATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAA
AAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCG
AGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATAC
TCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAA
CTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCT
CTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_006722833 ⟹ XP_006722896

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI

Sequence:

show sequence

CGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTCGGTCCCGCGCCCGCCATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCT
CGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGACGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTC
TTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACAAAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCA
CGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGC
TGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCC
TTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTC
CCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGC
AGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTT
GCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCA
GCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACC
TCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGAT
AACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCC
CTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTT
CTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCC
CTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTT
GAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGG
TGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCT
TCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCC
CTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTG
TCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCA
TACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTG
GGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTT
AATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACC
ACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCT
CTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCG
GTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGT
TTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTT
GGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTAC
TTGCTAAA

hide sequence

RefSeq Acc Id:

XM_006722836 ⟹ XP_006722899

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,270,577 - 3,297,076 (+)	NCBI

Sequence:

show sequence

GCGGCGGCACGTGGATGCCAGCCTGGCGCGCGTCTCCAGGCCGGTGGATGGCGCGGCCAATCCA
GGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGT
GCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCC
AGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGC
CCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCA
CACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCC
CTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCAC
GCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGA
TGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATG
AACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTC
CCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTG
GAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAA
ACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAAACTTTTCCGACTTCC
TTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCA
CATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCC
CACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTACTCATGTGACCAATAG
CCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGT
CTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTT
CTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGC
TGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAG
AAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAA
AAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAA
GCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTA
CTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACA
CACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCA
AAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_006722837 ⟹ XP_006722900

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,225,278 - 3,297,076 (+)	NCBI

Sequence:

show sequence

ACCCCCACCCCTTCCTCCCTCCCTCACCCCACTCTTTCCTGCCCGTTTGCCAGGGGAGCCTCGGGAACGCCGGCACCCCTCCCTGCCCCCCCACCCCCATTCATTCAGCCTCCCCAGGCCCCGTCGGG
GAAGTTTGCACCTGCGGACTCCATTGCTTTGGTTATTTTCACAAAGCCAGGCCGGCGGGGCAGGTCCGGCCGCGGGGGACACGGATGCCCAGGACCCCAGGCTAATCGGCTGTGCCTTCCTCACCTAC
TGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCT
GTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCG
TGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGG
CGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAG
CTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCA
CCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGC
CCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCA
GCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATC
GAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGG
CCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCAT
AAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTG
GGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATAT
ATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACAC
AGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGC
ACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGG
TACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGC
CCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGG
CCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAA
ATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTG
GACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAA
TGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACT
TGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCG
GCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGAT
TTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGG
TTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAA
AAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_006722838 ⟹ XP_006722901

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,271,173 - 3,297,076 (+)	NCBI

Sequence:

show sequence

GCCAACGGAGGTGGGGTGGGAGGGGTGGGGGGAGCAGGAGTCTGGAGCTCCTGCAGGTGCCCCC
CCATCTCTCCCCACCTCCCCTGGCACCCCCCCGCTTCCAGCCCAGAAGCTGGTCCCATCTGGTTGAAACCATCTCCCCTCCTGCCTCCAGCCTAGCAGGGTGTGGTACCCAGGTGGAAAGGGCCCCGA
TGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTC
GGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCAT
GCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCC
CCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTC
AACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCC
AGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACC
CCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGAC
ACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGC
AGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCC
CAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTC
TACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTC
GCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCA
AACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCAC
CACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGC
TGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTA
CTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCA
GCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTT
TTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAG
GGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAA
ACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAA
AAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGT
GTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCT
TTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTT
TTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTT
CAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_011528173 ⟹ XP_011526475

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,270,577 - 3,297,076 (+)	NCBI

Sequence:

show sequence

GGCGCGCGTCTCCAGGCCGATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGC
TGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCC
TTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTC
CCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGC
AGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTT
GCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCA
GCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACC
TCCCCCAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGAT
AACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCC
CTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTT
CTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCC
CTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTT
GAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGG
TGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCT
TCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCC
CTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTG
TCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCA
TACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTG
GGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTT
AATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACC
ACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCT
CTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCG
GTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGT
TTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTT
GGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTAC
TTGCTAAA

hide sequence

RefSeq Acc Id:

XM_011528174 ⟹ XP_011526476

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,271,170 - 3,297,076 (+)	NCBI

