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Gene: SYTL3 (synaptotagmin like 3) Homo sapiens

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Symbol:

SYTL3

Name:

synaptotagmin like 3

RGD ID:

1352944

HGNC Page

HGNC:15587

Description:

Predicted to enable neurexin family protein binding activity. Predicted to be involved in exocytosis. Predicted to be located in endomembrane system and membrane. Predicted to be active in exocytic vesicle and plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

exophilin-6; MGC105130; MGC118883; MGC118884; MGC118885; SLP3; synaptotagmin-like 3; synaptotagmin-like protein 3

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):	Sytl3 (synaptotagmin-like 3)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Sytl3 (synaptotagmin-like 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Sytl3 (synaptotagmin like 3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	SYTL3 (synaptotagmin like 3)	NCBI	Ortholog
Canis lupus familiaris (dog):	SYTL3 (synaptotagmin like 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Sytl3 (synaptotagmin like 3)	NCBI	Ortholog
Sus scrofa (pig):	SYTL3 (synaptotagmin like 3)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	SYTL3 (synaptotagmin like 3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Sytl3 (synaptotagmin like 3)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Frmd6 (FERM domain containing 6)	HGNC	OMA
Alliance orthologs ³
Mus musculus (house mouse):	Sytl3 (synaptotagmin-like 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Sytl3 (synaptotagmin-like 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	sytl3 (synaptotagmin-like 3)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Caenorhabditis elegans (roundworm):	Y48G8AR.2	Alliance	DIOPT (OrthoFinder\|PhylomeDB)
Xenopus laevis (African clawed frog):	sytl3.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	sytl3	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PhylomeDB)

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	6	158,644,936 - 158,764,871 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	158,650,014 - 158,764,876 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	159,071,086 - 159,185,903 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	6	158,991,034 - 159,105,889 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	6	159,041,508 - 159,156,311	NCBI
Celera	6	159,719,041 - 159,833,917 (+)	NCBI		Celera
Cytogenetic Map	6	q25.3	NCBI
HuRef	6	156,541,943 - 156,656,442 (+)	NCBI		HuRef
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	159,886,606 - 160,010,070 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (IAGP)

chromosome 6q24-q25 deletion syndrome (IAGP)

primary ciliary dyskinesia 32 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-demecolcine (EXP)

2,3',4,4',5-Pentachlorobiphenyl (ISO)

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

acetamide (ISO)

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP,ISO)

alpha-Zearalanol (ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[e]pyrene (EXP)

Benzo[ghi]perylene (ISO)

bisphenol A (EXP,ISO)

cadmium dichloride (ISO)

calcitriol (EXP)

carbon nanotube (ISO)

DDE (EXP)

Dibutyl phosphate (EXP)

disodium selenite (EXP)

doxorubicin (EXP)

endosulfan (ISO)

fulvestrant (EXP)

furan (ISO)

GW 4064 (ISO)

lead diacetate (ISO)

lipopolysaccharide (EXP)

methapyrilene (EXP)

methotrexate (EXP)

methoxychlor (ISO)

methyl methanesulfonate (EXP)

mono(2-ethylhexyl) phthalate (ISO)

nickel atom (EXP)

ozone (EXP)

paracetamol (ISO)

perfluorooctanoic acid (ISO)

potassium chromate (EXP)

propanal (EXP)

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

silicon dioxide (EXP,ISO)

sodium arsenite (EXP,ISO)

sunitinib (EXP)

temozolomide (EXP)

testosterone (ISO)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

triphenyl phosphate (EXP)

valproic acid (EXP)

vincristine (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

exocytosis (IBA,IEA,ISO)

intracellular protein transport (IEA)

Cellular Component

endomembrane system (IEA)

exocytic vesicle (IBA)

membrane (IEA)

plasma membrane (IBA,IEA)

Molecular Function

calcium-dependent phospholipid binding (IEA)

neurexin family protein binding (IBA,IEA)

phospholipid binding (IEA)

protein binding (IPI)

small GTPase binding (IEA)

References

References - curated

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

Additional References at PubMed

PMID:11243866	PMID:11327731	PMID:11773082	PMID:12049610	PMID:12477932	PMID:12590134	PMID:14702039	PMID:16344560	PMID:19913121	PMID:20628086	PMID:21873635	PMID:22308290
PMID:25940347	PMID:28514442	PMID:32296183	PMID:33657377	PMID:33961781

Genomics

Comparative Map Data

SYTL3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	158,650,014 - 158,764,876 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	159,071,086 - 159,185,903 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	6	158,991,034 - 159,105,889 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	6	159,041,508 - 159,156,311	NCBI
Celera	6	159,719,041 - 159,833,917 (+)	NCBI		Celera
Cytogenetic Map	6	q25.3	NCBI
HuRef	6	156,541,943 - 156,656,442 (+)	NCBI		HuRef
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	159,886,606 - 160,010,070 (+)	NCBI		T2T-CHM13v2.0

Sytl3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	17	6,925,633 - 7,005,449 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	17	6,926,492 - 7,005,443 (+)	Ensembl		GRCm39 Ensembl
GRCm38	17	6,658,133 - 6,738,070 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	17	6,659,093 - 6,738,044 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	17	6,877,960 - 6,942,393 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	17	6,523,269 - 6,587,494 (+)	NCBI		MGSCv36	mm8
Celera	15	14,732,754 - 14,737,852 (-)	NCBI		Celera
Cytogenetic Map	17	A1	NCBI
cM Map	17	4.33	NCBI

Sytl3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	49,300,935 - 49,372,533 (+)	NCBI		GRCr8
mRatBN7.2	1	46,896,308 - 46,967,461 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	46,911,217 - 46,967,460 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	47,460,176 - 47,516,406 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	53,447,437 - 53,503,677 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	47,535,610 - 47,591,852 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	47,216,988 - 47,287,372 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	47,231,093 - 47,287,371 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	48,520,061 - 48,591,365 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	41,121,373 - 41,177,695 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	1	42,598,861 - 42,655,031 (+)	NCBI		Celera
Cytogenetic Map	1	q11	NCBI

Sytl3
(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_004955439	3,741,185 - 3,813,670 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955439	3,740,044 - 3,825,954 (-)	NCBI	ChiLan1.0	ChiLan1.0

SYTL3
(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	5	178,751,597 - 178,868,789 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	6	176,655,495 - 176,774,134 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	6	156,537,572 - 156,655,272 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	6	161,552,602 - 161,669,609 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	6	161,559,559 - 161,669,609 (+)	Ensembl	panpan1.1		panPan2

SYTL3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	1	48,066,449 - 48,159,980 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	48,067,612 - 48,159,936 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	48,911,648 - 49,004,972 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	48,252,730 - 48,346,099 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	48,259,345 - 48,346,110 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	48,129,399 - 48,222,874 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	48,000,111 - 48,093,753 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	48,559,600 - 48,653,168 (+)	NCBI		UU_Cfam_GSD_1.0

