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Gene: LDB2 (LIM domain binding 2) Homo sapiens

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Symbol:

LDB2

Name:

LIM domain binding 2

RGD ID:

1317395

HGNC Page

HGNC:6533

Description:

Predicted to enable LIM domain binding activity and transcription coregulator activity. Predicted to be involved in several processes, including regulation of cell migration; regulation of kinase activity; and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including epithelial structure maintenance; hair follicle development; and somatic stem cell population maintenance. Located in nucleolus; nucleoplasm; and plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

carboxyl-terminal LIM domain-binding protein 1; CLIM-1; CLIM1; LDB-2; LDB1; LIM binding domain 2; LIM domain-binding factor CLIM1; LIM domain-binding factor-2; LIM domain-binding protein 2

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Ldb2 (LIM domain binding 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Ldb2 (LIM domain binding 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ldb2 (LIM domain binding 2)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	LDB2 (LIM domain binding 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	LDB2 (LIM domain binding 2)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ldb2 (LIM domain binding 2)	NCBI	Ortholog
Sus scrofa (pig):	LDB2 (LIM domain binding 2)	HGNC	Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	LDB2 (LIM domain binding 2)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ldb2 (LIM domain binding 2)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Fitm1 (fat storage-inducing transmembrane protein 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Ldb2 (LIM domain binding 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Ldb2 (LIM domain binding 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ldb2a (LIM domain binding 2a)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Danio rerio (zebrafish):	ldb2b (LIM domain binding 2b)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Drosophila melanogaster (fruit fly):	Chi	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	ldb2.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	ldb2	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	ldb2.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	16,501,541 - 16,898,678 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	16,503,164 - 16,900,268 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	16,112,262 - 16,509,425 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	16,179,434 - 16,576,596	NCBI
Celera	4	16,968,377 - 17,365,469 (-)	NCBI		Celera
Cytogenetic Map	4	p15.32	NCBI
HuRef	4	15,852,373 - 16,253,922 (-)	NCBI		HuRef
CHM1_1	4	16,501,239 - 16,898,326 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LDB2	Human	(1->4)-beta-D-glucan	multiple interactions	ISO	RGD:1317396	6480464	[perfluorooctane sulfonic acid co-treated with Cellulose] results in increased expression of LDB2 mRNA	CTD	PMID:36331819
LDB2	Human	1,1,1-trichloroethane	increases expression	ISO	RGD:1317396	6480464	1,1,1-trichloroethane results in increased expression of LDB2 mRNA	CTD	PMID:25270620
LDB2	Human	1,1-dichloroethene	decreases expression	ISO	RGD:1317396	6480464	vinylidene chloride results in decreased expression of LDB2 mRNA	CTD	PMID:26682919
LDB2	Human	1,2-dimethylhydrazine	decreases expression	ISO	RGD:1317396	6480464	1,2-Dimethylhydrazine results in decreased expression of LDB2 mRNA	CTD	PMID:22206623
LDB2	Human	17alpha-ethynylestradiol	affects expression	ISO	RGD:1317396	6480464	Ethinyl Estradiol affects the expression of LDB2 mRNA	CTD	PMID:17555576
LDB2	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	RGD:1307921	6480464	Tetrachlorodibenzodioxin results in decreased expression of LDB2 mRNA	CTD	PMID:32109520
LDB2	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	RGD:1307921	6480464	Tetrachlorodibenzodioxin results in increased expression of LDB2 mRNA	CTD	PMID:34747641
LDB2	Human	3-isobutyl-1-methyl-7H-xanthine	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] more ...	CTD	PMID:28628672
LDB2	Human	4,4'-sulfonyldiphenol	affects expression	ISO	RGD:1317396	6480464	bisphenol S affects the expression of LDB2 mRNA	CTD	PMID:30951980
LDB2	Human	4-hydroxyphenyl retinamide	increases expression	ISO	RGD:1317396	6480464	Fenretinide results in increased expression of LDB2 mRNA	CTD	PMID:28973697
LDB2	Human	6-propyl-2-thiouracil	increases expression	ISO	RGD:1307921	6480464	Propylthiouracil results in increased expression of LDB2 mRNA	CTD	PMID:24780913
LDB2	Human	acrylamide	decreases expression	ISO	RGD:1307921	6480464	Acrylamide results in decreased expression of LDB2 mRNA	CTD	PMID:28959563
LDB2	Human	aflatoxin B1	affects expression	EXP		6480464	Aflatoxin B1 affects the expression of LDB2 protein	CTD	PMID:20106945
LDB2	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of LDB2 intron	CTD	PMID:30157460
LDB2	Human	Aflatoxin B2 alpha	increases methylation	EXP		6480464	aflatoxin B2 results in increased methylation of LDB2 intron	CTD	PMID:30157460
LDB2	Human	antirheumatic drug	increases expression	EXP		6480464	Antirheumatic Agents results in increased expression of LDB2 mRNA	CTD	PMID:24449571
LDB2	Human	arsenous acid	decreases expression	EXP		6480464	Arsenic Trioxide results in decreased expression of LDB2 mRNA	CTD	PMID:26705709
LDB2	Human	atrazine	affects methylation	ISO	RGD:1307921	6480464	Atrazine affects the methylation of LDB2 gene	CTD	PMID:28931070
LDB2	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of LDB2 mRNA	CTD	PMID:20106945\|PMID:32234424
LDB2	Human	benzo[a]pyrene	increases methylation	ISO	RGD:1317396	6480464	Benzo(a)pyrene results in increased methylation of LDB2 intron	CTD	PMID:27901495
LDB2	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of LDB2 promoter	CTD	PMID:27901495
LDB2	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of LDB2 exon	CTD	PMID:27901495
LDB2	Human	benzo[a]pyrene	decreases expression	ISO	RGD:1317396	6480464	Benzo(a)pyrene results in decreased expression of LDB2 mRNA	CTD	PMID:27195522
LDB2	Human	benzo[a]pyrene diol epoxide I	decreases expression	EXP		6480464	7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide results in decreased expression of LDB2 mRNA	CTD	PMID:20382639
LDB2	Human	bis(2-chloroethyl) sulfide	increases expression	ISO	RGD:1317396	6480464	Mustard Gas results in increased expression of LDB2 mRNA	CTD	PMID:15674843
LDB2	Human	bis(2-ethylhexyl) phthalate	decreases expression	ISO	RGD:1317396	6480464	Diethylhexyl Phthalate results in decreased expression of LDB2 mRNA	CTD	PMID:34319233
LDB2	Human	bisphenol A	decreases expression	ISO	RGD:1307921	6480464	bisphenol A results in decreased expression of LDB2 mRNA	CTD	PMID:25181051
LDB2	Human	bisphenol A	increases expression	ISO	RGD:1317396	6480464	bisphenol A results in increased expression of LDB2 mRNA	CTD	PMID:37105096
LDB2	Human	bisphenol A	increases expression	EXP		6480464	bisphenol A results in increased expression of LDB2 mRNA	CTD	PMID:29275510
LDB2	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of LDB2 gene; [INS protein co-treated more ...	CTD	PMID:28628672\|PMID:31601247
LDB2	Human	bisphenol F	decreases expression	ISO	RGD:1317396	6480464	bisphenol F results in decreased expression of LDB2 mRNA	CTD	PMID:30951980
LDB2	Human	cadmium atom	multiple interactions	EXP		6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of LDB2 more ...	CTD	PMID:35301059
LDB2	Human	cadmium dichloride	decreases expression	ISO	RGD:1307921	6480464	Cadmium Chloride results in decreased expression of LDB2 mRNA	CTD	PMID:33453195
LDB2	Human	cadmium dichloride	multiple interactions	EXP		6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of LDB2 more ...	CTD	PMID:35301059
LDB2	Human	cadmium dichloride	increases expression	EXP		6480464	Cadmium Chloride results in increased expression of LDB2 mRNA	CTD	PMID:38568856
LDB2	Human	carbon nanotube	decreases expression	ISO	RGD:1317396	6480464	Nanotubes, Carbon analog results in decreased expression of LDB2 mRNA	CTD	PMID:25554681
LDB2	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to LDB2 gene]	CTD	PMID:28238834
LDB2	Human	cocaine	decreases expression	EXP		6480464	Cocaine results in decreased expression of LDB2 mRNA	CTD	PMID:12629581
LDB2	Human	cyclosporin A	decreases expression	EXP		6480464	Cyclosporine results in decreased expression of LDB2 mRNA	CTD	PMID:20106945
LDB2	Human	dexamethasone	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] more ...	CTD	PMID:28628672
LDB2	Human	diarsenic trioxide	decreases expression	EXP		6480464	Arsenic Trioxide results in decreased expression of LDB2 mRNA	CTD	PMID:26705709
LDB2	Human	diazinon	increases expression	ISO	RGD:1307921	6480464	Diazinon results in increased expression of LDB2 mRNA	CTD	PMID:29108742
LDB2	Human	diquat	decreases expression	ISO	RGD:1317396	6480464	Diquat results in decreased expression of LDB2 mRNA	CTD	PMID:36851058
LDB2	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
LDB2	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of LDB2 mRNA	CTD	PMID:29803840
LDB2	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of LDB2 gene	CTD	PMID:31601247
LDB2	Human	indometacin	multiple interactions	EXP		6480464	[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] more ...	CTD	PMID:28628672
LDB2	Human	lipopolysaccharide	increases expression	ISO	RGD:1317396	6480464	Lipopolysaccharides results in increased expression of LDB2 mRNA	CTD	PMID:12057914
LDB2	Human	methimazole	increases expression	ISO	RGD:1307921	6480464	Methimazole results in increased expression of LDB2 mRNA	CTD	PMID:38685447
LDB2	Human	methylmercury chloride	decreases expression	EXP		6480464	methylmercuric chloride results in decreased expression of LDB2 mRNA	CTD	PMID:28001369
LDB2	Human	nickel atom	decreases expression	EXP		6480464	Nickel results in decreased expression of LDB2 mRNA	CTD	PMID:25583101
LDB2	Human	O-methyleugenol	decreases expression	EXP		6480464	methyleugenol results in decreased expression of LDB2 mRNA	CTD	PMID:32234424
LDB2	Human	okadaic acid	decreases expression	EXP		6480464	Okadaic Acid results in decreased expression of LDB2 mRNA	CTD	PMID:38832940
LDB2	Human	oxaliplatin	multiple interactions	ISO	RGD:1307921	6480464	[oxaliplatin co-treated with Topotecan] results in increased expression of LDB2 mRNA	CTD	PMID:25729387
LDB2	Human	oxaliplatin	increases expression	ISO	RGD:1307921	6480464	oxaliplatin results in increased expression of LDB2 mRNA	CTD	PMID:25729387
LDB2	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of LDB2 mRNA	CTD	PMID:21420995
LDB2	Human	perfluorohexanesulfonic acid	increases expression	ISO	RGD:1317396	6480464	perfluorohexanesulfonic acid results in increased expression of LDB2 mRNA	CTD	PMID:37995155
LDB2	Human	perfluorooctane-1-sulfonic acid	multiple interactions	ISO	RGD:1317396	6480464	[perfluorooctane sulfonic acid co-treated with Cellulose] results in increased expression of LDB2 mRNA	CTD	PMID:36331819
LDB2	Human	phenylmercury acetate	decreases expression	EXP		6480464	Phenylmercuric Acetate results in decreased expression of LDB2 mRNA	CTD	PMID:26272509
LDB2	Human	phenylmercury acetate	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
LDB2	Human	phenytoin	increases expression	ISO	RGD:1307921	6480464	Phenytoin results in increased expression of LDB2 mRNA	CTD	PMID:20345932
LDB2	Human	progesterone	decreases expression	ISO	RGD:1317396	6480464	Progesterone results in decreased expression of LDB2 mRNA	CTD	PMID:17556502
LDB2	Human	progesterone	increases expression	ISO	RGD:1317396	6480464	Progesterone results in increased expression of LDB2 mRNA	CTD	PMID:22238285
LDB2	Human	progesterone	multiple interactions	ISO	RGD:1317396	6480464	NCOA2 protein affects the reaction [Progesterone results in decreased expression of LDB2 mRNA]	CTD	PMID:17556502
LDB2	Human	quercetin	affects expression	ISO	RGD:1307921	6480464	Quercetin affects the expression of LDB2 mRNA	CTD	PMID:18178720
LDB2	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased more ...	CTD	PMID:27188386
LDB2	Human	sodium arsenate	increases expression	ISO	RGD:1317396	6480464	sodium arsenate results in increased expression of LDB2 mRNA	CTD	PMID:21795629
LDB2	Human	Soman	decreases expression	ISO	RGD:1307921	6480464	Soman results in decreased expression of LDB2 mRNA	CTD	PMID:19281266
LDB2	Human	tamoxifen	affects expression	ISO	RGD:1317396	6480464	Tamoxifen affects the expression of LDB2 mRNA	CTD	PMID:17555576
LDB2	Human	tetrachloromethane	affects expression	ISO	RGD:1317396	6480464	Carbon Tetrachloride affects the expression of LDB2 mRNA	CTD	PMID:17484886
LDB2	Human	Theaflavin 3,3'-digallate	affects expression	EXP		6480464	theaflavin-3,3'-digallate affects the expression of LDB2 mRNA	CTD	PMID:34925699
LDB2	Human	titanium dioxide	decreases expression	ISO	RGD:1317396	6480464	titanium dioxide results in decreased expression of LDB2 mRNA	CTD	PMID:23557971
LDB2	Human	topotecan	increases expression	ISO	RGD:1307921	6480464	Topotecan results in increased expression of LDB2 mRNA	CTD	PMID:25729387
LDB2	Human	topotecan	multiple interactions	ISO	RGD:1307921	6480464	[oxaliplatin co-treated with Topotecan] results in increased expression of LDB2 mRNA	CTD	PMID:25729387
LDB2	Human	trichostatin A	increases expression	EXP		6480464	trichostatin A results in increased expression of LDB2 mRNA	CTD	PMID:24935251\|PMID:26272509
LDB2	Human	trichostatin A	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased more ...	CTD	PMID:27188386
LDB2	Human	triclosan	increases expression	EXP		6480464	Triclosan results in increased expression of LDB2 mRNA	CTD	PMID:30510588
LDB2	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of LDB2 mRNA	CTD	PMID:23179753
LDB2	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of LDB2 mRNA	CTD	PMID:25979313
LDB2	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of LDB2 mRNA	CTD	PMID:23179753\|PMID:24383497\|PMID:24935251\|PMID:26272509
LDB2	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased more ...	CTD	PMID:27188386
LDB2	Human	vitamin E	increases expression	EXP		6480464	Vitamin E results in increased expression of LDB2 mRNA	CTD	PMID:19244175
LDB2	Human	vorinostat	multiple interactions	EXP		6480464	[NOG protein co-treated with Vorinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased expression more ...	CTD	PMID:27188386
LDB2	Human	vorinostat	increases expression	EXP		6480464	vorinostat results in increased expression of LDB2 mRNA	CTD	PMID:26272509
LDB2	Human	zoledronic acid	increases expression	EXP		6480464	zoledronic acid results in increased expression of LDB2 mRNA	CTD	PMID:24714768