Sequence:

show sequence

GGGCCAACGGAGGTGGGGTGGGAGGGGTGGGGGGAGCAGGAGTCTGGAGCTCCTGCAGGTGCCC
CCCCATCTCTCCCCACCTCCCCTGGCACCCCCCCGCTTCCAGCCCAGAAGCTGGTCCCATCTGGTTGAAACCATCTCCCCTCCTGCCTCCAGCCTAGCAGGGTGTGGTACCCAGGTGGAAAGGGCCCC
GATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCG
GGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATG
CCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCC
CTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCA
ACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCA
GGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCC
CACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTTTGGAGACA
CGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCA
GCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCC
AGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCT
ACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCG
CTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAA
ACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACC
ACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCT
GCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTAC
TCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAG
CCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTT
TTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGG
GTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAA
CATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAA
AAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTG
TGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTT
TCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTT
TGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTC
AGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_017027111 ⟹ XP_016882600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,275,014 - 3,297,076 (+)	NCBI

Sequence:

show sequence

CTGATCTGTCTCTCTCTCTCCCTGATTCTCAGTCTCTCTGCTGGTTTCTCTCTCTCCCTCCCACCCCCATGAGTGACAGCTGCCGAGAGCGGTTTCCATAGTAACCCAGCTCACCGTCCCTAGGAGAT
GAAGCCACCACGTTCCCCATTACCAGGGAGCATGCAGTTACCCAAGGGGGCAGAGCTCACACAGGAGAGGCTGGCCCAGCTCCGGCCTCAGACCAGGTTCCAGCCCAGCCCCACCCAGCAGGGGGTCC
AGCCTGCCAAGGCCCCTGGTCCACTGAGCACGTGAACCCTCACTCCACTCCACAGATGGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCA
GCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCC
AGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCC
TTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGT
CAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGC
CCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCC
ATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGTCCCGAGGGCTGTAACCTGTTTATCTACCACCTCCCCCAGGAGTT
TGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCG
CCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGG
CATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTTGGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCT
GCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCGTGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAA
CGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAGATCTATAGACAGTATATATATATTTTGAGTACGGATCAT
GGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCA
CCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTCTCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGG
TCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTGGCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCAT
AGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCACCCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGA
ATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACTGGAGACGAACTTGATAATGACCTTCATACCTCTACAGAG
ATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATTTTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCT
TTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTCTTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAA
GAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGAGGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAA
AAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAGTTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGT
GTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCCGAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTA
CGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAA
CTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTA
CGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACTAAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence

RefSeq Acc Id:

XM_054321693 ⟹ XP_054177668

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321694 ⟹ XP_054177669

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321695 ⟹ XP_054177670

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,246,539 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321696 ⟹ XP_054177671

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,246,536 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321697 ⟹ XP_054177672

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,245,990 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321698 ⟹ XP_054177673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,200,157 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321699 ⟹ XP_054177674

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,246,014 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XM_054321700 ⟹ XP_054177675

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,250,381 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XR_001753733

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI

Sequence:

show sequence

CGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTCGGTCCCGCGCCCGCCATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCT
CGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGACGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTC
TTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACAAAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCA
CGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGCCGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACG
TGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGGCAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCAC
GCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACACGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCC
GTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACAACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCC
AGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCTGCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGC
TTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCCTTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGT
CCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAGCCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGAGTTTGGAGACACGGAGCTGACGCAGATG
TTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCAAGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAA
CGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACACCCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGACCTGCGTGATTTGT
ACAATGTACTTTATTTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTG
AGTTTTGTGTCAAAGAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAA
AAAAAAAAA

hide sequence

RefSeq Acc Id:

XR_007066936

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,270,577 - 3,297,076 (+)	NCBI

RefSeq Acc Id:

XR_008485175

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XR_008485176

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,199,540 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XR_008485177

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	3,245,994 - 3,272,447 (+)	NCBI

RefSeq Acc Id:

XR_430147

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	3,224,661 - 3,297,076 (+)	NCBI