Sytl3
(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_024404946	143,094,445 - 143,161,127 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936489	10,352,904 - 10,412,918 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936489	10,384,060 - 10,413,122 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SYTL3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	1	8,453,283 - 8,546,530 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	8,452,822 - 8,546,637 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	10,432,694 - 10,498,575 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SYTL3
(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	13	86,242,087 - 86,342,084 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	13	86,242,109 - 86,341,818 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666040	58,598,161 - 58,720,449 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Sytl3
(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_004624929	874,471 - 953,246 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624929	874,246 - 969,213 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SYTL3
44 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_001242384.1(SYTL3):c.394+2829C>T	single nucleotide variant	Lung cancer [RCV000096641]	Chr6:158685818 [GRCh38] Chr6:159106850 [GRCh37] Chr6:6q25.3	uncertain significance
GRCh38/hg38 6q24.1-27(chr6:141132990-169339571)x3	copy number gain	See cases [RCV000050604]	Chr6:141132990..169339571 [GRCh38] Chr6:141454127..169739666 [GRCh37] Chr6:141495820..169481591 [NCBI36] Chr6:6q24.1-27	pathogenic
GRCh38/hg38 6q25.2-27(chr6:152376338-170583214)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051902]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051902]\|See cases [RCV000051902]	Chr6:152376338..170583214 [GRCh38] Chr6:152697473..170892302 [GRCh37] Chr6:152739166..170734227 [NCBI36] Chr6:6q25.2-27	pathogenic
GRCh38/hg38 6q25.3(chr6:157827805-159726548)x3	copy number gain	See cases [RCV000051903]	Chr6:157827805..159726548 [GRCh38] Chr6:158248837..160147580 [GRCh37] Chr6:158168825..160067570 [NCBI36] Chr6:6q25.3	pathogenic
GRCh38/hg38 6q25.3-27(chr6:158664768-170612001)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051904]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051904]\|See cases [RCV000051904]	Chr6:158664768..170612001 [GRCh38] Chr6:159085800..170921089 [GRCh37] Chr6:159005788..170763014 [NCBI36] Chr6:6q25.3-27	pathogenic
GRCh38/hg38 6q25.2-27(chr6:154118058-170602152)x1	copy number loss	See cases [RCV000052207]	Chr6:154118058..170602152 [GRCh38] Chr6:154439193..170911240 [GRCh37] Chr6:154480885..170753165 [NCBI36] Chr6:6q25.2-27	pathogenic
GRCh38/hg38 6q25.2-25.3(chr6:154178964-159020369)x1	copy number loss	See cases [RCV000134896]	Chr6:154178964..159020369 [GRCh38] Chr6:154500098..159441401 [GRCh37] Chr6:154541790..159361389 [NCBI36] Chr6:6q25.2-25.3	likely pathogenic
GRCh38/hg38 6q25.2-27(chr6:154539655-170714507)x1	copy number loss	See cases [RCV000137381]	Chr6:154539655..170714507 [GRCh38] Chr6:154860789..171023595 [GRCh37] Chr6:154902481..170865520 [NCBI36] Chr6:6q25.2-27	pathogenic
GRCh38/hg38 6q25.3(chr6:158172635-158745586)x3	copy number gain	See cases [RCV000138111]	Chr6:158172635..158745586 [GRCh38] Chr6:158593667..159166618 [GRCh37] Chr6:158513655..159086606 [NCBI36] Chr6:6q25.3	uncertain significance
GRCh38/hg38 6q25.3-26(chr6:155378049-163133499)x1	copy number loss	See cases [RCV000137831]	Chr6:155378049..163133499 [GRCh38] Chr6:155699183..163554531 [GRCh37] Chr6:155740875..163474521 [NCBI36] Chr6:6q25.3-26	pathogenic
GRCh38/hg38 6q25.1-25.3(chr6:150381239-159553952)x1	copy number loss	See cases [RCV000139578]	Chr6:150381239..159553952 [GRCh38] Chr6:150702375..159974984 [GRCh37] Chr6:150744068..159894974 [NCBI36] Chr6:6q25.1-25.3	pathogenic
GRCh38/hg38 6q25.2-27(chr6:152793402-170610394)x1	copy number loss	See cases [RCV000141880]	Chr6:152793402..170610394 [GRCh38] Chr6:153114537..170919482 [GRCh37] Chr6:153156230..170761407 [NCBI36] Chr6:6q25.2-27	pathogenic
GRCh38/hg38 6q25.3(chr6:158174555-158762476)x3	copy number gain	See cases [RCV000141740]	Chr6:158174555..158762476 [GRCh38] Chr6:158595587..159183508 [GRCh37] Chr6:158515575..159103496 [NCBI36] Chr6:6q25.3	likely benign\|uncertain significance
GRCh38/hg38 6q25.2-27(chr6:152376338-170612001)x3	copy number gain	See cases [RCV000142594]	Chr6:152376338..170612001 [GRCh38] Chr6:152697473..170921089 [GRCh37] Chr6:152739166..170763014 [NCBI36] Chr6:6q25.2-27	pathogenic
GRCh38/hg38 6q23.2-27(chr6:133537271-165875545)x3	copy number gain	See cases [RCV000143444]	Chr6:133537271..165875545 [GRCh38] Chr6:133858409..166289033 [GRCh37] Chr6:133900102..166209023 [NCBI36] Chr6:6q23.2-27	pathogenic
GRCh38/hg38 6q25.3-26(chr6:158585724-160899783)x3	copy number gain	See cases [RCV000143618]	Chr6:158585724..160899783 [GRCh38] Chr6:159006756..161320815 [GRCh37] Chr6:158926744..161240805 [NCBI36] Chr6:6q25.3-26	uncertain significance
GRCh37/hg19 6q25.1-27(chr6:151214792-170892243)x3	copy number gain	See cases [RCV000449011]	Chr6:151214792..170892243 [GRCh37] Chr6:6q25.1-27	pathogenic
GRCh37/hg19 6q25.3(chr6:158392800-159229197)x3	copy number gain	See cases [RCV000447581]	Chr6:158392800..159229197 [GRCh37] Chr6:6q25.3	uncertain significance
GRCh37/hg19 6q25.3(chr6:155525920-159889169)x1	copy number loss	See cases [RCV000447692]	Chr6:155525920..159889169 [GRCh37] Chr6:6q25.3	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	copy number gain	See cases [RCV000512067]	Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	copy number gain	See cases [RCV000510595]	Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27	pathogenic
NM_001242394.2(SYTL3):c.1628C>G (p.Ala543Gly)	single nucleotide variant	not specified [RCV004307839]	Chr6:158763414 [GRCh38] Chr6:159184446 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.701C>T (p.Ala234Val)	single nucleotide variant	not specified [RCV004295104]	Chr6:158718192 [GRCh38] Chr6:159139224 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.874G>A (p.Asp292Asn)	single nucleotide variant	not specified [RCV004321107]	Chr6:158745498 [GRCh38] Chr6:159166530 [GRCh37] Chr6:6q25.3	likely benign
46,XX,der(6)(q25.1,q28)dn.seq[GRCh37/hg19]der(6)(6pter->6q25.2(+)(154768571)::q25.2(+)(154778901),q25.2(+)154778992::q25.2(-)(154774048),q25.2(-)(154768571)::q25.2(-)(154768571),q25.1(-)(~151443183-151443483))dn	complex	Coffin-Siris syndrome 1 [RCV000714957]	Chr6:151443333..171115067 [GRCh37] Chr6:6q25.1-27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3	copy number gain	not provided [RCV000745400]	Chr6:60107..171054786 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3	copy number gain	not provided [RCV000745404]	Chr6:165632..170919470 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3	copy number gain	not provided [RCV000745403]	Chr6:108666..170980171 [GRCh37] Chr6:6p25.3-q27	pathogenic
GRCh37/hg19 6q25.1-27(chr6:150284435-170919470)x3	copy number gain	not provided [RCV000746100]	Chr6:150284435..170919470 [GRCh37] Chr6:6q25.1-27	pathogenic
GRCh37/hg19 6q25.3-27(chr6:159155998-171054786)x3	copy number gain	not provided [RCV000746132]	Chr6:159155998..171054786 [GRCh37] Chr6:6q25.3-27	pathogenic
GRCh37/hg19 6q25.3-27(chr6:159006336-170713678)x3	copy number gain	not provided [RCV003312672]	Chr6:159006336..170713678 [GRCh37] Chr6:6q25.3-27	uncertain significance
GRCh37/hg19 6q25.3(chr6:157262571-160992289)x3	copy number gain	not provided [RCV000848057]	Chr6:157262571..160992289 [GRCh37] Chr6:6q25.3	uncertain significance
GRCh37/hg19 6q24.3-25.3(chr6:148195086-160127254)x3	copy number gain	not provided [RCV000846496]	Chr6:148195086..160127254 [GRCh37] Chr6:6q24.3-25.3	pathogenic
GRCh37/hg19 6q25.3(chr6:158392800-159229197)	copy number gain	not specified [RCV002053649]	Chr6:158392800..159229197 [GRCh37] Chr6:6q25.3	uncertain significance
GRCh37/hg19 6q25.3(chr6:155525920-159889169)	copy number loss	not specified [RCV002053642]	Chr6:155525920..159889169 [GRCh37] Chr6:6q25.3	pathogenic
GRCh37/hg19 6q25.2-26(chr6:153207930-164322346)	copy number loss	not specified [RCV002053640]	Chr6:153207930..164322346 [GRCh37] Chr6:6q25.2-26	pathogenic
NC_000006.11:g.(?_158532398)_(160114199_?)dup	duplication	Primary ciliary dyskinesia 32 [RCV001934131]	Chr6:158532398..160114199 [GRCh37] Chr6:6q25.3	uncertain significance
NC_000006.11:g.(?_158532398)_(162868359_?)del	deletion	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome [RCV003122912]\|not provided [RCV003122911]	Chr6:158532398..162868359 [GRCh37] Chr6:6q25.3-26	pathogenic\|no classifications from unflagged records
GRCh37/hg19 6q25.3-27(chr6:157318401-165233548)x1	copy number loss	See cases [RCV002287557]	Chr6:157318401..165233548 [GRCh37] Chr6:6q25.3-27	pathogenic
GRCh37/hg19 6q25.3-27(chr6:159121459-170919482)	copy number loss	Hydrocephalus [RCV002280751]	Chr6:159121459..170919482 [GRCh37] Chr6:6q25.3-27	pathogenic
NM_001242394.2(SYTL3):c.1169G>A (p.Arg390Gln)	single nucleotide variant	not specified [RCV004142044]	Chr6:158757242 [GRCh38] Chr6:159178274 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.191C>T (p.Ala64Val)	single nucleotide variant	not specified [RCV004078982]	Chr6:158665475 [GRCh38] Chr6:159086507 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.772T>C (p.Cys258Arg)	single nucleotide variant	not specified [RCV004162433]	Chr6:158725554 [GRCh38] Chr6:159146586 [GRCh37] Chr6:6q25.3	likely benign
NM_001242394.2(SYTL3):c.20T>A (p.Leu7Gln)	single nucleotide variant	not specified [RCV004230233]	Chr6:158663288 [GRCh38] Chr6:159084320 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.845G>T (p.Gly282Val)	single nucleotide variant	not specified [RCV004089213]	Chr6:158725627 [GRCh38] Chr6:159146659 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1670A>C (p.Gln557Pro)	single nucleotide variant	not specified [RCV004206427]	Chr6:158763456 [GRCh38] Chr6:159184488 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1384C>T (p.Arg462Trp)	single nucleotide variant	not specified [RCV004245216]	Chr6:158760715 [GRCh38] Chr6:159181747 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1330G>A (p.Val444Ile)	single nucleotide variant	not specified [RCV004109203]	Chr6:158760661 [GRCh38] Chr6:159181693 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1660G>T (p.Val554Phe)	single nucleotide variant	not specified [RCV004121198]	Chr6:158763446 [GRCh38] Chr6:159184478 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.257G>A (p.Arg86His)	single nucleotide variant	not specified [RCV004081410]	Chr6:158665541 [GRCh38] Chr6:159086573 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.322G>C (p.Glu108Gln)	single nucleotide variant	not specified [RCV004097414]	Chr6:158665606 [GRCh38] Chr6:159086638 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.470C>T (p.Thr157Ile)	single nucleotide variant	not specified [RCV004275783]	Chr6:158708345 [GRCh38] Chr6:159129377 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1778A>C (p.Gln593Pro)	single nucleotide variant	not specified [RCV004252652]	Chr6:158764549 [GRCh38] Chr6:159185581 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.941T>C (p.Ile314Thr)	single nucleotide variant	not specified [RCV004344228]	Chr6:158745565 [GRCh38] Chr6:159166597 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.611A>G (p.Gln204Arg)	single nucleotide variant	not specified [RCV004352526]	Chr6:158718102 [GRCh38] Chr6:159139134 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.266C>T (p.Ala89Val)	single nucleotide variant	not specified [RCV004344787]	Chr6:158665550 [GRCh38] Chr6:159086582 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1377C>T (p.Leu459=)	single nucleotide variant	not provided [RCV003429024]	Chr6:158760708 [GRCh38] Chr6:159181740 [GRCh37] Chr6:6q25.3	likely benign
GRCh37/hg19 6q25.2-27(chr6:152853218-170914297)x1	copy number loss	See cases [RCV004442824]	Chr6:152853218..170914297 [GRCh37] Chr6:6q25.2-27	pathogenic
NC_000006.12:g.(?_150381239)_(159553952_?)del	deletion	Chromosome 6q24-q25 deletion syndrome [RCV003884000]	Chr6:150381239..159553952 [GRCh38] Chr6:6q25.1-25.3	pathogenic
NM_001242394.2(SYTL3):c.821C>T (p.Ala274Val)	single nucleotide variant	not specified [RCV004466019]	Chr6:158725603 [GRCh38] Chr6:159146635 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1477C>T (p.Pro493Ser)	single nucleotide variant	not specified [RCV004466013]	Chr6:158762138 [GRCh38] Chr6:159183170 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.200A>G (p.Gln67Arg)	single nucleotide variant	not specified [RCV004466015]	Chr6:158665484 [GRCh38] Chr6:159086516 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1589A>C (p.Gln530Pro)	single nucleotide variant	not specified [RCV004466014]	Chr6:158763375 [GRCh38] Chr6:159184407 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.48G>C (p.Glu16Asp)	single nucleotide variant	not specified [RCV004466017]	Chr6:158663316 [GRCh38] Chr6:159084348 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1310C>T (p.Ala437Val)	single nucleotide variant	not specified [RCV004466012]	Chr6:158760641 [GRCh38] Chr6:159181673 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.616G>A (p.Asp206Asn)	single nucleotide variant	not specified [RCV004466018]	Chr6:158718107 [GRCh38] Chr6:159139139 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.950G>T (p.Cys317Phe)	single nucleotide variant	not specified [RCV004466020]	Chr6:158745574 [GRCh38] Chr6:159166606 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.109C>T (p.Arg37Trp)	single nucleotide variant	not specified [RCV004466009]	Chr6:158663377 [GRCh38] Chr6:159084409 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1187T>C (p.Val396Ala)	single nucleotide variant	not specified [RCV004466010]	Chr6:158757260 [GRCh38] Chr6:159178292 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1286G>A (p.Arg429His)	single nucleotide variant	not specified [RCV004466011]	Chr6:158757359 [GRCh38] Chr6:159178391 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.230G>A (p.Gly77Asp)	single nucleotide variant	not specified [RCV004466016]	Chr6:158665514 [GRCh38] Chr6:159086546 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1466C>T (p.Ala489Val)	single nucleotide variant	not specified [RCV004681883]	Chr6:158762127 [GRCh38] Chr6:159183159 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.71G>A (p.Arg24Gln)	single nucleotide variant	not specified [RCV004681884]	Chr6:158663339 [GRCh38] Chr6:159084371 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1295C>T (p.Pro432Leu)	single nucleotide variant	not specified [RCV004670998]	Chr6:158757368 [GRCh38] Chr6:159178400 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.275G>A (p.Arg92Gln)	single nucleotide variant	not specified [RCV004671003]	Chr6:158665559 [GRCh38] Chr6:159086591 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1690G>A (p.Asp564Asn)	single nucleotide variant	not specified [RCV004670999]	Chr6:158763476 [GRCh38] Chr6:159184508 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1321G>A (p.Glu441Lys)	single nucleotide variant	not specified [RCV004671000]	Chr6:158760652 [GRCh38] Chr6:159181684 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1668T>A (p.Asp556Glu)	single nucleotide variant	not specified [RCV004671001]	Chr6:158763454 [GRCh38] Chr6:159184486 [GRCh37] Chr6:6q25.3	uncertain significance
NM_001242394.2(SYTL3):c.1669C>A (p.Gln557Lys)	single nucleotide variant	not specified [RCV004671002]	Chr6:158763455 [GRCh38] Chr6:159184487 [GRCh37] Chr6:6q25.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	753
Count of miRNA genes:	293
Interacting mature miRNAs:	311
Transcripts:	ENST00000297239, ENST00000360448, ENST00000367081, ENST00000469735
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597446732	GWAS1542806_H	lipoprotein A measurement QTL GWAS1542806 (human)		5e-09	lipoprotein A measurement		6	158647682	158647683	Human
597035684	GWAS1131758_H	neuritic plaque measurement QTL GWAS1131758 (human)		0.000004	neuritic plaque measurement		6	158681417	158681418	Human
597606474	GWAS1663334_H	body weight gain QTL GWAS1663334 (human)		2e-11	body weight gain	body weight gain (CMO:0000420)	6	158694351	158694352	Human
1643404	BMD3_H	Bone mineral density QTL 3 (human)	2.42	0.0005	Bone mineral density		6	157563614	170805979	Human
597196864	GWAS1292938_H	memory performance QTL GWAS1292938 (human)		0.000009	memory performance		6	158701790	158701791	Human
597094815	GWAS1190889_H	lipoprotein A measurement QTL GWAS1190889 (human)		2e-13	lipoprotein A measurement		6	158684381	158684382	Human
597120876	GWAS1216950_H	lipoprotein A measurement QTL GWAS1216950 (human)		1e-11	lipoprotein A measurement		6	158665558	158665559	Human
407092328	GWAS741304_H	peripheral arterial disease QTL GWAS741304 (human)		0.0000008	peripheral arterial disease		6	158680261	158680262	Human
1643367	BW323_H	Body weight QTL 323 (human)	2.42	0.0005	Body fat amount		6	157563614	170805979	Human
596982954	GWAS1102473_H	memory performance QTL GWAS1102473 (human)		0.000009	memory performance		6	158701790	158701791	Human