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)
LDB2	Human	epithelial structure maintenance	acts_upstream_of_or_within	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	hair follicle development	acts_upstream_of_or_within	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	negative regulation of transcription by RNA polymerase II	involved_in	IBA	PANTHER:PTN001623859\|UniProtKB:F2Z5G6\|WB:WBGene00002261	150520179		GO_Central	GO_REF:0000033
LDB2	Human	nervous system development	involved_in	IBA	FB:FBgn0013764\|MGI:894762\|PANTHER:PTN000822352\|WB:WBGene00002261	150520179		GO_Central	GO_REF:0000033
LDB2	Human	positive regulation of cellular component biogenesis	acts_upstream_of_or_within	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	positive regulation of transcription by RNA polymerase II	involved_in	IBA	FB:FBgn0013764\|MGI:894670\|MGI:894762\|PANTHER:PTN001623859\|UniProtKB:Q86U70\|WB:WBGene00002261	150520179		GO_Central	GO_REF:0000033
LDB2	Human	positive regulation of transcription by RNA polymerase II	acts_upstream_of_or_within	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	regulation of cell migration	involved_in	ISS	UniProtKB:O55203	150520179		UniProt	GO_REF:0000024
LDB2	Human	regulation of cell migration	involved_in	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	regulation of kinase activity	involved_in	ISS	UniProtKB:O55203	150520179		UniProt	GO_REF:0000024
LDB2	Human	somatic stem cell population maintenance	acts_upstream_of_or_within	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107

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)
LDB2	Human	cell leading edge	located_in	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	cell leading edge	located_in	ISS	UniProtKB:O55203	150520179		UniProt	GO_REF:0000024
LDB2	Human	nucleolus	located_in	IDA		150520179		HPA	GO_REF:0000052
LDB2	Human	nucleoplasm	located_in	IDA		150520179		HPA	GO_REF:0000052
LDB2	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
LDB2	Human	nucleus	located_in	IDA		150520179	PMID:9853615	UniProt	PMID:9853615
LDB2	Human	nucleus	is_active_in	IBA	FB:FBgn0013764\|MGI:894762\|PANTHER:PTN001623859\|UniProtKB:O43679\|UniProtKB:Q86U70\|ZFIN:ZDB-GENE-990415-138	150520179		GO_Central	GO_REF:0000033
LDB2	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043
LDB2	Human	plasma membrane	located_in	IDA		150520179		HPA	GO_REF:0000052
LDB2	Human	transcription regulator complex	part_of	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	transcription regulator complex	part_of	IBA	MGI:894670\|MGI:894762\|PANTHER:PTN001623859\|UniProtKB:Q86U70	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)
LDB2	Human	enzyme binding	enables	IEA	UniProtKB:O55203\|ensembl:ENSMUSP00000067737	150520179		Ensembl	GO_REF:0000107
LDB2	Human	LIM domain binding	enables	IEA	UniRule:UR001503062	150520179		UniProt	GO_REF:0000104
LDB2	Human	LIM domain binding	enables	ISS	UniProtKB:P70662	150520179		UniProt	GO_REF:0000024
LDB2	Human	protein binding	enables	IPI	UniProtKB:P61968\|UniProtKB:Q9BWW4	150520179	PMID:20211142	IntAct	PMID:20211142
LDB2	Human	protein binding	enables	IPI	UniProtKB:P61968	150520179	PMID:15231748	IntAct	PMID:15231748
LDB2	Human	protein binding	enables	IPI	UniProtKB:O00560\|UniProtKB:O15182\|UniProtKB:P20618\|UniProtKB:P25791-3\|UniProtKB:P25800\|UniProtKB:P61968\|UniProtKB:Q68G74\|UniProtKB:Q6DKK2\|UniProtKB:Q7L775\|UniProtKB:Q86VI1\|UniProtKB:Q8TAP4-4\|UniProtKB:Q8TBB1\|UniProtKB:Q8WUI4-6\|UniProtKB:Q969H8\|UniProtKB:Q96GM5\|UniProtKB:Q96HA8\|UniProtKB:Q99598\|UniProtKB:Q9BVM4\|UniProtKB:Q9BY27\|UniProtKB:Q9H6Z9\|UniProtKB:Q9NWQ9	150520179	PMID:32296183	IntAct	PMID:32296183
LDB2	Human	protein binding	enables	IPI	UniProtKB:P61968\|UniProtKB:Q99598\|UniProtKB:Q9BWW4	150520179	PMID:18330356	IntAct	PMID:18330356
LDB2	Human	transcription coregulator activity	enables	IBA	MGI:894762\|PANTHER:PTN001623859\|TAIR:locus:2029137\|UniProtKB:F2Z5G6	150520179		GO_Central	GO_REF:0000033
LDB2	Human	transcription coregulator activity	enables	TAS		150520179	PMID:9880598	PINC	PMID:9880598

#	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:8125298	PMID:8918878	PMID:9192866	PMID:9799849	PMID:9853615	PMID:9880598	PMID:10083735	PMID:10431247	PMID:11882901	PMID:12477932	PMID:14702039	PMID:15231748
PMID:15489334	PMID:16344560	PMID:18330356	PMID:19997623	PMID:20211142	PMID:20379614	PMID:21873635	PMID:23534349	PMID:23585552	PMID:24925974	PMID:25609649	PMID:28946938
PMID:32296183	PMID:33656268	PMID:33849822	PMID:35914814	PMID:36473369

LDB2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	16,501,541 - 16,898,678 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	16,503,164 - 16,900,268 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	16,112,262 - 16,509,425 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	16,179,434 - 16,576,596	NCBI
Celera	4	16,968,377 - 17,365,469 (-)	NCBI		Celera
Cytogenetic Map	4	p15.32	NCBI
HuRef	4	15,852,373 - 16,253,922 (-)	NCBI		HuRef
CHM1_1	4	16,501,239 - 16,898,326 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI		T2T-CHM13v2.0

Ldb2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	44,593,292 - 44,957,466 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	44,629,474 - 44,957,022 (-)	Ensembl		GRCm39 Ensembl
GRCm38	5	44,435,955 - 44,799,759 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	44,472,132 - 44,799,680 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	44,863,372 - 45,190,946 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	44,760,963 - 45,087,867 (-)	NCBI		MGSCv36	mm8
Celera	5	41,894,726 - 42,234,169 (-)	NCBI		Celera
Cytogenetic Map	5	B3	NCBI
cM Map	5	24.24	NCBI