Sequence:

show sequence

CGCTCCAGCTGCGAGTCCGCCCGCCGCCCGCCGCCGCCGCCGCCGGCTCGGTCCCGCGCCCGCC
ATGGCCCGCCTGACGGAGAGCGAGGCGCGCCGGCAGCAGCAGCAGCTCCTGCAGCCGCGGCCCTCGCCCGTGGGCAGCAGCGGGCCCGAGCCCCCCGGGGGGCAGCCCGACGGCATGAAGGACCTGGA
CGCCATCAAACTCTTCGTGGGCCAGATCCCGCGGCACCTGGACGAGAAGGACCTCAAGCCGCTCTTCGAGCAGTTCGGCCGCATCTACGAGCTCACGGTGCTCAAAGACCCCTACACGGGGATGCACA
AAGGCTGTGCCTTCCTCACCTACTGTGCCAGGGATTCCGCCATCAAAGCTCAGACTGCCCTGCACGAGCAGAAGACCTTGCCCGGAATGGCGCGGCCAATCCAGGTGAAGCCTGCGGACAGTGAAAGC
CGCGGAGGTAGGGACCGGAAGCTGTTCGTGGGGATGCTGAACAAGCAGCAGTCGGAGGAGGACGTGCTGCGGCTGTTCCAGCCCTTCGGGGTCATTGACGAGTGCACCGTGCTCCGGGGGCCTGACGG
CAGCAGCAAAGGCTGTGCTTTCGTGAAGTTCTCCTCCCACACGGAGGCGCAGGCGGCCATCCACGCCTTGCATGGGAGCCAGACCATGCCGGGAGCCTCCTCCAGCCTGGTGGTCAAGTTCGCCGACA
CGGACAAGGAGCGGACGCTCCGGCGCATGCAGCAGATGGTGGGCCAGCTGGGCATCCTGACGCCGTCCCTCACATTGCCCTTCAGCCCCTACAGTGCCTACGCCCAGGCTCTCATGCAACAGCAGACA
ACAGTCCTGTCCACCTCGGGCAGCTACCTGAGTCCCGGCGTGGCCTTCTCACCCTGTCACATCCAGCAGATAGGCGCCGTCAGCCTCAACGGGCTGCCTGCCACACCCATCGCTCCTGCCTCTGGGCT
GCACTCACCCCCGCTGCTGGGCACCACCGCTGTGCCTGGCCTCGTGGCTCCCATCACCAATGGCTTTGCAGGTGTCGTGCCCTTTCCAGGTGGGCACCCTGCCCTGGAAACCGTCTATGCCAATGGCC
TTGTGCCCTACCCAGCTCAGAGCCCGACTGTGGCCGAGACACTGCATCCTGCCTTCTCCGGAGTCCAGCAGTACACAGCCATGTACCCCACCGCGGCCATCACGCCCATCGCGCACAGCGTCCCCCAG
CCGCCGCCCCTCCTGCAGCAGCAGCAGCGAGAAGGAGTTTGGAGACACGGAGCTGACGCAGATGTTCCTACCCTTCGGCAATATCATTTCCTCCAAGGTGTTTATGGATCGAGCTACCAACCAGAGCA
AGTGTTTCGGCTTCGTGAGCTTTGATAACCCGGCCAGCGCCCAGGCAGCCATCCAGGCCATGAACGGCTTCCAGATCGGCATGAAGAGGCTCAAAGTCCAGCTGAAGCGGCCCAAAGACCCGGGACAC
CCCTACTGACCGCGCCCACAGCCGCCCTGAGGCTGTAGGCATGGCCCAGGTGAGGGGCCTTCCCATCCCAGGAGGGTTTTCTGCTTCCAACCGATCCAGGACTTACCCATAAATTCCAACCGTTCTTT
GGACACCAGCCCTTTCCTCCCCTCTTCTCCCCTTGCCCTGCCCCTCTACTGGAGGCCACCTGGAGTGGCGAGGGGCCTTTGGGGTCTGTCCTGGGGCAGGGGCGGGGGTGGGGGAGGCTCCTGAATCG