Markers in Region

RH46204

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,185,688 - 159,185,845	UniSTS	GRCh37
Build 36	6	159,105,676 - 159,105,833	RGD	NCBI36
Celera	6	159,833,704 - 159,833,861	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,656,222 - 156,656,379	UniSTS
GeneMap99-GB4 RH Map	6	619.63	UniSTS
NCBI RH Map	6	1624.4	UniSTS

D6S1975

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,102,771 - 159,102,965	UniSTS	GRCh37
Build 36	6	159,022,759 - 159,022,953	RGD	NCBI36
Celera	6	159,750,773 - 159,750,967	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,573,586 - 156,573,780	UniSTS

SHGC-2438

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,102,771 - 159,102,847	UniSTS	GRCh37
Build 36	6	159,022,759 - 159,022,835	RGD	NCBI36
Celera	6	159,750,773 - 159,750,849	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,573,586 - 156,573,662	UniSTS

RH122273

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,090,069 - 159,090,401	UniSTS	GRCh37
Build 36	6	159,010,057 - 159,010,389	RGD	NCBI36
Celera	6	159,738,071 - 159,738,403	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,560,971 - 156,561,303	UniSTS
TNG Radiation Hybrid Map	6	79023.0	UniSTS

SHGC-132381

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,102,776 - 159,102,990	UniSTS	GRCh37
Build 36	6	159,022,764 - 159,022,978	RGD	NCBI36
Celera	6	159,750,778 - 159,750,992	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,573,591 - 156,573,805	UniSTS
TNG Radiation Hybrid Map	6	79019.0	UniSTS

SHGC-147444

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	159,124,510 - 159,124,825	UniSTS	GRCh37
Build 36	6	159,044,498 - 159,044,813	RGD	NCBI36
Celera	6	159,772,510 - 159,772,825	RGD
Cytogenetic Map	6	q25.3	UniSTS
HuRef	6	156,595,367 - 156,595,682	UniSTS
TNG Radiation Hybrid Map	6	79011.0	UniSTS

D16S325

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	9	q34.13	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	17	q21.2-q21.3	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	20	q13.32	UniSTS
Cytogenetic Map	1	p21.2	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	12	q13.2	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	1	p13.1	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	7	p22.2	UniSTS
Cytogenetic Map	7	q33	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	10	q11.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	3	q13.32	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	3	q22.1	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	6	q25.2-q25.3	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	3	q26.31	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	2	p13-p12	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	8	q21.13	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	4	q34.3	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	14	q21.2	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	9	p24.1-p23	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	10	pter-q25.3	UniSTS
Cytogenetic Map	6	q25.2-q27	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	15	q14	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	1	p36.3-p34.3	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	4	p15.2	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	2	q12.2	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	5	q22	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	12	q14.2	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	10	q26.11	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	6	q22.32	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	12	q23.3	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	19	qter	UniSTS
Cytogenetic Map	7	p13-p12	UniSTS
Cytogenetic Map	2	p22	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	19	q13.4	UniSTS

Expression

RNA-SEQ Expression

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	2433	2788	2246	4944	1724	2350	4	624	1949	465	2268	7291	6461	53	3710	1	851	1739	1615	173

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_029794	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001009991	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242384	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242395	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001318745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267218	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267222	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006715605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006715606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006715611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011536254	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011536255	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011495	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017011499	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024446588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419549	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419553	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419555	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419556	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419557	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419560	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047419562	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356794	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356797	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356798	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356804	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356805	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356806	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356808	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356809	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356818	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356819	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356822	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356823	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054356824	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AI674404	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055750	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK092729	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK304191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL567177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL589931	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC042966	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC085612	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC100828	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC100829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC100830	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC100831	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB175440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC394549	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000297239 ⟹ ENSP00000297239

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	158,661,319 - 158,764,869 (+)	Ensembl

Ensembl Acc Id:

ENST00000360448 ⟹ ENSP00000353631

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	158,650,014 - 158,764,869 (+)	Ensembl

Ensembl Acc Id:

ENST00000367081 ⟹ ENSP00000356048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	158,650,014 - 158,764,876 (+)	Ensembl

Ensembl Acc Id:

ENST00000469735

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	158,650,053 - 158,663,048 (+)	Ensembl

Ensembl Acc Id:

ENST00000611299 ⟹ ENSP00000483936

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	158,650,054 - 158,764,871 (+)	Ensembl

RefSeq Acc Id:

NM_001009991 ⟹ NP_001009991

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI
GRCh37	6	159,065,931 - 159,185,908 (+)	NCBI
Build 36	6	158,991,034 - 159,105,889 (+)	NCBI Archive
Celera	6	159,719,041 - 159,833,917 (+)	RGD
HuRef	6	156,541,943 - 156,656,442 (+)	ENTREZGENE
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

Sequence:

show sequence

CTCTTCTCTTGAAGCAGATGCGAAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGA
ATTGCAGTGATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCT
TGGGGCACTGAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGG
CGTTGCCCCTGCTGGCATAGTCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTCCTGCTGA
CCTGGAAACATCTTAAATGGAAGGGCGTGAGCGCTTGGTCCATGCAGTGAAGCTCTTCCAACCT
GGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGATCTGAGTGCTCTCAAGGAGTTAGA
ACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCGGTTCAAAACACAGAGGAGGAGAGG
ACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGAAAGGAGCGAAGAACACGGACTGGG
AGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCTGGGGTTCCTGCTGCACCGGGGCGC
CGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGCCGAGTGTTCCTGAGGGGGACCCAT
GCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCAAAATAAAAACTGGAGAATGGTTCT
ATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACATGAGACAGTTGGAGGGCAGCTCTT
GCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCTCCTACTCCACCTCCTGTCAGCGAG
AGCCAGTGCAGCCGCAGTCCTGGCAGGAAGGTCAGTGCACCAGATATTCTGAAACCTCTCAATC
AAGAGGATCCCAAATGCTCTACTAACCCTATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGC
ACCCAGTACCATATTCTCTGGAGGTTTTAGACACGGAAGTTTAATTAGCATTGACAGCACCTGT
ACAGAGATGGGCAATTTTGACAATGCTAATGTCACTGGAGAAATAGAATTTGCCATTCATTATT
GCTTCAAAACCCATTCTTTAGAAATATGCATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGA
AAAGAAGAAAAAGTGCAATCCGTATGTGAAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGA
AAGCGCAAGACTGGAGTCCAAAGGAACACCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATC
AGGTGGCCCCTGCCCAGCTGGTGACCCGGCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCT
GGCCCGGAGAGTGTTTCTTGGAGAAGTGATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGC
ACAACACAGTCCTTCCGCTGGCATCCGCTCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTC
CTCAGAGTAATGGAGAGCTCACAGTCCGGGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACT
CCAAGAGGCTCAAGAAGGGACAGATCAGCCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTA
GGAGCCAAGAATTTACCTGTGCGGCCAGATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCA
CTCTGCCAGACCAACAAAAACTGAGACTGAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCA
GTGGAAACACTCATTTGTCTTCAGTGGCGTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAG
TTAACTGTCTGGGATCAGGCCCTCTTTGGAATGAACGACCGCTTGCTTGGAGGAACCAGACTTG
GTTCAAAGGGAGACACAGCTGTTGGCGGGGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAA
AGTCCTTTCCAGCCCCAATCTATGGACAGACATGACTCTTGTCCTGCACTGACATGAAGGCCTC
AAGGTTCCAGGTTGCAGCAGGCGTGAGGCACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGC
AGGGTCCCAGCTGGAGACCCCTTTGACCTTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCT
TAACCGCCTATTGGTATCTGTGTATATTTACGTTAAACACAATTATGTTACCTAAGCCTCTGGT
GGGTTATCTCCTCTTTGAGATGTAGAAAATGGCCAGATTTTAATAAACGTTGTTACCCATGTC

hide sequence

RefSeq Acc Id:

NM_001242384 ⟹ NP_001229313

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI
GRCh37	6	159,065,931 - 159,185,908 (+)	NCBI
HuRef	6	156,541,943 - 156,656,442 (+)	ENTREZGENE
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

Sequence:

show sequence

CTCTTCTCTTGAAGCAGATGCGAAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGA
ATTGCAGTGATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCT
TGGGGCACTGAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGG
CGTTGCCCCTGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCA
TGATGGTTCCTGCTGACCTGGAAACATCTTAAATGGAAGGGCGTGAGCGCTTGGTCCATGCAGT
GAAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGATCTGAGTG
CTCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCGGTTCAAAA
CACAGAGGAGGAGAGGACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGAAAGGAGCG
AAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCTGGGGTTCC
TGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGCCGAGTGTT
CCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCAAAATAAAA
ACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACATGAGACAG
TTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCTCCTACTCC
ACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTACAGGAATTTGGTCAGTTT
AGAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTACCCACGTGAAAAAGCTCT
CCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGGCAGTGTGT
GGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGAAGGTCAGT
GCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCTATTTTGA
AGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTAGACACGG
AAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTAATGTCACT
GGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATGCATCAAGG
CCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTGAAGACCTA
CCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACACCGTGGAC
CCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCGGCAGCTGC
AGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTGATCATTCC
TCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGCTCCGGGCC
AAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCGGGCTAAGC
TGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAGCCATCACT
TCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAGATGGCACC
TTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACTGAAGTCGC
CAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGCGTAACCCC
AGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTGGAATGAAC
GACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGGGGATGCAT
GCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACAGACATGAC
TCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGGCACTGTGC
GTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACCTTGAGCAG
TCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATTTACGTTAA
ACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAAATGGCCAG
ATTTTAATAAACGTTGTTACCCATGTC

hide sequence

RefSeq Acc Id:

NM_001242394 ⟹ NP_001229323

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI
GRCh37	6	159,065,931 - 159,185,908 (+)	NCBI
HuRef	6	156,541,943 - 156,656,442 (+)	ENTREZGENE
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

Sequence:

show sequence

CTCTTCTCTTGAAGCAGATGCGAAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGA
ATTGCAGTGATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCT
TGGGGCACTGAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGG
CGTTGCCCCTGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCA
TGATGGTTCCTGCTGACCTGGAAACATCTTAAATGGAAGGTTAGCTTCTATGAGTCACTGATAC
TCTTTTTATTGCTATTTCTAAATTTCCTTGGCTTGAAAATTACTTCTGCTTTGCAGAAATTATC
TGCTTGCAGCTGTGGATAATTTATAACAATCTCTGGTGAAACCTCAGAAAAGAGATATGCTTTT
GTCTTAGATGGATGTCAGCAGCTGCTGCAGAACCCGGTGAAAACACCCCCCGGGTAGCACGAGG
CTCTGCGAGCCGTAACTCCGACAAACGCAGAACTTCTTGAGGCTTTCTTCTTCTAAGGAGTATG
ACACAGTTAAAAAGGAAAAAAGAACCACAAGCAAAACAGTTGCCAGTGAAATAGGAGAGGGAGC
TCTTTAAACAAGGCTGGCTGCAGCTGGCCTCCGCCGCTCATCTGCAGGGCGTGAGCGCTTGGTC
CATGCAGTGAAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGA
TCTGAGTGCTCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCG
GTTCAAAACACAGAGGAGGAGAGGACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGA
AAGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCT
GGGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGC
CGAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCA
AAATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACA
TGAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCT
CCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTACAGGAATTTG
GTCAGTTTAGAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTACCCACGTGAA
AAAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGG
CAGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGA
AGGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCC
TATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTT
AGACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTA
ATGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATG
CATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTG
AAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACA
CCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCG
GCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTG
ATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGC
TCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCG
GGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAG
CCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAG
ATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACT
GAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGC
GTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTG
GAATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGG
GGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACA
GACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGG
CACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACC
TTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATT
TACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAA
ATGGCCAGATTTTAATAAACGTTGTTACCCATGTC

hide sequence

RefSeq Acc Id:

NM_001242395 ⟹ NP_001229324

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI
GRCh37	6	159,065,931 - 159,185,908 (+)	NCBI
HuRef	6	156,541,943 - 156,656,442 (+)	ENTREZGENE
CHM1_1	6	159,333,606 - 159,448,611 (+)	NCBI
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