Ldb2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	14	70,489,243 - 70,810,573 (+)	NCBI		GRCr8
mRatBN7.2	14	66,277,044 - 66,598,071 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	14	66,277,085 - 66,597,778 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	14	70,673,511 - 70,993,888 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	14	71,957,095 - 72,277,709 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	14	68,383,948 - 68,704,320 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	14	70,780,605 - 71,112,857 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	14	70,780,623 - 71,112,552 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	14	70,817,435 - 70,817,796 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Rnor_5.0	14	70,920,028 - 71,144,813 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	14	71,374,621 - 71,695,965 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	14	71,377,028 - 71,698,910 (+)	NCBI
Celera	14	65,250,557 - 65,570,430 (+)	NCBI		Celera
Cytogenetic Map	14	q21	NCBI

Ldb2
(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_004955480	7,199,933 - 7,568,629 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955480	7,200,111 - 7,568,567 (+)	NCBI	ChiLan1.0	ChiLan1.0

LDB2
(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	3	16,771,454 - 17,168,732 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	4	16,969,178 - 17,366,385 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	4	10,930,160 - 11,327,367 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	4	16,226,042 - 16,621,851 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	4	16,227,146 - 16,622,167 (-)	Ensembl	panpan1.1		panPan2

LDB2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	3	63,508,721 - 63,883,842 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	3	63,508,247 - 63,883,717 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	3	66,026,288 - 66,401,935 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	3	63,985,593 - 64,361,307 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	3	63,985,615 - 64,362,099 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	3	63,476,565 - 63,852,008 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	3	63,680,390 - 64,055,540 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	3	64,040,117 - 64,415,250 (+)	NCBI		UU_Cfam_GSD_1.0

