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Gene: ARSJ (arylsulfatase family member J) Homo sapiens

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Symbol:

ARSJ

Name:

arylsulfatase family member J

RGD ID:

1606235

HGNC Page

HGNC:26286

Description:

Predicted to enable sulfuric ester hydrolase activity. Located in actin cytoskeleton.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

arylsulfatase family, member J; arylsulfatase J; ASJ; FLJ23548

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):	Arsj (arylsulfatase J)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Arsj (arylsulfatase family, member J)	HGNC	HomoloGene, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Arsj (arylsulfatase family member J)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ARSJ (arylsulfatase family member J)	NCBI	Ortholog
Canis lupus familiaris (dog):	ARSJ (arylsulfatase family member J)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Arsj (arylsulfatase family member J)	NCBI	Ortholog
Sus scrofa (pig):	ARSJ (arylsulfatase family member J)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ARSJ (arylsulfatase family member J)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Arsj (arylsulfatase family member J)	NCBI	Ortholog
Rattus rattus (black rat):	Arsj (arylsulfatase family member J)	NCBI	Ortholog
Other homologs ²
Mus musculus (house mouse):	Arsi (arylsulfatase i)	HGNC	OrthoMCL
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Arsj (arylsulfatase family, member J)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Arsj (arylsulfatase family, member J)	Alliance	DIOPT (HGNC)
Mus musculus (house mouse):	Arsj (arylsulfatase J)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	arsj (arylsulfatase family, member J)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Danio rerio (zebrafish):	arsj (arylsulfatase family, member J)	Alliance	DIOPT (ZFIN)
Drosophila melanogaster (fruit fly):	CG32191	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector)
Drosophila melanogaster (fruit fly):	CG7402	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG7408	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG8646	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|SonicParanoid)
Caenorhabditis elegans (roundworm):	sul-3	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	sul-3	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|SonicParanoid)
Xenopus laevis (African clawed frog):	arsj.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	arsj.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	arsj	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	113,900,284 - 113,979,727 (-)	Ensembl			hg38	GRCh38
GRCh37	4	114,821,440 - 114,900,803 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	115,040,889 - 115,120,327 (-)	NCBI	Build 36	Build 36	hg18	NCBI36
Celera	4	112,113,187 - 112,192,557 (-)	NCBI		Celera
Cytogenetic Map	4	q26	NCBI
HuRef	4	110,549,726 - 110,629,095 (-)	NCBI		HuRef
CHM1_1	4	114,797,941 - 114,877,327 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	117,209,000 - 117,288,314 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

1,2,4-trichloro-5-(2,5-dichlorophenyl)benzene (ISO)

17beta-estradiol (EXP,ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

2,4,4'-trichlorobiphenyl (ISO)

acetamide (ISO)

aflatoxin B1 (EXP)

aldehydo-D-glucose (ISO)

all-trans-retinoic acid (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

atrazine (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[b]fluoranthene (ISO)

bisphenol A (EXP,ISO)

chloroprene (ISO)

cisplatin (EXP)

cobalt dichloride (EXP)

copper atom (ISO)

copper(0) (ISO)

Cuprizon (ISO)

D-glucose (ISO)

divanadium pentaoxide (ISO)

doxorubicin (EXP)

fluoranthene (ISO)

fructose (ISO)

genistein (ISO)

glucose (ISO)

glyphosate (ISO)

lipopolysaccharide (EXP)

methylmercury chloride (EXP)

okadaic acid (EXP)

PCB138 (ISO)

pirinixic acid (ISO)

potassium chromate (EXP)

rifampicin (EXP)

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

sodium arsenite (EXP)

sulforaphane (EXP)

sunitinib (EXP)

tetrachloromethane (ISO)

trichostatin A (EXP)

triclosan (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Cellular Component

actin cytoskeleton (IDA)

endoplasmic reticulum lumen (TAS)

extracellular region (IEA)

Molecular Function

arylsulfatase activity (IEA,TAS)

hydrolase activity (IEA)

metal ion binding (IEA)

protein binding (IPI)

sulfuric ester hydrolase activity (IBA,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:12477932	PMID:12975309	PMID:15489334	PMID:16174644	PMID:16344560	PMID:16500042	PMID:20332099	PMID:24165912	PMID:25416956	PMID:35748872	PMID:37201587

Genomics

Comparative Map Data

ARSJ
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	113,900,284 - 113,979,727 (-)	Ensembl			hg38	GRCh38
GRCh37	4	114,821,440 - 114,900,803 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	115,040,889 - 115,120,327 (-)	NCBI	Build 36	Build 36	hg18	NCBI36
Celera	4	112,113,187 - 112,192,557 (-)	NCBI		Celera
Cytogenetic Map	4	q26	NCBI
HuRef	4	110,549,726 - 110,629,095 (-)	NCBI		HuRef
CHM1_1	4	114,797,941 - 114,877,327 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	117,209,000 - 117,288,314 (-)	NCBI		T2T-CHM13v2.0