TGGGCAGAAGTGTTCACACGCCCCCCCTGCTTTGGGAAACGCTCTCGCTTCTTCCCCACAAAACTTGGTGACTTCCCCAAACTAAATCACACCTTTTCCTATATATATATATATGCATATATATATAG
ATCTATAGACAGTATATATATATTTTGAGTACGGATCATGGGACCAAACTTTTCCGACTTCCTTCCATCCGAGTAGAGTGACCCTGGGCCGGTCACTCAGCGGGGGACACAGGAAGGGCTGAGGTTGG
CGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCCTGGCTGGCACATCCCACCAGGAACCCGCCAACACAACATACCTCCAGGACTTTTGGCACCCCCCACCACCAATTC
TCCAGGGCCGTTGGGCTCTGCCAGCTTCAGTGTCCCTGGTCCCAGCTGCAGCCTCCAGACCCCACCTCGCCCCTTCGTCCCAGAGCCCTGCCCTCCGGGATGGATATAGGTACAACAGAGACGCTCTG
GCCTGCCTCAGCCCTTCTCTGCTCCCCTGCCCGAGTCATAGCCTTACTCATGTGACCAATAGCCCTTAGCTTTCCGTCGGAGGGGGGGGGCGGACAGGGTTGGGGGGAGCCCCCCTGCCCCTCACCAC
CCCCTCCCAAGGCCAGGCAGCCATTGTCCCTGCCTTCGAATCACCAGCCTCGAATTTAAGGTCTTGTAACCAGGATTGCCAAGCGTAGCGGAAGACCCTACCCGGACCGGCCAAGCACCCCTTTAACT
GGAGACGAACTTGATAATGACCTTCATACCTCTACAGAGATTTTTTTTTTTTTCCGGTCTTTCTGAGCAGGTACAAAGAAGAAAAGAGAAGAAAAAGATGGGGGGAAAAAATCAAACCACAATGGATT
TTTGTTTCCTAGTTGGGAGTGGGGTGGGGTGGGGTGTCTTTGTGAGGGTGCCTCTGTACAGCTGCCCAATCCGCGACACCCACGTCAAAGCACAGCATCAAGTTCGTTTGGACATCCGGCAAGGCCTC
TTACCAAATGAGGCGCCAGATAACTTAATAAGCTCAAAAGAAAAAAACATTTAAAAAGAAAGAAAAAAAAAAAAAAAAAAACCAAGCATTTCCTTTTCTTTCTACCAAAATGTGTTGACTGACCCGGA
GGGGGGGCGGTAGGGTGGGGGAAACCACACAGAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAAAAAAATAGAAAAGAAAAAAAAAAATCTTCTGAACCAACTTGTTTCGATATTCCAGAG
TTTGATAATTGTTTCGAGACTCTCCTCTAGCGTGCCTGTGTTCCGTGTGTCCCCGTGTGCAAGCGTGTGCCATGCCAATCTGCCTCGAGGGGGCCTCACCCGTGTCCGCGGCGCCCGCCGAGGCCCCC
GAGGGCCTGCTTGGGAGTGTGTGCCGGTGTGCAGTTGTACGTGTCTTTCTGGTCCATGTTTACTGGCTGTAAATACCATTTTTATACTCCACATCGCAGACCTGCGTGATTTGTACAATGTACTTTAT
TTCTGCTACGAGTAATTTCATGAAGTTTCAACTTGCAAACTGACTTTTGGGACAAACCAACACACACACAGAAGAGAAAGCAAAGAACTTGGAACTTTGGGTTGACTCGGTTTGAGTTTTGTGTCAAA
GAAGATTTCCCGCGGCTGAAGAGGTTGGTGTTCCTGTTACGTGTTTCAGGTGAGAAGCAGCAAAGCGTCTTAATGTTCAAAACGCCTCTCTTTGGTCTGGAGAAAAAAAAAAAAAAAAAAAAACAACT
AAAAATTTATTTAATAAAAGTTTTACTTGCTAAA