Ldb2
(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_024405285	57,497,602 - 57,837,007 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936477	11,199,003 - 11,538,728 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936477	11,199,200 - 11,538,699 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LDB2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	8	11,641,064 - 12,037,265 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	8	11,641,060 - 12,037,388 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	8	11,335,352 - 11,566,827 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LDB2
(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	27	33,303,801 - 33,698,460 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666047	80,035,660 - 80,430,270 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ldb2
(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_004624755	14,962,317 - 15,359,814 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624755	14,962,538 - 15,358,771 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in LDB2
32 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 4p16.3-15.1(chr4:72555-28066309)x1	copy number loss	See cases [RCV000051642]	Chr4:72555..28066309 [GRCh38] Chr4:72447..28067931 [GRCh37] Chr4:62447..27677029 [NCBI36] Chr4:4p16.3-15.1	pathogenic
GRCh38/hg38 4p15.33-15.31(chr4:14061129-20121834)x1	copy number loss	See cases [RCV000051220]	Chr4:14061129..20121834 [GRCh38] Chr4:14062753..20123457 [GRCh37] Chr4:13671851..19732555 [NCBI36] Chr4:4p15.33-15.31	pathogenic
GRCh38/hg38 4p16.3-15.2(chr4:51519-26519788)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051752]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051752]\|See cases [RCV000051752]	Chr4:51519..26519788 [GRCh38] Chr4:51413..26521410 [GRCh37] Chr4:41413..26130508 [NCBI36] Chr4:4p16.3-15.2	pathogenic
GRCh38/hg38 4p16.3-15.1(chr4:72555-33130620)x3	copy number gain	See cases [RCV000051753]	Chr4:72555..33130620 [GRCh38] Chr4:72447..33132242 [GRCh37] Chr4:62447..32808637 [NCBI36] Chr4:4p16.3-15.1	pathogenic
GRCh38/hg38 4p16.3-14(chr4:85149-38700366)x3	copy number gain	See cases [RCV000051757]	Chr4:85149..38700366 [GRCh38] Chr4:85040..38701987 [GRCh37] Chr4:75040..38378382 [NCBI36] Chr4:4p16.3-14	pathogenic
GRCh38/hg38 4p15.33-15.31(chr4:14659764-18274924)x3	copy number gain	See cases [RCV000051769]	Chr4:14659764..18274924 [GRCh38] Chr4:14661388..18276547 [GRCh37] Chr4:14270486..17885645 [NCBI36] Chr4:4p15.33-15.31	pathogenic
GRCh38/hg38 4p16.3-15.2(chr4:85149-22450018)x3	copy number gain	See cases [RCV000051755]	Chr4:85149..22450018 [GRCh38] Chr4:85040..22451641 [GRCh37] Chr4:75040..22060739 [NCBI36] Chr4:4p16.3-15.2	pathogenic
GRCh38/hg38 4p16.3-15.32(chr4:85149-17486742)x1	copy number loss	See cases [RCV000051679]	Chr4:85149..17486742 [GRCh38] Chr4:85040..17488365 [GRCh37] Chr4:75040..17097463 [NCBI36] Chr4:4p16.3-15.32	pathogenic
NM_001130834.2(LDB2):c.615+29471T>G	single nucleotide variant	Lung cancer [RCV000094285]	Chr4:16556451 [GRCh38] Chr4:16558074 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001130834.2(LDB2):c.236-7334A>G	single nucleotide variant	Lung cancer [RCV000094288]	Chr4:16603209 [GRCh38] Chr4:16604832 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001130834.2(LDB2):c.132+25534A>T	single nucleotide variant	Lung cancer [RCV000094301]	Chr4:16872820 [GRCh38] Chr4:16874443 [GRCh37] Chr4:4p15.32	uncertain significance
GRCh37/hg19 4p15.32-15.31(chr4:16830399-17805183)x3	copy number gain	See cases [RCV000184072]	Chr4:16830399..17805183 [GRCh37] Chr4:4p15.32-15.31	uncertain significance
GRCh38/hg38 4p16.3-14(chr4:72555-39477144)x3	copy number gain	See cases [RCV000133677]	Chr4:72555..39477144 [GRCh38] Chr4:72447..39478764 [GRCh37] Chr4:62447..39155159 [NCBI36] Chr4:4p16.3-14	pathogenic
GRCh38/hg38 4p16.3-15.32(chr4:72555-17278013)x1	copy number loss	See cases [RCV000135657]	Chr4:72555..17278013 [GRCh38] Chr4:72447..17279636 [GRCh37] Chr4:62447..16888734 [NCBI36] Chr4:4p16.3-15.32	pathogenic
GRCh38/hg38 4p16.3-15.31(chr4:51519-17798196)x3	copy number gain	See cases [RCV000137071]	Chr4:51519..17798196 [GRCh38] Chr4:51413..17799819 [GRCh37] Chr4:41413..17408917 [NCBI36] Chr4:4p16.3-15.31	pathogenic
GRCh38/hg38 4p16.3-12(chr4:36424-47491595)x3	copy number gain	See cases [RCV000137261]	Chr4:36424..47491595 [GRCh38] Chr4:36424..47493612 [GRCh37] Chr4:26424..47188369 [NCBI36] Chr4:4p16.3-12	pathogenic
GRCh38/hg38 4p16.3-15.31(chr4:72555-21022414)x3	copy number gain	See cases [RCV000138305]	Chr4:72555..21022414 [GRCh38] Chr4:72447..21024037 [GRCh37] Chr4:62447..20633135 [NCBI36] Chr4:4p16.3-15.31	pathogenic
GRCh38/hg38 4p15.32(chr4:15868863-16925081)x1	copy number loss	See cases [RCV000140878]	Chr4:15868863..16925081 [GRCh38] Chr4:15870486..16926704 [GRCh37] Chr4:15479584..16535802 [NCBI36] Chr4:4p15.32	uncertain significance
GRCh38/hg38 4p16.3-15.32(chr4:4426403-17460549)x1	copy number loss	See cases [RCV000141502]	Chr4:4426403..17460549 [GRCh38] Chr4:4428130..17462172 [GRCh37] Chr4:4479031..17071270 [NCBI36] Chr4:4p16.3-15.32	pathogenic
GRCh38/hg38 4p16.3-15.31(chr4:68453-20385608)x1	copy number loss	See cases [RCV000143713]	Chr4:68453..20385608 [GRCh38] Chr4:68345..20387231 [GRCh37] Chr4:58345..19996329 [NCBI36] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-15.31(chr4:44020-19796182)x1	copy number loss	See cases [RCV000203431]	Chr4:44020..19796182 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-15.1(chr4:71552-29006745)x1	copy number loss	See cases [RCV000240003]	Chr4:71552..29006745 [GRCh37] Chr4:4p16.3-15.1	pathogenic
GRCh37/hg19 4p16.1-15.31(chr4:6447048-20490737)x3	copy number gain	See cases [RCV000240007]	Chr4:6447048..20490737 [GRCh37] Chr4:4p16.1-15.31	pathogenic
GRCh37/hg19 4p16.3-11(chr4:12440-49064044)x3	copy number gain	See cases [RCV000240562]	Chr4:12440..49064044 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-11(chr4:68345-49089361)x3	copy number gain	not specified [RCV003986479]	Chr4:68345..49089361 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p15.32-15.31(chr4:16834640-17818885)x3	copy number gain	See cases [RCV000599152]	Chr4:16834640..17818885 [GRCh37] Chr4:4p15.32-15.31	uncertain significance
GRCh37/hg19 4p16.3-15.31(chr4:68345-20533787)x1	copy number loss	See cases [RCV000449197]	Chr4:68345..20533787 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	copy number gain	See cases [RCV000446653]	Chr4:12440..190904441 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-11(chr4:68345-49093788)x3	copy number gain	See cases [RCV000446451]	Chr4:68345..49093788 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p15.32-15.31(chr4:16826659-17818949)x3	copy number gain	See cases [RCV000448351]	Chr4:16826659..17818949 [GRCh37] Chr4:4p15.32-15.31	uncertain significance
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	copy number gain	See cases [RCV000510453]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p15.32(chr4:15974221-16897124)x3	copy number gain	See cases [RCV000510880]	Chr4:15974221..16897124 [GRCh37] Chr4:4p15.32	uncertain significance
GRCh37/hg19 4p15.32(chr4:15836236-16942209)x3	copy number gain	See cases [RCV000510810]	Chr4:15836236..16942209 [GRCh37] Chr4:4p15.32	uncertain significance
GRCh37/hg19 4p16.3-q13.1(chr4:68345-66440622)x3	copy number gain	See cases [RCV000511193]	Chr4:68345..66440622 [GRCh37] Chr4:4p16.3-q13.1	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	copy number gain	See cases [RCV000512241]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-11(chr4:68345-49089361)x3	copy number gain	not provided [RCV000682363]	Chr4:68345..49089361 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-15.1(chr4:4165334-33324781)x1	copy number loss	not provided [RCV000682373]	Chr4:4165334..33324781 [GRCh37] Chr4:4p16.3-15.1	pathogenic
GRCh37/hg19 4p15.32(chr4:16518224-16575820)x1	copy number loss	not provided [RCV000682389]	Chr4:16518224..16575820 [GRCh37] Chr4:4p15.32	likely benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3	copy number gain	not provided [RCV000743155]	Chr4:49450..190915650 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p15.32-15.31(chr4:16822918-17818885)x3	copy number gain	not provided [RCV000743429]	Chr4:16822918..17818885 [GRCh37] Chr4:4p15.32-15.31	benign
GRCh37/hg19 4p15.32-15.31(chr4:16825299-17809538)x3	copy number gain	not provided [RCV000743430]	Chr4:16825299..17809538 [GRCh37] Chr4:4p15.32-15.31	benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3	copy number gain	not provided [RCV000743156]	Chr4:49450..190963766 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3	copy number gain	not provided [RCV000743147]	Chr4:11525..191028879 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-11(chr4:1356924-49659859)x3	copy number gain	not provided [RCV000743201]	Chr4:1356924..49659859 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-12(chr4:49450-46339070)x3	copy number gain	not provided [RCV000743154]	Chr4:49450..46339070 [GRCh37] Chr4:4p16.3-12	pathogenic
NM_001290.5(LDB2):c.1001T>G (p.Met334Arg)	single nucleotide variant	not specified [RCV004286491]	Chr4:16502764 [GRCh38] Chr4:16504387 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.204A>G (p.Ser68=)	single nucleotide variant	not provided [RCV000965670]	Chr4:16759189 [GRCh38] Chr4:16760812 [GRCh37] Chr4:4p15.32	benign
GRCh37/hg19 4p15.33-15.1(chr4:12778849-27760141)	copy number loss	not provided [RCV000767707]	Chr4:12778849..27760141 [GRCh37] Chr4:4p15.33-15.1	pathogenic
GRCh37/hg19 4p16.2-15.32(chr4:5914109-17264668)x1	copy number loss	not provided [RCV001005519]	Chr4:5914109..17264668 [GRCh37] Chr4:4p16.2-15.32	likely pathogenic
NC_000004.12:g.8398067_17505522inv	inversion	Dihydropteridine reductase deficiency [RCV000768549]	Chr4:8398067..17505522 [GRCh38] Chr4:4p16.1-15.32	pathogenic
GRCh37/hg19 4p15.32-15.31(chr4:16826786-17818949)x3	copy number gain	not provided [RCV001005526]	Chr4:16826786..17818949 [GRCh37] Chr4:4p15.32-15.31	likely benign
GRCh37/hg19 4p15.33-15.2(chr4:13529798-22750583)x1	copy number loss	not provided [RCV000998337]	Chr4:13529798..22750583 [GRCh37] Chr4:4p15.33-15.2	uncertain significance
GRCh37/hg19 4p16.3-15.2(chr4:68345-27423424)x3	copy number gain	not provided [RCV001005510]	Chr4:68345..27423424 [GRCh37] Chr4:4p16.3-15.2	pathogenic
GRCh37/hg19 4p16.3-15.2(chr4:49450-24280482)x1	copy number loss	See cases [RCV001007422]	Chr4:49450..24280482 [GRCh37] Chr4:4p16.3-15.2	pathogenic
GRCh37/hg19 4p16.3-11(chr4:49450-49620898)x3	copy number gain	See cases [RCV001194594]	Chr4:49450..49620898 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-15.1(chr4:69671-29702595)x3	copy number gain	not provided [RCV001537928]	Chr4:69671..29702595 [GRCh37] Chr4:4p16.3-15.1	pathogenic
GRCh37/hg19 4p16.3-15.31(chr4:68598-18912995)x1	copy number loss	not provided [RCV001537927]	Chr4:68598..18912995 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-15.1(chr4:68345-34512694)	copy number gain	4p16.3 microduplication syndrome [RCV003319592]	Chr4:68345..34512694 [GRCh37] Chr4:4p16.3-15.1	pathogenic
GRCh37/hg19 4p15.32-15.31(chr4:16826659-17818949)	copy number gain	not specified [RCV002053408]	Chr4:16826659..17818949 [GRCh37] Chr4:4p15.32-15.31	uncertain significance
GRCh37/hg19 4p16.3-15.31(chr4:68345-20587167)x1	copy number loss	not provided [RCV001829146]	Chr4:68345..20587167 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-11(chr4:68345-49089361)x3	copy number gain	See cases [RCV002292704]	Chr4:68345..49089361 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-15.31(chr4:68345-20964575)x1	copy number loss	See cases [RCV002286359]	Chr4:68345..20964575 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-12(chr4:114784-47569569)x3	copy number gain	FETAL DEMISE [RCV002282978]	Chr4:114784..47569569 [GRCh37] Chr4:4p16.3-12	pathogenic
GRCh37/hg19 4p15.32-15.2(chr4:16249194-24864955)x1	copy number loss	not provided [RCV002474848]	Chr4:16249194..24864955 [GRCh37] Chr4:4p15.32-15.2	uncertain significance
NM_001290.5(LDB2):c.290T>C (p.Val97Ala)	single nucleotide variant	not specified [RCV004107676]	Chr4:16595821 [GRCh38] Chr4:16597444 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.622G>A (p.Val208Ile)	single nucleotide variant	not specified [RCV004116449]	Chr4:16512098 [GRCh38] Chr4:16513721 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.397A>G (p.Met133Val)	single nucleotide variant	not specified [RCV004173589]	Chr4:16595714 [GRCh38] Chr4:16597337 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.730G>T (p.Ala244Ser)	single nucleotide variant	not specified [RCV004079525]	Chr4:16511990 [GRCh38] Chr4:16513613 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.989C>A (p.Ala330Glu)	single nucleotide variant	not specified [RCV004177286]	Chr4:16502776 [GRCh38] Chr4:16504399 [GRCh37] Chr4:4p15.32	uncertain significance
GRCh38/hg38 4p15.33-14(chr4:11399082-38137335)	copy number loss	4p partial monosomy syndrome [RCV003155905]	Chr4:11399082..38137335 [GRCh38] Chr4:4p15.33-14	pathogenic
GRCh38/hg38 4p16.3-13(chr4:2904667-42963232)x3	copy number gain	Neurodevelopmental disorder [RCV003327612]	Chr4:2904667..42963232 [GRCh38] Chr4:4p16.3-13	pathogenic
GRCh38/hg38 4p16.3-11(chr4:1-49062177)x3	copy number gain	Neurodevelopmental disorder [RCV003327611]	Chr4:1..49062177 [GRCh38] Chr4:4p16.3-11	pathogenic
GRCh38/hg38 4p16.3-q12(chr4:85624-57073230)x3	copy number gain	Neurodevelopmental disorder [RCV003327613]	Chr4:85624..57073230 [GRCh38] Chr4:4p16.3-q12	pathogenic
GRCh37/hg19 4p16.3-15.32(chr4:85622-16900108)x1	copy number loss	not provided [RCV003334269]	Chr4:85622..16900108 [GRCh37] Chr4:4p16.3-15.32	pathogenic
GRCh37/hg19 4p15.33-15.2(chr4:12238766-23083496)x1	copy number loss	not provided [RCV003485415]	Chr4:12238766..23083496 [GRCh37] Chr4:4p15.33-15.2	likely pathogenic
GRCh37/hg19 4p16.3-15.31(chr4:68345-19103550)x1	copy number loss	not specified [RCV003986512]	Chr4:68345..19103550 [GRCh37] Chr4:4p16.3-15.31	pathogenic
GRCh37/hg19 4p16.3-15.31(chr4:68345-21143236)x1	copy number loss	not specified [RCV003986488]	Chr4:68345..21143236 [GRCh37] Chr4:4p16.3-15.31	pathogenic
NM_001290.5(LDB2):c.286G>T (p.Gly96Trp)	single nucleotide variant	EBV-positive nodal T- and NK-cell lymphoma [RCV004557773]	Chr4:16595825 [GRCh38] Chr4:16597448 [GRCh37] Chr4:4p15.32	likely benign
NM_001290.5(LDB2):c.1006G>A (p.Asp336Asn)	single nucleotide variant	not specified [RCV004412591]	Chr4:16502759 [GRCh38] Chr4:16504382 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.470C>T (p.Thr157Ile)	single nucleotide variant	not specified [RCV004412592]	Chr4:16588771 [GRCh38] Chr4:16590394 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.73A>G (p.Met25Val)	single nucleotide variant	not specified [RCV004412593]	Chr4:16898413 [GRCh38] Chr4:16900036 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.757C>G (p.Pro253Ala)	single nucleotide variant	not specified [RCV004642244]	Chr4:16508669 [GRCh38] Chr4:16510292 [GRCh37] Chr4:4p15.32	uncertain significance
NM_001290.5(LDB2):c.399G>A (p.Met133Ile)	single nucleotide variant	not specified [RCV004940022]	Chr4:16595712 [GRCh38] Chr4:16597335 [GRCh37] Chr4:4p15.32	uncertain significance
GRCh37/hg19 4p16.3-15.32(chr4:68346-16744084)x3	copy number gain	not provided [RCV004819301]	Chr4:68346..16744084 [GRCh37] Chr4:4p16.3-15.32	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	4773
Count of miRNA genes:	976
Interacting mature miRNAs:	1182
Transcripts:	ENST00000304523, ENST00000441778, ENST00000502640, ENST00000503153, ENST00000503178, ENST00000503829, ENST00000504189, ENST00000504886, ENST00000506732, ENST00000507464, ENST00000508804, ENST00000508918, ENST00000509803, ENST00000510825, ENST00000512345, ENST00000513457, ENST00000515064
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597095829	GWAS1191903_H	protein measurement QTL GWAS1191903 (human)		7e-09	protein measurement		4	16545521	16545522	Human
596972433	GWAS1091952_H	radiation-induced disorder QTL GWAS1091952 (human)		0.000004	radiation-induced disorder		4	16616089	16616090	Human
597212703	GWAS1308777_H	protein measurement QTL GWAS1308777 (human)		4e-09	protein measurement		4	16545521	16545522	Human
597060380	GWAS1156454_H	metabolic syndrome QTL GWAS1156454 (human)		5e-09	metabolic syndrome		4	16885671	16885672	Human
597060379	GWAS1156453_H	metabolic syndrome QTL GWAS1156453 (human)		9e-09	metabolic syndrome		4	16599170	16599171	Human
597173640	GWAS1269714_H	body mass index QTL GWAS1269714 (human)		1e-09	body mass index	body mass index (BMI) (CMO:0000105)	4	16599041	16599042	Human
597173641	GWAS1269715_H	body mass index QTL GWAS1269715 (human)		9e-09	body mass index	body mass index (BMI) (CMO:0000105)	4	16860132	16860133	Human
597276427	GWAS1372501_H	insomnia QTL GWAS1372501 (human)		4e-08	insomnia		4	16725994	16725995	Human
597143748	GWAS1239822_H	severe acute respiratory syndrome, COVID-19 QTL GWAS1239822 (human)		0.0000003	severe acute respiratory syndrome, COVID-19		4	16525171	16525172	Human
597276426	GWAS1372500_H	insomnia QTL GWAS1372500 (human)		2e-10	insomnia		4	16725163	16725164	Human
597173643	GWAS1269717_H	body mass index QTL GWAS1269717 (human)		1e-08	body mass index	body mass index (BMI) (CMO:0000105)	4	16890406	16890407	Human
596960640	GWAS1080159_H	metabolic syndrome QTL GWAS1080159 (human)		5e-09	metabolic syndrome		4	16885671	16885672	Human
597210382	GWAS1306456_H	protein measurement QTL GWAS1306456 (human)		2e-09	protein measurement		4	16545521	16545522	Human
597348748	GWAS1444822_H	Abdominal Aortic Aneurysm QTL GWAS1444822 (human)		3e-11	Abdominal Aortic Aneurysm		4	16883832	16883833	Human
597025346	GWAS1121420_H	body mass index QTL GWAS1121420 (human)		7e-08	body mass index	body mass index (BMI) (CMO:0000105)	4	16891547	16891548	Human
597332098	GWAS1428172_H	smoking initiation QTL GWAS1428172 (human)		1e-10	smoking initiation		4	16841093	16841094	Human
597230339	GWAS1326413_H	mortality QTL GWAS1326413 (human)		0.000001	mortality	ratio of deaths to total study population during a period of time (CMO:0001023)	4	16585051	16585052	Human
597099656	GWAS1195730_H	protein measurement QTL GWAS1195730 (human)		1e-08	protein measurement		4	16545521	16545522	Human
597169784	GWAS1265858_H	body mass index QTL GWAS1265858 (human)		5e-09	body mass index	body mass index (BMI) (CMO:0000105)	4	16614646	16614647	Human
597113206	GWAS1209280_H	protein measurement QTL GWAS1209280 (human)		6e-09	protein measurement		4	16545521	16545522	Human
597310648	GWAS1406722_H	vaginal microbiome measurement QTL GWAS1406722 (human)		0.0000002	vaginal microbiome measurement		4	16549953	16549954	Human
597167930	GWAS1264004_H	radiation-induced disorder QTL GWAS1264004 (human)		0.000004	radiation-induced disorder		4	16616089	16616090	Human
597145534	GWAS1241608_H	COVID-19 QTL GWAS1241608 (human)		0.000001	COVID-19		4	16664384	16664385	Human
596960639	GWAS1080158_H	metabolic syndrome QTL GWAS1080158 (human)		9e-09	metabolic syndrome		4	16599170	16599171	Human
406895852	GWAS544828_H	QT interval QTL GWAS544828 (human)		0.000007	QT interval	QT interval (CMO:0000235)	4	16892270	16892271	Human
596956537	GWAS1076056_H	body mass index QTL GWAS1076056 (human)		5e-09	body mass index		4	16599041	16599042	Human
407055342	GWAS704318_H	trauma exposure measurement QTL GWAS704318 (human)		0.000002	trauma exposure measurement		4	16727694	16727695	Human
597529203	GWAS1625277_H	body mass index QTL GWAS1625277 (human)		3e-08	body mass index	body mass index (BMI) (CMO:0000105)	4	16603555	16603556	Human
597101432	GWAS1197506_H	protein measurement QTL GWAS1197506 (human)		7e-11	protein measurement		4	16545521	16545522	Human
597097894	GWAS1193968_H	protein measurement QTL GWAS1193968 (human)		9e-11	protein measurement		4	16545521	16545522	Human
597211182	GWAS1307256_H	protein measurement QTL GWAS1307256 (human)		1e-09	protein measurement		4	16545521	16545522	Human
597209902	GWAS1305976_H	liver fibrosis measurement QTL GWAS1305976 (human)		0.000002	liver integrity trait (VT:0010547)	liver fibrotic lesion measurement (CMO:0001088)	4	16842287	16842288	Human
597189281	GWAS1285355_H	systemic lupus erythematosus QTL GWAS1285355 (human)		2e-08	systemic lupus erythematosus		4	16516592	16516593	Human
597025263	GWAS1121337_H	body mass index QTL GWAS1121337 (human)		5e-09	body mass index	body mass index (BMI) (CMO:0000105)	4	16599041	16599042	Human
597276771	GWAS1372845_H	diet measurement QTL GWAS1372845 (human)		2e-09	eating behavior trait (VT:0001431)	food intake measurement (CMO:0000772)	4	16892316	16892321	Human
597207972	GWAS1304046_H	protein measurement QTL GWAS1304046 (human)		2e-08	protein measurement		4	16545521	16545522	Human
597172900	GWAS1268974_H	smoking initiation QTL GWAS1268974 (human)		1e-12	smoking initiation		4	16819979	16819980	Human
407026300	GWAS675276_H	rhegmatogenous retinal detachment QTL GWAS675276 (human)		0.000005	rhegmatogenous retinal detachment		4	16512785	16512786	Human
597599968	GWAS1656828_H	human papilloma virus infection QTL GWAS1656828 (human)		0.0000003	human papilloma virus infection		4	16517334	16517335	Human

