Advanced Search (OLGA)

Gene: TXK (TXK tyrosine kinase) Homo sapiens

Subscribe to Updates

Analyze

Symbol:

TXK

Name:

TXK tyrosine kinase

RGD ID:

1315122

HGNC Page

HGNC:12434

Description:

Predicted to enable non-membrane spanning protein tyrosine kinase activity. Involved in positive regulation of macromolecule biosynthetic process; positive regulation of type II interferon-mediated signaling pathway; and protein autophosphorylation. Located in cytosol; nuclear lumen; and plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

BTKL; MGC22473; protein-tyrosine kinase 4; PSCTK5; PTK4; PTK4 protein tyrosine kinase 4; resting lymphocyte kinase; RLK; TKL; tyrosine kinase; tyrosine-protein kinase TXK

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):	Txk (TXK tyrosine kinase)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Txk (TXK tyrosine kinase)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Txk (TXK tyrosine kinase)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	TXK (TXK tyrosine kinase)	NCBI	Ortholog
Canis lupus familiaris (dog):	TXK (TXK tyrosine kinase)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Txk (TXK tyrosine kinase)	NCBI	Ortholog
Sus scrofa (pig):	TXK (TXK tyrosine kinase)	HGNC	Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	TXK (TXK tyrosine kinase)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Txk (TXK tyrosine kinase)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Stimate (STIM activating enhancer)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Txk (TXK tyrosine kinase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Txk (TXK tyrosine kinase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	txk (TXK tyrosine kinase)	Alliance	DIOPT (OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Drosophila melanogaster (fruit fly):	Btk29A	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	48,066,393 - 48,134,250 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	48,063,158 - 48,134,250 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	48,068,410 - 48,136,267 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	47,763,167 - 47,831,030 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	47,909,688 - 47,977,201	NCBI
Celera	4	48,517,268 - 48,584,988 (-)	NCBI		Celera
Cytogenetic Map	4	p12	NCBI
HuRef	4	47,388,494 - 47,456,038 (-)	NCBI		HuRef
CHM1_1	4	48,067,554 - 48,135,380 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	48,033,459 - 48,101,082 (-)	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)
TXK	Human	1,2-dichloroethane	decreases expression	ISO	RGD:1315123	6480464	ethylene dichloride results in decreased expression of TXK mRNA	CTD	PMID:28960355
TXK	Human	1,2-dimethylhydrazine	decreases expression	ISO	RGD:1315123	6480464	1,2-Dimethylhydrazine results in decreased expression of TXK mRNA	CTD	PMID:22206623
TXK	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	RGD:1315123	6480464	Tetrachlorodibenzodioxin results in decreased expression of TXK mRNA	CTD	PMID:23238561
TXK	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	RGD:1306481	6480464	Tetrachlorodibenzodioxin affects the expression of TXK mRNA	CTD	PMID:34747641
TXK	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	RGD:1306481	6480464	Tetrachlorodibenzodioxin results in increased expression of TXK mRNA	CTD	PMID:23238561\|PMID:33387578
TXK	Human	2,4-dibromophenyl 2,4,5-tribromophenyl ether	affects expression	ISO	RGD:1315123	6480464	2,2',4,4',5-brominated diphenyl ether affects the expression of TXK mRNA	CTD	PMID:38648751
TXK	Human	acetamide	increases expression	ISO	RGD:1306481	6480464	acetamide results in increased expression of TXK mRNA	CTD	PMID:31881176
TXK	Human	aflatoxin M1	decreases expression	EXP		6480464	Aflatoxin M1 results in decreased expression of TXK mRNA	CTD	PMID:30928695
TXK	Human	all-trans-retinoic acid	increases expression	EXP		6480464	Tretinoin results in increased expression of TXK mRNA	CTD	PMID:21934132\|PMID:23830798\|PMID:33167477
TXK	Human	alpha-Zearalanol	increases expression	ISO	RGD:1306481	6480464	Zeranol results in increased expression of TXK mRNA	CTD	PMID:35163327
TXK	Human	benzo[a]pyrene	decreases expression	ISO	RGD:1315123	6480464	Benzo(a)pyrene results in decreased expression of TXK mRNA	CTD	PMID:21569818
TXK	Human	bisphenol A	increases expression	ISO	RGD:1315123	6480464	bisphenol A results in increased expression of TXK mRNA	CTD	PMID:26063408
TXK	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of TXK gene	CTD	PMID:31601247
TXK	Human	bisphenol A	increases expression	ISO	RGD:1306481	6480464	bisphenol A results in increased expression of TXK mRNA	CTD	PMID:25181051
TXK	Human	carbon nanotube	decreases expression	ISO	RGD:1315123	6480464	Nanotubes, Carbon analog results in decreased expression of TXK mRNA; Nanotubes, Carbon results in decreased more ...	CTD	PMID:25554681
TXK	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to TXK gene]	CTD	PMID:28238834
TXK	Human	dimethylarsinic acid	multiple interactions	ISO	RGD:1315123	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results more ...	CTD	PMID:34876320
TXK	Human	diquat	decreases expression	ISO	RGD:1315123	6480464	Diquat results in decreased expression of TXK mRNA	CTD	PMID:36851058
TXK	Human	endosulfan	increases expression	ISO	RGD:1306481	6480464	Endosulfan results in increased expression of TXK mRNA	CTD	PMID:29391264
TXK	Human	formaldehyde	decreases expression	EXP		6480464	Formaldehyde results in decreased expression of TXK mRNA	CTD	PMID:18849615
TXK	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in decreased methylation of TXK gene	CTD	PMID:31601247
TXK	Human	furan	increases methylation	ISO	RGD:1306481	6480464	furan results in increased methylation of TXK gene	CTD	PMID:22079235
TXK	Human	genistein	decreases expression	ISO	RGD:1315123	6480464	Genistein results in decreased expression of TXK mRNA	CTD	PMID:32186404
TXK	Human	gentamycin	increases expression	ISO	RGD:1306481	6480464	Gentamicins results in increased expression of TXK mRNA	CTD	PMID:22061828\|PMID:33387578
TXK	Human	GW 4064	decreases expression	ISO	RGD:1315123	6480464	GW 4064 results in decreased expression of TXK mRNA	CTD	PMID:26655953
TXK	Human	imidacloprid	increases expression	ISO	RGD:1306481	6480464	imidacloprid results in increased expression of TXK mRNA	CTD	PMID:27782041
TXK	Human	isotretinoin	increases expression	EXP		6480464	Isotretinoin results in increased expression of TXK mRNA	CTD	PMID:18769122
TXK	Human	isotretinoin	multiple interactions	EXP		6480464	[vorinostat co-treated with Isotretinoin] results in increased expression of TXK mRNA	CTD	PMID:18769122
TXK	Human	methapyrilene	increases expression	ISO	RGD:1306481	6480464	Methapyrilene results in increased expression of TXK mRNA	CTD	PMID:30467583
TXK	Human	methylarsonic acid	multiple interactions	ISO	RGD:1315123	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results more ...	CTD	PMID:34876320
TXK	Human	mono(2-ethylhexyl) phthalate	increases expression	ISO	RGD:1306481	6480464	mono-(2-ethylhexyl)phthalate results in increased expression of TXK mRNA	CTD	PMID:16809437
TXK	Human	nickel atom	increases expression	EXP		6480464	Nickel results in increased expression of TXK mRNA	CTD	PMID:24768652\|PMID:25583101
TXK	Human	okadaic acid	increases expression	EXP		6480464	Okadaic Acid results in increased expression of TXK mRNA	CTD	PMID:38832940
TXK	Human	oxaliplatin	multiple interactions	ISO	RGD:1306481	6480464	[oxaliplatin co-treated with Topotecan] results in increased expression of TXK mRNA	CTD	PMID:25729387
TXK	Human	paracetamol	increases expression	EXP		6480464	Acetaminophen results in increased expression of TXK mRNA	CTD	PMID:26690555
TXK	Human	pirinixic acid	increases expression	ISO	RGD:1315123	6480464	pirinixic acid results in increased expression of TXK mRNA	CTD	PMID:20813756
TXK	Human	S-nitrosoglutathione	decreases expression	EXP		6480464	S-Nitrosoglutathione results in decreased expression of TXK mRNA	CTD	PMID:38825487
TXK	Human	silicon dioxide	increases expression	ISO	RGD:1315123	6480464	Silicon Dioxide results in increased expression of TXK mRNA	CTD	PMID:29341224
TXK	Human	sodium arsenate	multiple interactions	ISO	RGD:1315123	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results more ...	CTD	PMID:34876320
TXK	Human	sodium arsenite	multiple interactions	ISO	RGD:1315123	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results more ...	CTD	PMID:34876320
TXK	Human	sodium arsenite	decreases expression	ISO	RGD:1315123	6480464	sodium arsenite results in decreased expression of TXK mRNA	CTD	PMID:37682722
TXK	Human	sotorasib	multiple interactions	EXP		6480464	[sotorasib co-treated with trametinib co-treated with NVP-BKM120] results in decreased expression of TXK mRNA	CTD	PMID:36139627
TXK	Human	titanium dioxide	decreases expression	ISO	RGD:1315123	6480464	titanium dioxide results in decreased expression of TXK mRNA	CTD	PMID:27760801\|PMID:29264374
TXK	Human	titanium dioxide	increases expression	ISO	RGD:1315123	6480464	titanium dioxide results in increased expression of TXK mRNA	CTD	PMID:23557971
TXK	Human	topotecan	multiple interactions	ISO	RGD:1306481	6480464	[oxaliplatin co-treated with Topotecan] results in increased expression of TXK mRNA	CTD	PMID:25729387
TXK	Human	trametinib	multiple interactions	EXP		6480464	[sotorasib co-treated with trametinib co-treated with NVP-BKM120] results in decreased expression of TXK mRNA	CTD	PMID:36139627
TXK	Human	trichloroethene	increases expression	ISO	RGD:1306481	6480464	Trichloroethylene results in increased expression of TXK mRNA	CTD	PMID:33387578
TXK	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of TXK mRNA	CTD	PMID:37042841
TXK	Human	vorinostat	multiple interactions	EXP		6480464	[vorinostat co-treated with Isotretinoin] results in increased expression of TXK mRNA	CTD	PMID:18769122

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)
TXK	Human	adaptive immune response	involved_in	IEA	UniProtKB-KW:KW-1064	150520179		UniProt	GO_REF:0000043
TXK	Human	adaptive immune response	involved_in	IBA	MGI:102960\|MGI:88216\|MGI:96621\|PANTHER:PTN000700360	150520179		GO_Central	GO_REF:0000033
TXK	Human	adaptive immune response	involved_in	ISS	UniProtKB:P42682	150520179		UniProt	GO_REF:0000024
TXK	Human	immune system process	involved_in	IEA	UniProtKB-KW:KW-0391	150520179		UniProt	GO_REF:0000043
TXK	Human	NK T cell differentiation	acts_upstream_of_or_within	ISO	MGI:96621	9068941	PMID:18292523	MGI	PMID:18292523
TXK	Human	positive regulation of cytokine production	involved_in	ISS	UniProtKB:P42682	150520179		UniProt	GO_REF:0000024
TXK	Human	positive regulation of transcription by RNA polymerase II	involved_in	IDA		150520179	PMID:11859127	NTNU_SB	PMID:11859127
TXK	Human	positive regulation of type II interferon production	involved_in	IDA		150520179	PMID:10523612, PMID:11859127	UniProt	PMID:10523612\|PMID:11859127
TXK	Human	positive regulation of type II interferon-mediated signaling pathway	involved_in	IDA		150520179	PMID:11859127	UniProt	PMID:11859127
TXK	Human	protein autophosphorylation	involved_in	IDA		150520179	PMID:12081135, PMID:17177976	UniProt	PMID:12081135\|PMID:17177976
TXK	Human	protein phosphorylation	involved_in	IDA		150520179	PMID:17177976	UniProt	PMID:17177976
TXK	Human	regulation of gene expression	involved_in	IDA		150520179	PMID:11859127	GO_Central	PMID:11859127
TXK	Human	T cell receptor signaling pathway	involved_in	ISS	UniProtKB:P42682	150520179		UniProt	GO_REF:0000024
TXK	Human	T cell receptor signaling pathway	involved_in	IBA	MGI:102960\|MGI:96621\|PANTHER:PTN000700360	150520179		GO_Central	GO_REF:0000033