Arsj
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	3	126,157,566 - 126,234,025 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	3	126,157,333 - 126,234,024 (+)	Ensembl		GRCm39 Ensembl		GRCm39
GRCm38	3	126,363,852 - 126,440,374 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	3	126,363,684 - 126,440,375 (+)	Ensembl			mm10	GRCm38
MGSCv37	3	126,066,770 - 126,143,292 (+)	NCBI	MGSCv37	MGSCv37	mm9	NCBIm37
MGSCv36	3	126,355,874 - 126,432,396 (+)	NCBI		MGSCv36	mm8
Celera	3	132,806,992 - 132,894,155 (+)	NCBI		Celera
Cytogenetic Map	3	G1	NCBI
cM Map	3	55.97	NCBI

Arsj
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	2	217,449,147 - 217,529,142 (+)	NCBI	GRCr8	GRCr8		GRCr8
GRCr8 Ensembl	2	217,449,147 - 217,529,142 (+)	Ensembl				GRCr8
mRatBN7.2	2	214,774,631 - 214,854,614 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	214,774,654 - 214,854,612 (+)	Ensembl				mRatBN7.2
UTH_Rnor_SHR_Utx	2	222,432,586 - 222,517,509 (+)	NCBI	UTH_Rnor_SHR_Utx	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	2	220,332,519 - 220,417,442 (+)	NCBI	UTH_Rnor_SHRSP_BbbUtx_1.0	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	2	215,186,721 - 215,271,647 (+)	NCBI	UTH_Rnor_WKY_Bbb_1.0	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	2	230,163,014 - 230,662,084 (+)	NCBI	Rnor_6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_5.0	2	249,516,525 - 249,516,927 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
Rnor_5.0	2	250,012,102 - 250,013,503 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
RGSC_v3.4	2	223,574,825 - 223,666,259 (+)	NCBI	RGSC_v3.4	RGSC_v3.4	rn4
Celera	2	207,110,820 - 207,186,084 (+)	NCBI		Celera
RGSC_v3.1	2	223,561,467 - 223,652,939 (+)	NCBI
Cytogenetic Map	2	q42	NCBI

Arsj
(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_004955428	25,373,664 - 25,437,506 (+)	Ensembl
ChiLan1.0	NW_004955428	25,373,664 - 25,436,251 (+)	NCBI	ChiLan1.0	ChiLan1.0

ARSJ
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	3	112,001,869 - 112,082,620 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	4	112,285,049 - 112,374,062 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	4	106,413,083 - 106,493,804 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	4	116,977,450 - 117,055,778 (-)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	4	116,977,450 - 117,055,778 (-)	Ensembl			panPan2	panpan1.1

ARSJ
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	32	33,636,117 - 33,715,867 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	32	33,635,467 - 33,716,434 (-)	Ensembl			canFam3	CanFam3.1
Dog10K_Boxer_Tasha	32	8,316,578 - 8,396,341 (+)	NCBI	Dog10K_Boxer_Tasha	Dog10K_Boxer_Tasha
ROS_Cfam_1.0	32	33,862,066 - 33,942,038 (-)	NCBI	ROS_Cfam_1.0	ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	32	33,861,117 - 33,942,038 (-)	Ensembl				ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	32	33,840,343 - 33,920,028 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	32	33,609,619 - 33,689,546 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	32	6,172,634 - 6,252,363 (+)	NCBI	UU_Cfam_GSD_1.0	UU_Cfam_GSD_1.0

Arsj
(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_024405301	7,180,989 - 7,256,670 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936563	4,652,711 - 4,728,884 (-)	Ensembl		SpeTri2.0 Ensembl
SpeTri2.0	NW_004936563	4,653,070 - 4,728,820 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ARSJ
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	8	108,726,113 - 108,803,559 (+)	Ensembl			susScr11	Sscrofa11.1
Sscrofa11.1	8	108,710,636 - 108,804,846 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	16	82,531,767 - 82,538,491 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ARSJ
(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	7	61,710,123 - 61,787,875 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	7	61,712,063 - 61,786,876 (-)	Ensembl		ChlSab1.1 Ensembl	chlSab2	Vervet-AGM
Vero_WHO_p1.0	NW_023666037	40,473,821 - 40,559,290 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Arsj
(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_004624867	481,293 - 567,142 (-)	Ensembl		HetGla_female_1.0 Ensembl	hetGla2	HetGla_female_1.0 Ensembl
HetGla 1.0	NW_004624867	480,714 - 567,988 (-)	NCBI	HetGla 1.0	HetGla 1.0	hetGla2

Arsj
(Rattus rattus - black rat)

Black Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Black Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Rrattus_CSIRO_v1	3	33,031,289 - 33,102,290 (-)	NCBI		Rrattus_CSIRO_v1