D4S1525

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,583,446 - 16,583,709	UniSTS	GRCh37
Build 36	4	16,192,544 - 16,192,807	RGD	NCBI36
Celera	4	17,048,518 - 17,048,807	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,937,073 - 15,937,328	UniSTS
Marshfield Genetic Map	4	29.68	UniSTS
Marshfield Genetic Map	4	29.68	RGD
deCODE Assembly Map	4	31.19	UniSTS

D4S590

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,814,138 - 16,814,479	UniSTS	GRCh37
Build 36	4	16,423,236 - 16,423,577	RGD	NCBI36
Celera	4	17,279,228 - 17,279,567	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,167,514 - 16,167,853	UniSTS

D4S599

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,814,095 - 16,814,472	UniSTS	GRCh37
Build 36	4	16,423,193 - 16,423,570	RGD	NCBI36
Celera	4	17,279,185 - 17,279,560	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,167,471 - 16,167,846	UniSTS
TNG Radiation Hybrid Map	4	11008.0	UniSTS
Stanford-G3 RH Map	4	1058.0	UniSTS
NCBI RH Map	4	158.3	UniSTS

RH121731

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,516,016 - 16,516,357	UniSTS	GRCh37
Build 36	4	16,125,114 - 16,125,455	RGD	NCBI36
Celera	4	16,981,232 - 16,981,573	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,865,227 - 15,865,568	UniSTS
TNG Radiation Hybrid Map	4	10843.0	UniSTS

RH123952

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,677,143 - 16,677,428	UniSTS	GRCh37
Build 36	4	16,286,241 - 16,286,526	RGD	NCBI36
Celera	4	17,142,247 - 17,142,532	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,030,643 - 16,030,928	UniSTS
TNG Radiation Hybrid Map	4	10929.0	UniSTS

D4S731

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,858,872 - 16,859,035	UniSTS	GRCh37
Build 36	4	16,467,970 - 16,468,133	RGD	NCBI36
Celera	4	17,323,973 - 17,324,136	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,212,366 - 16,212,529	UniSTS

SHGC-149811

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,585,574 - 16,585,845	UniSTS	GRCh37
Build 36	4	16,194,672 - 16,194,943	RGD	NCBI36
Celera	4	17,050,672 - 17,050,943	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,939,193 - 15,939,464	UniSTS
TNG Radiation Hybrid Map	4	10888.0	UniSTS

GDB:3755021

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,833,425 - 16,833,507	UniSTS	GRCh37
Build 36	4	16,442,523 - 16,442,605	RGD	NCBI36
Celera	4	17,298,513 - 17,298,595	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,186,905 - 16,186,987	UniSTS

SHGC-67928

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,639,015 - 16,639,201	UniSTS	GRCh37
Build 36	4	16,248,113 - 16,248,299	RGD	NCBI36
Celera	4	17,104,114 - 17,104,300	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,992,514 - 15,992,700	UniSTS
TNG Radiation Hybrid Map	4	10910.0	UniSTS
GeneMap99-GB4 RH Map	4	73.05	UniSTS

SHGC-155343

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,744,199 - 16,744,524	UniSTS	GRCh37
Build 36	4	16,353,297 - 16,353,622	RGD	NCBI36
Celera	4	17,209,284 - 17,209,609	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,097,726 - 16,098,051	UniSTS
TNG Radiation Hybrid Map	4	10947.0	UniSTS

SHGC-156280

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,708,186 - 16,708,376	UniSTS	GRCh37
Build 36	4	16,317,284 - 16,317,474	RGD	NCBI36
Celera	4	17,173,277 - 17,173,467	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,061,708 - 16,061,898	UniSTS
TNG Radiation Hybrid Map	4	10940.0	UniSTS

LDB2_2122

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,502,976 - 16,503,823	UniSTS	GRCh37
Build 36	4	16,112,074 - 16,112,921	RGD	NCBI36
Celera	4	16,968,189 - 16,969,036	RGD
HuRef	4	15,852,185 - 15,853,032	UniSTS

AB046090

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,547,668 - 16,547,810	UniSTS	GRCh37
Build 36	4	16,156,766 - 16,156,908	RGD	NCBI36
Celera	4	17,012,865 - 17,013,007	RGD
HuRef	4	15,897,254 - 15,897,396	UniSTS

SHGC-59820

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,832,876 - 16,833,028	UniSTS	GRCh37
Build 36	4	16,441,974 - 16,442,126	RGD	NCBI36
Celera	4	17,297,964 - 17,298,116	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,186,356 - 16,186,508	UniSTS
GeneMap99-GB4 RH Map	4	78.23	UniSTS

G09887

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,718,723 - 16,718,903	UniSTS	GRCh37
Build 36	4	16,327,821 - 16,328,001	RGD	NCBI36
Celera	4	17,183,814 - 17,183,994	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,072,249 - 16,072,429	UniSTS

SHGC-50314

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,583,683 - 16,583,800	UniSTS	GRCh37
Build 36	4	16,192,781 - 16,192,898	RGD	NCBI36
Celera	4	17,048,781 - 17,048,898	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,937,302 - 15,937,419	UniSTS
TNG Radiation Hybrid Map	4	10891.0	UniSTS

G34137

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,858,673 - 16,858,874	UniSTS	GRCh37
Build 36	4	16,467,771 - 16,467,972	RGD	NCBI36
Celera	4	17,323,774 - 17,323,975	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	16,212,167 - 16,212,368	UniSTS

D4S2642

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,519,395 - 16,519,636	UniSTS	GRCh37
Build 36	4	16,128,493 - 16,128,734	RGD	NCBI36
Celera	4	16,984,606 - 16,984,847	RGD
Cytogenetic Map	4	p16	UniSTS
HuRef	4	15,868,601 - 15,868,838	UniSTS
Marshfield Genetic Map	4	29.68	UniSTS
Whitehead-YAC Contig Map	4		UniSTS

LDB2

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	16,510,167 - 16,510,306	UniSTS	GRCh37
Celera	4	16,975,383 - 16,975,522	UniSTS
HuRef	4	15,859,379 - 15,859,518	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2340	2788	2232	4922	1711	2179	3	612	1441	451	2234	6680	5962	44	3720	1	805	1663	1461	168	1


RefSeq Transcripts	NM_001130834	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001290	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001304434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001304435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_130734	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005248197	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005248201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005248202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713976	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713980	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713981	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713982	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006713983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011513905	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008822	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454278	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416390	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416391	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351198	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351199	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351200	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351210	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351212	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351213	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054351215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC005690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC097515	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC105353	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC106894	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF047337	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF052389	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF064492	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF064493	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF068651	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095238	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097013	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK226029	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300119	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832772	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC034019	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG704168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX089082	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471069	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA166898	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA521198	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB352456	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584466	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000304523 ⟹ ENSP00000306772