hide sequence


Protein RefSeqs	NP_001166144	(Get FASTA)	NCBI Sequence Viewer
	NP_068757	(Get FASTA)	NCBI Sequence Viewer
	XP_006722895	(Get FASTA)	NCBI Sequence Viewer
	XP_006722896	(Get FASTA)	NCBI Sequence Viewer
	XP_006722899	(Get FASTA)	NCBI Sequence Viewer
	XP_006722900	(Get FASTA)	NCBI Sequence Viewer
	XP_006722901	(Get FASTA)	NCBI Sequence Viewer
	XP_011526475	(Get FASTA)	NCBI Sequence Viewer
	XP_011526476	(Get FASTA)	NCBI Sequence Viewer
	XP_016882600	(Get FASTA)	NCBI Sequence Viewer
	XP_054177668	(Get FASTA)	NCBI Sequence Viewer
	XP_054177669	(Get FASTA)	NCBI Sequence Viewer
	XP_054177670	(Get FASTA)	NCBI Sequence Viewer
	XP_054177671	(Get FASTA)	NCBI Sequence Viewer
	XP_054177672	(Get FASTA)	NCBI Sequence Viewer
	XP_054177673	(Get FASTA)	NCBI Sequence Viewer
	XP_054177674	(Get FASTA)	NCBI Sequence Viewer
	XP_054177675	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAC27666	(Get FASTA)	NCBI Sequence Viewer
	AAF86231	(Get FASTA)	NCBI Sequence Viewer
	AAH28101	(Get FASTA)	NCBI Sequence Viewer
	AAK07476	(Get FASTA)	NCBI Sequence Viewer
	BAD92304	(Get FASTA)	NCBI Sequence Viewer
	BAG57444	(Get FASTA)	NCBI Sequence Viewer
	EAW69327	(Get FASTA)	NCBI Sequence Viewer
	EAW69328	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000292672
	ENSP00000292672.1
	ENSP00000443498
	ENSP00000443498.1
	ENSP00000468503
GenBank Protein	Q8N6W0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001166144 ⟸ NM_001172673
- Peptide Label:	isoform 2
- UniProtKB:	Q8N6W0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARLTESEARRQQQQLLQPRPSPVGSSGPEPPGGQPDGMKDLDAIKLFVGQIPRHLDEKDLKPLFEQFGRIYELTVLKDPYTGMHKGCAFLTYCARDSAIKAQTALHEQKTLPGMARPIQVKPADSES RGGRDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAFVKFSSHTEAQAAIHALHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQT TVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGVWRHGADADVPTL RQYHFLQGVYGSSYQPEQVFRLREL hide sequence

RefSeq Acc Id:	NP_068757 ⟸ NM_021938
- Peptide Label:	isoform 1
- UniProtKB:	Q9BZC0 (UniProtKB/Swiss-Prot), Q86VW6 (UniProtKB/Swiss-Prot), Q59GP2 (UniProtKB/Swiss-Prot), O75253 (UniProtKB/Swiss-Prot), D6W614 (UniProtKB/Swiss-Prot), Q9NR86 (UniProtKB/Swiss-Prot), Q8N6W0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARLTESEARRQQQQLLQPRPSPVGSSGPEPPGGQPDGMKDLDAIKLFVGQIPRHLDEKDLKPL FEQFGRIYELTVLKDPYTGMHKGCAFLTYCARDSAIKAQTALHEQKTLPGMARPIQVKPADSESRGGRDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAFVKFSSHTEAQAAIH ALHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQTTVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGLHSPPLLGTTAVPGLVAPITNG FAGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGPEGCNLFIYHLPQEFGDTELTQMFLPFGNIISSKVFMDRATNQSKCFGFVSF DNPASAQAAIQAMNGFQIGMKRLKVQLKRPKDPGHPY hide sequence

RefSeq Acc Id:	XP_006722895 ⟸ XM_006722832
- Peptide Label:	isoform X1
- UniProtKB:	Q9BZC0 (UniProtKB/Swiss-Prot), Q86VW6 (UniProtKB/Swiss-Prot), Q59GP2 (UniProtKB/Swiss-Prot), O75253 (UniProtKB/Swiss-Prot), D6W614 (UniProtKB/Swiss-Prot), Q9NR86 (UniProtKB/Swiss-Prot), Q8N6W0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARLTESEARRQQQQLLQPRPSPVGSSGPEPPGGQPDGMKDLDAIKLFVGQIPRHLDEKDLKPL FEQFGRIYELTVLKDPYTGMHKGCAFLTYCARDSAIKAQTALHEQKTLPGMARPIQVKPADSESRGGRDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAFVKFSSHTEAQAAIH ALHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQTTVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGLHSPPLLGTTAVPGLVAPITNG FAGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGPEGCNLFIYHLPQEFGDTELTQMFLPFGNIISSKVFMDRATNQSKCFGFVSF DNPASAQAAIQAMNGFQIGMKRLKVQLKRPKDPGHPY hide sequence

RefSeq Acc Id:

XP_006722896 ⟸ XM_006722833

- Peptide Label:

isoform X2

- Sequence:

show sequence

MARLTESEARRQQQQLLQPRPSPVGSSGPEPPGGQPDGMKDLDAIKLFVGQIPRHLDEKDLKPL
FEQFGRIYELTVLKDPYTGMHKGCAFLTYCARDSAIKAQTALHEQKTLPGMARPIQVKPADSESRGGDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAFVKFSSHTEAQAAIHA
LHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQTTVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGLHSPPLLGTTAVPGLVAPITNGF
AGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGPEGCNLFIYHLPQEFGDTELTQMFLPFGNIISSKVFMDRATNQSKCFGFVSFD
NPASAQAAIQAMNGFQIGMKRLKVQLKRPKDPGHPY

hide sequence

RefSeq Acc Id:

XP_006722900 ⟸ XM_006722837

- Peptide Label:

isoform X3

- Sequence:

show sequence

MARPIQVKPADSESRGGRDRKLFVGMLNKQQSEEDVLRLFQPFGVIDECTVLRGPDGSSKGCAF
VKFSSHTEAQAAIHALHGSQTMPGASSSLVVKFADTDKERTLRRMQQMVGQLGILTPSLTLPFSPYSAYAQALMQQQTTVLSTSGSYLSPGVAFSPCHIQQIGAVSLNGLPATPIAPASGLHSPPLLG
TTAVPGLVAPITNGFAGVVPFPGGHPALETVYANGLVPYPAQSPTVAETLHPAFSGVQQYTAMYPTAAITPIAHSVPQPPPLLQQQQREGPEGCNLFIYHLPQEFGDTELTQMFLPFGNIISSKVFMD
RATNQSKCFGFVSFDNPASAQAAIQAMNGFQIGMKRLKVQLKRPKDPGHPY

hide sequence

Protein Domains

RRM

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8N6W0-F1-model_v2	AlphaFold	Q8N6W0	1-485	view protein structure

RGD ID:

7237999

Promoter ID:

EPDNEW_H24746

Type:

initiation region

Name:

CELF5_1

Description:

CUGBP Elav-like family member 5

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	19	3,224,725 - 3,224,785	EPDNEW

RGD ID:

6811513

Promoter ID:

HG_ACW:39236

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

BRUNOL5.EAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	3,235,621 - 3,236,121 (+)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	CELF5	COSMIC
Ensembl Genes	ENSG00000161082	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000292672	ENTREZGENE
	ENST00000292672.7	UniProtKB/Swiss-Prot
	ENST00000334293	ENTREZGENE
	ENST00000541430	ENTREZGENE
	ENST00000541430.6	UniProtKB/Swiss-Prot
	ENST00000588350	ENTREZGENE
Gene3D-CATH	3.30.70.330	UniProtKB/Swiss-Prot
GTEx	ENSG00000161082	GTEx
HGNC ID	HGNC:14058	ENTREZGENE
Human Proteome Map	CELF5	Human Proteome Map
InterPro	CELF3/4/5/6_RRM1	UniProtKB/Swiss-Prot
	Nucleotide-bd_a/b_plait_sf	UniProtKB/Swiss-Prot
	RBD_domain_sf	UniProtKB/Swiss-Prot
	RRM_dom	UniProtKB/Swiss-Prot
KEGG Report	hsa:60680	UniProtKB/Swiss-Prot
NCBI Gene	60680	ENTREZGENE
OMIM	612680	OMIM
PANTHER	RNA BINDING PROTEIN	UniProtKB/Swiss-Prot
Pfam	RRM_1	UniProtKB/Swiss-Prot
PharmGKB	PA25429	PharmGKB
PROSITE	RRM	UniProtKB/Swiss-Prot
SMART	RRM	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF54928	UniProtKB/Swiss-Prot
UniProt	B4DFI3_HUMAN	UniProtKB/TrEMBL
	CELF5_HUMAN	UniProtKB/Swiss-Prot
	D6W614	ENTREZGENE
	K7ES14_HUMAN	UniProtKB/TrEMBL
	O75253	ENTREZGENE
	Q59GP2	ENTREZGENE
	Q86VW6	ENTREZGENE
	Q8N6W0	ENTREZGENE
	Q9BZC0	ENTREZGENE
	Q9NR86	ENTREZGENE
UniProt Secondary	D6W614	UniProtKB/Swiss-Prot
	O75253	UniProtKB/Swiss-Prot
	Q59GP2	UniProtKB/Swiss-Prot
	Q86VW6	UniProtKB/Swiss-Prot
	Q9BZC0	UniProtKB/Swiss-Prot
	Q9NR86	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2017-01-24	CELF5	CUGBP Elav-like family member 5		CUGBP, Elav-like family member 5	Symbol and/or name change	5135510	APPROVED
2011-07-27	CELF5	CUGBP, Elav-like family member 5	BRUNOL5	bruno-like 5, RNA binding protein (Drosophila)	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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Imported Disease Annotations - ClinVar