Variants

Variants in ARSJ
48 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 4q22.2-32.3(chr4:92913386-165299707)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051775]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051775]\|See cases [RCV000051775]	Chr4:92913386..165299707 [GRCh38] Chr4:93834537..166220859 [GRCh37] Chr4:94053560..166440309 [NCBI36] Chr4:4q22.2-32.3	pathogenic
GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	copy number gain	See cases [RCV000051776]	Chr4:96092893..136410207 [GRCh38] Chr4:97014044..137331362 [GRCh37] Chr4:97233067..137550812 [NCBI36] Chr4:4q22.3-28.3	pathogenic
NM_024590.3(ARSJ):c.1157C>T (p.Ser386Leu)	single nucleotide variant	Malignant melanoma [RCV000074315]	Chr4:113902917 [GRCh38] Chr4:114824073 [GRCh37] Chr4:115043522 [NCBI36] Chr4:4q26	not provided
GRCh38/hg38 4q25-26(chr4:111069785-116691879)x1	copy number loss	See cases [RCV000134955]	Chr4:111069785..116691879 [GRCh38] Chr4:111990941..117613035 [GRCh37] Chr4:112210390..117832483 [NCBI36] Chr4:4q25-26	likely pathogenic
NC_000004.10:g.111994000_115504000del3510001	deletion	Congenital aniridia [RCV005419942]	Chr4:110853395..114363395 [GRCh38] Chr4:111774551..115284551 [GRCh37] Chr4:111994000..115504000 [NCBI36] Chr4:4q25-26	pathogenic
t(4;14)(q26;q12)	translocation	Rett syndrome, congenital variant [RCV000601500]	Chr4:114869960..114871254 [GRCh37] Chr14:29630531..29631032 [GRCh37] Chr14:14q12 Chr4:4q26	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	copy number gain	See cases [RCV000446653]	Chr4:12440..190904441 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4q25-26(chr4:112857598-115434654)x1	copy number loss	See cases [RCV000448547]	Chr4:112857598..115434654 [GRCh37] Chr4:4q25-26	likely pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	copy number gain	See cases [RCV000510453]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4q25-35.2(chr4:109199664-189752726)x3	copy number gain	See cases [RCV000511945]	Chr4:109199664..189752726 [GRCh37] Chr4:4q25-35.2	pathogenic
GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3	copy number gain	See cases [RCV000510970]	Chr4:93071152..190957473 [GRCh37] Chr4:4q22.1-35.2	pathogenic
NM_024590.4(ARSJ):c.974C>T (p.Ser325Phe)	single nucleotide variant	not specified [RCV004323584]	Chr4:113903100 [GRCh38] Chr4:114824256 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	copy number gain	See cases [RCV000512241]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3	copy number gain	not provided [RCV000743155]	Chr4:49450..190915650 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3	copy number gain	not provided [RCV000743156]	Chr4:49450..190963766 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3	copy number gain	not provided [RCV000743147]	Chr4:11525..191028879 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
NM_024590.4(ARSJ):c.1244G>A (p.Arg415Gln)	single nucleotide variant	not provided [RCV000905819]	Chr4:113902830 [GRCh38] Chr4:114823986 [GRCh37] Chr4:4q26	likely benign
GRCh37/hg19 4q26(chr4:114579245-115640604)x3	copy number gain	not provided [RCV000846546]	Chr4:114579245..115640604 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114635932-115251586)x3	copy number gain	not provided [RCV002473673]	Chr4:114635932..115251586 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114868539-115175427)x1	copy number loss	not provided [RCV001005590]	Chr4:114868539..115175427 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114868539-114954676)x1	copy number loss	not provided [RCV001005591]	Chr4:114868539..114954676 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26-28.3(chr4:114872547-138005267)x1	copy number loss	not provided [RCV001795851]	Chr4:114872547..138005267 [GRCh37] Chr4:4q26-28.3	pathogenic
GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	copy number gain	not provided [RCV001827738]	Chr4:52866944..143582507 [GRCh37] Chr4:4q12-31.21	pathogenic
GRCh37/hg19 4q24-31.21(chr4:104715235-145252595)	copy number gain	not specified [RCV002053446]	Chr4:104715235..145252595 [GRCh37] Chr4:4q24-31.21	pathogenic
GRCh37/hg19 4q25-26(chr4:112849108-115434557)	copy number loss	not specified [RCV002053449]	Chr4:112849108..115434557 [GRCh37] Chr4:4q25-26	likely pathogenic
NM_024590.4(ARSJ):c.23G>A (p.Gly8Glu)	single nucleotide variant	not specified [RCV004331487]	Chr4:113978812 [GRCh38] Chr4:114899968 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114661111-115170981)x3	copy number gain	not provided [RCV002472659]	Chr4:114661111..115170981 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1154T>C (p.Ile385Thr)	single nucleotide variant	not specified [RCV004118016]	Chr4:113902920 [GRCh38] Chr4:114824076 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114535234-115262363)x1	copy number loss	not provided [RCV002475569]	Chr4:114535234..115262363 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1759G>C (p.Val587Leu)	single nucleotide variant	not specified [RCV004139989]	Chr4:113902315 [GRCh38] Chr4:114823471 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.853A>G (p.Ile285Val)	single nucleotide variant	not specified [RCV004233659]	Chr4:113903221 [GRCh38] Chr4:114824377 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.980A>G (p.Asp327Gly)	single nucleotide variant	not specified [RCV004144037]	Chr4:113903094 [GRCh38] Chr4:114824250 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1219A>G (p.Ile407Val)	single nucleotide variant	not specified [RCV004202967]	Chr4:113902855 [GRCh38] Chr4:114824011 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1465A>G (p.Thr489Ala)	single nucleotide variant	not specified [RCV004180315]	Chr4:113902609 [GRCh38] Chr4:114823765 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1532G>A (p.Arg511Lys)	single nucleotide variant	not specified [RCV004194561]	Chr4:113902542 [GRCh38] Chr4:114823698 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.232C>G (p.Leu78Val)	single nucleotide variant	not specified [RCV004196893]	Chr4:113978603 [GRCh38] Chr4:114899759 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.998C>T (p.Thr333Met)	single nucleotide variant	not specified [RCV004230138]	Chr4:113903076 [GRCh38] Chr4:114824232 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.520G>A (p.Val174Ile)	single nucleotide variant	not specified [RCV004232302]	Chr4:113903554 [GRCh38] Chr4:114824710 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1796G>T (p.Gly599Val)	single nucleotide variant	not specified [RCV004126377]	Chr4:113902278 [GRCh38] Chr4:114823434 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.883G>T (p.Ala295Ser)	single nucleotide variant	not specified [RCV004168830]	Chr4:113903191 [GRCh38] Chr4:114824347 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1772C>G (p.Thr591Ser)	single nucleotide variant	not specified [RCV004089339]	Chr4:113902302 [GRCh38] Chr4:114823458 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.286T>G (p.Ser96Ala)	single nucleotide variant	not specified [RCV004110804]	Chr4:113978549 [GRCh38] Chr4:114899705 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.20C>A (p.Ala7Glu)	single nucleotide variant	not specified [RCV004096133]	Chr4:113978815 [GRCh38] Chr4:114899971 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.598C>T (p.Leu200Phe)	single nucleotide variant	not specified [RCV004081123]	Chr4:113903476 [GRCh38] Chr4:114824632 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.736G>A (p.Val246Ile)	single nucleotide variant	not specified [RCV004264072]	Chr4:113903338 [GRCh38] Chr4:114824494 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.23G>C (p.Gly8Ala)	single nucleotide variant	not specified [RCV004272184]	Chr4:113978812 [GRCh38] Chr4:114899968 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1781C>T (p.Ser594Leu)	single nucleotide variant	not specified [RCV004365278]	Chr4:113902293 [GRCh38] Chr4:114823449 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q26(chr4:114874186-114954676)x1	copy number loss	not provided [RCV003485434]	Chr4:114874186..114954676 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	copy number gain	not specified [RCV003986496]	Chr4:101203509..190957473 [GRCh37] Chr4:4q24-35.2	pathogenic
NM_024590.4(ARSJ):c.1004G>A (p.Gly335Glu)	single nucleotide variant	not specified [RCV004418269]	Chr4:113903070 [GRCh38] Chr4:114824226 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1358A>G (p.His453Arg)	single nucleotide variant	not specified [RCV004418271]	Chr4:113902716 [GRCh38] Chr4:114823872 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1607C>A (p.Pro536His)	single nucleotide variant	not specified [RCV004418273]	Chr4:113902467 [GRCh38] Chr4:114823623 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.838G>A (p.Glu280Lys)	single nucleotide variant	not specified [RCV004418277]	Chr4:113903236 [GRCh38] Chr4:114824392 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.838G>C (p.Glu280Gln)	single nucleotide variant	not specified [RCV004418278]	Chr4:113903236 [GRCh38] Chr4:114824392 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.848G>T (p.Arg283Leu)	single nucleotide variant	not specified [RCV004418279]	Chr4:113903226 [GRCh38] Chr4:114824382 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.331G>A (p.Val111Ile)	single nucleotide variant	not specified [RCV004418274]	Chr4:113978504 [GRCh38] Chr4:114899660 [GRCh37] Chr4:4q26	uncertain significance
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	copy number gain	not provided [RCV003885507]	Chr4:45455621..191003541 [GRCh37] Chr4:4p12-q35.2	pathogenic
NM_024590.4(ARSJ):c.767C>T (p.Thr256Ile)	single nucleotide variant	not specified [RCV004418276]	Chr4:113903307 [GRCh38] Chr4:114824463 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1309G>C (p.Gly437Arg)	single nucleotide variant	not specified [RCV004418270]	Chr4:113902765 [GRCh38] Chr4:114823921 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1531A>T (p.Arg511Trp)	single nucleotide variant	not specified [RCV004418272]	Chr4:113902543 [GRCh38] Chr4:114823699 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.725A>G (p.Tyr242Cys)	single nucleotide variant	not specified [RCV004418275]	Chr4:113903349 [GRCh38] Chr4:114824505 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.536T>G (p.Leu179Trp)	single nucleotide variant	not specified [RCV004658807]	Chr4:113903538 [GRCh38] Chr4:114824694 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.785A>G (p.Tyr262Cys)	single nucleotide variant	not specified [RCV004850156]	Chr4:113903289 [GRCh38] Chr4:114824445 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.319G>A (p.Ala107Thr)	single nucleotide variant	not specified [RCV004850164]	Chr4:113978516 [GRCh38] Chr4:114899672 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1645G>A (p.Gly549Arg)	single nucleotide variant	not specified [RCV004850168]	Chr4:113902429 [GRCh38] Chr4:114823585 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.347A>G (p.Tyr116Cys)	single nucleotide variant	not specified [RCV004855287]	Chr4:113978488 [GRCh38] Chr4:114899644 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.848G>A (p.Arg283Gln)	single nucleotide variant	not specified [RCV004855272]	Chr4:113903226 [GRCh38] Chr4:114824382 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.689G>C (p.Trp230Ser)	single nucleotide variant	not specified [RCV004855276]	Chr4:113903385 [GRCh38] Chr4:114824541 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.1120C>T (p.Leu374Phe)	single nucleotide variant	not specified [RCV005259740]	Chr4:113902954 [GRCh38] Chr4:114824110 [GRCh37] Chr4:4q26	uncertain significance
NM_024590.4(ARSJ):c.837C>G (p.Phe279Leu)	single nucleotide variant	not specified [RCV005259750]	Chr4:113903237 [GRCh38] Chr4:114824393 [GRCh37] Chr4:4q26	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	1932
Count of miRNA genes:	850
Interacting mature miRNAs:	977
Transcripts:	ENST00000315366, ENST00000503013, ENST00000509829, ENST00000541197
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