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,501,541 - 16,898,645 (-)	Ensembl

Ensembl Acc Id:

ENST00000441778 ⟹ ENSP00000392089

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,501,541 - 16,898,594 (-)	Ensembl

Ensembl Acc Id:

ENST00000502640 ⟹ ENSP00000423963

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,501,546 - 16,898,634 (-)	Ensembl

Ensembl Acc Id:

ENST00000503153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,512,005 - 16,653,819 (-)	Ensembl

Ensembl Acc Id:

ENST00000503829

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,585,976 - 16,626,993 (-)	Ensembl

Ensembl Acc Id:

ENST00000504189

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,750,850 - 16,898,378 (-)	Ensembl

Ensembl Acc Id:

ENST00000504886

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,585,950 - 16,726,502 (-)	Ensembl

Ensembl Acc Id:

ENST00000506732 ⟹ ENSP00000421767

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,585,972 - 16,898,660 (-)	Ensembl

Ensembl Acc Id:

ENST00000507464 ⟹ ENSP00000425754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,502,042 - 16,595,875 (-)	Ensembl

Ensembl Acc Id:

ENST00000508804

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,588,709 - 16,759,375 (-)	Ensembl

Ensembl Acc Id:

ENST00000508918 ⟹ ENSP00000424770

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,502,794 - 16,898,634 (-)	Ensembl

Ensembl Acc Id:

ENST00000509803

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,501,544 - 16,507,227 (-)	Ensembl

Ensembl Acc Id:

ENST00000510825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,741,455 - 16,898,678 (-)	Ensembl

Ensembl Acc Id:

ENST00000512345 ⟹ ENSP00000424676

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,511,985 - 16,898,621 (-)	Ensembl

Ensembl Acc Id:

ENST00000513457

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,588,710 - 16,826,560 (-)	Ensembl

Ensembl Acc Id:

ENST00000515064 ⟹ ENSP00000422552

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	16,501,541 - 16,898,562 (-)	Ensembl

RefSeq Acc Id:

NM_001130834 ⟹ NP_001124306

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI
GRCh37	4	16,503,164 - 16,900,424 (-)	RGD
Celera	4	16,968,377 - 17,365,469 (-)	RGD
HuRef	4	15,852,373 - 16,253,922 (-)	RGD
CHM1_1	4	16,501,232 - 16,898,334 (-)	NCBI
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

Sequence:

show sequence

AGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACT
CTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATC
TATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGTACCTGGGCTAGGAGCGATCCCGAACTGCAGCCTCAACCCTGGGAGGGATGGAGACCTGTGTCATTCAACAGCAGTGACCCCTTCTGGCCAATTTAAGGAGAAGCA
TTGAGGGGCCCTGAAAGGAGTCACTTCCAGTCCTCCTCAGAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACAC
GCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCAC
CCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAAT
ATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCAC
TGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAG
GATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTT
GGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGAC
TCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATC
CAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATAT
TTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATG
TAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

NM_001290 ⟹ NP_001281

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI
GRCh37	4	16,503,164 - 16,900,424 (-)	RGD
Build 36	4	16,112,262 - 16,509,425 (-)	NCBI Archive
Celera	4	16,968,377 - 17,365,469 (-)	RGD
HuRef	4	15,852,373 - 16,253,922 (-)	RGD
CHM1_1	4	16,501,232 - 16,898,334 (-)	NCBI
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

Sequence:

show sequence

AGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACT
CTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATC
TATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGC
CAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAAT
AAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACC
ACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAA
TGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATG
CCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAA
TGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAG
TGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGC
CATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCA
CCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGC
TCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

NM_001304434 ⟹ NP_001291363

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI
CHM1_1	4	16,501,232 - 16,898,334 (-)	NCBI
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

Sequence:

show sequence

AGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACT
CTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATC
TATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGG
CATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATG
ATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATG
ATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAG
AAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAAC
CTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACC
TTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGA
AACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTA
ATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGT
TCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTG
TGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

NM_001304435 ⟹ NP_001291364

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI
CHM1_1	4	16,501,232 - 16,898,334 (-)	NCBI
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

Sequence:

show sequence

AGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACT
CTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATC
TATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGTACCTATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAA
TCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTC
CCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCG
GCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCA
ATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAA
CCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAA
AATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATA
TGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTA
AATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCA
AGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAA
GCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCT
CACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTG
GCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

NR_130734

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,750,850 - 16,898,645 (-)	NCBI
CHM1_1	4	16,750,540 - 16,898,334 (-)	NCBI
T2T-CHM13v2.0	4	16,732,654 - 16,880,253 (-)	NCBI

Sequence:

show sequence

AGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACT
CTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATC
TATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGCCTCAGAAAACCAATTTGTTTCTTTTCTCATTTGATATTTCTGCTACTTCTGTCTCTCTATATCTACCTGGGAGCCCAC
AGCCGTGAATTACGGTATGAATCATGATAATATGTTACATTTCCTGGAGCACTTTGCATTTTAGGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGATACACTTATTCTGGAT
TCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACAGAAC
CAAGAATTTAAGACCAATTGGGGAAAAAATGAATATTAATGGAAAATGGTGTTGCTGCCAGAATTTATTGTTTGGGGACTGGAGAAGAGAACTGTTCTACACAATAAAAAATTATTGAGAAACACA

hide sequence

RefSeq Acc Id:

XM_005248197 ⟹ XP_005248254

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI
GRCh37	4	16,503,164 - 16,900,424 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAAC
ACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGG
CATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGC
CACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAAC
ACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACC
TTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACAT
CACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCT
GCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAAC
AGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAAT
CACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCA
AATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAA
AAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGG
TAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCA
TAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAA
GACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGG
TTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTT
GTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_006713975 ⟹ XP_006714038

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCCGTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAG
AGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGG
ACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGC
CAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGCCTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGAT
ACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGC
CAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAAT
AAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACC
ACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAA
TGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATG
CCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAA
TGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAG
TGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGC
CATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCA
CCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGC
TCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_006713976 ⟹ XP_006714039

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCCGTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAG
AGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGG
ACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGC
CAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGCCTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGAT
ACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAAC
CTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAA
CGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAG
ATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACA
ATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGA
GAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCG
AACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGT
ACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGC
TGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCAT
GTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_006713977 ⟹ XP_006714040

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCC
GTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTG
TGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACAT
GACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGC
CTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGATACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCT
TTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGG
GTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTAC
AGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTC
AGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAAC
CTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCAC
TTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGT
TTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGT
AAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTT
ACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATG
ACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATG
CATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGT
TTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAAT
TTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAAT
TGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_006713982 ⟹ XP_006714045

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCCGTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAG
AGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGG
ACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGC
CAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGCCTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGAT
ACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGGTACCTATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAA
TCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTC
CCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCG
GCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCA
ATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAA
CCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAA
AATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATA
TGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTA
AATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCA
AGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAA
GCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCT
CACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTG
GCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_006713983 ⟹ XP_006714046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCCGTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAG
AGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGG
ACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGC
CAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGCCTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGAT
ACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACC
AAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGG
TGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTT
ACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTA
CCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGC
CAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCA
AACCTGAGTCTGTCCAGTCAGATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAAT
ATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTA
ATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAAC
GGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGA
TGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAA
TGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAG
AGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGA
ACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTA
CCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCT
GAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATG
TAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_017008812 ⟹ XP_016864301

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCC
GTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTG
TGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACAT
GACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGC
CTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGATACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCT
TTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGG
GTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTAC
AGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTC
AGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAAC
CTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTC
CAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTG
GGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAA
CCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACA
GGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACC
CTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCAT
CAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTC
TTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTA
TGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGG
ACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTT
GACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATT
AATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAAT
GACCAAA

hide sequence

RefSeq Acc Id:

XM_017008813 ⟹ XP_016864302

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCC
TGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGG
CAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTC
GCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTC
ATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCAC
CCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCC
CGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCA
ATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAA
ACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGATGTGATGG
TGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCA
CCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCC
GTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCT
AATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTT
AACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAA
ATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCAT
TGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGAC
ACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAAC
CTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAA
CTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCT
TTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_017008815 ⟹ XP_016864304

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCC
GTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTG
TGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACAT
GACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGC
CTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGATACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCT
TTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGG
GTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTAC
AGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTC
AGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAAC
CTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTC
CAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCAC
TAAGGACATAAACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGT
CCTAGATTCCCCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGG
TGAGTTTGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGA
ACAGTAAACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTT
TACTTACAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTT
CCATGACCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTT
TTATGCATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTG
AGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAG
GTAATTTATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAG
ACAATTGGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA
CCTGAGTTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATA
AGAGAATTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACT
GTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_017008816 ⟹ XP_016864305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

CTTCCTCCATACCAACCTCCCTCCCTCTCTGGAGCTCCTGCTCTCTCCCTCTCCCTCCTCTCCC
GTGCTCCCTCCCTCCCTCCCTCTTTCCCTCCCTCCTCTCCTCTCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTG
TGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAACACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACAT
GACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGGCATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATCTCTACATGGC
CTCAGAAAACCAATTGTGCCACATCATTGGGAACTATGATGATGATGACGACGATGACGACGATACACTTATTCTGGATTCTATCAGCAAATTAAATAATGATAGTGACAACCTCTGGTGGGACGCCT
TTGCCACTGAATTTTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGG
GTGACCGACCTGTATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTAC
AGAAGGCAGACTGATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTC
AGGTCCTGGATCAGCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAAC
CTCAGTCCCCGAGACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTC
CAACAGCAGCGCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGA
CATAAACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGA
TTCCCCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTT
TGGGGACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTA
AACCTCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTA
CAGGAGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGA
CCCTTTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGC
ATCAAACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTT
TCTTGTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATT
TATGGTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATT
GGACCCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAG
TTGACCATCCTTTCTTTTTATAGTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAA
TTAATTTTTCCATTTGCATATTAATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTA
ATGACCAAA

hide sequence

RefSeq Acc Id:

XM_017008818 ⟹ XP_016864307

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,778,923 (-)	NCBI

Sequence:

show sequence

GCTCCCACTGATTCTACATTATGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATT
TTTTGAAGATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGT
ATTACATTCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTG
ATCTTGGAGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCA
GCTGTCCAAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAG
ACTGCCTGAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGC
GCTGGGAACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGA
CGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTC
CCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAG
AGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTT
CTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAA
CGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGT
TTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGT
TGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCC
TTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_017008819 ⟹ XP_016864308