Sequence:

show sequence

CTCTTCTCTTGAAGCAGATGCGAAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGA
ATTGCAGTGATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCT
TGGGGCACTGAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGG
CGTTGCCCCTGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCA
TGATGGTTCCTGCTGACCTGGAAACATCTTAAATGGAAGGTTAGCTTCTATGAGTCACTGATAC
TCTTTTTATTGCTATTTCTAAATTTCCTTGGCTTGAAAATTACTTCTGCTTTGCAGAAATTATC
TGCTTGCAGCTGTGGATAATTTATAACAATCTCTGGTGAAACCTCAGAAAAGAGATATGCTTTT
GTCTTAGATGGATGTCAGCAGCTGCTGCAGAACCCGGTGAAAACACCCCCCGGGTAGCACGAGG
CTCTGCGAGCCGTAACTCCGACAAACGCAGAACTTCTTGAGGCTTTCTTCTTCTAAGGAGTATG
ACACAGTTAAAAAGGAAAAAAGAACCACAAGCAAAACAGTTGCCAGTGAAATAGGAGAGGGAGC
TCTTTAAACAAGGCTGGCTGCAGCTGGCCTCCGCCGCTCATCTGCAGGGCGTGAGCGCTTGGTC
CATGCAGTGAAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGA
TCTGAGTGCTCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCG
GTTCAAAACACAGAGGAGGAGAGGACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGA
AAGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCT
GGGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGC
CGAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCA
AAATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACA
TGAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCT
CCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGAAGGTCAGTGCAC
CAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCTATTTTGAAGCA
ACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTAGACACGGAAGT
TTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTAATGTCACTGGAG
AAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATGCATCAAGGCCTG
TAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTGAAGACCTACCTG
TTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACACCGTGGACCCGA
CCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCGGCAGCTGCAGGT
CTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTGATCATTCCTCTG
GCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGCTCCGGGCCAAGG
CGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCGGGCTAAGCTGGT
TCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAGCCATCACTTCAT
GGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAGATGGCACCTTGA
ACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACTGAAGTCGCCAGT
CCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGCGTAACCCCAGCT
CAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTGGAATGAACGACC
GCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGGGGATGCATGCTC
ACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACAGACATGACTCTT
GTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGGCACTGTGCGTCT
GCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACCTTGAGCAGTCTC
CATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATTTACGTTAAACAC
AATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAAATGGCCAGATTT
TAATAAACGTTGTTACCCATGTC

hide sequence

RefSeq Acc Id:

NM_001318745 ⟹ NP_001305674

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,662,947 - 158,764,871 (+)	NCBI
CHM1_1	6	159,346,998 - 159,448,611 (+)	NCBI
T2T-CHM13v2.0	6	159,908,180 - 160,010,070 (+)	NCBI

Sequence:

show sequence

AGAAAAGAGATATGCTTTTGTCTTAGATGGATGTCAGCAGCTGCTGCAGAACCCGGTGAAAACA
CCCCCCGGGTAGCACGAGGCTCTGCGAGCCGTAACTCCGACAAACGCAGAACTTCTTGAGGCTT
TCTTCTTCTAAGGAGTATGACACAGTTAAAAAGGAAAAAAGAACCACAAGCAAAACAGTTGCCA
GTGAAATAGGAGAGGGAGCTCTTTAAACAAGGCTGGCTGCAGCTGGCCTCCGCCGCTCATCTGC
AGGGCGTGAGCGCTTGGTCCATGCAGTGAAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAG
AAATGGCCCAAGAAATAGATCTGAGTGCTCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGT
CCTGTACCGAGACCAGGCGGTTCAAAACACAGAGGAGGAGAGGACACGGTAGGCTGCCCTTCCC
GGGGGGTCACTTTGGGTGTTTAGCTTTCTCTGCTTGGGGCCTGCCACTCCGTCGCCAATGCTGT
TTGCTTACAAATCACTACCCACCTGCTGCTGGGCTTCGTGCCTGAGAAGGGTCCTAACGAAGGT
CTGTTGGTGGAGATGATCCTCCTTATGTAACTAAACGTAGAGGACGCTCAGGAGGAGGAGGGAG
GCCGCTCTTGTTATTCATTTAAAACGGTGCCTTTGGGCGGAAACTGAAAACACACCTGCAGCAT
CTCCGGTGGAAAGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCC
AGCAGGTGCTGGGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTG
TGCCCAGTGCCGAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGAC
AGGAATGTCAAAATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTG
GAGGCAAACATGAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTC
TGTGGTTCCTCCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTA
CAGGAATTTGGTCAGTTTAGAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTA
CCCACGTGAAAAAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCAC
GGGCCCCAGGCAGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTC
ACCACCAGGAAGGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCT
CTACTAACCCTATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTC
TGGAGGTTTTAGACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTT
GACAATGCTAATGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTT
TAGAAATATGCATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAA
TCCGTATGTGAAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTC
CAAAGGAACACCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGC
TGGTGACCCGGCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCT
TGGAGAAGTGATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGC
TGGCATCCGCTCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGC
TCACAGTCCGGGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGG
GACAGATCAGCCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCT
GTGCGGCCAGATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAA
AACTGAGACTGAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGT
CTTCAGTGGCGTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAG
GCCCTCTTTGGAATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAG
CTGTTGGCGGGGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAA
TCTATGGACAGACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGC
AGGCGTGAGGCACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGAC
CCCTTTGACCTTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATC
TGTGTATATTTACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGA
GATGTAGAAAATGGCCAGATTTTAATAAACGTTGTTACCCATGTC

hide sequence

RefSeq Acc Id:

XM_005267222 ⟹ XP_005267279

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,708,322 - 158,764,871 (+)	NCBI
GRCh37	6	159,065,931 - 159,185,908 (+)	NCBI

Sequence:

show sequence

ATTTCTGTGGTTCCTCCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCA
GGAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGG
CAGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGA
AGGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCC
TATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTT
AGACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTA
ATGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATG
CATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTG
AAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACA
CCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCG
GCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTG
ATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGC
TCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCG
GGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAG
CCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAG
ATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACT
GAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGC
GTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTG
GAATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGG
GGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACA
GACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGG
CACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACC
TTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATT
TACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAA
ATGGCCAGATTTTAATAAACGTTGTTACCCATGTCCTCCAGTGCTTATCAAATGAGGTAAAAGG
CCGGCTGGTGGGCATGGTAACTCCCCCCTGTAATCCCAGCAACTTTGGGAGGCTGCAGTGGATG
GCTTGAGCTCAGAAGTGTGAGATCAGCCCAGGCAACATAGATACCCTGTCTACAAAAAAACCAA
AAAATTATCCAGGTGTGGTGGTACACACCTGTAGTCCCAGTTACTCAGGAGGCTGAACCGGGAG
GATTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCCCGATCATGCAACTGTGCTCCAGCCTGGGC
CAAAGTAAGACCCTGTCTCAAGGCGGGGGGGGGAGTCACAGCTTCGCTGTGAGAAGCACTTTAT
TTTTTGAGACGGAGTCTCCCCGTCACCAGGCTGGAGTGCAGTGGCACGATCTTGGCTTGCTGCA
AGCTCCGCCTCCCGGGTTCTAGCAATTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTATAGG
TATGCACCACCACACCAGGCTAATTTTCGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGC
CAGGATGGTCTCGATCTCCTGACCTCGTGATCCGACCACCTCGGCCTCCCAAAGTGCTGGGATT
ACAGGTGTGAGCCACTGTGCCCGGCTATGAGGAGCATTTTAGAGGAGCCTGATGAGTGTTGGAG
CAGTCTTTCTCTCCTGTGGAAACCATCTCGAGGAGGTTAGGTGACCCATGGAGCACCATGTCTT
GGGTTGGTCAGCTCCAACTTACCAGTGTACCCCCAGGGACACCACGGCCCCTCACGAAACCTGG
CCAGAGGACAGCATAGAGCCCAGACGAGTCGGCGGTAGCCCTCCCACCCCACACACAAGCACAC
ACCCGTGCTGCTTCGTGCCTTTGCAAAGCTTTTATTTCATGTCTGCGGCATGGAATCCACCTGC
ACATGGCATCTTAGCTGTGAAGGAGAAAGCAGTGCACGAGAAGGAATGAGTGGGCGGAACCAAC
GGCCTCCACAAGCTGCCTTCCAGCAGCCTGCCAAGGCCATGGCAGAGAGAGACTGCAAACAAAC
AAACACAAGCAAACAGAGTCTCTTCACAGCTGGAGTCTGAAAGCTCATAGTGGCATGTGTGAAT
CTGACAAAATTAAAAGTGTGCATAGTCCATTACATGCATAAAACACTAATAATAATCCTGTTTA
CACGTGACTGCAGCAGGCAGGTCCAGCTCCACCACTGCCCTCCTGCCACATCACATCAAGTGCC
ATGGTTTAGAGGGTTTTTCATATGTAATTCTTTTATTCTGTAAAAGGTAACAAAATATACAGAA
CAAAACTTTCCCTTTTTAAAACTAATGTTACAAATCTGTATTATCACTTGTATATAAATAGTAT
ATAGCTGATCATTAATAAGGTGTATAAGTACAATGTATTCTAAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_006715606 ⟹ XP_006715669

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

Sequence:

show sequence

CTGAATTCGCCTCTCCTCCTGTCCTCTGGGAGGTGGTAGTTTCCATGGGAATCCGTGAGGGTAG
CCGGGCAGCTCCCTAAACCTTAGCAACAGAAACAAAACACACGTACAAAAGGCAGTCCTGGAGG
GGAAGCGTGGTCCCGGCCCCTCCTCCGGTTTGTACTGTGTGGATTGACGCGGACGTTCAAACCC
GCTCGGACACCTGGCAACAAACTCGAAAGTGACTGCTGAAGGCAGTGCGCCCGGTGAGACGTTG
TTGCAGTTCCCTTGGGGACTGGGATTGGCATGCTTTAGCTATCTGAACGAAACTTCCCTTTGGG
GAGTTAAGTTTTCCAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGAATTGCAGTG
ATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCTTGGGGCACT
GAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGGCGTTGCCCC
TGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTC
CTGCTGACCTGGAAACATCTTAAATGGAAGATGGATGTCAGCAGCTGCTGCAGAACCCGGTGAA
AACACCCCCCGGGTAGCACGAGGCTCTGCGAGCCGTAACTCCGACAAACGCAGAACTTCTTGAG
GCTTTCTTCTTCTAAGGAGTATGACACAGTTAAAAAGGAAAAAAGAACCACAAGCAAAACAGTT
GCCAGTGAAATAGGAGAGGGAGCTCTTTAAACAAGGCTGGCTGCAGCTGGCCTCCGCCGCTCAT
CTGCAGGGCGTGAGCGCTTGGTCCATGCAGTGAAGCTCTTCCAACCTGGGTCAACGAAAACGGA
GAAGAAATGGCCCAAGAAATAGATCTGAGTGCTCTCAAGGAGTTAGAACGCGAGGCCATTCTCC
AGGTCCTGTACCGAGACCAGGCGGTTCAAAACACAGAGGAGGAGAGGACACGGAAACTGAAAAC
ACACCTGCAGCATCTCCGGTGGAAAGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGC
TGTGCGCGCTGCCAGCAGGTGCTGGGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCA
GCCACCGCGTGTGTGCCCAGTGCCGAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGT
GTGCTTCGAGGACAGGAATGTCAAAATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAG
AAATTTCCAACTGGAGGCAAACATGAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGC
TGAGCAAAATTTCTGTGGTTCCTCCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAG
TCCTGGCAGGTTACAGGAATTTGGTCAGTTTAGAGGATTTAATAAGTCCGTGGAAAATTTGTTT
CTGTCTCTTGCTACCCACGTGAAAAAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGC
ATCTTCTCGCCACGGGCCCCAGGCAGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACAC
TGCGGTCAACGTCACCACCAGGAAGGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAG
GATCCCAAATGCTCTACTAACCCTATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCA
GTACCATATTCTCTGGAGGTTTTAGACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGA
GATGGGCAATTTTGACAATGCTAATGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTC
AAAACCCATTCTTTAGAAATATGCATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGA
AGAAAAAGTGCAATCCGTATGTGAAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCG
CAAGACTGGAGTCCAAAGGAACACCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTG
GCCCCTGCCCAGCTGGTGACCCGGCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCC
GGAGAGTGTTTCTTGGAGAAGTGATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAAC
ACAGTCCTTCCGCTGGCATCCGCTCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAG
AGTAATGGAGAGCTCACAGTCCGGGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAG
AGGCTCAAGAAGGGACAGATCAGCCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGC
CAAGAATTTACCTGTGCGGCCAGATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTG
CCAGACCAACAAAAACTGAGACTGAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGA
AACACTCATTTGTCTTCAGTGGCGTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAAC
TGTCTGGGATCAGGCCCTCTTTGGAATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCA
AAGGGAGACACAGCTGTTGGCGGGGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCC
TTTCCAGCCCCAATCTATGGACAGACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGT
TCCAGGTTGCAGCAGGCGTGAGGCACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGT
CCCAGCTGGAGACCCCTTTGACCTTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACC
GCCTATTGGTATCTGTGTATATTTACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTT
ATCTCCTCTTTGAGATGTAGAAAATGGCCAGATTTTAATAAACGTTGTTACCCATGTCCTCCAG
TGCTTATCAAATGAGGTAAAAGGCCGGCTGGTGGGCATGGTAACTCCCCCCTGTAATCCCAGCA
ACTTTGGGAGGCTGCAGTGGATGGCTTGAGCTCAGAAGTGTGAGATCAGCCCAGGCAACATAGA
TACCCTGTCTACAAAAAAACCAAAAAATTATCCAGGTGTGGTGGTACACACCTGTAGTCCCAGT
TACTCAGGAGGCTGAACCGGGAGGATTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCCCGATCA
TGCAACTGTGCTCCAGCCTGGGCCAAAGTAAGACCCTGTCTCAAGGCGGGGGGGGGAGTCACAG
CTTCGCTGTGAGAAGCACTTTATTTTTTGAGACGGAGTCTCCCCGTCACCAGGCTGGAGTGCAG
TGGCACGATCTTGGCTTGCTGCAAGCTCCGCCTCCCGGGTTCTAGCAATTCTCCTGCCCCAGCC
TCCCAAGTAGCTGGGATTATAGGTATGCACCACCACACCAGGCTAATTTTCGTATTTTTAGTAA
AGATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGACCACCT
CGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCTATGAGGAGCATTTTA
GAGGAGCCTGATGAGTGTTGGAGCAGTCTTTCTCTCCTGTGGAAACCATCTCGAGGAGGTTAGG
TGACCCATGGAGCACCATGTCTTGGGTTGGTCAGCTCCAACTTACCAGTGTACCCCCAGGGACA
CCACGGCCCCTCACGAAACCTGGCCAGAGGACAGCATAGAGCCCAGACGAGTCGGCGGTAGCCC
TCCCACCCCACACACAAGCACACACCCGTGCTGCTTCGTGCCTTTGCAAAGCTTTTATTTCATG
TCTGCGGCATGGAATCCACCTGCACATGGCATCTTAGCTGTGAAGGAGAAAGCAGTGCACGAGA
AGGAATGAGTGGGCGGAACCAACGGCCTCCACAAGCTGCCTTCCAGCAGCCTGCCAAGGCCATG
GCAGAGAGAGACTGCAAACAAACAAACACAAGCAAACAGAGTCTCTTCACAGCTGGAGTCTGAA
AGCTCATAGTGGCATGTGTGAATCTGACAAAATTAAAAGTGTGCATAGTCCATTACATGCATAA
AACACTAATAATAATCCTGTTTACACGTGACTGCAGCAGGCAGGTCCAGCTCCACCACTGCCCT
CCTGCCACATCACATCAAGTGCCATGGTTTAGAGGGTTTTTCATATGTAATTCTTTTATTCTGT
AAAAGGTAACAAAATATACAGAACAAAACTTTCCCTTTTTAAAACTAATGTTACAAATCTGTAT
TATCACTTGTATATAAATAGTATATAGCTGATCATTAATAAGGTGTATAAGTACAATGTATTCT
AAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_006715611 ⟹ XP_006715674