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
TXK	Human	cytoplasm	located_in	IDA		150520179	PMID:10523612, PMID:17177976	UniProt	PMID:10523612\|PMID:17177976
TXK	Human	cytoplasm	located_in	IEA	UniProtKB-KW:KW-0963	150520179		UniProt	GO_REF:0000043
TXK	Human	cytoplasm	located_in	IEA	UniProtKB-SubCell:SL-0086	150520179		UniProt	GO_REF:0000044
TXK	Human	cytosol	located_in	IEA	ARBA:ARBA00029243	150520179		UniProt	GO_REF:0000117
TXK	Human	cytosol	located_in	IDA		150520179		HPA	GO_REF:0000052
TXK	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
TXK	Human	nucleolus	located_in	IDA		150520179		HPA	GO_REF:0000052
TXK	Human	nucleoplasm	located_in	IDA		150520179		HPA	GO_REF:0000052
TXK	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043
TXK	Human	nucleus	located_in	IDA		150520179	PMID:10523612, PMID:17177976	UniProt	PMID:10523612\|PMID:17177976
TXK	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
TXK	Human	plasma membrane	located_in	IEA	UniProtKB-SubCell:SL-0039	150520179		UniProt	GO_REF:0000044
TXK	Human	plasma membrane	is_active_in	IBA	FB:FBgn0000017\|FB:FBgn0000723\|FB:FBgn0003502\|MGI:1858308\|MGI:87860\|MGI:95481\|MGI:95527\|MGI:95602\|MGI:96892\|MGI:98397\|MGI:99147\|MGI:99515\|MGI:99613\|PANTHER:PTN002521457\|RGD:3443\|RGD:620795\|RGD:621017\|RGD:628758\|UniProtKB:P00523\|UniProtKB:P06239\|UniProtKB:P06241\|UniProtKB:P07332\|UniProtKB:P07947\|UniProtKB:P07948\|UniProtKB:P08631\|UniProtKB:P09769\|UniProtKB:P12931\|UniProtKB:P16591\|UniProtKB:P41240\|UniProtKB:P42680\|UniProtKB:P42681\|UniProtKB:P43403\|UniProtKB:P43405\|UniProtKB:P51813\|UniProtKB:Q00944\|UniProtKB:Q06187\|UniProtKB:Q07912\|UniProtKB:Q13882\|UniProtKB:Q6J9G0\|WB:WBGene00000812\|WB:WBGene00001487\|WB:WBGene00004962\|WB:WBGene00005077	150520179		GO_Central	GO_REF:0000033
TXK	Human	plasma membrane	located_in	IEA	UniProtKB-KW:KW-1003	150520179		UniProt	GO_REF:0000043
TXK	Human	plasma membrane	located_in	IDA		150520179		HPA	GO_REF:0000052

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)
TXK	Human	ATP binding	enables	IEA	UniProtKB-KW:KW-0067	150520179		UniProt	GO_REF:0000043
TXK	Human	ATP binding	enables	IEA	UniRule:UR001503341	150520179		UniProt	GO_REF:0000104
TXK	Human	ATP binding	enables	IEA	InterPro:IPR000719\|InterPro:IPR017441	150520179		InterPro	GO_REF:0000002
TXK	Human	kinase activity	enables	IEA	UniProtKB-KW:KW-0418	150520179		UniProt	GO_REF:0000043
TXK	Human	non-membrane spanning protein tyrosine kinase activity	enables	IEA	EC:2.7.10.2	150520179		UniProt	GO_REF:0000003
TXK	Human	non-membrane spanning protein tyrosine kinase activity	enables	IBA	PANTHER:PTN001231474\|UniProtKB:P42680\|UniProtKB:P51813\|UniProtKB:Q06187\|UniProtKB:Q08881	150520179		GO_Central	GO_REF:0000033
TXK	Human	nucleotide binding	enables	IEA	UniProtKB-KW:KW-0547	150520179		UniProt	GO_REF:0000043
TXK	Human	nucleotide binding	enables	IEA	UniRule:UR001503341	150520179		UniProt	GO_REF:0000104
TXK	Human	protein binding	enables	IPI	UniProtKB:P09874\|UniProtKB:P68104	150520179	PMID:17177976	UniProt	PMID:17177976
TXK	Human	protein binding	enables	IPI	UniProtKB:O14543\|UniProtKB:O14544\|UniProtKB:O43639\|UniProtKB:O60496\|UniProtKB:O75564-2\|UniProtKB:P27986-2\|UniProtKB:P46108\|UniProtKB:P62993\|UniProtKB:Q13322-4\|UniProtKB:Q13422-7\|UniProtKB:Q16828\|UniProtKB:Q3KQV3\|UniProtKB:Q5JST6\|UniProtKB:Q8IZW8\|UniProtKB:Q8NA61-2\|UniProtKB:Q96SQ5\|UniProtKB:Q9GZV8\|UniProtKB:Q9H2S9\|UniProtKB:Q9NYW8\|UniProtKB:Q9UGK3\|UniProtKB:Q9Y2P0	150520179	PMID:32296183	IntAct	PMID:32296183
TXK	Human	protein binding	enables	IPI	UniProtKB:P10721	150520179	PMID:24728074	IntAct	PMID:24728074
TXK	Human	protein kinase activity	enables	IEA	InterPro:IPR000719\|InterPro:IPR001245\|InterPro:IPR008266	150520179		InterPro	GO_REF:0000002
TXK	Human	protein tyrosine kinase activity	enables	IEA	UniProtKB-KW:KW-0829	150520179		UniProt	GO_REF:0000043
TXK	Human	protein tyrosine kinase activity	enables	IEA	RHEA:10596	150520179		RHEA	GO_REF:0000116
TXK	Human	protein tyrosine kinase activity	enables	IEA	InterPro:IPR020635	150520179		InterPro	GO_REF:0000002
TXK	Human	transferase activity	enables	IEA	UniProtKB-KW:KW-0808	150520179		UniProt	GO_REF:0000043

#	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:7528718	PMID:7951233	PMID:8632917	PMID:8702662	PMID:9047237	PMID:9813138	PMID:10523612	PMID:10587356	PMID:10660534	PMID:11353545	PMID:11859127	PMID:12081135
PMID:12477932	PMID:14684750	PMID:15175272	PMID:16273093	PMID:16344560	PMID:16809408	PMID:17177976	PMID:18941202	PMID:19913121	PMID:20379614	PMID:20628086	PMID:20800603
PMID:21873635	PMID:22623531	PMID:22973453	PMID:23128233	PMID:24728074	PMID:25593320	PMID:25814554	PMID:31586073	PMID:32296183	PMID:33961781	PMID:39085785

TXK
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	48,066,393 - 48,134,250 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	48,063,158 - 48,134,250 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	48,068,410 - 48,136,267 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	47,763,167 - 47,831,030 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	47,909,688 - 47,977,201	NCBI
Celera	4	48,517,268 - 48,584,988 (-)	NCBI		Celera
Cytogenetic Map	4	p12	NCBI
HuRef	4	47,388,494 - 47,456,038 (-)	NCBI		HuRef
CHM1_1	4	48,067,554 - 48,135,380 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	48,033,459 - 48,101,082 (-)	NCBI		T2T-CHM13v2.0

Txk
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	72,853,321 - 72,910,337 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	72,853,321 - 72,910,120 (-)	Ensembl		GRCm39 Ensembl
GRCm38	5	72,695,978 - 72,752,992 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	72,695,978 - 72,752,777 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	73,087,217 - 73,144,012 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	72,975,117 - 73,015,737 (-)	NCBI		MGSCv36	mm8
Celera	5	69,944,742 - 70,002,864 (-)	NCBI		Celera
Cytogenetic Map	5	C3.2	NCBI
cM Map	5	38.44	NCBI

Txk
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	14	35,817,270 - 35,873,454 (+)	NCBI		GRCr8
mRatBN7.2	14	35,463,369 - 35,519,448 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	14	35,463,944 - 35,519,448 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	14	35,828,243 - 35,884,548 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	14	37,132,987 - 37,189,292 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	14	35,621,349 - 35,677,656 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	14	38,029,809 - 38,085,822 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	14	38,030,189 - 38,085,919 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	14	37,840,106 - 37,896,117 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	14	37,867,565 - 37,923,075 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	14	37,870,891 - 37,926,425 (+)	NCBI
Celera	14	34,718,226 - 34,773,309 (+)	NCBI		Celera
Cytogenetic Map	14	p11	NCBI

Txk
(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_004955443	474,099 - 556,697 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955443	474,099 - 556,697 (+)	NCBI	ChiLan1.0	ChiLan1.0

TXK
(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	79,730,977 - 79,801,494 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	4	79,992,362 - 80,063,009 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	4	74,039,292 - 74,086,744 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	4	84,750,804 - 84,818,671 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	4	84,750,804 - 84,818,671 (+)	Ensembl	panpan1.1		panPan2

TXK
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	13	43,911,881 - 43,977,499 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	13	43,914,534 - 43,976,655 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	13	43,865,388 - 43,929,029 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	13	44,512,768 - 44,576,339 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	13	44,514,039 - 44,576,331 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	13	44,190,147 - 44,253,820 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	13	43,722,001 - 43,785,908 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	13	44,605,279 - 44,668,806 (-)	NCBI		UU_Cfam_GSD_1.0

Txk
(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	32,066,522 - 32,108,331 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936482	14,190,409 - 14,245,943 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936482	14,190,409 - 14,231,690 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

TXK
(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	37,977,986 - 38,046,933 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	8	37,977,222 - 38,047,876 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	8	40,028,569 - 40,096,747 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