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
598090727	GWAS1810026_H	body height QTL GWAS1810026 (human)		3e-14	body height		4	113975748	113975749	Human
628916088	GWAS2824317_H	body height QTL GWAS2824317 (human)		5e-20	body height		4	113901423	113901424	Human
628539071	GWAS2447300_H	body height QTL GWAS2447300 (human)		3e-13	body height		4	113968498	113968499	Human
407017864	GWAS666840_H	body height QTL GWAS666840 (human)		1e-15	body height		4	113968218	113968219	Human
628819444	GWAS2727673_H	body height QTL GWAS2727673 (human)		8e-15	body height		4	113968498	113968499	Human
597299467	GWAS1395541_H	body height QTL GWAS1395541 (human)		3e-14	body height		4	113975748	113975749	Human
406985943	GWAS634919_H	behavioural disinhibition measurement QTL GWAS634919 (human)		0.0000009	behavioural disinhibition measurement		4	113934816	113934817	Human
406928278	GWAS577254_H	body height QTL GWAS577254 (human)		5e-20	body height		4	113901423	113901424	Human
628909349	GWAS2817578_H	body height QTL GWAS2817578 (human)		3e-08	body height		4	113901423	113901424	Human
628620653	GWAS2528882_H	body height QTL GWAS2528882 (human)		1e-15	body height		4	113968218	113968219	Human
597034312	GWAS1130386_H	body height QTL GWAS1130386 (human)		1e-15	body height		4	113968218	113968219	Human
407020962	GWAS669938_H	body height QTL GWAS669938 (human)		3e-08	body height		4	113901423	113901424	Human
1643256	BW127_H	Body Weight QTL 127 (human)	1.31	0.007	Body weight	body mass index	4	106319694	132319694	Human
597138993	GWAS1235067_H	body height QTL GWAS1235067 (human)		5e-20	body height		4	113901423	113901424	Human
597114111	GWAS1210185_H	behavioural disinhibition measurement QTL GWAS1210185 (human)		0.0000009	behavior trait (VT:0010442)		4	113934816	113934817	Human
407269486	GWAS918462_H	body height QTL GWAS918462 (human)		3e-56	body height		4	113958625	113958626	Human
407269487	GWAS918463_H	body height QTL GWAS918463 (human)		2e-89	body height		4	113970601	113970602	Human
628801232	GWAS2709461_H	COVID-19 QTL GWAS2709461 (human)		0.000005	COVID-19		4	113911048	113911049	Human
628536732	GWAS2444961_H	body height QTL GWAS2444961 (human)		3e-14	body height		4	113975748	113975749	Human
598057870	GWAS1777169_H	body height QTL GWAS1777169 (human)		3e-08	body height		4	113901423	113901424	Human
597216564	GWAS1312638_H	body height QTL GWAS1312638 (human)		2e-105	body height		4	113901423	113901424	Human
597216565	GWAS1312639_H	body height QTL GWAS1312639 (human)		3e-56	body height		4	113958625	113958626	Human
598033675	GWAS1752974_H	body height QTL GWAS1752974 (human)		8e-15	body height		4	113968498	113968499	Human
407269481	GWAS918457_H	body height QTL GWAS918457 (human)		2e-105	body height		4	113901423	113901424	Human
406903215	GWAS552191_H	COVID-19 QTL GWAS552191 (human)		0.000005	COVID-19		4	113911048	113911049	Human
598061909	GWAS1781208_H	body height QTL GWAS1781208 (human)		2e-105	body height		4	113901423	113901424	Human
597995412	GWAS1714711_H	body height QTL GWAS1714711 (human)		1e-15	body height		4	113968218	113968219	Human
625824767	GWAS2245689_H	body height QTL GWAS2245689 (human)		3e-13	body height		4	113968498	113968499	Human
598061911	GWAS1781210_H	body height QTL GWAS1781210 (human)		2e-89	body height		4	113970601	113970602	Human
597336041	GWAS1432115_H	COVID-19 QTL GWAS1432115 (human)		0.000005	COVID-19		4	113911048	113911049	Human
598061910	GWAS1781209_H	body height QTL GWAS1781209 (human)		3e-56	body height		4	113958625	113958626	Human
597129955	GWAS1226029_H	body height QTL GWAS1226029 (human)		3e-08	body height		4	113901423	113901424	Human
407048951	GWAS697927_H	systolic blood pressure, response to high sodium diet, response to dietary potassium supplementation QTL GWAS697927 (human)		0.0000002	arterial blood pressure trait (VT:2000000)	systolic blood pressure (CMO:0000004)	4	113940144	113940145	Human
597216812	GWAS1312886_H	body height QTL GWAS1312886 (human)		2e-89	body height		4	113970601	113970602	Human
407048635	GWAS697611_H	mean arterial pressure, response to high sodium diet, response to dietary potassium supplementation QTL GWAS697611 (human)		0.000003	arterial blood pressure trait (VT:2000000)	mean arterial blood pressure (CMO:0000009)	4	113940144	113940145	Human
597307297	GWAS1403371_H	body height QTL GWAS1403371 (human)		8e-15	body height		4	113968498	113968499	Human
407312444	GWAS961420_H	body height QTL GWAS961420 (human)		3e-14	body height		4	113975748	113975749	Human
596977449	GWAS1096968_H	body height QTL GWAS1096968 (human)		8e-15	body height		4	113968498	113968499	Human
598056859	GWAS1776158_H	body height QTL GWAS1776158 (human)		5e-20	body height		4	113901423	113901424	Human