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

Sequence:

show sequence

CTGAATTCGCCTCTCCTCCTGTCCTCTGGGAGGTGGTAGTTTCCATGGGAATCCGTGAGGGTAG
CCGGGCAGCTCCCTAAACCTTAGCAACAGAAACAAAACACACGTACAAAAGGCAGTCCTGGAGG
GGAAGCGTGGTCCCGGCCCCTCCTCCGGTTTGTACTGTGTGGATTGACGCGGACGTTCAAACCC
GCTCGGACACCTGGCAACAAACTCGAAAGTGACTGCTGAAGGCAGTGCGCCCGGTGAGACGTTG
TTGCAGTTCCCTTGGGGACTGGGATTGGCATGCTTTAGCTATCTGAACGAAACTTCCCTTTGGG
GAGTTAAGTTTTCCAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGAATTGCAGTG
ATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCTTGGGGCACT
GAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGGCGTTGCCCC
TGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTC
CTGCTGACCTGGAAACATCTTAAATGGAAGGGCTGCAGGAAACTGAAAACACACCTGCAGCATC
TCCGGTGGAAAGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCA
GCAGGTGCTGGGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGT
GCCCAGTGCCGAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACA
GGAATGTCAAAATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGG
AGGCAAACATGAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCT
GTGGTTCCTCCTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTAC
AGGAATTTGGTCAGTTTAGAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTAC
CCACGTGAAAAAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACG
GGCCCCAGGCAGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCA
CCACCAGGAAGGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTC
TACTAACCCTATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCT
GGAGGTTTTAGACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTG
ACAATGCTAATGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTT
AGAAATATGCATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAAT
CCGTATGTGAAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCC
AAAGGAACACCGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCT
GGTGACCCGGCAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTT
GGAGAAGTGATCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCT
GGCATCCGCTCCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCT
CACAGTCCGGGCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGG
ACAGATCAGCCATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTG
TGCGGCCAGATGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAA
ACTGAGACTGAAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTC
TTCAGTGGCGTAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGG
CCCTCTTTGGAATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGC
TGTTGGCGGGGATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAAT
CTATGGACAGACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCA
GGCGTGAGGCACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACC
CCTTTGACCTTGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCT
GTGTATATTTACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAG
ATGTAGAAAATGGCCAGATTTTAATAAACGTTGTTACCCATGTCCTCCAGTGCTTATCAAATGA
GGTAAAAGGCCGGCTGGTGGGCATGGTAACTCCCCCCTGTAATCCCAGCAACTTTGGGAGGCTG
CAGTGGATGGCTTGAGCTCAGAAGTGTGAGATCAGCCCAGGCAACATAGATACCCTGTCTACAA
AAAAACCAAAAAATTATCCAGGTGTGGTGGTACACACCTGTAGTCCCAGTTACTCAGGAGGCTG
AACCGGGAGGATTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCCCGATCATGCAACTGTGCTCC
AGCCTGGGCCAAAGTAAGACCCTGTCTCAAGGCGGGGGGGGGAGTCACAGCTTCGCTGTGAGAA
GCACTTTATTTTTTGAGACGGAGTCTCCCCGTCACCAGGCTGGAGTGCAGTGGCACGATCTTGG
CTTGCTGCAAGCTCCGCCTCCCGGGTTCTAGCAATTCTCCTGCCCCAGCCTCCCAAGTAGCTGG
GATTATAGGTATGCACCACCACACCAGGCTAATTTTCGTATTTTTAGTAAAGATGGGGTTTCAC
CATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGACCACCTCGGCCTCCCAAAGT
GCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCTATGAGGAGCATTTTAGAGGAGCCTGATGA
GTGTTGGAGCAGTCTTTCTCTCCTGTGGAAACCATCTCGAGGAGGTTAGGTGACCCATGGAGCA
CCATGTCTTGGGTTGGTCAGCTCCAACTTACCAGTGTACCCCCAGGGACACCACGGCCCCTCAC
GAAACCTGGCCAGAGGACAGCATAGAGCCCAGACGAGTCGGCGGTAGCCCTCCCACCCCACACA
CAAGCACACACCCGTGCTGCTTCGTGCCTTTGCAAAGCTTTTATTTCATGTCTGCGGCATGGAA
TCCACCTGCACATGGCATCTTAGCTGTGAAGGAGAAAGCAGTGCACGAGAAGGAATGAGTGGGC
GGAACCAACGGCCTCCACAAGCTGCCTTCCAGCAGCCTGCCAAGGCCATGGCAGAGAGAGACTG
CAAACAAACAAACACAAGCAAACAGAGTCTCTTCACAGCTGGAGTCTGAAAGCTCATAGTGGCA
TGTGTGAATCTGACAAAATTAAAAGTGTGCATAGTCCATTACATGCATAAAACACTAATAATAA
TCCTGTTTACACGTGACTGCAGCAGGCAGGTCCAGCTCCACCACTGCCCTCCTGCCACATCACA
TCAAGTGCCATGGTTTAGAGGGTTTTTCATATGTAATTCTTTTATTCTGTAAAAGGTAACAAAA
TATACAGAACAAAACTTTCCCTTTTTAAAACTAATGTTACAAATCTGTATTATCACTTGTATAT
AAATAGTATATAGCTGATCATTAATAAGGTGTATAAGTACAATGTATTCTAAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_011536254 ⟹ XP_011534556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

Sequence:

show sequence

CTGAATTCGCCTCTCCTCCTGTCCTCTGGGAGGTGGTAGTTTCCATGGGAATCCGTGAGGGTAG
CCGGGCAGCTCCCTAAACCTTAGCAACAGAAACAAAACACACGTACAAAAGGCAGTCCTGGAGG
GGAAGCGTGGTCCCGGCCCCTCCTCCGGTTTGTACTGTGTGGATTGACGCGGACGTTCAAACCC
GCTCGGACACCTGGCAACAAACTCGAAAGTGACTGCTGAAGGCAGTGCGCCCGGTGAGACGTTG
TTGCAGTTCCCTTGGGGACTGGGATTGGCATGCTTTAGCTATCTGAACGAAACTTCCCTTTGGG
GAGTTAAGTTTTCCAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGAATTGCAGTG
ATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCTTGGGGCACT
GAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGGCGTTGCCCC
TGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTC
CTGCTGACCTGGAAACATCTTAAATGGAAGGGCGTGAGCGCTTGGTCCATGCAGTGAAGCTCTT
CCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGATCTGAGTGCTCTCAAGG
AGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCGGTTCAAAACACAGAGGA
GGAGAGGACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGAAAGGAGCGAAGAACACG
GACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCTGGGGTTCCTGCTGCACC
GGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGCCGAGTGTTCCTGAGGGG
GACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCAAAATAAAAACTGGAGAA
TGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACATGAGACAGTTGGAGGGC
AGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCTCCTACTCCACCTCCTGT
CAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTACAGGAATTTGGTCAGTTTAGAGGATTT
AATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTACCCACGTGAAAAAGCTCTCCAAATCCC
AGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGGCAGTGTGTGGGACAGAC
AGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGAAGGTCAGTGCACCAGAT
ATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCTATTTTGAAGCAACAGA
ATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTAGACACGGAAGTTTAAT
TAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTAATGTCACTGGAGAAATA
GAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATGCATCAAGGCCTGTAAGA
ACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTGAAGACCTACCTGTTGCC
CGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACACCGTGGACCCGACCTTT
CAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCGGCAGCTGCAGGTCTCGG
TGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTGATCATTCCTCTGGCCAC
GTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGCTCCGGGCCAAGGCGGAG
AAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCGGGCTAAGCTGGTTCTCC
CTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAGCCATCACTTCATGGTCA
ACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAGATGGCACCTTGAACTCA
TTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACTGAAGTCGCCAGTCCTGA
GGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGCGTAACCCCAGCTCAGCT
GAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTGGAATGAACGACCGCTTG
CTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGGGGATGCATGCTCACTAT
CGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACAGACATGACTCTTGTCCT
GCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGGCACTGTGCGTCTGCAGA
GGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACCTTGAGCAGTCTCCATCT
GCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATTTACGTTAAACACAATTA
TGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAAATGGCCAGATTTTAATA
AACGTTGTTACCCATGTCCTCCAGTGCTTATCAAATGAGGTAAAAGGCCGGCTGGTGGGCATGG
TAACTCCCCCCTGTAATCCCAGCAACTTTGGGAGGCTGCAGTGGATGGCTTGAGCTCAGAAGTG
TGAGATCAGCCCAGGCAACATAGATACCCTGTCTACAAAAAAACCAAAAAATTATCCAGGTGTG
GTGGTACACACCTGTAGTCCCAGTTACTCAGGAGGCTGAACCGGGAGGATTGAGCCCAGGAGGT
TGAGGCTGCAGTAAGCCCCGATCATGCAACTGTGCTCCAGCCTGGGCCAAAGTAAGACCCTGTC
TCAAGGCGGGGGGGGGAGTCACAGCTTCGCTGTGAGAAGCACTTTATTTTTTGAGACGGAGTCT
CCCCGTCACCAGGCTGGAGTGCAGTGGCACGATCTTGGCTTGCTGCAAGCTCCGCCTCCCGGGT
TCTAGCAATTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTATAGGTATGCACCACCACACCA
GGCTAATTTTCGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCT
CCTGACCTCGTGATCCGACCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTG
TGCCCGGCTATGAGGAGCATTTTAGAGGAGCCTGATGAGTGTTGGAGCAGTCTTTCTCTCCTGT
GGAAACCATCTCGAGGAGGTTAGGTGACCCATGGAGCACCATGTCTTGGGTTGGTCAGCTCCAA
CTTACCAGTGTACCCCCAGGGACACCACGGCCCCTCACGAAACCTGGCCAGAGGACAGCATAGA
GCCCAGACGAGTCGGCGGTAGCCCTCCCACCCCACACACAAGCACACACCCGTGCTGCTTCGTG
CCTTTGCAAAGCTTTTATTTCATGTCTGCGGCATGGAATCCACCTGCACATGGCATCTTAGCTG
TGAAGGAGAAAGCAGTGCACGAGAAGGAATGAGTGGGCGGAACCAACGGCCTCCACAAGCTGCC
TTCCAGCAGCCTGCCAAGGCCATGGCAGAGAGAGACTGCAAACAAACAAACACAAGCAAACAGA
GTCTCTTCACAGCTGGAGTCTGAAAGCTCATAGTGGCATGTGTGAATCTGACAAAATTAAAAGT
GTGCATAGTCCATTACATGCATAAAACACTAATAATAATCCTGTTTACACGTGACTGCAGCAGG
CAGGTCCAGCTCCACCACTGCCCTCCTGCCACATCACATCAAGTGCCATGGTTTAGAGGGTTTT
TCATATGTAATTCTTTTATTCTGTAAAAGGTAACAAAATATACAGAACAAAACTTTCCCTTTTT
AAAACTAATGTTACAAATCTGTATTATCACTTGTATATAAATAGTATATAGCTGATCATTAATA
AGGTGTATAAGTACAATGTATTCTAAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_011536255 ⟹ XP_011534557