TXK
(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	2,120,429 - 2,186,950 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	27	2,140,685 - 2,190,398 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666047	48,133,664 - 48,203,278 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Txk
(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_004624761	18,841,795 - 18,897,458 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624761	18,841,795 - 18,897,564 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in TXK
49 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 4p13-q13.1(chr4:44356201-62245882)x3	copy number gain	See cases [RCV000050683]	Chr4:44356201..62245882 [GRCh38] Chr4:44358218..63111600 [GRCh37] Chr4:44052975..62794195 [NCBI36] Chr4:4p13-q13.1	pathogenic
GRCh38/hg38 4p13-11(chr4:44577678-49081273)x3	copy number gain	See cases [RCV000051770]	Chr4:44577678..49081273 [GRCh38] Chr4:44579695..49083290 [GRCh37] Chr4:44274452..48778047 [NCBI36] Chr4:4p13-11	pathogenic
NM_003328.2(TXK):c.956+2609C>A	single nucleotide variant	Lung cancer [RCV000094862]	Chr4:48083857 [GRCh38] Chr4:48085874 [GRCh37] Chr4:4p12	uncertain significance
GRCh38/hg38 4p14-11(chr4:40496476-49579850)x3	copy number gain	See cases [RCV000134946]	Chr4:40496476..49579850 [GRCh38] Chr4:40498493..49581867 [GRCh37] Chr4:40193250..49276624 [NCBI36] Chr4:4p14-11	pathogenic
GRCh38/hg38 4p12-11(chr4:47383124-48851860)x3	copy number gain	See cases [RCV000138576]	Chr4:47383124..48851860 [GRCh38] Chr4:47385141..48853877 [GRCh37] Chr4:47079898..48548634 [NCBI36] Chr4:4p12-11	uncertain significance
GRCh37/hg19 4p14-11(chr4:38532827-49064044)x3	copy number gain	See cases [RCV000240190]	Chr4:38532827..49064044 [GRCh37] Chr4:4p14-11	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 4p16.3-11(chr4:68345-49089361)x3	copy number gain	See cases [RCV002292704]	Chr4:68345..49089361 [GRCh37] Chr4:4p16.3-11	pathogenic
GRCh37/hg19 4p16.3-11(chr4:68345-49093788)x3	copy number gain	See cases [RCV000446451]	Chr4:68345..49093788 [GRCh37] Chr4:4p16.3-11	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-q35.2(chr4:68346-190957473)	copy number gain	See cases [RCV000510453]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
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
NM_003328.3(TXK):c.836G>A (p.Ser279Asn)	single nucleotide variant	not specified [RCV004331881]	Chr4:48086586 [GRCh38] Chr4:48088603 [GRCh37] Chr4:4p12	uncertain significance
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 4p12(chr4:47828849-48182073)x1	copy number loss	not provided [RCV000682399]	Chr4:47828849..48182073 [GRCh37] Chr4:4p12	uncertain significance
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 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 4p12-11(chr4:47951905-48323818)x3	copy number gain	not provided [RCV000849578]	Chr4:47951905..48323818 [GRCh37] Chr4:4p12-11	uncertain significance
GRCh37/hg19 4p12-11(chr4:45868775-48273513)x3	copy number gain	Autism [RCV000993707]	Chr4:45868775..48273513 [GRCh37] Chr4:4p12-11	likely 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
NM_003328.3(TXK):c.877C>T (p.His293Tyr)	single nucleotide variant	not specified [RCV004098708]	Chr4:48086545 [GRCh38] Chr4:48088562 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.562G>A (p.Val188Ile)	single nucleotide variant	not specified [RCV004189867]	Chr4:48095162 [GRCh38] Chr4:48097179 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1543G>A (p.Glu515Lys)	single nucleotide variant	not specified [RCV004154256]	Chr4:48067678 [GRCh38] Chr4:48069695 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.958A>C (p.Lys320Gln)	single nucleotide variant	not specified [RCV004133337]	Chr4:48080127 [GRCh38] Chr4:48082144 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.793G>A (p.Glu265Lys)	single nucleotide variant	not specified [RCV004247185]	Chr4:48086629 [GRCh38] Chr4:48088646 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1061A>C (p.Tyr354Ser)	single nucleotide variant	not specified [RCV004213232]	Chr4:48080024 [GRCh38] Chr4:48082041 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.639G>T (p.Trp213Cys)	single nucleotide variant	not specified [RCV004135448]	Chr4:48094147 [GRCh38] Chr4:48096164 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.683T>A (p.Ile228Asn)	single nucleotide variant	not specified [RCV004150456]	Chr4:48094103 [GRCh38] Chr4:48096120 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.514G>T (p.Ala172Ser)	single nucleotide variant	not specified [RCV004079888]	Chr4:48095210 [GRCh38] Chr4:48097227 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.959A>G (p.Lys320Arg)	single nucleotide variant	not specified [RCV004116516]	Chr4:48080126 [GRCh38] Chr4:48082143 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1180A>G (p.Arg394Gly)	single nucleotide variant	not specified [RCV004103837]	Chr4:48076460 [GRCh38] Chr4:48078477 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.29A>G (p.Gln10Arg)	single nucleotide variant	not specified [RCV004150325]	Chr4:48114390 [GRCh38] Chr4:48116407 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.665A>G (p.Gln222Arg)	single nucleotide variant	not specified [RCV004083817]	Chr4:48094121 [GRCh38] Chr4:48096138 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1555G>A (p.Ala519Thr)	single nucleotide variant	not specified [RCV004124423]	Chr4:48067666 [GRCh38] Chr4:48069683 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.367A>G (p.Arg123Gly)	single nucleotide variant	not specified [RCV004119058]	Chr4:48112320 [GRCh38] Chr4:48114337 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.598A>G (p.Ile200Val)	single nucleotide variant	not specified [RCV004219520]	Chr4:48094188 [GRCh38] Chr4:48096205 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1552C>T (p.Arg518Trp)	single nucleotide variant	not specified [RCV004177653]	Chr4:48067669 [GRCh38] Chr4:48069686 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1426G>A (p.Val476Met)	single nucleotide variant	not specified [RCV004275708]	Chr4:48071606 [GRCh38] Chr4:48073623 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.220C>T (p.Pro74Ser)	single nucleotide variant	not specified [RCV004276286]	Chr4:48112467 [GRCh38] Chr4:48114484 [GRCh37] Chr4:4p12	uncertain significance
GRCh38/hg38 4p16.3-q12(chr4:85624-57073230)x3	copy number gain	Neurodevelopmental disorder [RCV003327613]	Chr4:85624..57073230 [GRCh38] Chr4:4p16.3-q12	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
NM_003328.3(TXK):c.1103T>A (p.Leu368Gln)	single nucleotide variant	not specified [RCV004350690]	Chr4:48079982 [GRCh38] Chr4:48081999 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1414A>C (p.Asn472His)	single nucleotide variant	not specified [RCV004346946]	Chr4:48071618 [GRCh38] Chr4:48073635 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.373C>T (p.Arg125Cys)	single nucleotide variant	not specified [RCV004338594]	Chr4:48112314 [GRCh38] Chr4:48114331 [GRCh37] Chr4:4p12	uncertain significance
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	copy number gain	not provided [RCV003885507]	Chr4:45455621..191003541 [GRCh37] Chr4:4p12-q35.2	pathogenic
NM_003328.3(TXK):c.1187G>A (p.Cys396Tyr)	single nucleotide variant	not specified [RCV004483940]	Chr4:48076453 [GRCh38] Chr4:48078470 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1195A>G (p.Ser399Gly)	single nucleotide variant	not specified [RCV004483941]	Chr4:48076445 [GRCh38] Chr4:48078462 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1264A>G (p.Ser422Gly)	single nucleotide variant	not specified [RCV004483942]	Chr4:48074028 [GRCh38] Chr4:48076045 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1361T>A (p.Val454Asp)	single nucleotide variant	not specified [RCV004483943]	Chr4:48071671 [GRCh38] Chr4:48073688 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1414A>G (p.Asn472Asp)	single nucleotide variant	not specified [RCV004483945]	Chr4:48071618 [GRCh38] Chr4:48073635 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1435A>G (p.Ile479Val)	single nucleotide variant	not specified [RCV004483946]	Chr4:48071597 [GRCh38] Chr4:48073614 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1512T>G (p.His504Gln)	single nucleotide variant	not specified [RCV004483947]	Chr4:48071520 [GRCh38] Chr4:48073537 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.442T>C (p.Tyr148His)	single nucleotide variant	not specified [RCV004483949]	Chr4:48110542 [GRCh38] Chr4:48112559 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.670A>G (p.Ile224Val)	single nucleotide variant	not specified [RCV004483950]	Chr4:48094116 [GRCh38] Chr4:48096133 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.905A>G (p.Asn302Ser)	single nucleotide variant	not specified [RCV004483951]	Chr4:48086517 [GRCh38] Chr4:48088534 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.374G>A (p.Arg125His)	single nucleotide variant	not specified [RCV004683078]	Chr4:48112313 [GRCh38] Chr4:48114330 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.85C>G (p.Gln29Glu)	single nucleotide variant	not specified [RCV004683079]	Chr4:48113296 [GRCh38] Chr4:48115313 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.587C>T (p.Thr196Met)	single nucleotide variant	not specified [RCV004683080]	Chr4:48094199 [GRCh38] Chr4:48096216 [GRCh37] Chr4:4p12	likely benign
NM_003328.3(TXK):c.125A>G (p.Tyr42Cys)	single nucleotide variant	not specified [RCV004683081]	Chr4:48113256 [GRCh38] Chr4:48115273 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1471G>A (p.Ala491Thr)	single nucleotide variant	not specified [RCV004683082]	Chr4:48071561 [GRCh38] Chr4:48073578 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1157A>G (p.Tyr386Cys)	single nucleotide variant	not specified [RCV004881281]	Chr4:48079928 [GRCh38] Chr4:48081945 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.1541C>T (p.Ala514Val)	single nucleotide variant	not specified [RCV004881282]	Chr4:48067680 [GRCh38] Chr4:48069697 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.927G>C (p.Glu309Asp)	single nucleotide variant	not specified [RCV004881284]	Chr4:48086495 [GRCh38] Chr4:48088512 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.148C>G (p.Leu50Val)	single nucleotide variant	not specified [RCV004881285]	Chr4:48113233 [GRCh38] Chr4:48115250 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.839G>A (p.Gly280Asp)	single nucleotide variant	not specified [RCV004881286]	Chr4:48086583 [GRCh38] Chr4:48088600 [GRCh37] Chr4:4p12	uncertain significance
NM_003328.3(TXK):c.871C>T (p.Arg291Trp)	single nucleotide variant	not specified [RCV004881287]	Chr4:48086551 [GRCh38] Chr4:48088568 [GRCh37] Chr4:4p12	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	1491
Count of miRNA genes:	545
Interacting mature miRNAs:	621
Transcripts:	ENST00000264316, ENST00000506073, ENST00000507351, ENST00000509681, ENST00000510457, ENST00000514937
Prediction methods:	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
597054592	GWAS1150666_H	multiple sclerosis QTL GWAS1150666 (human)		1e-11	multiple sclerosis		4	48125245	48125246	Human
597101407	GWAS1197481_H	platelet component distribution width QTL GWAS1197481 (human)		2e-20	platelet size trait (VT:0010457)	platelet distribution width (CMO:0001350)	4	48070143	48070144	Human
597296338	GWAS1392412_H	ceramide measurement QTL GWAS1392412 (human)		1e-09	ceramide measurement		4	48130172	48130173	Human
406968188	GWAS617164_H	platelet component distribution width QTL GWAS617164 (human)		5e-11	platelet size trait (VT:0010457)	platelet distribution width (CMO:0001350)	4	48087441	48087442	Human

D2S2579

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	85,885,392 - 85,885,546	UniSTS	GRCh37
Build 36	2	85,738,903 - 85,739,057	RGD	NCBI36
Celera	2	85,713,691 - 85,713,845	RGD
Cytogenetic Map	2	p12-p11.2	UniSTS
Cytogenetic Map	4	p12	UniSTS
HuRef	2	85,782,717 - 85,782,871	UniSTS
TNG Radiation Hybrid Map	2	53817.0	UniSTS
Stanford-G3 RH Map	2	3925.0	UniSTS
GeneMap99-G3 RH Map	2	4337.0	UniSTS

D4S3133

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	48,069,332 - 48,069,648	UniSTS	GRCh37
Build 36	4	47,764,089 - 47,764,405	RGD	NCBI36
Celera	4	48,518,190 - 48,518,506	RGD
Cytogenetic Map	4	p12	UniSTS
HuRef	4	47,389,416 - 47,389,732	UniSTS
Whitehead-YAC Contig Map	4		UniSTS

SHGC-59740

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	48,088,152 - 48,088,498	UniSTS	GRCh37
Build 36	4	47,782,909 - 47,783,255	RGD	NCBI36
Celera	4	48,537,041 - 48,537,387	RGD
Cytogenetic Map	4	p12	UniSTS
HuRef	4	47,408,201 - 47,408,547	UniSTS
GeneMap99-GB4 RH Map	4	250.48	UniSTS

RH70607

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	48,068,779 - 48,069,001	UniSTS	GRCh37
Build 36	4	47,763,536 - 47,763,758	RGD	NCBI36
Celera	4	48,517,637 - 48,517,859	RGD
Cytogenetic Map	4	p12	UniSTS
HuRef	4	47,388,863 - 47,389,085	UniSTS
GeneMap99-GB4 RH Map	4	250.36	UniSTS

G20621

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	48,068,397 - 48,068,534	UniSTS	GRCh37
Build 36	4	47,763,154 - 47,763,291	RGD	NCBI36
Celera	4	48,517,255 - 48,517,392	RGD
Cytogenetic Map	4	p12	UniSTS
HuRef	4	47,388,481 - 47,388,618	UniSTS

A005Z18

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	48,068,397 - 48,068,534	UniSTS	GRCh37
Build 36	4	47,763,154 - 47,763,291	RGD	NCBI36
Celera	4	48,517,255 - 48,517,392	RGD
Cytogenetic Map	4	p12	UniSTS
HuRef	4	47,388,481 - 47,388,618	UniSTS
GeneMap99-GB4 RH Map	4	249.98	UniSTS

D11S3316

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	10	q11.1	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	7	p15-p14	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	4	p12	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	p12-p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	11	q12-q13.2	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	1	p36.32	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	4	q31.3	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	10	q26.13	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	10	q26.1	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	14	q31	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
1204	2431	2785	2238	4789	1717	2334	5	617	1942	458	2257	7258	6440	52	3564	1	846	1731	1607	170


RefSeq Transcripts	NM_003328	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011513747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011513748	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008582	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454200	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416123	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416125	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350777	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007057955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008487028	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_925166	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC079118	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC096749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH000846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH005334	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC017829	(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
	DB103575	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L27071	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000264316 ⟹ ENSP00000264316

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,066,393 - 48,134,250 (-)	Ensembl

Ensembl Acc Id:

ENST00000506073 ⟹ ENSP00000422798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,063,158 - 48,114,545 (-)	Ensembl

Ensembl Acc Id:

ENST00000507351 ⟹ ENSP00000423481

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,067,161 - 48,080,177 (-)	Ensembl

Ensembl Acc Id:

ENST00000509681 ⟹ ENSP00000424070

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,067,388 - 48,080,178 (-)	Ensembl

Ensembl Acc Id:

ENST00000510457

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,089,385 - 48,134,229 (-)	Ensembl

Ensembl Acc Id:

ENST00000514937 ⟹ ENSP00000422139

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	48,066,677 - 48,080,066 (-)	Ensembl

RefSeq Acc Id:

NM_003328 ⟹ NP_003319

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,134,250 (-)	NCBI
GRCh37	4	48,068,410 - 48,136,273 (-)	ENTREZGENE
Build 36	4	47,763,167 - 47,831,030 (-)	NCBI Archive
HuRef	4	47,388,494 - 47,456,038 (-)	ENTREZGENE
CHM1_1	4	48,067,554 - 48,135,380 (-)	NCBI
T2T-CHM13v2.0	4	48,033,459 - 48,101,082 (-)	NCBI

Sequence:

show sequence

AGTTGAAAGATGTGTTTTTGTGAGTAGAGCACCGCAGAAGAACTGAAGACTGTTGTGTGCTCCCCGCAGAAGGGGCTACCATGATCCTTTCCTCCTATAACACCATCCAGTCGGTTTTCTGTTGCTGC
TGTTGCTGTTCAGTGCAGAAGCGACAAATGAGAACACAGATAAGCCTGAGCACAGATGAAGAGCTTCCAGAAAAATACACCCAGCGTCGCAGGCCGTGGCTCAGCCAATTGTCAAATAAGAAGCAATC
CAACACGGGCCGTGTGCAGCCGTCAAAACGAAAGCCACTGCCTCCCCTCCCACCCTCTGAGGTTGCTGAAGAGAAGATCCAAGTCAAGGCACTTTATGATTTTCTGCCCAGAGAACCCTGTAATTTAG
CCTTAAGGAGAGCAGAAGAATACCTGATACTGGAGAAATACAATCCTCACTGGTGGAAGGCAAGAGACCGTTTGGGGAATGAAGGCTTAATCCCAAGCAACTATGTGACTGAAAACAAAATAACTAAT
TTAGAAATATATGAGTGGTACCATAGAAACATTACCAGAAATCAGGCAGAACATCTATTGAGACAAGAGTCTAAAGAAGGTGCATTTATTGTCAGAGATTCAAGACATTTAGGATCCTACACAATTTC
CGTATTTATGGGAGCTAGAAGAAGTACGGAGGCTGCCATAAAACATTATCAGATAAAAAAGAATGACTCAGGACAGTGGTATGTGGCTGAAAGACACGCCTTTCAATCAATCCCTGAGTTAATCTGGT
ATCACCAGCACAATGCAGCCGGTCTCATGACTCGTCTCCGATATCCAGTTGGGCTGATGGGCAGTTGTTTACCAGCCACAGCTGGGTTTAGCTACGAAAAGTGGGAGATAGATCCATCTGAGTTGGCT
TTTATAAAGGAGATTGGAAGCGGTCAGTTTGGAGTGGTCCATTTAGGTGAATGGCGGTCACATATCCAGGTAGCTATCAAGGCCATCAATGAAGGCTCCATGTCTGAAGAGGATTTCATTGAAGAGGC
CAAAGTGATGATGAAATTATCTCATTCAAAGCTAGTGCAACTTTATGGAGTCTGTATACAGCGGAAGCCCCTTTACATTGTGACAGAGTTCATGGAAAATGGCTGCCTGCTTAACTATCTCAGGGAGA
ATAAAGGAAAGCTTAGGAAGGAAATGCTACTGAGTGTATGCCAGGATATATGTGAAGGAATGGAATATCTGGAGAGGAATGGCTATATTCATAGGGATTTGGCGGCAAGGAATTGTTTGGTCAGTTCA
ACATGCATAGTAAAAATTTCAGACTTTGGAATGACAAGGTACGTTTTGGATGATGAGTATGTCAGTTCTTTTGGAGCCAAGTTCCCAATCAAGTGGTCCCCTCCTGAAGTTTTTCTTTTCAATAAGTA
CAGCAGTAAATCTGATGTCTGGTCATTTGGAGTTTTAATGTGGGAAGTTTTTACAGAAGGAAAAATGCCTTTTGAAAATAAGTCAAATTTGCAAGTCGTGGAAGCTATTTCTGAAGGCTTCAGGCTAT
ATCGCCCTCACCTGGCACCAATGTCCATATATGAAGTCATGTACAGCTGCTGGCATGAGAAACCTGAAGGCCGCCCTACATTTGCCGAGCTGCTGCGGGCTGTCACAGAGATTGCGGAAACCTGGTGA
CCGGAAACAGAATGCCAACCCAAAGAGTCATCTTGCAAAACTGTCATTTATTGTGAATATCTTCACCATATGGGGTCACTTATGGTGAATATCTTTCTTCAGAGTTGCTGACTCTTGAAAACAGTGCA
AAGATCACAGTTTTTAAAAGTTTTAAAAATTTAAGAATATTCACACAATCGTTTTTCTATGTGTGAGAGGGATTTGCACACTCTTATTTTTCTGTAAAATATTTCACATCCCAAATGTGAAGAAGTGA
AAAAGACTTCGCAGCAGTCTTCATTGTGGTGCTCTTCATGATCATAGCCCCAGGAACCCTTGAGGTTCTTCTTCACAAGGCTGAGAGTGCTTCCTTCTTGAAGACGAGTGACATTCATCACTTCAGTG
ATCCATGCATAGAATATGAAAATAAATTCTTCCAACTCATGGGATAAAGGGGACTCCCTTGAAGAATTTCATGTTTTTGGGCTGTATAGCTCTTTACAGAAAATGCACCTTTATAAATCACATGAATG
TTAGTATTCTGGAAATGTCTTTTGTTAATATAATCTTCCCATGTTATTTAACAAATTGTTTTTGCACATATCTGATTATATTGAAAGCAGTTTTTTGCATTCGAGTTTTAAACACTGTTATAAAATGT
AGCCAAAGCTCACCTTTGAACAGATCCCGGTGACATTCTATTTCCAGGAAAATCCGGAACCTGATTTTAGTTCTGTGATTTTACACTTTTTACATGTGAGATTGGACAGTTTCAGAGGCCTTATTTTG
TCATACTAAGTGTCTCCTGTAATTTTCAGGAAGATGATTTGTTCTTTCCAGAAGAGGAGACAAAAGCAAGATAGCCAAATGTGACATCAAGCTCCATTGTTTCGGAAATCCAGGATTTTGAATTCGAG
ATGAAACAACCAGCAATCACAGTTAAATCTTAACTTTGCCTGCACTCTTTGTAGGAATGATCAGAAATTTATCTTTATCATTCTGAGTGCTTCAGGAGTACAATAGGAAGAAAGATACTGGAGAAAGC
ACTAATGTAATCACCATGAAGTCTGACAACAGGAGCCCATTATTTGCGTACTGTCCCACCCTGTATCATGGTTCTCTGGGAACAAGCTTTATGATTCTCATTAGAGTTTATTTGTTGATTGTCAGTAG
TTGCGACTTTTAAATTATATTTCCCCCACTCAAAGAATGGTATCTTTATATATCAATGACATTCAATAAATGTGTATTATTTCTAATGAGAA

hide sequence

RefSeq Acc Id:

XM_011513747 ⟹ XP_011512049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,114,336 (-)	NCBI

Sequence:

show sequence

GGTTTTCTGTTGCTGCTGTTGCTGTTCAGTGCAGAAGCGATGAGGAAATTGAAGATTAGAGAGGTTACATTGCTTACCCAAGGCCACACTATGAAATGGTGGAGCTGGGATTCAAACTCTTGTTCCTA
ATCACTATACCATGTCTATTTATAACAAAAAGACACCATCAAATGAGACAAATGAGAACACAGATAAGCCTGAGCACAGATGAAGAGCTTCCAGAAAAATACACCCAGCGTCGCAGGCCGTGGCTCAG
CCAATTGTCAAATAAGAAGCAATCCAACACGGGCCGTGTGCAGCCGTCAAAACGAAAGCCACTGCCTCCCCTCCCACCCTCTGAGGTTGCTGAAGAGAAGATCCAAGTCAAGGCACTTTATGATTTTC
TGCCCAGAGAACCCTGTAATTTAGCCTTAAGGAGAGCAGAAGAATACCTGATACTGGAGAAATACAATCCTCACTGGTGGAAGGCAAGAGACCGTTTGGGGTGGTACCATAGAAACATTACCAGAAAT
CAGGCAGAACATCTATTGAGACAAGAGTCTAAAGAAGGTGCATTTATTGTCAGAGATTCAAGACATTTAGGATCCTACACAATTTCCGTATTTATGGGAGCTAGAAGAAGTACGGAGGCTGCCATAAA
ACATTATCAGATAAAAAAGAATGACTCAGGACAGTGGTATGTGGCTGAAAGACACGCCTTTCAATCAATCCCTGAGTTAATCTGGTATCACCAGCACAATGCAGCCGGTCTCATGACTCGTCTCCGAT
ATCCAGTTGGGCTGATGGGCAGTTGTTTACCAGCCACAGCTGGGTTTAGCTACGAAAAGTGGGAGATAGATCCATCTGAGTTGGCTTTTATAAAGGAGATTGGAAGCGGTCAGTTTGGAGTGGTCCAT
TTAGGTGAATGGCGGTCACATATCCAGGTAGCTATCAAGGCCATCAATGAAGGCTCCATGTCTGAAGAGGATTTCATTGAAGAGGCCAAAGTGATGATGAAATTATCTCATTCAAAGCTAGTGCAACT
TTATGGAGTCTGTATACAGCGGAAGCCCCTTTACATTGTGACAGAGTTCATGGAAAATGGCTGCCTGCTTAACTATCTCAGGGAGAATAAAGGAAAGCTTAGGAAGGAAATGCTACTGAGTGTATGCC
AGGATATATGTGAAGGAATGGAATATCTGGAGAGGAATGGCTATATTCATAGGGATTTGGCGGCAAGGAATTGTTTGGTCAGTTCAACATGCATAGTAAAAATTTCAGACTTTGGAATGACAAGGTAC
GTTTTGGATGATGAGTATGTCAGTTCTTTTGGAGCCAAGTTCCCAATCAAGTGGTCCCCTCCTGAAGTTTTTCTTTTCAATAAGTACAGCAGTAAATCTGATGTCTGGTCATTTGGAGTTTTAATGTG
GGAAGTTTTTACAGAAGGAAAAATGCCTTTTGAAAATAAGTCAAATTTGCAAGTCGTGGAAGCTATTTCTGAAGGCTTCAGGCTATATCGCCCTCACCTGGCACCAATGTCCATATATGAAGTCATGT
ACAGCTGCTGGCATGAGAAACCTGAAGGCCGCCCTACATTTGCCGAGCTGCTGCGGGCTGTCACAGAGATTGCGGAAACCTGGTGACCGGAAACAGAATGCCAACCCAAAGAGTCATCTTGCAAAACT
GTCATTTATTGTGAATATCTTCACCATATGGGGTCACTTATGGTGAATATCTTTCTTCAGAGTTGCTGACTCTTGAAAACAGTGCAAAGATCACAGTTTTTAAAAGTTTTAAAAATTTAAGAATATTC
ACACAATCGTTTTTCTATGTGTGAGAGGGATTTGCACACTCTTATTTTTCTGTAAAATATTTCACATCCCAAATGTGAAGAAGTGAAAAAGACTTCGCAGCAGTCTTCATTGTGGTGCTCTTCATGAT
CATAGCCCCAGGAACCCTTGAGGTTCTTCTTCACAAGGCTGAGAGTGCTTCCTTCTTGAAGACGAGTGACATTCATCACTTCAGTGATCCATGCATAGAATATGAAAATAAATTCTTCCAACTCATGG
GATAAAGGGGACTCCCTTGAAGAATTTCATGTTTTTGGGCTGTATAGCTCTTTACAGAAAATGCACCTTTATAAATCACATGAATGTTAGTATTCTGGAAATGTCTTTTGTTAATATAATCTTCCCAT
GTTATTTAACAAATTGTTTTTGCACATATCTGATTATATTGAAAGCAGTTTTTTGCATTCGAGTTTTAAACACTGTTATAAAATGTAGCCAAAGCTCACCTTTGAACAGATCCCGGTGACATTCTATT
TCCAGGAAAATCCGGAACCTGATTTTAGTTCTGTGATTTTACACTTTTTACATGTGAGATTGGACAGTTTCAGAGGCCTTATTTTGTCATACTAAGTGTCTCCTGTAATTTTCAGGAAGATGATTTGT
TCTTTCCAGAAGAGGAGACAAAAGCAAGATAGCCAAATGTGACATCAAGCTCCATTGTTTCGGAAATCCAGGATTTTGAATTCGAGATGAAACAACCAGCAATCACAGTTAAATCTTAACTTTGCCTG
CACTCTTTGTAGGAATGATCAGAAATTTATCTTTATCATTCTGAGTGCTTCAGGAGTACAATAGGAAGAAAGATACTGGAGAAAGCACTAATGTAATCACCATGAAGTCTGACAACAGGAGCCCATTA
TTTGCGTACTGTCCCACCCTGTATCATGGTTCTCTGGGAACAAGCTTTATGATTCTCATTAGAGTTTATTTGTTGATTGTCAGTAGTTGCGACTTTTAAATTATATTTCCCCCACTCAAAGAATGGTA
TCTTTATATATCAATGACATTCAATAAATGTGTATTATTTCTAATGAGAATCAGTTACAAGAGGAGACTTGATAGTTCAAGTAGTGGTCTCAGAAATGTTTGGGCTGAATGTGGTGGCTCATGCCTAT
AATCCCAGCACTTTGGGAGGCCAAGGTGGGAAGATAACTTGAGCCCAGTTTGAGACCAGCCTGGGCAACAAAGTGAGATCCTATCTCTATTACAAGAAAAAAGAAAAAAGAAAAAAAAAGCTAGGTGT
AGTGGTGCATGCATGCACGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGCCCAGGAGATCAAGGCTGCAGTGAGCCATGATTGTGCCACTGCACTCCAGCCTGGGTGATAGAGCGAGACCCTGTC
TCAAAAACAGAAACAAGTTTGTATGAGATGCTAGGCTGTTTCTGAGACTATCACACCCCCTTTCCTATGACTCCTGTTACGGTGAGGAAAGACAGAAGGCTGTTATTACTGAGACCTCAATTCACATA
ACATGAATTTACATAAGATAGTCTAGCTCAAGAAGACATGAGACTACTAAACAGCAAAAGCAGATGGAAGGGAGGTTAATATTATGACATAGGAAATAATGTAGTATCAATATATGGCTGCAGTAAGT
TGCCCTTTCCAGGTTTTACTCAGCTTGGAAGTCCCCATTTCTCTCAAAAAGAAAGAAAGAAAAAACCCAGCAAAGCCAAACACTGAAAAGCTAGGACTGAGTATGGAGCATCTGCCATCACTATAGTT
GTACCAGGTACAGAGCAAAGAGTGACACCCAGAGGCAAATCATTCTAAGAGGGCAACAACTATGACAGTGCCTGGCACTTCTAAGAGGGTGCAGCACTTCTAAGGTGCTAGGCAAGCTCTATTCCTTT
TGTTTTAACACCTCGGGAAAATTTGAGGTACCAAATTAGGTACAAGAATAACTGGGGGTATGTCCTAGGTAACTAAGAGTCCAGATAATGTGTGAATTTTGAATGTGCGTGGAAAGAGATTTACCATT
CTTTGTCTAACTAAACAAAAAAGTTTCCTTAAGAGGTAGTCAGCCAGGCACAATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCATCTGAGGTCAGGAGTTAGAGATCAG
CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACGAAAAGTTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTG
GAAGTTGCGGTGAGCTGAGACTGTGCTACTGCCCTCTATCCTGGGTGACAGAGTGAGACTCTGTCAAAAAAAAAAGAGATAGTTATACAAGTTCTCCTGGAAAGGAACTATGTTTTGCAACCAATCTT
AATATTAGTTATTGATATGAGGGTTCTCTGGGTCATTTGAGGTGAGATAGTGCAATATTTAAACAGCTCTGCATAAAAAAATGAATAGGAGGTTTAGGGGTCAATTGTAGAGTCCTAAAAAGGAGAAT
ATAGGAGGTCAACAGACAGCGAGGAGGCTCAGAAAAATGGAAGGAATTTGGAGGCCAAGCGGAATATATAATCAGTGAAAATAACCTTTTGGCAAGAATAGATAAAGGAATTTAGTAAACTTTTTATT
GAAGTGCAATACATGGTACCACCATGGTATTGGGAACATGTTTGGACTGGCAAGCAAACTGATGAGATACAATAGCATTTAGCCTAGCACTAAATTTGCTTAGCTTTATAGTAGGATACAGGACAGGA
AATTAAGCATGCATGATGCTTGGGTCCCTCCTCACCTGCCTAAAGAGCGTGCATGAGCTTGTGGTATTTGGATGAGGTTGTGGTATGTGGGGGTTTGCCTTGATGCAAAGAAGCTTCTATGTGGGTTT
CCCACCAGTCATATAGGCCTACGGTTCACAGGTCTCCCAGCCCCATGTACTGTCCCATAGATTGTAGGTTTCACAGTGCACAAAATGGATGTCTGTCCCTGGTACCCAATATTCCAAATTTATCTTAA
TTTGGGTCATTTACAAGAAACTCGTGCTGGGATAAGACAAACCTAAAATTTCCCAAGCAGGCATAGTTCTGGGAGAAAAATGGTACAGACCTGCTATTAACTCTTTGCTCACACATACATAAAGAAAA
GTACACAAATCATGAGTATGTAACATCATTGATATTGGCAAAGTGAATACATCTCTGTAACCAGACTCAGATCAAGAAATGATACATTCTGGCCAGGTGTGGTGGCTCATGCCTGTAATCTCAGCACT
TTGGCAGGCCAAGGTGGGTGGATCACTTGAGGCCAGGAGTTCGAGACCAGTGTGGCCAACATGGTGAAACCCCACCTCTACTAAACACACATACACACCCACAAATTAGCCAGGTGCAGTGGTACATT
CGTGTAATCCCAGCTACTTGGGAGGCTGAGGTGCACAAGTGAGAATCGCTTGAGCCTGGGAGGCAGATGTTGCAGTGAGCCAAGATGGTGCCACTATACTCCAGCCTGGGCAACAGAGTGAAACTCTG
TCAAAAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAGAAAAGAAAGAAAGAAAACATTCTAGAATTCCAGAAGCCATTCTCATTCCCTATTTAAGTCACTAACCCAAGAGTAATTAATATCCTGAG
TTCCAACACCTTGGATTTGTATGGGTTATTTTTAAACCTTCTATAAATGGAATTTTATGATATGTTTGTTTGATCCACCTATGTTGTATGTAGTTGTATTTCATTTATTCCCATTTCTGCATTGTCTT
GAATTGTACAACTATTTTACATATTTATCTATTCTAATTTCAATGGATATTTGAGTTGTTTCCAATTTTTAACTATTTTTTAAAATTATACTCTAAGTTCAATAAACATACATGTGCATGTGT