Markers in Region

RH104453

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,822,416 - 114,822,591	UniSTS	GRCh37
Build 36	4	115,041,865 - 115,042,040	RGD	NCBI36
Celera	4	112,114,163 - 112,114,338	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,550,702 - 110,550,877	UniSTS
GeneMap99-GB4 RH Map	4	529.82	UniSTS

STS-W81455

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,823,654 - 114,823,817	UniSTS	GRCh37
Build 36	4	115,043,103 - 115,043,266	RGD	NCBI36
Celera	4	112,115,357 - 112,115,520	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,551,896 - 110,552,059	UniSTS
TNG Radiation Hybrid Map	4	71476.0	UniSTS
GeneMap99-GB4 RH Map	4	529.6	UniSTS

D4S1343

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,848,386 - 114,848,540	UniSTS	GRCh37
Build 36	4	115,067,835 - 115,067,989	RGD	NCBI36
Celera	4	112,140,085 - 112,140,239	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,576,626 - 110,576,780	UniSTS

SHGC-51089

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,848,384 - 114,848,508	UniSTS	GRCh37
Build 36	4	115,067,833 - 115,067,957	RGD	NCBI36
Celera	4	112,140,083 - 112,140,207	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,576,624 - 110,576,748	UniSTS
TNG Radiation Hybrid Map	4	71483.0	UniSTS

WI-11180

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,883,731 - 114,883,881	UniSTS	GRCh37
Build 36	4	115,103,180 - 115,103,330	RGD	NCBI36
Celera	4	112,175,411 - 112,175,561	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,611,947 - 110,612,097	UniSTS
TNG Radiation Hybrid Map	4	71501.0	UniSTS
Whitehead-RH Map	4	578.9	UniSTS

WI-21570

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	114,823,594 - 114,823,858	UniSTS	GRCh37
Build 36	4	115,043,043 - 115,043,307	RGD	NCBI36
Celera	4	112,115,297 - 112,115,561	RGD
Cytogenetic Map	4	q26	UniSTS
HuRef	4	110,551,836 - 110,552,100	UniSTS
GeneMap99-GB4 RH Map	4	529.49	UniSTS
Whitehead-RH Map	4	578.9	UniSTS
NCBI RH Map	4	1186.1	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	renal system	reproductive system	respiratory system	sensory system
1204	2428	2788	2230	4953	1714	2331	3	615	1202	458	2267	6550	5730	44	3710	850	1735	1603	172