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,718,249 - 158,764,871 (+)	NCBI

Sequence:

show sequence

AAAAAAAAAAAAAAAGCCTGAGTTTTAGTGAGAGGTTGACCAACGTGCCTAATGTCACATAGTG
AATGAGAGATGGAGCCAGGAGCAGACCTGGGATTTGACTCTGAATTCTAAACTCTATGTTCCCA
TAAGAAGGACAAATGAGGACCGCTGAAGAAAGAGGGTTCAGGAAGGGGCGTGTGGAAGCATGAG
TAATTATCTTACTTGCTTGAGTCACAGGAAACCACTCAGAGGCTAACACTGACTTGGGGTTAAC
CAGATGCCTGGCATTGTTCTCAGCGTAATGCCCTTCAGAGGTATTTAGCCTTTGTAATCCTTAA
GACAGCCCTATGAAGTTGGTACTGTTCCTGTCCCTACTAAAGACAGGGACACTGGGGCAAAGAG
ATGACCAAGAGCTAGGTGAAGCCTGCTCCAGAGACCAACCACACCCTGTCCACGCCCCAGAGAA
GGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCT
ATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTA
GACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTAA
TGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATGC
ATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTGA
AGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACAC
CGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCGG
CAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTGA
TCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGCT
CCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCGG
GCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAGC
CATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAGA
TGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACTG
AAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGCG
TAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTGG
AATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGGG
GATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACAG
ACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGGC
ACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACCT
TGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATTT
ACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAAA
TGGCCAGATTTTAATAAACGTTGTTACCCATGTCCTCCAGTGCTTATCAAATGAGGTAAAAGGC
CGGCTGGTGGGCATGGTAACTCCCCCCTGTAATCCCAGCAACTTTGGGAGGCTGCAGTGGATGG
CTTGAGCTCAGAAGTGTGAGATCAGCCCAGGCAACATAGATACCCTGTCTACAAAAAAACCAAA
AAATTATCCAGGTGTGGTGGTACACACCTGTAGTCCCAGTTACTCAGGAGGCTGAACCGGGAGG
ATTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCCCGATCATGCAACTGTGCTCCAGCCTGGGCC
AAAGTAAGACCCTGTCTCAAGGCGGGGGGGGGAGTCACAGCTTCGCTGTGAGAAGCACTTTATT
TTTTGAGACGGAGTCTCCCCGTCACCAGGCTGGAGTGCAGTGGCACGATCTTGGCTTGCTGCAA
GCTCCGCCTCCCGGGTTCTAGCAATTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTATAGGT
ATGCACCACCACACCAGGCTAATTTTCGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCC
AGGATGGTCTCGATCTCCTGACCTCGTGATCCGACCACCTCGGCCTCCCAAAGTGCTGGGATTA
CAGGTGTGAGCCACTGTGCCCGGCTATGAGGAGCATTTTAGAGGAGCCTGATGAGTGTTGGAGC
AGTCTTTCTCTCCTGTGGAAACCATCTCGAGGAGGTTAGGTGACCCATGGAGCACCATGTCTTG
GGTTGGTCAGCTCCAACTTACCAGTGTACCCCCAGGGACACCACGGCCCCTCACGAAACCTGGC
CAGAGGACAGCATAGAGCCCAGACGAGTCGGCGGTAGCCCTCCCACCCCACACACAAGCACACA
CCCGTGCTGCTTCGTGCCTTTGCAAAGCTTTTATTTCATGTCTGCGGCATGGAATCCACCTGCA
CATGGCATCTTAGCTGTGAAGGAGAAAGCAGTGCACGAGAAGGAATGAGTGGGCGGAACCAACG
GCCTCCACAAGCTGCCTTCCAGCAGCCTGCCAAGGCCATGGCAGAGAGAGACTGCAAACAAACA
AACACAAGCAAACAGAGTCTCTTCACAGCTGGAGTCTGAAAGCTCATAGTGGCATGTGTGAATC
TGACAAAATTAAAAGTGTGCATAGTCCATTACATGCATAAAACACTAATAATAATCCTGTTTAC
ACGTGACTGCAGCAGGCAGGTCCAGCTCCACCACTGCCCTCCTGCCACATCACATCAAGTGCCA
TGGTTTAGAGGGTTTTTCATATGTAATTCTTTTATTCTGTAAAAGGTAACAAAATATACAGAAC
AAAACTTTCCCTTTTTAAAACTAATGTTACAAATCTGTATTATCACTTGTATATAAATAGTATA
TAGCTGATCATTAATAAGGTGTATAAGTACAATGTATTCTAAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_017011496 ⟹ XP_016866985

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,663,301 - 158,764,871 (+)	NCBI

Sequence:

show sequence

CTGAATTCGCCTCTCCTCCTGTCCTCTGGGAGGTGGTAGTTTCCATGGGAATCCGTGAGGGTAG
CCGGGCAGCTCCCTAAACCTTAGCAACAGAAACAAAACACACGTACAAAAGGCAGTCCTGGAGG
GGAAGCGTGGTCCCGGCCCCTCCTCCGGTTTGTACTGTGTGGATTGACGCGGACGTTCAAACCC
GCTCGGACACCTGGCAACAAACTCGAAAGTGACTGCTGAAGGCAGTGCGCCCGGTGAGACGTTG
TTGCAGTTCCCTTGGGGACTGGGATTGGCATGCTTTAGCTATCTGAACGAAACTTCCCTTTGGG
GAGTTAAGTTTTCCAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGAATTGCAGTG
ATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCTTGGGGCACT
GAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGGCGTTGCCCC
TGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTC
CTGCTGACCTGGAAACATCTTAAATGGAAGGTTAGCTTCTATGAGTCACTGATACTCTTTTTAT
TGCTATTTCTAAATTTCCTTGGCTTGAAAATTACTTCTGCTTTGCAGAAATTATCTGCTTGCAG
CTGTGGATAATTTATAACAATCTCTGGTGAAACCTCAGAAAAGAGATATGCTTTTGTCTTAGAT
GGATGTCAGCAGCTGCTGCAGAACCCGGTGAAAACACCCCCCGGGTAGCACGAGGCTCTGCGAG
CCGTAACTCCGACAAACGCAGAACTTCTTGAGGCTTTCTTCTTCTAAGGAGTATGACACAGTTA
AAAAGGAAAAAAGAACCACAAGCAAAACAGTTGCCAGTGAAATAGGAGAGGGAGCTCTTTAAAC
AAGGCTGGCTGCAGCTGGCCTCCGCCGCTCATCTGCAGGGCGTGAGCGCTTGGTCCATGCAGTG
AAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGATCTGAGTGC
TCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCGGTTCAAAAC
ACAGAGGAGGAGAGGACACGGGCTGCAGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGAA
AGGAGCGAAGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCTG
GGGTTCCTGCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGCC
GAGTGTTCCTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCAA
AATAAAAACTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACAT
GAGACAGTTGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCTC
CTACTCCACCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTACAGGAATTTGG
TCAGTTTAGAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTACCCACGTGAAA
AAGCTCTCCAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGGC
AGTGTGTGGGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGAA
GGTCAGTGCACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCT
ATTTTGAAGCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTA
GACACGGAAGTTTAATTAGCATTGACAGCACCTGTACAGAGATGGGCAATTTTGACAATGCTAA
TGTCACTGGAGAAATAGAATTTGCCATTCATTATTGCTTCAAAACCCATTCTTTAGAAATATGC
ATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTATGTGA
AGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGGAACAC
CGTGGACCCGACCTTTCAGGAGACCTTGAAGTATCAGGTGGCCCCTGCCCAGCTGGTGACCCGG
CAGCTGCAGGTCTCGGTGTGGCATCTGGGCACGCTGGCCCGGAGAGTGTTTCTTGGAGAAGTGA
TCATTCCTCTGGCCACGTGGGACTTTGAAGACAGCACAACACAGTCCTTCCGCTGGCATCCGCT
CCGGGCCAAGGCGGAGAAATACGAAGACAGCGTTCCTCAGAGTAATGGAGAGCTCACAGTCCGG
GCTAAGCTGGTTCTCCCTTCACGGCCCAGAAAACTCCAAGAGGCTCAAGAAGGGACAGATCAGC
CATCACTTCATGGTCAACTTTGTTTGGTAGTGCTAGGAGCCAAGAATTTACCTGTGCGGCCAGA
TGGCACCTTGAACTCATTTGTTAAGGGCTGTCTCACTCTGCCAGACCAACAAAAACTGAGACTG
AAGTCGCCAGTCCTGAGGAAGCAGGCTTGCCCCCAGTGGAAACACTCATTTGTCTTCAGTGGCG
TAACCCCAGCTCAGCTGAGGCAGTCAAGCTTGGAGTTAACTGTCTGGGATCAGGCCCTCTTTGG
AATGAACGACCGCTTGCTTGGAGGAACCAGACTTGGTTCAAAGGGAGACACAGCTGTTGGCGGG
GATGCATGCTCACTATCGAAGCTCCAGTGGCAGAAAGTCCTTTCCAGCCCCAATCTATGGACAG
ACATGACTCTTGTCCTGCACTGACATGAAGGCCTCAAGGTTCCAGGTTGCAGCAGGCGTGAGGC
ACTGTGCGTCTGCAGAGGGGCTACGAACCAGGTGCAGGGTCCCAGCTGGAGACCCCTTTGACCT
TGAGCAGTCTCCATCTGCGGCCCTGTCCCATGGCTTAACCGCCTATTGGTATCTGTGTATATTT
ACGTTAAACACAATTATGTTACCTAAGCCTCTGGTGGGTTATCTCCTCTTTGAGATGTAGAAAA
TGGCCAGATTTTAATAAACGTTGTTACCCATGTCCTCCAGTGCTTATCAAATGAGGTAAAAGGC
CGGCTGGTGGGCATGGTAACTCCCCCCTGTAATCCCAGCAACTTTGGGAGGCTGCAGTGGATGG
CTTGAGCTCAGAAGTGTGAGATCAGCCCAGGCAACATAGATACCCTGTCTACAAAAAAACCAAA
AAATTATCCAGGTGTGGTGGTACACACCTGTAGTCCCAGTTACTCAGGAGGCTGAACCGGGAGG
ATTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCCCGATCATGCAACTGTGCTCCAGCCTGGGCC
AAAGTAAGACCCTGTCTCAAGGCGGGGGGGGGAGTCACAGCTTCGCTGTGAGAAGCACTTTATT
TTTTGAGACGGAGTCTCCCCGTCACCAGGCTGGAGTGCAGTGGCACGATCTTGGCTTGCTGCAA
GCTCCGCCTCCCGGGTTCTAGCAATTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTATAGGT
ATGCACCACCACACCAGGCTAATTTTCGTATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCC
AGGATGGTCTCGATCTCCTGACCTCGTGATCCGACCACCTCGGCCTCCCAAAGTGCTGGGATTA
CAGGTGTGAGCCACTGTGCCCGGCTATGAGGAGCATTTTAGAGGAGCCTGATGAGTGTTGGAGC
AGTCTTTCTCTCCTGTGGAAACCATCTCGAGGAGGTTAGGTGACCCATGGAGCACCATGTCTTG
GGTTGGTCAGCTCCAACTTACCAGTGTACCCCCAGGGACACCACGGCCCCTCACGAAACCTGGC
CAGAGGACAGCATAGAGCCCAGACGAGTCGGCGGTAGCCCTCCCACCCCACACACAAGCACACA
CCCGTGCTGCTTCGTGCCTTTGCAAAGCTTTTATTTCATGTCTGCGGCATGGAATCCACCTGCA
CATGGCATCTTAGCTGTGAAGGAGAAAGCAGTGCACGAGAAGGAATGAGTGGGCGGAACCAACG
GCCTCCACAAGCTGCCTTCCAGCAGCCTGCCAAGGCCATGGCAGAGAGAGACTGCAAACAAACA
AACACAAGCAAACAGAGTCTCTTCACAGCTGGAGTCTGAAAGCTCATAGTGGCATGTGTGAATC
TGACAAAATTAAAAGTGTGCATAGTCCATTACATGCATAAAACACTAATAATAATCCTGTTTAC
ACGTGACTGCAGCAGGCAGGTCCAGCTCCACCACTGCCCTCCTGCCACATCACATCAAGTGCCA
TGGTTTAGAGGGTTTTTCATATGTAATTCTTTTATTCTGTAAAAGGTAACAAAATATACAGAAC
AAAACTTTCCCTTTTTAAAACTAATGTTACAAATCTGTATTATCACTTGTATATAAATAGTATA
TAGCTGATCATTAATAAGGTGTATAAGTACAATGTATTCTAAAACTGTTAAGC

hide sequence

RefSeq Acc Id:

XM_017011499 ⟹ XP_016866988

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,662,947 - 158,752,030 (+)	NCBI

Sequence:

show sequence

CTGAATTCGCCTCTCCTCCTGTCCTCTGGGAGGTGGTAGTTTCCATGGGAATCCGTGAGGGTAG
CCGGGCAGCTCCCTAAACCTTAGCAACAGAAACAAAACACACGTACAAAAGGCAGTCCTGGAGG
GGAAGCGTGGTCCCGGCCCCTCCTCCGGTTTGTACTGTGTGGATTGACGCGGACGTTCAAACCC
GCTCGGACACCTGGCAACAAACTCGAAAGTGACTGCTGAAGGCAGTGCGCCCGGTGAGACGTTG
TTGCAGTTCCCTTGGGGACTGGGATTGGCATGCTTTAGCTATCTGAACGAAACTTCCCTTTGGG
GAGTTAAGTTTTCCAGGCTCCCCGAATGAGAAAGAATACTCGGAATCAGCGGTGAATTGCAGTG
ATCTTTCAGAGAAAGCGCCTGTTCAACTTTGTCCTCTCTCAGAGACTCAGAGCCTTGGGGCACT
GAGGGATGCCAGTTCTGCCTGTTCATCTGGAACCTGGATCTAAGGAGGGAAGAGGCGTTGCCCC
TGCTGGCATAGTCAGGTACCAGCCCAGCCAGGTATTGAACGGGCTGAGCTTTTCATGATGGTTC
CTGCTGACCTGGAAACATCTTAAATGGAAGGTTAGCTTCTATGAGTCACTGATACTCTTTTTAT
TGCTATTTCTAAATTTCCTTGGCTTGAAAATTACTTCTGCTTTGCAGAAATTATCTGCTTGCAG
CTGTGGATAATTTATAACAATCTCTGGTGAAACCTCAGAAAAGAGATATGCTTTTGTCTTAGAT
GGATGTCAGCAGCTGCTGCAGAACCCGGTGAAAACACCCCCCGGGTAGCACGAGGCTCTGCGAG
CCGTAACTCCGACAAACGCAGAACTTCTTGAGGCTTTCTTCTTCTAAGGAGTATGACACAGTTA
AAAAGGAAAAAAGAACCACAAGCAAAACAGTTGCCAGTGAAATAGGAGAGGGAGCTCTTTAAAC
AAGGCTGGCTGCAGCTGGCCTCCGCCGCTCATCTGCAGGGCGTGAGCGCTTGGTCCATGCAGTG
AAGCTCTTCCAACCTGGGTCAACGAAAACGGAGAAGAAATGGCCCAAGAAATAGATCTGAGTGC
TCTCAAGGAGTTAGAACGCGAGGCCATTCTCCAGGTCCTGTACCGAGACCAGGCGGTTCAAAAC
ACAGAGGAGGAGAGGACACGGAAACTGAAAACACACCTGCAGCATCTCCGGTGGAAAGGAGCGA
AGAACACGGACTGGGAGCACAAAGAGAAGTGCTGTGCGCGCTGCCAGCAGGTGCTGGGGTTCCT
GCTGCACCGGGGCGCCGTGTGCCGGGGCTGCAGCCACCGCGTGTGTGCCCAGTGCCGAGTGTTC
CTGAGGGGGACCCATGCCTGGAAGTGCACGGTGTGCTTCGAGGACAGGAATGTCAAAATAAAAA
CTGGAGAATGGTTCTATGAGGAACGAGCCAAGAAATTTCCAACTGGAGGCAAACATGAGACAGT
TGGAGGGCAGCTCTTGCAATCTTATCAGAAGCTGAGCAAAATTTCTGTGGTTCCTCCTACTCCA
CCTCCTGTCAGCGAGAGCCAGTGCAGCCGCAGTCCTGGCAGGTTACAGGAATTTGGTCAGTTTA
GAGGATTTAATAAGTCCGTGGAAAATTTGTTTCTGTCTCTTGCTACCCACGTGAAAAAGCTCTC
CAAATCCCAGAATGATATGACTTCTGAGAAGCATCTTCTCGCCACGGGCCCCAGGCAGTGTGTG
GGACAGACAGAGAGACGGAGCCAGTCTGACACTGCGGTCAACGTCACCACCAGGAAGGTCAGTG
CACCAGATATTCTGAAACCTCTCAATCAAGAGGATCCCAAATGCTCTACTAACCCTATTTTGAA
GCAACAGAATCTCCCATCCAGTCCGGCACCCAGTACCATATTCTCTGGAGGTTTTAGACACAAA
TATGCATCAAGGCCTGTAAGAACCTTGCCTATGGAGAAGAAAAGAAGAAAAAGTGCAATCCGTA
TGTGAAGACCTACCTGTTGCCCGACAGATCCTCCCAGGGAAAGCGCAAGACTGGAGTCCAAAGG
AACACCGTGGACCCGACCTTTCAGGAGACCTTGAAG

hide sequence

RefSeq Acc Id:

XM_047419549 ⟹ XP_047275505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419550 ⟹ XP_047275506

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419551 ⟹ XP_047275507

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419552 ⟹ XP_047275508

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419553 ⟹ XP_047275509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419554 ⟹ XP_047275510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419555 ⟹ XP_047275511

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419556 ⟹ XP_047275512

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419557 ⟹ XP_047275513

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419558 ⟹ XP_047275514

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419559 ⟹ XP_047275515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,704,408 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419560 ⟹ XP_047275516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,936 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419561 ⟹ XP_047275517

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,662,947 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_047419562 ⟹ XP_047275518

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,665,510 - 158,764,871 (+)	NCBI

RefSeq Acc Id:

XM_054356793 ⟹ XP_054212768

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356794 ⟹ XP_054212769

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356795 ⟹ XP_054212770

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356796 ⟹ XP_054212771

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356797 ⟹ XP_054212772

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356798 ⟹ XP_054212773

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356799 ⟹ XP_054212774

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356800 ⟹ XP_054212775

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356801 ⟹ XP_054212776

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,886,606 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356802 ⟹ XP_054212777

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356803 ⟹ XP_054212778

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356804 ⟹ XP_054212779

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,886,606 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356805 ⟹ XP_054212780

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,906,637 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356806 ⟹ XP_054212781

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356807 ⟹ XP_054212782

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356808 ⟹ XP_054212783

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356809 ⟹ XP_054212784

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356810 ⟹ XP_054212785

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356811 ⟹ XP_054212786

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356812 ⟹ XP_054212787

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,081 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356813 ⟹ XP_054212788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,895,281 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356814 ⟹ XP_054212789

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,886,606 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356815 ⟹ XP_054212790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,963,416 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356816 ⟹ XP_054212791

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,949,815 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356817 ⟹ XP_054212792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,953,462 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356818 ⟹ XP_054212793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,086 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356819 ⟹ XP_054212794

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,086 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356820 ⟹ XP_054212795

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,908,180 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356821 ⟹ XP_054212796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,906,641 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356822 ⟹ XP_054212797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,906,641 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356823 ⟹ XP_054212798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,908,534 - 160,010,070 (+)	NCBI

RefSeq Acc Id:

XM_054356824 ⟹ XP_054212799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	6	159,890,068 - 159,997,220 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001009991	(Get FASTA)	NCBI Sequence Viewer
	NP_001229313	(Get FASTA)	NCBI Sequence Viewer
	NP_001229323	(Get FASTA)	NCBI Sequence Viewer
	NP_001229324	(Get FASTA)	NCBI Sequence Viewer
	NP_001305674	(Get FASTA)	NCBI Sequence Viewer
	XP_005267279	(Get FASTA)	NCBI Sequence Viewer
	XP_006715669	(Get FASTA)	NCBI Sequence Viewer
	XP_006715674	(Get FASTA)	NCBI Sequence Viewer
	XP_011534556	(Get FASTA)	NCBI Sequence Viewer
	XP_011534557	(Get FASTA)	NCBI Sequence Viewer
	XP_016866985	(Get FASTA)	NCBI Sequence Viewer
	XP_016866988	(Get FASTA)	NCBI Sequence Viewer
	XP_047275505	(Get FASTA)	NCBI Sequence Viewer
	XP_047275506	(Get FASTA)	NCBI Sequence Viewer
	XP_047275507	(Get FASTA)	NCBI Sequence Viewer
	XP_047275508	(Get FASTA)	NCBI Sequence Viewer
	XP_047275509	(Get FASTA)	NCBI Sequence Viewer
	XP_047275510	(Get FASTA)	NCBI Sequence Viewer
	XP_047275511	(Get FASTA)	NCBI Sequence Viewer
	XP_047275512	(Get FASTA)	NCBI Sequence Viewer
	XP_047275513	(Get FASTA)	NCBI Sequence Viewer
	XP_047275514	(Get FASTA)	NCBI Sequence Viewer
	XP_047275515	(Get FASTA)	NCBI Sequence Viewer
	XP_047275516	(Get FASTA)	NCBI Sequence Viewer
	XP_047275517	(Get FASTA)	NCBI Sequence Viewer
	XP_047275518	(Get FASTA)	NCBI Sequence Viewer
	XP_054212768	(Get FASTA)	NCBI Sequence Viewer
	XP_054212769	(Get FASTA)	NCBI Sequence Viewer
	XP_054212770	(Get FASTA)	NCBI Sequence Viewer
	XP_054212771	(Get FASTA)	NCBI Sequence Viewer
	XP_054212772	(Get FASTA)	NCBI Sequence Viewer
	XP_054212773	(Get FASTA)	NCBI Sequence Viewer
	XP_054212774	(Get FASTA)	NCBI Sequence Viewer
	XP_054212775	(Get FASTA)	NCBI Sequence Viewer
	XP_054212776	(Get FASTA)	NCBI Sequence Viewer
	XP_054212777	(Get FASTA)	NCBI Sequence Viewer
	XP_054212778	(Get FASTA)	NCBI Sequence Viewer
	XP_054212779	(Get FASTA)	NCBI Sequence Viewer
	XP_054212780	(Get FASTA)	NCBI Sequence Viewer
	XP_054212781	(Get FASTA)	NCBI Sequence Viewer
	XP_054212782	(Get FASTA)	NCBI Sequence Viewer
	XP_054212783	(Get FASTA)	NCBI Sequence Viewer
	XP_054212784	(Get FASTA)	NCBI Sequence Viewer
	XP_054212785	(Get FASTA)	NCBI Sequence Viewer
	XP_054212786	(Get FASTA)	NCBI Sequence Viewer
	XP_054212787	(Get FASTA)	NCBI Sequence Viewer
	XP_054212788	(Get FASTA)	NCBI Sequence Viewer
	XP_054212789	(Get FASTA)	NCBI Sequence Viewer
	XP_054212790	(Get FASTA)	NCBI Sequence Viewer
	XP_054212791	(Get FASTA)	NCBI Sequence Viewer
	XP_054212792	(Get FASTA)	NCBI Sequence Viewer
	XP_054212793	(Get FASTA)	NCBI Sequence Viewer
	XP_054212794	(Get FASTA)	NCBI Sequence Viewer
	XP_054212795	(Get FASTA)	NCBI Sequence Viewer
	XP_054212796	(Get FASTA)	NCBI Sequence Viewer
	XP_054212797	(Get FASTA)	NCBI Sequence Viewer
	XP_054212798	(Get FASTA)	NCBI Sequence Viewer
	XP_054212799	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH85612	(Get FASTA)	NCBI Sequence Viewer
	AAI00831	(Get FASTA)	NCBI Sequence Viewer
	AAI00832	(Get FASTA)	NCBI Sequence Viewer
	BAC85142	(Get FASTA)	NCBI Sequence Viewer
	BAG60868	(Get FASTA)	NCBI Sequence Viewer
	BAG65071	(Get FASTA)	NCBI Sequence Viewer
	EAW47648	(Get FASTA)	NCBI Sequence Viewer
	EAW47649	(Get FASTA)	NCBI Sequence Viewer
	EAW47650	(Get FASTA)	NCBI Sequence Viewer
	EAW47651	(Get FASTA)	NCBI Sequence Viewer
	EAW47652	(Get FASTA)	NCBI Sequence Viewer
	EAW47653	(Get FASTA)	NCBI Sequence Viewer
	EAW47654	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000353631
	ENSP00000353631.4
	ENSP00000356048
	ENSP00000356048.4
	ENSP00000483936
	ENSP00000483936.1
GenBank Protein	Q4VX76	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001009991 ⟸ NM_001009991
- Peptide Label:	isoform 2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRKVSAPDILKPLNQEDPKCST NPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLE ICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLV TRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELT VRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKL RLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAV GGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	NP_001229323 ⟸ NM_001242394
- Peptide Label:	isoform 1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRLQEFGQFRGFNKSVENLFLS LATHVKKLSKSQNDMTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDP KCSTNPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKT HSLEICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAP AQLVTRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSN GELTVRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPD QQKLRLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKG DTAVGGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	NP_001229324 ⟸ NM_001242395
- Peptide Label:	isoform 2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRKVSAPDILKPLNQEDPKCST NPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLE ICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLV TRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELT VRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKL RLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAV GGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	NP_001229313 ⟸ NM_001242384
- Peptide Label:	isoform 1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRLQEFGQFRGFNKSVENLFLS LATHVKKLSKSQNDMTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDP KCSTNPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKT HSLEICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAP AQLVTRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSN GELTVRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPD QQKLRLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKG DTAVGGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	XP_005267279 ⟸ XM_005267222
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDPKCSTNPILKQQNLP SSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLEICIKACKNLA YGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLVTRQLQVSVWH LGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELTVRAKLVLPSR PRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKLRLKSPVLRKQ ACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAVGGDACSLSKL QWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	XP_006715669 ⟸ XM_006715606
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRLQEFGQFRGFNKSVENLFLS LATHVKKLSKSQNDMTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDP KCSTNPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKT HSLEICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAP AQLVTRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSN GELTVRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPD QQKLRLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKG DTAVGGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	XP_006715674 ⟸ XM_006715611
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDPKCSTNPILKQQNLP SSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLEICIKACKNLA YGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLVTRQLQVSVWH LGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELTVRAKLVLPSR PRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKLRLKSPVLRKQ ACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAVGGDACSLSKL QWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	XP_011534556 ⟸ XM_011536254
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRLQEFGQFRGFNKSVENLFLS LATHVKKLSKSQNDMTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDP KCSTNPILKQQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKT HSLEICIKACKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAP AQLVTRQLQVSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSN GELTVRAKLVLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPD QQKLRLKSPVLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKG DTAVGGDACSLSKLQWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:

XP_011534557 ⟸ XM_011536255

- Peptide Label:

isoform X3

- Sequence:

show sequence

MKLVLFLSLLKTGTLGQRDDQELGEACSRDQPHPVHAPEKVSAPDILKPLNQEDPKCSTNPILK
QQNLPSSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLEICIKA
CKNLAYGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLVTRQLQ
VSVWHLGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELTVRAKL
VLPSRPRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKLRLKSP
VLRKQACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAVGGDAC
SLSKLQWQKVLSSPNLWTDMTLVLH

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RefSeq Acc Id:	NP_001305674 ⟸ NM_001318745
- Peptide Label:	isoform 3
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDPKCSTNPILKQQNLP SSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLEICIKACKNLA YGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLVTRQLQVSVWH LGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELTVRAKLVLPSR PRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKLRLKSPVLRKQ ACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAVGGDACSLSKL QWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:	XP_016866985 ⟸ XM_017011496
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDPKCSTNPILKQQNLP SSPAPSTIFSGGFRHGSLISIDSTCTEMGNFDNANVTGEIEFAIHYCFKTHSLEICIKACKNLA YGEEKKKKCNPYVKTYLLPDRSSQGKRKTGVQRNTVDPTFQETLKYQVAPAQLVTRQLQVSVWH LGTLARRVFLGEVIIPLATWDFEDSTTQSFRWHPLRAKAEKYEDSVPQSNGELTVRAKLVLPSR PRKLQEAQEGTDQPSLHGQLCLVVLGAKNLPVRPDGTLNSFVKGCLTLPDQQKLRLKSPVLRKQ ACPQWKHSFVFSGVTPAQLRQSSLELTVWDQALFGMNDRLLGGTRLGSKGDTAVGGDACSLSKL QWQKVLSSPNLWTDMTLVLH hide sequence

RefSeq Acc Id:

XP_016866988 ⟸ XM_017011499

- Peptide Label:

isoform X6

- Sequence:

show sequence

MAQEIDLSALKELEREAILQVLYRDQAVQNTEEERTRKLKTHLQHLRWKGAKNTDWEHKEKCCA
RCQQVLGFLLHRGAVCRGCSHRVCAQCRVFLRGTHAWKCTVCFEDRNVKIKTGEWFYEERAKKF
PTGGKHETVGGQLLQSYQKLSKISVVPPTPPPVSESQCSRSPGRLQEFGQFRGFNKSVENLFLS
LATHVKKLSKSQNDMTSEKHLLATGPRQCVGQTERRSQSDTAVNVTTRKVSAPDILKPLNQEDP
KCSTNPILKQQNLPSSPAPSTIFSGGFRHKYASRPVRTLPMEKKRRKSAIRM

hide sequence

Ensembl Acc Id:

ENSP00000353631 ⟸ ENST00000360448

Ensembl Acc Id:

ENSP00000483936 ⟸ ENST00000611299

Ensembl Acc Id:

ENSP00000297239 ⟸ ENST00000297239

Ensembl Acc Id:

ENSP00000356048 ⟸ ENST00000367081

RefSeq Acc Id:	XP_047275512 ⟸ XM_047419556
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275516 ⟸ XM_047419560
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275508 ⟸ XM_047419552
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275513 ⟸ XM_047419557
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275509 ⟸ XM_047419553
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275506 ⟸ XM_047419550
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275510 ⟸ XM_047419554
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275505 ⟸ XM_047419549
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275511 ⟸ XM_047419555
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275514 ⟸ XM_047419558
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275507 ⟸ XM_047419551
- Peptide Label:	isoform X1
- UniProtKB:	Q4VX76 (UniProtKB/Swiss-Prot), Q496J6 (UniProtKB/Swiss-Prot), Q496J4 (UniProtKB/Swiss-Prot), Q5U3B9 (UniProtKB/Swiss-Prot), B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275517 ⟸ XM_047419561
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275518 ⟸ XM_047419562
- Peptide Label:	isoform X5
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047275515 ⟸ XM_047419559
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212779 ⟸ XM_054356804
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212776 ⟸ XM_054356801
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212789 ⟸ XM_054356814
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212799 ⟸ XM_054356824
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054212781 ⟸ XM_054356806
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212768 ⟸ XM_054356793
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212769 ⟸ XM_054356794
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212786 ⟸ XM_054356811
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212773 ⟸ XM_054356798
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212772 ⟸ XM_054356797
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212784 ⟸ XM_054356809
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212778 ⟸ XM_054356803
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212782 ⟸ XM_054356807
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212775 ⟸ XM_054356800
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212787 ⟸ XM_054356812
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212794 ⟸ XM_054356819
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212793 ⟸ XM_054356818
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212777 ⟸ XM_054356802
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212771 ⟸ XM_054356796
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212783 ⟸ XM_054356808
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212770 ⟸ XM_054356795
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212785 ⟸ XM_054356810
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212788 ⟸ XM_054356813
- Peptide Label:	isoform X2
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212774 ⟸ XM_054356799
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212780 ⟸ XM_054356805
- Peptide Label:	isoform X1
- UniProtKB:	B4DQA6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212797 ⟸ XM_054356822
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212796 ⟸ XM_054356821
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212795 ⟸ XM_054356820
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212798 ⟸ XM_054356823
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212791 ⟸ XM_054356816
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212792 ⟸ XM_054356817
- Peptide Label:	isoform X4
- UniProtKB:	B4E2A9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054212790 ⟸ XM_054356815
- Peptide Label:	isoform X3

Protein Domains

C2 RabBD

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q4VX76-F1-model_v2	AlphaFold	Q4VX76	1-610	view protein structure

Promoters

RGD ID:

7209555

Promoter ID:

EPDNEW_H10523

Type:

initiation region

Name:

SYTL3_2

Description:

synaptotagmin like 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H10524 EPDNEW_H10525

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,644,933 - 158,644,993	EPDNEW

RGD ID:

7209557

Promoter ID:

EPDNEW_H10524

Type:

initiation region

Name:

SYTL3_1

Description:

synaptotagmin like 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H10523 EPDNEW_H10525

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,650,054 - 158,650,114	EPDNEW

RGD ID:

7209559

Promoter ID:

EPDNEW_H10525

Type:

initiation region

Name:

SYTL3_3

Description:

synaptotagmin like 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H10523 EPDNEW_H10524

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	158,663,131 - 158,663,191	EPDNEW

RGD ID:

6804836

Promoter ID:

HG_KWN:55622

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, K562, Lymphoblastoid, NB4

Transcripts:

NM_001009991, OTTHUMT00000042877

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	6	158,990,526 - 158,991,057 (+)	MPROMDB

RGD ID:

6804834

Promoter ID:

HG_KWN:55623

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell

Transcripts:

UC003QRP.1, UC003QRQ.1, UC003QRR.1, UC003QRS.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	6	159,001,441 - 159,001,941 (+)	MPROMDB

RGD ID:

6816484

Promoter ID:

HG_SPT:55033

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

AA313891, AI091450, AI674404, AL567177, BG059681, BU633217, CA450395, DB320403, DB331640, N64362

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	6	159,105,426 - 159,105,926 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:15587	AgrOrtholog
COSMIC	SYTL3	COSMIC
Ensembl Genes	ENSG00000164674	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000360448	ENTREZGENE
	ENST00000360448.8	UniProtKB/Swiss-Prot
	ENST00000367081	ENTREZGENE
	ENST00000367081.7	UniProtKB/Swiss-Prot
	ENST00000611299	ENTREZGENE
	ENST00000611299.5	UniProtKB/Swiss-Prot
Gene3D-CATH	2.60.40.150	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	3.30.40.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000164674	GTEx
HGNC ID	HGNC:15587	ENTREZGENE
Human Proteome Map	SYTL3	Human Proteome Map
InterPro	C2_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	C2_domain_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	FYVE_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Rab_BD	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SYTL1-5_C2B	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_FYVE_PHD	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_RING/FYVE/PHD	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:94120	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	94120	ENTREZGENE
OMIM	620973	OMIM
PANTHER	BITESIZE, ISOFORM I	UniProtKB/Swiss-Prot
	BITESIZE, ISOFORM I	UniProtKB/Swiss-Prot
	BITESIZE, ISOFORM I	UniProtKB/TrEMBL
	BITESIZE, ISOFORM I	UniProtKB/TrEMBL
	PTHR45716:SF1	UniProtKB/TrEMBL
Pfam	FYVE_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PF00168	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37986	PharmGKB
PROSITE	PS50004	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	RABBD	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	SM00239	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	FYVE/PHD zinc finger	UniProtKB/TrEMBL
	SSF49562	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF57903	UniProtKB/Swiss-Prot
UniProt	B4DQA6	ENTREZGENE, UniProtKB/TrEMBL
	B4E2A9	ENTREZGENE, UniProtKB/TrEMBL
	Q496J4	ENTREZGENE
	Q496J6	ENTREZGENE
	Q4VX76	ENTREZGENE
	Q5U3B9	ENTREZGENE
	SYTL3_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q496J4	UniProtKB/Swiss-Prot
	Q496J6	UniProtKB/Swiss-Prot
	Q5U3B9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-11-24	SYTL3	synaptotagmin like 3		synaptotagmin-like 3	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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Imported Disease Annotations - ClinVar