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAAC
ACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGG
CATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGC
CACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAAC
ACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACC
TTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACAT
CACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCT
GCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAAC
AGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTAC
ACATCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTT
ATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTA
ATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGAC
CAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGAT
AAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACA
GGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTC
CATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAA
AAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATT
GGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCAT
TTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATA
GTATATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATT
AATATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_017008820 ⟹ XP_016864309

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAAC
ACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGG
CATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGC
CACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAAC
ACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACC
TTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACAT
CACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCT
GCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCA
AACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTACACA
TCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTTATT
TTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATC
ACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAA
ATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAA
AACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGT
AATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCAT
AAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAG
ACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGT
TCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTG
TAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTA
TATTTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAAT
ATGTTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_017008821 ⟹ XP_016864310

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAAC
ACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGG
CATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGC
CACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAAC
ACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACC
TTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACAT
CACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCT
GCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCAAAC
AGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATAAACTCGCGTGGTTGTTACACATCA
GGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCCCCGACTCCTCCCACTGTTATTTTA
AGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGACGAAAGGCTAATCACT
AGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCACTCAAGAGACCAAATC
AGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAACAGAAGAGATAAAAAC
TTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAGGCCTTCACAGGTAAT
ACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGCCATATTGTCCATAAA
TGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTAAAAAAAGAAAAGACA
AAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTGATGTCAATTGGTTCT
TGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAATTTATGCATTTGTAA
AGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTACCTGAGTTGACCATCCTTTCTTTTTATAGTATAT
TTCTTGTATGATATTTTGTAAAGCTCTCACCTGGTTCTTTTATGGGGACTTTTCGTTTTTGGGCAACTCCAGTGTATTTATGTGAAACTTTATAAGAGAATTAATTTTTCCATTTGCATATTAATATG
TTCCTCCACACATGTAAAGGCACAGTGGCTCCGTGTGTTAAAAAACAGCTGTATTTTATGTATGCTTTACTGATAAGTGTGCCAATAATAAACTGTGTTAATGACCAAA

hide sequence

RefSeq Acc Id:

XM_024454278 ⟹ XP_024310046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,898,645 (-)	NCBI

Sequence:

show sequence

TCCCTCTCCTCTCCTGCTATAGAGGGCTCCGACAGCAGTTCCCAGCCAGCGTGTTCAGCCTGCCTGCCTGCCTGCCTCTGTGTGTGTGTGAGCGTGTGTGCGTGCGTCTACTTTGTACTGGGAAGAAC
ACAGCCCATGTGCTCTGCATGGACGTTACTGATACTCTGTTTAGCTTGATTTTCGAAAAGCAGGCAAGATGTCCAGCACACCACATGACCCCTTCTATTCTTCTCCTTTCGGCCCATTTTATAGGAGG
CATACACCATACATGGTACAGCCAGAGTACCGAATCTATGAGATGAACAAGAGACTGCAGTCTCGCACAGAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAAGATGACGC
CACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACATTCTCAAAC
ACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGGAGTTCACC
TTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCCAAAAACAT
CACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCTGAAGACCT
GCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGAACAATGCA
AACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTGGGCTAGGAGCGATCCCGAACTGCAGCCTCAACCCTGGGAGGGATGGAGACCTGTGTCATTCAAC
AGCAGTGACCCCTTCTGGCCAATTTAAGGAGAAGCATTGAGGGGCCCTGAAAGGAGTCACTTCCAGTCCTCCTCAGAGATTGCTAGCATTGCTCGTTCTCCAGTGTCAGGCTGCGCACTAAGGACATA
AACTCGCGTGGTTGTTACACATCAGGAGGCGATGTTTATTTCCTGTAGAAATCAAATATGCGTCTCGGCCCCCGACATTGAGACTTGACCCCGTTGTACAGTACACGAGTGTGTCTGTCCTAGATTCC
CCGACTCCTCCCACTGTTATTTTAAGCTGAGCTTCTCTCTCCCAAGGTTTCCCTGTAATAATGTCAGCTGCTGTTCACAGGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGG
GACGAGGACGAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACC
TCCCGCCACTCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGG
AGAGGAAACAGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCT
TTCTTGGAGGCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCA
AACGAAGGCCATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTT
GTTTCAGTAAAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATG
GTTGAGCTGATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGAC
CCTTAAGAATTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_024454280 ⟹ XP_024310048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,814,244 (-)	NCBI

Sequence:

show sequence

TCTCTAGATGGAAACCATTTTTTTCTTCTGAACTTGTGTCCTGCTATTCAAGATTCAAAGTCACAGGAGAGAGAATCCAACTGTCTGAATCTAGGTTCTGCTATTGACACATGGTTGCCCTGGAACAG
ACGAGTAGCCACAGGACTCCCTCAGCTTCCGCGGGTAGCTTGGTTCATTTCCCAACCTGGCCTGTGCACACTAAGCAAAGGATAGTGACAACCTCTGGTGGGACGCCTTTGCCACTGAATTTTTTGAA
GATGACGCCACATTAACCCTTTCATTTTGTTTGGAAGATGGACCAAAGCGATACACTATCGGCAGGACCCTCATCCCCCGTTACTTTAGCACTGTGTTTGAAGGAGGGGTGACCGACCTGTATTACAT
TCTCAAACACTCGAAAGAGTCATACCACAACTCATCCATCACGGTGGACTGCGACCAGTGTACCATGGTCACCCAGCACGGGAAGCCCATGTTTACCAAGGTATGTACAGAAGGCAGACTGATCTTGG
AGTTCACCTTTGATGATCTCATGAGAATCAAAACATGGCACTTTACCATTAGACAATACCGAGAGTTAGTCCCGAGAAGCATCCTAGCCATGCATGCACAAGATCCTCAGGTCCTGGATCAGCTGTCC
AAAAACATCACCAGGATGGGGCTAACAAACTTCACCCTCAACTACCTCAGGTTGTGTGTAATATTGGAGCCAATGCAGGAACTGATGTCGAGACATAAAACTTACAACCTCAGTCCCCGAGACTGCCT
GAAGACCTGCTTGTTTCAGAAGTGGCAGAGGATGGTGGCTCCGCCAGCAGAACCCACAAGGCAACCAACAACCAAACGGAGAAAAAGGAAAAATTCCACCAGCAGCACTTCCAACAGCAGCGCTGGGA
ACAATGCAAACAGCACTGGCAGCAAGAAGAAGACCACAGCTGCAAACCTGAGTCTGTCCAGTCAGGTACCTGATGTGATGGTGGTAGGAGAGCCAACTCTGATGGGAGGTGAGTTTGGGGACGAGGAC
GAAAGGCTAATCACTAGATTAGAAAACACGCAATATGATGCGGCCAACGGCATGGACGACGAGGAGGACTTCAACAATTCACCCGCGCTGGGGAACAACAGCCCGTGGAACAGTAAACCTCCCGCCAC
TCAAGAGACCAAATCAGAAAACCCCCCACCCCAGGCTTCCCAATAAGATGATCGGCACCAGAATCCACTGTCAATAGGCCCGTGGGTGATCATTACAATTGCAAATCTTTACTTACAGGAGAGGAAAC
AGAAGAGATAAAAACTTTTCCATGCAAATATCTATTTCTAAACCACAATGATCTGATTTTCTTTCTTCTTTCTTTTTTTCTAATTGAGAGGATTATTCCCAGTAAGCTTCCATGACCCTTTCTTGGAG
GCCTTCACAGGTAATACAGATACTGGCACTGATTGTAATTAAAATGAGAGAAAACTCTAGCGCATCTTCTGGCACGGTTTTAACAACGTGTTTGTGTTGAATTTCCTTTTTATGCATCAAACGAAGGC
CATATTGTCCATAAATGCTCAGTGCTCAGGATCTCATTAATATGCCGAACCTAACTACAGATGACTTTTTAATATTGTAAAATATTTTCTGCTTTTTGACTTGCATCTGAGAGTTTCTTGTTTCAGTA
AAAAAAGAAAAGACAAAAAAATCAGCTTTGGAAAGTAATTTAAATGTACCTTATTTTTTTTTTCTTTATGTTTTCTTTCATTGGGCAACAGCTAAGAGGGCCCAGCAAGGTAATTTATGGTTGAGCTG
ATGTCAATTGGTTCTTGTCTTGAGTCGACTCAATTTAGCCCAAGTGCTGAAACAAGAAATGTCATTTTTTTCATCAAAGACACCAGGGCAGATTTTTAAGTAAAGAAAGACAATTGGACCCTTAAGAA
TTTATGCATTTGTAAAGTTGCTGTTGATCCAAATATTTTCAAGCCATGTAATCCATTGGTTTTGTGGGCAGTTTAATAAACCTGAACCTTTGTGTGTTTTCTAATTGTA

hide sequence

RefSeq Acc Id:

XM_047416390 ⟹ XP_047272346

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,752,431 (-)	NCBI

RefSeq Acc Id:

XM_047416391 ⟹ XP_047272347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,501,541 - 16,778,911 (-)	NCBI

RefSeq Acc Id:

XM_054351198 ⟹ XP_054207173

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351199 ⟹ XP_054207174

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351200 ⟹ XP_054207175

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351201 ⟹ XP_054207176

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351202 ⟹ XP_054207177

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351203 ⟹ XP_054207178

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351204 ⟹ XP_054207179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351205 ⟹ XP_054207180

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351206 ⟹ XP_054207181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351207 ⟹ XP_054207182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351208 ⟹ XP_054207183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351209 ⟹ XP_054207184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,760,696 (-)	NCBI

RefSeq Acc Id:

XM_054351210 ⟹ XP_054207185

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351211 ⟹ XP_054207186

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351212 ⟹ XP_054207187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,880,253 (-)	NCBI

RefSeq Acc Id:

XM_054351213 ⟹ XP_054207188

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,734,227 (-)	NCBI

RefSeq Acc Id:

XM_054351214 ⟹ XP_054207189

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,760,684 (-)	NCBI

RefSeq Acc Id:

XM_054351215 ⟹ XP_054207190

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	16,483,292 - 16,797,564 (-)	NCBI