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001354210	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001354211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024590	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532238	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532239	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008592	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008593	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008595	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008597	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024454216	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416154	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047416157	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC104779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI087279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307532	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AM049401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX206967	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY875938	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC032010	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033156	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC089445	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC132879	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC132881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC142701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC144265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC151213	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG661302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471057	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA031262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA884606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000315366 ⟹ ENSP00000320219

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	113,900,284 - 113,979,647 (-)	Ensembl

Ensembl Acc Id:

ENST00000503013

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	113,946,192 - 113,979,727 (-)	Ensembl

Ensembl Acc Id:

ENST00000509829 ⟹ ENSP00000421327

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	113,902,352 - 113,979,647 (-)	Ensembl

Ensembl Acc Id:

ENST00000636527

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	113,903,505 - 113,979,611 (-)	Ensembl

RefSeq Acc Id:

NM_001354210 ⟹ NP_001341139

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI
T2T-CHM13v2.0	4	117,209,000 - 117,288,314 (-)	NCBI

Sequence:

show sequence

AGTTTGCAGCGCCTGCGCCGGGTGCGCCAACTACGCAAAGACCAAGCGGGCTCCGCGCGGACCG
GCCGCGGGGCTAGGGACCCGGCTTTGGCCTTCAGGCTCCCTAGCAGCGGGGAAAAGGAATTGCT
GCCCGGAGTTTCTGCGGAGGTGGAGGGAGATCAGGAAACGGCTTCTTCCTCACTTCGCCGCCTG
GTGAGTGTCGGGGAGATTGGCAAACGCCTAGGAAAGGACTGGGGAAAATAGCCCTGGGAAAGTG
GAGAAGGTGATCAGGAGGCCGGTCCACTACGGCAGTTTATCTGTCTGATCAGAGCCAGACGCGA
CGCGTCCACTTCGCAGTTCTTTCCAGGTGTGGGGACCGCAGGACAGACGGCCGATCCCGCCGCC
CTCCGTACCAGCACTCCCAGGAGAGTCAGCCTCGCTCCCCAACGTCGAGGGCGCTCTGGCCACG
AAAAGTTCCTGTCCACTGTGATTCTCAATTCCTTGCTTGGTTTTTTTCTCCAGAGAACTTTTGG
GTGGAGATATTAACTTTTTTCTTTTTTTTTTCCTTGGTGGAAGCTGCTCTAGGGAGGGGGGAGG
AGGAGGAGAAAGTGAAATGTGCTGGAGAAGAGCGAGCCCTCCTTGTTCTTCCGGAGTCCCATCC
ATTAAGCCATCACTTCTGGAAGATTAAAGTTGTCGGACATGGTGACAGCTGAGAGGAGAGGAGG
ATTTCTTGCCAGGTGGAGAGTCTTCACCGTCTGTTGGGTGCATGTGTGCGCCCGCAGCGGCGCG
GGGCGCGTGGTTCTCCGCGTGGAGTCTCACCTGGGACCTGAGTGAATGGCTCCCAGGGGCTGTG
CGGGGCATCCGCCTCCGCCTTCTCCACAGGCCTGTGTCTGTCCTGGAAAGATGCTAGCAATGGG
GGCGCTGGCAGGATTCTGGATCCTCTGCCTCCTCACTTATGGTTACCTGTCCTGGGGCCAGGCC
TTAGAAGAGGAGGAAGAAGGGGCCTTACTAGCTCAAGCTGGAGAGAAACTAGAGCCCAGCACAA