hide sequence

RefSeq Acc Id:

XM_011513748 ⟹ XP_011512050

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,095,224 (-)	NCBI

Sequence:

show sequence

CAGTCTAAAGAAGGTGCATTTATTGTCAGAGATTCAAGACATTTAGGATCCTACACAATTTCCGTATTTATGGGAGCTAGAAGGTCTCATGACTCGTCTCCGATATCCAGTTGGGCTGATGGGCAGTT
GTTTACCAGCCACAGCTGGGTTTAGCTACGAAAAGTGGGAGATAGATCCATCTGAGTTGGCTTTTATAAAGGAGATTGGAAGCGGTCAGTTTGGAGTGGTCCATTTAGGTGAATGGCGGTCACATATC
CAGGTAGCTATCAAGGCCATCAATGAAGGCTCCATGTCTGAAGAGGATTTCATTGAAGAGGCCAAAGTGATGATGAAATTATCTCATTCAAAGCTAGTGCAACTTTATGGAGTCTGTATACAGCGGAA
GCCCCTTTACATTGTGACAGAGTTCATGGAAAATGGCTGCCTGCTTAACTATCTCAGGGAGAATAAAGGAAAGCTTAGGAAGGAAATGCTACTGAGTGTATGCCAGGATATATGTGAAGGAATGGAAT
ATCTGGAGAGGAATGGCTATATTCATAGGGATTTGGCGGCAAGGAATTGTTTGGTCAGTTCAACATGCATAGTAAAAATTTCAGACTTTGGAATGACAAGGTACGTTTTGGATGATGAGTATGTCAGT
TCTTTTGGAGCCAAGTTCCCAATCAAGTGGTCCCCTCCTGAAGTTTTTCTTTTCAATAAGTACAGCAGTAAATCTGATGTCTGGTCATTTGGAGTTTTAATGTGGGAAGTTTTTACAGAAGGAAAAAT
GCCTTTTGAAAATAAGTCAAATTTGCAAGTCGTGGAAGCTATTTCTGAAGGCTTCAGGCTATATCGCCCTCACCTGGCACCAATGTCCATATATGAAGTCATGTACAGCTGCTGGCATGAGAAACCTG
AAGGCCGCCCTACATTTGCCGAGCTGCTGCGGGCTGTCACAGAGATTGCGGAAACCTGGTGACCGGAAACAGAATGCCAACCCAAAGAGTCATCTTGCAAAACTGTCATTTATTGTGAATATCTTCAC
CATATGGGGTCACTTATGGTGAATATCTTTCTTCAGAGTTGCTGACTCTTGAAAACAGTGCAAAGATCACAGTTTTTAAAAGTTTTAAAAATTTAAGAATATTCACACAATCGTTTTTCTATGTGTGA
GAGGGATTTGCACACTCTTATTTTTCTGTAAAATATTTCACATCCCAAATGTGAAGAAGTGAAAAAGACTTCGCAGCAGTCTTCATTGTGGTGCTCTTCATGATCATAGCCCCAGGAACCCTTGAGGT
TCTTCTTCACAAGGCTGAGAGTGCTTCCTTCTTGAAGACGAGTGACATTCATCACTTCAGTGATCCATGCATAGAATATGAAAATAAATTCTTCCAACTCATGGGATAAAGGGGACTCCCTTGAAGAA
TTTCATGTTTTTGGGCTGTATAGCTCTTTACAGAAAATGCACCTTTATAAATCACATGAATGTTAGTATTCTGGAAATGTCTTTTGTTAATATAATCTTCCCATGTTATTTAACAAATTGTTTTTGCA
CATATCTGATTATATTGAAAGCAGTTTTTTGCATTCGAGTTTTAAACACTGTTATAAAATGTAGCCAAAGCTCACCTTTGAACAGATCCCGGTGACATTCTATTTCCAGGAAAATCCGGAACCTGATT
TTAGTTCTGTGATTTTACACTTTTTACATGTGAGATTGGACAGTTTCAGAGGCCTTATTTTGTCATACTAAGTGTCTCCTGTAATTTTCAGGAAGATGATTTGTTCTTTCCAGAAGAGGAGACAAAAG
CAAGATAGCCAAATGTGACATCAAGCTCCATTGTTTCGGAAATCCAGGATTTTGAATTCGAGATGAAACAACCAGCAATCACAGTTAAATCTTAACTTTGCCTGCACTCTTTGTAGGAATGATCAGAA
ATTTATCTTTATCATTCTGAGTGCTTCAGGAGTACAATAGGAAGAAAGATACTGGAGAAAGCACTAATGTAATCACCATGAAGTCTGACAACAGGAGCCCATTATTTGCGTACTGTCCCACCCTGTAT
CATGGTTCTCTGGGAACAAGCTTTATGATTCTCATTAGAGTTTATTTGTTGATTGTCAGTAGTTGCGACTTTTAAATTATATTTCCCCCACTCAAAGAATGGTATCTTTATATATCAATGACATTCAA
TAAATGTGTATTATTTCTAATGAGAATCAGTTACAAGAGGAGACTTGATAGTTCAAGTAGTGGTCTCAGAAATGTTTGGGCTGAATGTGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAA
GGTGGGAAGATAACTTGAGCCCAGTTTGAGACCAGCCTGGGCAACAAAGTGAGATCCTATCTCTATTACAAGAAAAAAGAAAAAAGAAAAAAAAAGCTAGGTGTAGTGGTGCATGCATGCACGTAGTC
CCAGCTACTTGGGAGGCTGAGACAGGAGCCCAGGAGATCAAGGCTGCAGTGAGCCATGATTGTGCCACTGCACTCCAGCCTGGGTGATAGAGCGAGACCCTGTCTCAAAAACAGAAACAAGTTTGTAT
GAGATGCTAGGCTGTTTCTGAGACTATCACACCCCCTTTCCTATGACTCCTGTTACGGTGAGGAAAGACAGAAGGCTGTTATTACTGAGACCTCAATTCACATAACATGAATTTACATAAGATAGTCT
AGCTCAAGAAGACATGAGACTACTAAACAGCAAAAGCAGATGGAAGGGAGGTTAATATTATGACATAGGAAATAATGTAGTATCAATATATGGCTGCAGTAAGTTGCCCTTTCCAGGTTTTACTCAGC
TTGGAAGTCCCCATTTCTCTCAAAAAGAAAGAAAGAAAAAACCCAGCAAAGCCAAACACTGAAAAGCTAGGACTGAGTATGGAGCATCTGCCATCACTATAGTTGTACCAGGTACAGAGCAAAGAGTG
ACACCCAGAGGCAAATCATTCTAAGAGGGCAACAACTATGACAGTGCCTGGCACTTCTAAGAGGGTGCAGCACTTCTAAGGTGCTAGGCAAGCTCTATTCCTTTTGTTTTAACACCTCGGGAAAATTT
GAGGTACCAAATTAGGTACAAGAATAACTGGGGGTATGTCCTAGGTAACTAAGAGTCCAGATAATGTGTGAATTTTGAATGTGCGTGGAAAGAGATTTACCATTCTTTGTCTAACTAAACAAAAAAGT
TTCCTTAAGAGGTAGTCAGCCAGGCACAATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCATCTGAGGTCAGGAGTTAGAGATCAGCCTGGCCAACATGGTGAAACCCTG
TCTCTACTAAAAATACGAAAAGTTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAAGTTGCGGTGAGCTGAGACTGT
GCTACTGCCCTCTATCCTGGGTGACAGAGTGAGACTCTGTCAAAAAAAAAAGAGATAGTTATACAAGTTCTCCTGGAAAGGAACTATGTTTTGCAACCAATCTTAATATTAGTTATTGATATGAGGGT
TCTCTGGGTCATTTGAGGTGAGATAGTGCAATATTTAAACAGCTCTGCATAAAAAAATGAATAGGAGGTTTAGGGGTCAATTGTAGAGTCCTAAAAAGGAGAATATAGGAGGTCAACAGACAGCGAGG
AGGCTCAGAAAAATGGAAGGAATTTGGAGGCCAAGCGGAATATATAATCAGTGAAAATAACCTTTTGGCAAGAATAGATAAAGGAATTTAGTAAACTTTTTATTGAAGTGCAATACATGGTACCACCA
TGGTATTGGGAACATGTTTGGACTGGCAAGCAAACTGATGAGATACAATAGCATTTAGCCTAGCACTAAATTTGCTTAGCTTTATAGTAGGATACAGGACAGGAAATTAAGCATGCATGATGCTTGGG
TCCCTCCTCACCTGCCTAAAGAGCGTGCATGAGCTTGTGGTATTTGGATGAGGTTGTGGTATGTGGGGGTTTGCCTTGATGCAAAGAAGCTTCTATGTGGGTTTCCCACCAGTCATATAGGCCTACGG
TTCACAGGTCTCCCAGCCCCATGTACTGTCCCATAGATTGTAGGTTTCACAGTGCACAAAATGGATGTCTGTCCCTGGTACCCAATATTCCAAATTTATCTTAATTTGGGTCATTTACAAGAAACTCG
TGCTGGGATAAGACAAACCTAAAATTTCCCAAGCAGGCATAGTTCTGGGAGAAAAATGGTACAGACCTGCTATTAACTCTTTGCTCACACATACATAAAGAAAAGTACACAAATCATGAGTATGTAAC
ATCATTGATATTGGCAAAGTGAATACATCTCTGTAACCAGACTCAGATCAAGAAATGATACATTCTGGCCAGGTGTGGTGGCTCATGCCTGTAATCTCAGCACTTTGGCAGGCCAAGGTGGGTGGATC
ACTTGAGGCCAGGAGTTCGAGACCAGTGTGGCCAACATGGTGAAACCCCACCTCTACTAAACACACATACACACCCACAAATTAGCCAGGTGCAGTGGTACATTCGTGTAATCCCAGCTACTTGGGAG
GCTGAGGTGCACAAGTGAGAATCGCTTGAGCCTGGGAGGCAGATGTTGCAGTGAGCCAAGATGGTGCCACTATACTCCAGCCTGGGCAACAGAGTGAAACTCTGTCAAAAAAAGAAAAAGAAAAAGAA
AAAGAAAAAGAAAAGAAAAGAAAGAAAGAAAACATTCTAGAATTCCAGAAGCCATTCTCATTCCCTATTTAAGTCACTAACCCAAGAGTAATTAATATCCTGAGTTCCAACACCTTGGATTTGTATGG
GTTATTTTTAAACCTTCTATAAATGGAATTTTATGATATGTTTGTTTGATCCACCTATGTTGTATGTAGTTGTATTTCATTTATTCCCATTTCTGCATTGTCTTGAATTGTACAACTATTTTACATAT
TTATCTATTCTAATTTCAATGGATATTTGAGTTGTTTCCAATTTTTAACTATTTTTTAAAATTATACTCTAAGTTCAATAAACATACATGTGCATGTGT

hide sequence

RefSeq Acc Id:

XM_017008581 ⟹ XP_016864070

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,134,250 (-)	NCBI

Sequence:

show sequence

CTGCATAATATTCCACGGTGTATATGTACCACATTTTCTTTATCCAGCCTATCATTGATGGGCATTTTGGTTGCTAACCATGCACAACTTTTAACTGACTTGTAGCTCATTGAAGGAGTCGGTCCTGG
CACACTCTACCTTACTATCACTGTCAGCCTTTTCTCCTTCCTTCCTGACCTTCCCTCCTCCCATCCCATACTTCCCTTTTCACCTTGAGGAGCTACGGGAAGTACTAGGTGGTATGAAAGAGAGTGAG
GAGAAGATAGAGTCCCTGTCCTAATGGTCAGTGTATGCTTTTTATGGGAAAACAAGATAGATAGCACCTGGCAACATTTGTCAACATTTCCTTCAAAAATCTTTAAATATTTTTCACTAAGACTTAGA
AAAAAAGTTTTATACGAAAGCATAACAAAGGCAAAAGGTGAAGTAAAAATAACAGTCATCACCCAGAATGCTAAGGAGACCTTAATCTAAACCAGGAAATTGGAAGGGCGATTAGAATATGCTGTGTC
TTCATTAAAGTTGCTCTGTTAATTAGTTGACACATGGTTATGCTTTCCAGTGGGATGAAGTGAAACTCCCAAGTGTGTTTTGTATTGTTGGTGTTTTTATATTTCTCAGCCATCCCCCAATCACATTT
TAGGGTTATTACTAGATTGACTTCCCCCAAATAAAGTGTCTGCTGAGTGGGAGGATGGAACATTCTAAACTCAATATTCCAGAGCCTAGAATCTAATTGTTTCTGCCACTCACGGTGTGGCCTTGGGC
AAGTCCCTTATTCTGTCTGTGCCTTCATTTCCTTCCCAGTCCAGAGAGGGCAGTTTGATTTGATAATTTTAAAGGTGCCTTTTACCAAAATTTTGTGATTTCTTGAAAATGATGTTTGCGAGTCACCC
ACACCTTTGGGGATGAGAGACTAATAGCAGATACCCTCAGAGATTGGGATGGAGATTACTGAGCTTTCTTATATATGCCATTGGTTGTCATTTATACTCTTCTGAGGTTTTCAGAACAGGAAAATAGG
TGGGGTTAACTCTGCCCGTGAGAAACATCTTGAGCGAACTATGATTTCAGTTGAAAGATGTGTTTTTGTGAGTAGAGCACCGCAGAAGAACTGAAGACTGTTGTGTGCTCCCCGCAGAAGGGGCTACC
ATGATCCTTTCCTCCTACAAATGAGAACACAGATAAGCCTGAGCACAGATGAAGAGCTTCCAGAAAAATACACCCAGCGTCGCAGGCCGTGGCTCAGCCAATTGTCAAATAAGAAGCAATCCAACACG
GGCCGTGTGCAGCCGTCAAAACGAAAGCCACTGCCTCCCCTCCCACCCTCTGAGGTTGCTGAAGAGAAGATCCAAGTCAAGGCACTTTATGATTTTCTGCCCAGAGAACCCTGTAATTTAGCCTTAAG
GAGAGCAGAAGAATACCTGATACTGGAGAAATACAATCCTCACTGGTGGAAGGCAAGAGACCGTTTGGGGAATGAAGGCTTAATCCCAAGCAACTATGTGACTGAAAACAAAATAACTAATTTAGAAA
TATATGAGTGGTACCATAGAAACATTACCAGAAATCAGGCAGAACATCTATTGAGACAAGAGTCTAAAGAAGGTGCATTTATTGTCAGAGATTCAAGACATTTAGGATCCTACACAATTTCCGTATTT
ATGGGAGCTAGAAGAAGTACGGAGGCTGCCATAAAACATTATCAGATAAAAAAGAATGACTCAGGACAGTGGTATGTGGCTGAAAGACACGCCTTTCAATCAATCCCTGAGTTAATCTGGTATCACCA
GCACAATGCAGCCGGTCTCATGACTCGTCTCCGATATCCAGTTGGGCTGATGGGCAGTTGTTTACCAGCCACAGCTGGGTTTAGCTACGAAAAGTGGGAGATAGATCCATCTGAGTTGGCTTTTATAA
AGGAGATTGGAAGCGGTCAGTTTGGAGTGGTCCATTTAGGTGAATGGCGGTCACATATCCAGGTAGCTATCAAGGCCATCAATGAAGGCTCCATGTCTGAAGAGGATTTCATTGAAGAGGCCAAAGTG
ATGATGAAATTATCTCATTCAAAGCTAGTGCAACTTTATGGAGTCTGTATACAGCGGAAGCCCCTTTACATTGTGACAGAGTTCATGGAAAATGGCTGCCTGCTTAACTATCTCAGGGAGAATAAAGG
AAAGCTTAGGAAGGAAATGCTACTGAGTGTATGCCAGGATATATGTGAAGGAATGGAATATCTGGAGAGGAATGGCTATATTCATAGGGATTTGGCGGCAAGGAATTGTTTGGTCAGTTCAACATGCA
TAGTAAAAATTTCAGACTTTGGAATGACAAGGTACGTTTTGGATGATGAGTATGTCAGTTCTTTTGGAGCCAAGTTCCCAATCAAGTGGTCCCCTCCTGAAGTTTTTCTTTTCAATAAGTACAGCAGT
AAATCTGATGTCTGGTCATTTGGAGTTTTAATGTGGGAAGTTTTTACAGAAGGAAAAATGCCTTTTGAAAATAAGTCAAATTTGCAAGTCGTGGAAGCTATTTCTGAAGGCTTCAGGCTATATCGCCC
TCACCTGGCACCAATGTCCATATATGAAGTCATGTACAGCTGCTGGCATGAGAAACCTGAAGGCCGCCCTACATTTGCCGAGCTGCTGCGGGCTGTCACAGAGATTGCGGAAACCTGGTGACCGGAAA
CAGAATGCCAACCCAAAGAGTCATCTTGCAAAACTGTCATTTATTGTGAATATCTTCACCATATGGGGTCACTTATGGTGAATATCTTTCTTCAGAGTTGCTGACTCTTGAAAACAGTGCAAAGATCA
CAGTTTTTAAAAGTTTTAAAAATTTAAGAATATTCACACAATCGTTTTTCTATGTGTGAGAGGGATTTGCACACTCTTATTTTTCTGTAAAATATTTCACATCCCAAATGTGAAGAAGTGAAAAAGAC
TTCGCAGCAGTCTTCATTGTGGTGCTCTTCATGATCATAGCCCCAGGAACCCTTGAGGTTCTTCTTCACAAGGCTGAGAGTGCTTCCTTCTTGAAGACGAGTGACATTCATCACTTCAGTGATCCATG
CATAGAATATGAAAATAAATTCTTCCAACTCATGGGATAAAGGGGACTCCCTTGAAGAATTTCATGTTTTTGGGCTGTATAGCTCTTTACAGAAAATGCACCTTTATAAATCACATGAATGTTAGTAT
TCTGGAAATGTCTTTTGTTAATATAATCTTCCCATGTTATTTAACAAATTGTTTTTGCACATATCTGATTATATTGAAAGCAGTTTTTTGCATTCGAGTTTTAAACACTGTTATAAAATGTAGCCAAA
GCTCACCTTTGAACAGATCCCGGTGACATTCTATTTCCAGGAAAATCCGGAACCTGATTTTAGTTCTGTGATTTTACACTTTTTACATGTGAGATTGGACAGTTTCAGAGGCCTTATTTTGTCATACT
AAGTGTCTCCTGTAATTTTCAGGAAGATGATTTGTTCTTTCCAGAAGAGGAGACAAAAGCAAGATAGCCAAATGTGACATCAAGCTCCATTGTTTCGGAAATCCAGGATTTTGAATTCGAGATGAAAC
AACCAGCAATCACAGTTAAATCTTAACTTTGCCTGCACTCTTTGTAGGAATGATCAGAAATTTATCTTTATCATTCTGAGTGCTTCAGGAGTACAATAGGAAGAAAGATACTGGAGAAAGCACTAATG
TAATCACCATGAAGTCTGACAACAGGAGCCCATTATTTGCGTACTGTCCCACCCTGTATCATGGTTCTCTGGGAACAAGCTTTATGATTCTCATTAGAGTTTATTTGTTGATTGTCAGTAGTTGCGAC
TTTTAAATTATATTTCCCCCACTCAAAGAATGGTATCTTTATATATCAATGACATTCAATAAATGTGTATTATTTCTAATGAGAATCAGTTACAAGAGGAGACTTGATAGTTCAAGTAGTGGTCTCAG
AAATGTTTGGGCTGAATGTGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGAAGATAACTTGAGCCCAGTTTGAGACCAGCCTGGGCAACAAAGTGAGATCCTATCTCTATTAC
AAGAAAAAAGAAAAAAGAAAAAAAAAGCTAGGTGTAGTGGTGCATGCATGCACGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGCCCAGGAGATCAAGGCTGCAGTGAGCCATGATTGTGCCACT
GCACTCCAGCCTGGGTGATAGAGCGAGACCCTGTCTCAAAAACAGAAACAAGTTTGTATGAGATGCTAGGCTGTTTCTGAGACTATCACACCCCCTTTCCTATGACTCCTGTTACGGTGAGGAAAGAC
AGAAGGCTGTTATTACTGAGACCTCAATTCACATAACATGAATTTACATAAGATAGTCTAGCTCAAGAAGACATGAGACTACTAAACAGCAAAAGCAGATGGAAGGGAGGTTAATATTATGACATAGG
AAATAATGTAGTATCAATATATGGCTGCAGTAAGTTGCCCTTTCCAGGTTTTACTCAGCTTGGAAGTCCCCATTTCTCTCAAAAAGAAAGAAAGAAAAAACCCAGCAAAGCCAAACACTGAAAAGCTA
GGACTGAGTATGGAGCATCTGCCATCACTATAGTTGTACCAGGTACAGAGCAAAGAGTGACACCCAGAGGCAAATCATTCTAAGAGGGCAACAACTATGACAGTGCCTGGCACTTCTAAGAGGGTGCA
GCACTTCTAAGGTGCTAGGCAAGCTCTATTCCTTTTGTTTTAACACCTCGGGAAAATTTGAGGTACCAAATTAGGTACAAGAATAACTGGGGGTATGTCCTAGGTAACTAAGAGTCCAGATAATGTGT
GAATTTTGAATGTGCGTGGAAAGAGATTTACCATTCTTTGTCTAACTAAACAAAAAAGTTTCCTTAAGAGGTAGTCAGCCAGGCACAATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCCGAGGC
GGGTGGATCATCTGAGGTCAGGAGTTAGAGATCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACGAAAAGTTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCGGGAG
GCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAAGTTGCGGTGAGCTGAGACTGTGCTACTGCCCTCTATCCTGGGTGACAGAGTGAGACTCTGTCAAAAAAAAAAGAGATAGTTATACAAGTT
CTCCTGGAAAGGAACTATGTTTTGCAACCAATCTTAATATTAGTTATTGATATGAGGGTTCTCTGGGTCATTTGAGGTGAGATAGTGCAATATTTAAACAGCTCTGCATAAAAAAATGAATAGGAGGT
TTAGGGGTCAATTGTAGAGTCCTAAAAAGGAGAATATAGGAGGTCAACAGACAGCGAGGAGGCTCAGAAAAATGGAAGGAATTTGGAGGCCAAGCGGAATATATAATCAGTGAAAATAACCTTTTGGC
AAGAATAGATAAAGGAATTTAGTAAACTTTTTATTGAAGTGCAATACATGGTACCACCATGGTATTGGGAACATGTTTGGACTGGCAAGCAAACTGATGAGATACAATAGCATTTAGCCTAGCACTAA
ATTTGCTTAGCTTTATAGTAGGATACAGGACAGGAAATTAAGCATGCATGATGCTTGGGTCCCTCCTCACCTGCCTAAAGAGCGTGCATGAGCTTGTGGTATTTGGATGAGGTTGTGGTATGTGGGGG
TTTGCCTTGATGCAAAGAAGCTTCTATGTGGGTTTCCCACCAGTCATATAGGCCTACGGTTCACAGGTCTCCCAGCCCCATGTACTGTCCCATAGATTGTAGGTTTCACAGTGCACAAAATGGATGTC
TGTCCCTGGTACCCAATATTCCAAATTTATCTTAATTTGGGTCATTTACAAGAAACTCGTGCTGGGATAAGACAAACCTAAAATTTCCCAAGCAGGCATAGTTCTGGGAGAAAAATGGTACAGACCTG
CTATTAACTCTTTGCTCACACATACATAAAGAAAAGTACACAAATCATGAGTATGTAACATCATTGATATTGGCAAAGTGAATACATCTCTGTAACCAGACTCAGATCAAGAAATGATACATTCTGGC
CAGGTGTGGTGGCTCATGCCTGTAATCTCAGCACTTTGGCAGGCCAAGGTGGGTGGATCACTTGAGGCCAGGAGTTCGAGACCAGTGTGGCCAACATGGTGAAACCCCACCTCTACTAAACACACATA
CACACCCACAAATTAGCCAGGTGCAGTGGTACATTCGTGTAATCCCAGCTACTTGGGAGGCTGAGGTGCACAAGTGAGAATCGCTTGAGCCTGGGAGGCAGATGTTGCAGTGAGCCAAGATGGTGCCA
CTATACTCCAGCCTGGGCAACAGAGTGAAACTCTGTCAAAAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAGAAAAGAAAGAAAGAAAACATTCTAGAATTCCAGAAGCCATTCTCATTCCCTATT
TAAGTCACTAACCCAAGAGTAATTAATATCCTGAGTTCCAACACCTTGGATTTGTATGGGTTATTTTTAAACCTTCTATAAATGGAATTTTATGATATGTTTGTTTGATCCACCTATGTTGTATGTAG
TTGTATTTCATTTATTCCCATTTCTGCATTGTCTTGAATTGTACAACTATTTTACATATTTATCTATTCTAATTTCAATGGATATTTGAGTTGTTTCCAATTTTTAACTATTTTTTAAAATTATACTC
TAAGTTCAATAAACATACATGTGCATGTGT

hide sequence

RefSeq Acc Id:

XM_024454200 ⟹ XP_024309968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,114,336 (-)	NCBI

Sequence:

show sequence

GTTTTCTGTTGCTGCTGTTGCTGTTCAGTGCAGAAGCGATGAGGAAATTGAAGATTAGAGAGGT
TACATTGCTTACCCAAGGCCACACTATGAAATGGTGGAGCTGGGATTCAAACTCTTGTTCCTAATCACTATACCATGTCTATTTATAACAAAAAGACACCATCAAATGAGACAAATGAGAACACAGAT
AAGCCTGAGCACAGATGAAGAGCTTCCAGAAAAATACACCCAGCGTCGCAGGCCGTGGCTCAGCCAATTGTCAAATAAGAAGCAATCCAACACGGGCCGTGTGCAGCCGTCAAAACGAAAGCCACTGC
CTCCCCTCCCACCCTCTGAGGTTGCTGAAGAGAAGATCCAAGTCAAGGCACTTTATGATTTTCTGCCCAGAGAACCCTGTAATTTAGCCTTAAGGAGAGCAGAAGAATACCTGATACTGGAGAAATAC
AATCCTCACTGGTGGAAGGCAAGAGACCGTTTGGGGAATGAAGGCTTAATCCCAAGCAACTATGTGACTGAAAACAAAATAACTAATTTAGAAATATATGAGTGGTACCATAGAAACATTACCAGAAA
TCAGGCAGAACATCTATTGAGACAAGAGTCTAAAGAAGGTGCATTTATTGTCAGAGATTCAAGACATTTAGGATCCTACACAATTTCCGTATTTATGGGAGCTAGAAGAAGTACGGAGGCTGCCATAA
AACATTATCAGATAAAAAAGAATGACTCAGGACAGTGGTATGTGGCTGAAAGACACGCCTTTCAATCAATCCCTGAGTTAATCTGGTATCACCAGCACAATGCAGCCGGTCTCATGACTCGTCTCCGA
TATCCAGTTGGGCTGATGGGCAGTTGTTTACCAGCCACAGCTGGGTTTAGCTACGAAAAGTGGGAGATAGATCCATCTGAGTTGGCTTTTATAAAGGAGATTGGAAGCGGTCAGTTTGGAGTGGTCCA
TTTAGGTGAATGGCGGTCACATATCCAGGTAGCTATCAAGGCCATCAATGAAGGCTCCATGTCTGAAGAGGATTTCATTGAAGAGGCCAAAGTGATGATGAAATTATCTCATTCAAAGCTAGTGCAAC
TTTATGGAGTCTGTATACAGCGGAAGCCCCTTTACATTGTGACAGAGTTCATGGAAAATGGCTGCCTGCTTAACTATCTCAGGGAGAATAAAGGAAAGCTTAGGAAGGAAATGCTACTGAGTGTATGC
CAGGATATATGTGAAGGAATGGAATATCTGGAGAGGAATGGCTATATTCATAGGGATTTGGCGGCAAGGAATTGTTTGGTCAGTTCAACATGCATAGTAAAAATTTCAGACTTTGGAATGACAAGGTA
CGTTTTGGATGATGAGTATGTCAGTTCTTTTGGAGCCAAGTTCCCAATCAAGTGGTCCCCTCCTGAAGTTTTTCTTTTCAATAAGTACAGCAGTAAATCTGATGTCTGGTCATTTGGAGTTTTAATGT
GGGAAGTTTTTACAGAAGGAAAAATGCCTTTTGAAAATAAGTCAAATTTGCAAGTCGTGGAAGCTATTTCTGAAGGCTTCAGGCTATATCGCCCTCACCTGGCACCAATGTCCATATATGAAGTCATG
TACAGCTGCTGGCATGAGAAACCTGAAGGCCGCCCTACATTTGCCGAGCTGCTGCGGGCTGTCACAGAGATTGCGGAAACCTGGTGACCGGAAACAGAATGCCAACCCAAAGAGTCATCTTGCAAAAC
TGTCATTTATTGTGAATATCTTCACCATATGGGGTCACTTATGGTGAATATCTTTCTTCAGAGTTGCTGACTCTTGAAAACAGTGCAAAGATCACAGTTTTTAAAAGTTTTAAAAATTTAAGAATATT
CACACAATCGTTTTTCTATGTGTGAGAGGGATTTGCACACTCTTATTTTTCTGTAAAATATTTCACATCCCAAATGTGAAGAAGTGAAAAAGACTTCGCAGCAGTCTTCATTGTGGTGCTCTTCATGA
TCATAGCCCCAGGAACCCTTGAGGTTCTTCTTCACAAGGCTGAGAGTGCTTCCTTCTTGAAGACGAGTGACATTCATCACTTCAGTGATCCATGCATAGAATATGAAAATAAATTCTTCCAACTCATG
GGATAAAGGGGACTCCCTTGAAGAATTTCATGTTTTTGGGCTGTATAGCTCTTTACAGAAAATGCACCTTTATAAATCACATGAATGTTAGTATTCTGGAAATGTCTTTTGTTAATATAATCTTCCCA
TGTTATTTAACAAATTGTTTTTGCACATATCTGATTATATTGAAAGCAGTTTTTTGCATTCGAGTTTTAAACACTGTTATAAAATGTAGCCAAAGCTCACCTTTGAACAGATCCCGGTGACATTCTAT
TTCCAGGAAAATCCGGAACCTGATTTTAGTTCTGTGATTTTACACTTTTTACATGTGAGATTGGACAGTTTCAGAGGCCTTATTTTGTCATACTAAGTGTCTCCTGTAATTTTCAGGAAGATGATTTG
TTCTTTCCAGAAGAGGAGACAAAAGCAAGATAGCCAAATGTGACATCAAGCTCCATTGTTTCGGAAATCCAGGATTTTGAATTCGAGATGAAACAACCAGCAATCACAGTTAAATCTTAACTTTGCCT
GCACTCTTTGTAGGAATGATCAGAAATTTATCTTTATCATTCTGAGTGCTTCAGGAGTACAATAGGAAGAAAGATACTGGAGAAAGCACTAATGTAATCACCATGAAGTCTGACAACAGGAGCCCATT
ATTTGCGTACTGTCCCACCCTGTATCATGGTTCTCTGGGAACAAGCTTTATGATTCTCATTAGAGTTTATTTGTTGATTGTCAGTAGTTGCGACTTTTAAATTATATTTCCCCCACTCAAAGAATGGT
ATCTTTATATATCAATGACATTCAATAAATGTGTATTATTTCTAATGAGAATCAGTTACAAGAGGAGACTTGATAGTTCAAGTAGTGGTCTCAGAAATGTTTGGGCTGAATGTGGTGGCTCATGCCTA
TAATCCCAGCACTTTGGGAGGCCAAGGTGGGAAGATAACTTGAGCCCAGTTTGAGACCAGCCTGGGCAACAAAGTGAGATCCTATCTCTATTACAAGAAAAAAGAAAAAAGAAAAAAAAAGCTAGGTG
TAGTGGTGCATGCATGCACGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGCCCAGGAGATCAAGGCTGCAGTGAGCCATGATTGTGCCACTGCACTCCAGCCTGGGTGATAGAGCGAGACCCTGT
CTCAAAAACAGAAACAAGTTTGTATGAGATGCTAGGCTGTTTCTGAGACTATCACACCCCCTTTCCTATGACTCCTGTTACGGTGAGGAAAGACAGAAGGCTGTTATTACTGAGACCTCAATTCACAT
AACATGAATTTACATAAGATAGTCTAGCTCAAGAAGACATGAGACTACTAAACAGCAAAAGCAGATGGAAGGGAGGTTAATATTATGACATAGGAAATAATGTAGTATCAATATATGGCTGCAGTAAG
TTGCCCTTTCCAGGTTTTACTCAGCTTGGAAGTCCCCATTTCTCTCAAAAAGAAAGAAAGAAAAAACCCAGCAAAGCCAAACACTGAAAAGCTAGGACTGAGTATGGAGCATCTGCCATCACTATAGT
TGTACCAGGTACAGAGCAAAGAGTGACACCCAGAGGCAAATCATTCTAAGAGGGCAACAACTATGACAGTGCCTGGCACTTCTAAGAGGGTGCAGCACTTCTAAGGTGCTAGGCAAGCTCTATTCCTT
TTGTTTTAACACCTCGGGAAAATTTGAGGTACCAAATTAGGTACAAGAATAACTGGGGGTATGTCCTAGGTAACTAAGAGTCCAGATAATGTGTGAATTTTGAATGTGCGTGGAAAGAGATTTACCAT
TCTTTGTCTAACTAAACAAAAAAGTTTCCTTAAGAGGTAGTCAGCCAGGCACAATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCATCTGAGGTCAGGAGTTAGAGATCA
GCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACGAAAAGTTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGT
GGAAGTTGCGGTGAGCTGAGACTGTGCTACTGCCCTCTATCCTGGGTGACAGAGTGAGACTCTGTCAAAAAAAAAAGAGATAGTTATACAAGTTCTCCTGGAAAGGAACTATGTTTTGCAACCAATCT
TAATATTAGTTATTGATATGAGGGTTCTCTGGGTCATTTGAGGTGAGATAGTGCAATATTTAAACAGCTCTGCATAAAAAAATGAATAGGAGGTTTAGGGGTCAATTGTAGAGTCCTAAAAAGGAGAA
TATAGGAGGTCAACAGACAGCGAGGAGGCTCAGAAAAATGGAAGGAATTTGGAGGCCAAGCGGAATATATAATCAGTGAAAATAACCTTTTGGCAAGAATAGATAAAGGAATTTAGTAAACTTTTTAT
TGAAGTGCAATACATGGTACCACCATGGTATTGGGAACATGTTTGGACTGGCAAGCAAACTGATGAGATACAATAGCATTTAGCCTAGCACTAAATTTGCTTAGCTTTATAGTAGGATACAGGACAGG
AAATTAAGCATGCATGATGCTTGGGTCCCTCCTCACCTGCCTAAAGAGCGTGCATGAGCTTGTGGTATTTGGATGAGGTTGTGGTATGTGGGGGTTTGCCTTGATGCAAAGAAGCTTCTATGTGGGTT
TCCCACCAGTCATATAGGCCTACGGTTCACAGGTCTCCCAGCCCCATGTACTGTCCCATAGATTGTAGGTTTCACAGTGCACAAAATGGATGTCTGTCCCTGGTACCCAATATTCCAAATTTATCTTA
ATTTGGGTCATTTACAAGAAACTCGTGCTGGGATAAGACAAACCTAAAATTTCCCAAGCAGGCATAGTTCTGGGAGAAAAATGGTACAGACCTGCTATTAACTCTTTGCTCACACATACATAAAGAAA
AGTACACAAATCATGAGTATGTAACATCATTGATATTGGCAAAGTGAATACATCTCTGTAACCAGACTCAGATCAAGAAATGATACATTCTGGCCAGGTGTGGTGGCTCATGCCTGTAATCTCAGCAC
TTTGGCAGGCCAAGGTGGGTGGATCACTTGAGGCCAGGAGTTCGAGACCAGTGTGGCCAACATGGTGAAACCCCACCTCTACTAAACACACATACACACCCACAAATTAGCCAGGTGCAGTGGTACAT
TCGTGTAATCCCAGCTACTTGGGAGGCTGAGGTGCACAAGTGAGAATCGCTTGAGCCTGGGAGGCAGATGTTGCAGTGAGCCAAGATGGTGCCACTATACTCCAGCCTGGGCAACAGAGTGAAACTCT
GTCAAAAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAGAAAAGAAAGAAAGAAAACATTCTAGAATTCCAGAAGCCATTCTCATTCCCTATTTAAGTCACTAACCCAAGAGTAATTAATATCCTGA
GTTCCAACACCTTGGATTTGTATGGGTTATTTTTAAACCTTCTATAAATGGAATTTTATGATATGTTTGTTTGATCCACCTATGTTGTATGTAGTTGTATTTCATTTATTCCCATTTCTGCATTGTCT
TGAATTGTACAACTATTTTACATATTTATCTATTCTAATTTCAATGGATATTTGAGTTGTTTCCAATTTTTAACTATTTTTTAAAATTATACTCTAAGTTCAATAAACATACATGTGCATGTGT

hide sequence

RefSeq Acc Id:

XM_047416122 ⟹ XP_047272078

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,071,534 - 48,114,340 (-)	NCBI