Protein RefSeqs	NP_001124306	(Get FASTA)	NCBI Sequence Viewer
	NP_001281	(Get FASTA)	NCBI Sequence Viewer
	NP_001291363	(Get FASTA)	NCBI Sequence Viewer
	NP_001291364	(Get FASTA)	NCBI Sequence Viewer
	XP_005248254	(Get FASTA)	NCBI Sequence Viewer
	XP_006714038	(Get FASTA)	NCBI Sequence Viewer
	XP_006714039	(Get FASTA)	NCBI Sequence Viewer
	XP_006714040	(Get FASTA)	NCBI Sequence Viewer
	XP_006714045	(Get FASTA)	NCBI Sequence Viewer
	XP_006714046	(Get FASTA)	NCBI Sequence Viewer
	XP_016864301	(Get FASTA)	NCBI Sequence Viewer
	XP_016864302	(Get FASTA)	NCBI Sequence Viewer
	XP_016864304	(Get FASTA)	NCBI Sequence Viewer
	XP_016864305	(Get FASTA)	NCBI Sequence Viewer
	XP_016864307	(Get FASTA)	NCBI Sequence Viewer
	XP_016864308	(Get FASTA)	NCBI Sequence Viewer
	XP_016864309	(Get FASTA)	NCBI Sequence Viewer
	XP_016864310	(Get FASTA)	NCBI Sequence Viewer
	XP_024310046	(Get FASTA)	NCBI Sequence Viewer
	XP_024310048	(Get FASTA)	NCBI Sequence Viewer
	XP_047272346	(Get FASTA)	NCBI Sequence Viewer
	XP_047272347	(Get FASTA)	NCBI Sequence Viewer
	XP_054207173	(Get FASTA)	NCBI Sequence Viewer
	XP_054207174	(Get FASTA)	NCBI Sequence Viewer
	XP_054207175	(Get FASTA)	NCBI Sequence Viewer
	XP_054207176	(Get FASTA)	NCBI Sequence Viewer
	XP_054207177	(Get FASTA)	NCBI Sequence Viewer
	XP_054207178	(Get FASTA)	NCBI Sequence Viewer
	XP_054207179	(Get FASTA)	NCBI Sequence Viewer
	XP_054207180	(Get FASTA)	NCBI Sequence Viewer
	XP_054207181	(Get FASTA)	NCBI Sequence Viewer
	XP_054207182	(Get FASTA)	NCBI Sequence Viewer
	XP_054207183	(Get FASTA)	NCBI Sequence Viewer
	XP_054207184	(Get FASTA)	NCBI Sequence Viewer
	XP_054207185	(Get FASTA)	NCBI Sequence Viewer
	XP_054207186	(Get FASTA)	NCBI Sequence Viewer
	XP_054207187	(Get FASTA)	NCBI Sequence Viewer
	XP_054207188	(Get FASTA)	NCBI Sequence Viewer
	XP_054207189	(Get FASTA)	NCBI Sequence Viewer
	XP_054207190	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAC13274	(Get FASTA)	NCBI Sequence Viewer
	AAC28342	(Get FASTA)	NCBI Sequence Viewer
	AAC28343	(Get FASTA)	NCBI Sequence Viewer
	AAC77817	(Get FASTA)	NCBI Sequence Viewer
	AAC83552	(Get FASTA)	NCBI Sequence Viewer
	AAH34019	(Get FASTA)	NCBI Sequence Viewer
	AAY40912	(Get FASTA)	NCBI Sequence Viewer
	BAH11819	(Get FASTA)	NCBI Sequence Viewer
	BAH13216	(Get FASTA)	NCBI Sequence Viewer
	EAW92765	(Get FASTA)	NCBI Sequence Viewer
	EAW92766	(Get FASTA)	NCBI Sequence Viewer
	EAW92767	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000306772
	ENSP00000306772.5
	ENSP00000392089
	ENSP00000392089.2
	ENSP00000422552
	ENSP00000423963
	ENSP00000425754
GenBank Protein	O43679	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001281 ⟸ NM_001290
- Peptide Label:	isoform a
- UniProtKB:	O60619 (UniProtKB/Swiss-Prot), O75480 (UniProtKB/Swiss-Prot), O43679 (UniProtKB/Swiss-Prot), B7Z6D0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MSSTPHDPFYSSPFGPFYRRHTPYMVQPEYRIYEMNKRLQSRTEDSDNLWWDAFATEFFEDDATLTLSFCLEDGPKRYTIGRTLIPRYFSTVFEGGVTDLYYILKHSKESYHNSSITVDCDQCTMVTQ HGKPMFTKVCTEGRLILEFTFDDLMRIKTWHFTIRQYRELVPRSILAMHAQDPQVLDQLSKNITRMGLTNFTLNYLRLCVILEPMQELMSRHKTYNLSPRDCLKTCLFQKWQRMVAPPAEPTRQPTTK RRKRKNSTSSTSNSSAGNNANSTGSKKKTTAANLSLSSQVPDVMVVGEPTLMGGEFGDEDERLITRLENTQYDAANGMDDEEDFNNSPALGNNSPWNSKPPATQETKSENPPPQASQ hide sequence

RefSeq Acc Id:	NP_001124306 ⟸ NM_001130834
- Peptide Label:	isoform b
- UniProtKB:	O43679 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSSTPHDPFYSSPFGPFYRRHTPYMVQPEYRIYEMNKRLQSRTEDSDNLWWDAFATEFFEDDATLTLSFCLEDGPKRYTIGRTLIPRYFSTVFEGGVTDLYYILKHSKESYHNSSITVDCDQCTMVTQ HGKPMFTKVCTEGRLILEFTFDDLMRIKTWHFTIRQYRELVPRSILAMHAQDPQVLDQLSKNITRMGLTNFTLNYLRLCVILEPMQELMSRHKTYNLSPRDCLKTCLFQKWQRMVAPPAEPTRQPTTK RRKRKNSTSSTSNSSAGNNANSTGSKKKTTAANLSLSSQVPGLGAIPNCSLNPGRDGDLCHSTAVTPSGQFKEKH hide sequence

RefSeq Acc Id:	XP_005248254 ⟸ XM_005248197
- Peptide Label:	isoform X5
- UniProtKB:	B7Z6D0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MSSTPHDPFYSSPFGPFYRRHTPYMVQPEYRIYEMNKRLQSRTEDSDNLWWDAFATEFFEDDATLTLSFCLEDGPKRYTIGRTLIPRYFSTVFEGGVTDLYYILKHSKESYHNSSITVDCDQCTMVTQ HGKPMFTKVCTEGRLILEFTFDDLMRIKTWHFTIRQYRELVPRSILAMHAQDPQVLDQLSKNITRMGLTNFTLNYLRLCVILEPMQELMSRHKTYNLSPRDCLKTCLFQKWQRMVAPPEPTRQPTTKR RKRKNSTSSTSNSSAGNNANSTGSKKKTTAANLSLSSQVPDVMVVGEPTLMGGEFGDEDERLITRLENTQYDAANGMDDEEDFNNSPALGNNSPWNSKPPATQETKSENPPPQASQ hide sequence

RefSeq Acc Id:

XP_006714039 ⟸ XM_006713976

- Peptide Label:

isoform X2

- Sequence:

show sequence

MSSTPHDPFYSSPFGPFYRRHTPYMVQPEYRIYEMNKRLQSRTEDLYMASENQLCHIIGNYDDDDDDDDDTLILDSISKLNNDSDNLWWDAFATEFFEDDATLTLSFCLEDGPKRYTIGRTLIPRYFS
TVFEGGVTDLYYILKHSKESYHNSSITVDCDQCTMVTQHGKPMFTKVCTEGRLILEFTFDDLMRIKTWHFTIRQYRELVPRSILAMHAQDPQVLDQLSKNITRMGLTNFTLNYLRLCVILEPMQELMS
RHKTYNLSPRDCLKTCLFQKWQRMVAPPEPTRQPTTKRRKRKNSTSSTSNSSAGNNANSTGSKKKTTAANLSLSSQVPDVMVVGEPTLMGGEFGDEDERLITRLENTQYDAANGMDDEEDFNNSPALG
NNSPWNSKPPATQETKSENPPPQASQ

hide sequence

RefSeq Acc Id:

XP_006714040 ⟸ XM_006713977

- Peptide Label:

isoform X3

- Sequence:

show sequence

MSSTPHDPFYSSPFGPFYRRHTPYMVQPEYRIYEMNKRLQSRTEDLYMASENQLCHIIGNYDDD
DDDDDDTLILDSISKLNNDSDNLWWDAFATEFFEDDATLTLSFCLEDGPKRYTIGRTLIPRYFSTVFEGGVTDLYYILKHSKESYHNSSITVDCDQCTMVTQHGKPMFTKVCTEGRLILEFTFDDLMR
IKTWHFTIRQYRELVPRSILAMHAQDPQVLDQLSKNITRMGLTNFTLNYLRLCVILEPMQELMSRHKTYNLSPRDCLKTCLFQKWQRMVAPPAEPTRQPTTKRRKRKNSTSSTSNSSAGNNANSTGSK
KKTTAANLSLSSQDVMVVGEPTLMGGEFGDEDERLITRLENTQYDAANGMDDEEDFNNSPALGNNSPWNSKPPATQETKSENPPPQASQ

hide sequence

Protein Domains

LIM interaction LIM interaction domain (LID)

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O43679-F1-model_v2	AlphaFold	O43679	1-373	view protein structure

RGD ID:

6867088

Promoter ID:

EPDNEW_H6709

Type:

initiation region

Name:

LDB2_1

Description:

LIM domain binding 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6710

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,898,634 - 16,898,694	EPDNEW

RGD ID:

6867090

Promoter ID:

EPDNEW_H6710

Type:

initiation region

Name:

LDB2_2

Description:

LIM domain binding 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6709

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	16,898,779 - 16,898,839	EPDNEW

Database	Acc Id	Source(s)
COSMIC	LDB2	COSMIC
Ensembl Genes	ENSG00000169744	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000304523	ENTREZGENE
	ENST00000304523.10	UniProtKB/Swiss-Prot
	ENST00000441778	ENTREZGENE
	ENST00000441778.6	UniProtKB/Swiss-Prot
	ENST00000502640	ENTREZGENE
	ENST00000507464	ENTREZGENE
	ENST00000515064	ENTREZGENE
Gene3D-CATH	Cysteine Rich Protein	UniProtKB/Swiss-Prot
GTEx	ENSG00000169744	GTEx
HGNC ID	HGNC:6533	ENTREZGENE
Human Proteome Map	LDB2	Human Proteome Map
InterPro	LID	UniProtKB/Swiss-Prot
	LIM-bd/SEUSS	UniProtKB/Swiss-Prot
KEGG Report	hsa:9079	UniProtKB/Swiss-Prot
NCBI Gene	9079	ENTREZGENE
OMIM	603450	OMIM
PANTHER	PTHR10378	UniProtKB/Swiss-Prot
Pfam	LID	UniProtKB/Swiss-Prot
	LIM_bind	UniProtKB/Swiss-Prot
PharmGKB	PA30317	PharmGKB
PROSITE	LID	UniProtKB/Swiss-Prot
UniProt	B7Z6D0	ENTREZGENE, UniProtKB/TrEMBL
	D6RAT1_HUMAN	UniProtKB/TrEMBL
	E7EX95_HUMAN	UniProtKB/TrEMBL
	E9PFI4	ENTREZGENE, UniProtKB/TrEMBL
	E9PGU0_HUMAN	UniProtKB/TrEMBL
	G5E9Y7	ENTREZGENE, UniProtKB/TrEMBL
	H0YA09	ENTREZGENE, UniProtKB/TrEMBL
	LDB2_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	O60619	ENTREZGENE
	O75480	ENTREZGENE
	Q4W5E7_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	O60619	UniProtKB/Swiss-Prot
	O75480	UniProtKB/Swiss-Prot

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


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


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

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