RefSeq Acc Id:

XM_047416123 ⟹ XP_047272079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,066,393 - 48,110,529 (-)	NCBI

RefSeq Acc Id:

XM_047416125 ⟹ XP_047272081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,086,818 - 48,114,340 (-)	NCBI

RefSeq Acc Id:

XM_054350773 ⟹ XP_054206748

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,033,459 - 48,081,170 (-)	NCBI

RefSeq Acc Id:

XM_054350774 ⟹ XP_054206749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,033,459 - 48,081,170 (-)	NCBI

RefSeq Acc Id:

XM_054350775 ⟹ XP_054206750

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,033,459 - 48,101,082 (-)	NCBI

RefSeq Acc Id:

XM_054350776 ⟹ XP_054206751

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,038,602 - 48,081,174 (-)	NCBI

RefSeq Acc Id:

XM_054350777 ⟹ XP_054206752

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,033,459 - 48,077,363 (-)	NCBI

RefSeq Acc Id:

XM_054350778 ⟹ XP_054206753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,033,459 - 48,062,300 (-)	NCBI

RefSeq Acc Id:

XM_054350779 ⟹ XP_054206754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,053,619 - 48,081,174 (-)	NCBI

RefSeq Acc Id:

XR_007057955

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,086,550 - 48,114,340 (-)	NCBI

RefSeq Acc Id:

XR_008487028

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	48,053,625 - 48,081,174 (-)	NCBI


Protein RefSeqs	NP_003319	(Get FASTA)	NCBI Sequence Viewer
	XP_011512049	(Get FASTA)	NCBI Sequence Viewer
	XP_011512050	(Get FASTA)	NCBI Sequence Viewer
	XP_016864070	(Get FASTA)	NCBI Sequence Viewer
	XP_024309968	(Get FASTA)	NCBI Sequence Viewer
	XP_047272078	(Get FASTA)	NCBI Sequence Viewer
	XP_047272079	(Get FASTA)	NCBI Sequence Viewer
	XP_047272081	(Get FASTA)	NCBI Sequence Viewer
	XP_054206748	(Get FASTA)	NCBI Sequence Viewer
	XP_054206749	(Get FASTA)	NCBI Sequence Viewer
	XP_054206750	(Get FASTA)	NCBI Sequence Viewer
	XP_054206751	(Get FASTA)	NCBI Sequence Viewer
	XP_054206752	(Get FASTA)	NCBI Sequence Viewer
	XP_054206753	(Get FASTA)	NCBI Sequence Viewer
	XP_054206754	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA19597	(Get FASTA)	NCBI Sequence Viewer
	AAA19598	(Get FASTA)	NCBI Sequence Viewer
	AAA19599	(Get FASTA)	NCBI Sequence Viewer
	AAA19600	(Get FASTA)	NCBI Sequence Viewer
	AAA74557	(Get FASTA)	NCBI Sequence Viewer
	AAB60412	(Get FASTA)	NCBI Sequence Viewer
	BAG61927	(Get FASTA)	NCBI Sequence Viewer
	EAW93051	(Get FASTA)	NCBI Sequence Viewer
	EAW93052	(Get FASTA)	NCBI Sequence Viewer
	EAW93053	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000264316
	ENSP00000264316.4
GenBank Protein	P42681	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_003319 ⟸ NM_003328

- UniProtKB:

Q14220 (UniProtKB/Swiss-Prot), P42681 (UniProtKB/Swiss-Prot), E7EQN8 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MILSSYNTIQSVFCCCCCCSVQKRQMRTQISLSTDEELPEKYTQRRRPWLSQLSNKKQSNTGRVQPSKRKPLPPLPPSEVAEEKIQVKALYDFLPREPCNLALRRAEEYLILEKYNPHWWKARDRLGN
EGLIPSNYVTENKITNLEIYEWYHRNITRNQAEHLLRQESKEGAFIVRDSRHLGSYTISVFMGARRSTEAAIKHYQIKKNDSGQWYVAERHAFQSIPELIWYHQHNAAGLMTRLRYPVGLMGSCLPAT
AGFSYEKWEIDPSELAFIKEIGSGQFGVVHLGEWRSHIQVAIKAINEGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPLYIVTEFMENGCLLNYLRENKGKLRKEMLLSVCQDICEGMEYLERN
GYIHRDLAARNCLVSSTCIVKISDFGMTRYVLDDEYVSSFGAKFPIKWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPFENKSNLQVVEAISEGFRLYRPHLAPMSIYEVMYSCWHEKPEGRPT
FAELLRAVTEIAETW

hide sequence

RefSeq Acc Id:	XP_011512049 ⟸ XM_011513747
- Peptide Label:	isoform X2
- UniProtKB:	E7EQN8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVELGFKLLFLITIPCLFITKRHHQMRQMRTQISLSTDEELPEKYTQRRRPWLSQLSNKKQSNT GRVQPSKRKPLPPLPPSEVAEEKIQVKALYDFLPREPCNLALRRAEEYLILEKYNPHWWKARDRLGWYHRNITRNQAEHLLRQESKEGAFIVRDSRHLGSYTISVFMGARRSTEAAIKHYQIKKNDSG QWYVAERHAFQSIPELIWYHQHNAAGLMTRLRYPVGLMGSCLPATAGFSYEKWEIDPSELAFIKEIGSGQFGVVHLGEWRSHIQVAIKAINEGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPL YIVTEFMENGCLLNYLRENKGKLRKEMLLSVCQDICEGMEYLERNGYIHRDLAARNCLVSSTCIVKISDFGMTRYVLDDEYVSSFGAKFPIKWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPF ENKSNLQVVEAISEGFRLYRPHLAPMSIYEVMYSCWHEKPEGRPTFAELLRAVTEIAETW hide sequence

RefSeq Acc Id:

XP_011512050 ⟸ XM_011513748

- Peptide Label:

isoform X6

- Sequence:

show sequence

MTRLRYPVGLMGSCLPATAGFSYEKWEIDPSELAFIKEIGSGQFGVVHLGEWRSHIQVAIKAIN
EGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPLYIVTEFMENGCLLNYLRENKGKLRKEMLLSVCQDICEGMEYLERNGYIHRDLAARNCLVSSTCIVKISDFGMTRYVLDDEYVSSFGAKFPI
KWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPFENKSNLQVVEAISEGFRLYRPHLAPMSIYEVMYSCWHEKPEGRPTFAELLRAVTEIAETW

hide sequence

RefSeq Acc Id:	XP_016864070 ⟸ XM_017008581
- Peptide Label:	isoform X3
- UniProtKB:	E7EQN8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRTQISLSTDEELPEKYTQRRRPWLSQLSNKKQSNTGRVQPSKRKPLPPLPPSEVAEEKIQVKALYDFLPREPCNLALRRAEEYLILEKYNPHWWKARDRLGNEGLIPSNYVTENKITNLEIYEWYHR NITRNQAEHLLRQESKEGAFIVRDSRHLGSYTISVFMGARRSTEAAIKHYQIKKNDSGQWYVAERHAFQSIPELIWYHQHNAAGLMTRLRYPVGLMGSCLPATAGFSYEKWEIDPSELAFIKEIGSGQ FGVVHLGEWRSHIQVAIKAINEGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPLYIVTEFMENGCLLNYLRENKGKLRKEMLLSVCQDICEGMEYLERNGYIHRDLAARNCLVSSTCIVKISDF GMTRYVLDDEYVSSFGAKFPIKWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPFENKSNLQVVEAISEGFRLYRPHLAPMSIYEVMYSCWHEKPEGRPTFAELLRAVTEIAETW hide sequence

RefSeq Acc Id:	XP_024309968 ⟸ XM_024454200
- Peptide Label:	isoform X1
- UniProtKB:	E7EQN8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MVELGFKLLFLITIPCLFITKRHHQMRQMRTQISLSTDEELPEKYTQRRRPWLSQLSNKKQSNTGRVQPSKRKPLPPLPPSEVAEEKIQVKALYDFLPREPCNLALRRAEEYLILEKYNPHWWKARDR LGNEGLIPSNYVTENKITNLEIYEWYHRNITRNQAEHLLRQESKEGAFIVRDSRHLGSYTISVFMGARRSTEAAIKHYQIKKNDSGQWYVAERHAFQSIPELIWYHQHNAAGLMTRLRYPVGLMGSCL PATAGFSYEKWEIDPSELAFIKEIGSGQFGVVHLGEWRSHIQVAIKAINEGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPLYIVTEFMENGCLLNYLRENKGKLRKEMLLSVCQDICEGMEYL ERNGYIHRDLAARNCLVSSTCIVKISDFGMTRYVLDDEYVSSFGAKFPIKWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPFENKSNLQVVEAISEGFRLYRPHLAPMSIYEVMYSCWHEKPEG RPTFAELLRAVTEIAETW hide sequence

Protein Domains

Protein kinase SH2 SH3

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P42681-F1-model_v2	AlphaFold	P42681	1-527	view protein structure

RGD ID:

6802681

Promoter ID:

HG_KWN:48181

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Lymphoblastoid

Transcripts:

OTTHUMT00000219869, UC003GXY.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	4	47,831,046 - 47,831,546 (-)	MPROMDB

RGD ID:

6867364

Promoter ID:

EPDNEW_H6847

Type:

initiation region

Name:

TXK_2

Description:

TXK tyrosine kinase

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6848 EPDNEW_H6849

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,080,066 - 48,080,126	EPDNEW

RGD ID:

6867366

Promoter ID:

EPDNEW_H6848

Type:

initiation region

Name:

TXK_1

Description:

TXK tyrosine kinase

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6847 EPDNEW_H6849

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,134,250 - 48,134,310	EPDNEW

RGD ID:

6867368

Promoter ID:

EPDNEW_H6849

Type:

multiple initiation site

Name:

TXK_3

Description:

TXK tyrosine kinase

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6847 EPDNEW_H6848

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	48,135,847 - 48,135,907	EPDNEW

Database	Acc Id	Source(s)
COSMIC	TXK	COSMIC
Ensembl Genes	ENSG00000074966	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000264316	ENTREZGENE
	ENST00000264316.9	UniProtKB/Swiss-Prot
Gene3D-CATH	3.30.505.10	UniProtKB/Swiss-Prot
	SH3 Domains	UniProtKB/Swiss-Prot
	Transferase(Phosphotransferase) domain 1	UniProtKB/Swiss-Prot
GTEx	ENSG00000074966	GTEx
HGNC ID	HGNC:12434	ENTREZGENE
Human Proteome Map	TXK	Human Proteome Map
InterPro	Kinase-like_dom_sf	UniProtKB/Swiss-Prot
	Non-receptor_tyrosine_kinases	UniProtKB/Swiss-Prot
	Prot_kinase_dom	UniProtKB/Swiss-Prot
	Protein_kinase_ATP_BS	UniProtKB/Swiss-Prot
	Ser-Thr/Tyr_kinase_cat_dom	UniProtKB/Swiss-Prot
	SH2	UniProtKB/Swiss-Prot
	SH2_dom_sf	UniProtKB/Swiss-Prot
	SH3-like_dom_sf	UniProtKB/Swiss-Prot
	SH3_domain	UniProtKB/Swiss-Prot
	Txk_SH2	UniProtKB/Swiss-Prot
	TXK_SH3	UniProtKB/Swiss-Prot
	Tyr_kinase_AS	UniProtKB/Swiss-Prot
	Tyr_kinase_cat_dom	UniProtKB/Swiss-Prot
KEGG Report	hsa:7294	UniProtKB/Swiss-Prot
NCBI Gene	7294	ENTREZGENE
OMIM	600058	OMIM
PANTHER	TYROSINE-PROTEIN KINASE	UniProtKB/Swiss-Prot
Pfam	Pkinase_Tyr	UniProtKB/Swiss-Prot
	SH2	UniProtKB/Swiss-Prot
	SH3_1	UniProtKB/Swiss-Prot
PharmGKB	PA37090	PharmGKB, RGD
PRINTS	SH2DOMAIN	UniProtKB/Swiss-Prot
	TYRKINASE	UniProtKB/Swiss-Prot
PROSITE	PROTEIN_KINASE_ATP	UniProtKB/Swiss-Prot
	PROTEIN_KINASE_DOM	UniProtKB/Swiss-Prot
	PROTEIN_KINASE_TYR	UniProtKB/Swiss-Prot
	SH2	UniProtKB/Swiss-Prot
	SH3	UniProtKB/Swiss-Prot
SMART	SH2	UniProtKB/Swiss-Prot
	SH3	UniProtKB/Swiss-Prot
	TyrKc	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF50044	UniProtKB/Swiss-Prot
	SSF55550	UniProtKB/Swiss-Prot
	SSF56112	UniProtKB/Swiss-Prot
UniProt	D6R9F2_HUMAN	UniProtKB/TrEMBL
	D6RA14_HUMAN	UniProtKB/TrEMBL
	D6RBM7_HUMAN	UniProtKB/TrEMBL
	E7EQN8	ENTREZGENE, UniProtKB/TrEMBL
	P42681	ENTREZGENE
	Q14220	ENTREZGENE
	Q6LD13_HUMAN	UniProtKB/TrEMBL
	Q6LD14_HUMAN	UniProtKB/TrEMBL
	TXK_HUMAN	UniProtKB/Swiss-Prot
	V9GZ99_HUMAN	UniProtKB/TrEMBL
	V9GZA3_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	Q14220	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
		Excel (Download)

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

Send us a Message