CTTCCACCTCCCAGCCCCATCTCATTTTCATCCTAGCGGATGATCAGGGATTTAGAGATGTGGG
TTACCACGGATCTGAGATTAAAACACCTACTCTTGACAAGCTCGCTGCCGAAGGAGTTAAACTG
GAGAACTACTATGTCCAGCCTATTTGCACACCATCCAGGAGTCAGTTTATTACTGGAAAGTATC
AGATACACACCGGACTTCAACATTCTATCATAAGACCTACCCAACCCAACTGTTTACCTCTGGA
CAATGCCACCCTACCTCAGAAACTGAAGGAGGTTGGATATTCAACGCATATGGTCGGAAAATGG
CACTTGGGTTTTTACAGAAAAGAATGCATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTT
CCCTTTTGGGAAGTGGGGATTACTATACACACTACAAATGTGACAGTCCTGGGATGTGTGGCTA
TGACTTGTATGAAAACGACAATGCTGCCTGGGACTATGACAATGGCATATACTCCACACAGATG
TACACTCAGAGAGTACAGCAAATCTTAGCTTCCCATAACCCCACAAAGCCTATATTTTTATATA
TTGCCTATCAAGCTGTTCATTCACCACTGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATC
CATTATCAACATAAACAGGAGGAGATATGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAAC
AACGTGACATTGGCTCTAAAGACTTATGGTTTCTATAACAACAGCATTATCATTTACTCTTCAG
ATAATGGTGGCCAGCCTACGGCAGGAGGGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATA
TTGGGAAGGAGGGATCCGGGCTGTAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACA
GTGTGTAAGGAACTTGTGCACATCACTGACTGGTACCCCACTCTCATTTCACTGGCTGAAGGAC
AGATTGATGAGGACATTCAACTAGATGGCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCG
CTCACCCCGAGTAGATATTTTGCATAACATTGACCCCATATACACCAAGGCAAAAAATGGCTCC
TGGGCAGCAGGCTATGGGATCTGGAACACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGA
AATTGCTTACAGGAAATCCTGGCTACAGCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGG
ACCGAACCGGTGGCACAATGAACGGATCACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAAC
ATCACAGCCGACCCATATGAGAGGGTGGACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGC
TCCTACGGAGGCTCTCACAGTTCAACAAAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCC
CAGAAGTAACCCTAGGCTCAATGGAGGGGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAA
AAGAAGCCAAGCAAAAATCAGGCTGAGAAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAAC
AGCAGAAAGCAGTCTCAGGTAAACCAGCAAATTTGGCTCGATAATATCGCTGGCCTAAGCGTCA
GGCTTGTTTTCATGCTGTGCCACTCCAGAGACTTCTGCCACCTGGCCGCCACACTGAAAACTGT
CCTGCTCAGTGCCAAGGTGCTACTCTTGCAAGCCACACTTAGAGAGAGTGGAGATGTTTATTTC
TCTTGCTCCTTTAGAAAACGTGGTGAGTCCTGAGTTCCACTGCTGTGCTTCAGTCAACTGACCA
AACACTGCTTTGAATTATAGGAGGAGAACAATAACCTACCATCCGCAAGCATGCTAATTTGATG
GAAGTTACAGGGTATACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTAGCATGATT
AAAACTACCTTTGATAAATTACAGTCAAAGATTGTGTCACCTCAAAGGCCTTGAAGAATATATT
TTCTTGGTGAATTTTTGTATGTCTGTCATATGACACTTGGGTTTTTTAATTAATTCTATTTTAT
ATATATATATATGTTTCTTTTCCTGTGAAAAGCTGTTTTTCTCACATGTGAACAGCTTGCACCT
CATTTTACCATGCGTGAGGGAATGGCAAATAAGAATGTTTGAGCACACTGCCCACAATGAATGT
AACTATTTTCTAAACACTTTACTAGAAGAACATTTCAGTATAAAAAACCTAATTTATTTTTACA
GAAAAATATTTTGTTGTTTTTATAAAAAGTTATGCAAATGACTTTATTTTATTTTTATTTCCTG
CATACCATTAGAATAATTTTATTTCATTTCTTCAAATTACCAAGCACTGTAATACTATAAATTA
ATGTAATACTGTGTGAATTCAGACTATAAAAAACATCATTCAGAAAACTTTATAATCGTCATTG
TTCAACCAAGATTTTGAATGTAATAAGATGAATATATTCCTTACAAATTACTTGGAAATTCAAT
GTTTGTGCAGAGTTGAGACAACTTTATTGTTTCTATCATAAACTATTTATGTATCTTAATTATT
AAAATGATTTACTTTATGGCACTAGAAAATTTACTGTGGCTTTTCTGATCTAACTTCTAGCTAA
AATTGTATCATTGGTCCTAAAAAATAAAAATCTTTACTAATAGGCAATTGAAGGAATGGTTTGC
TAACAACCACAGTAATATAATATGATTTTACAGATAGATGCTTCCCCTTGGCTATGACATGGAG
AAAGATTTTCCCATAATAATAACTAACATTTATATTAGGTTGGTGCAAAACTAGTTGCGGTTTT
TCCCATTAAAAGTAATAAACTTACTCTTATACAAAGTGGACACTGTGGGGAGATACAGAGAAAT
GGAAGATACGGATCCTGCCTGGAGTAGGTAACCTTGCTTGGAAACCCCACATGCAAACGTCATG
AGGAGAATTAAAGGAGTATTATCAGTAATGAAGTTTATCATGGGTCATCAATGAGCATAGATTG
GTGTGGATCCTGTAGACCCTGGTGTTTTCTTTGAAGTGCCCTCTCCTAATGCAGAGGCCTTGAA
GCTTACAGTATACACTTGAAAAGTCACAGATAGCTAGAATTATGATCTTTGAAGTTATAACTGT
GATCTGAAAATGTGTGTGGTGGTATGACAGCATACCATTAAATACATTTACATCACAGCTCAAA
GGACTGTGATATAATCCATTTATATCACAACTCAAAGGACTGTGATATAATCCATTTATATCAC
AGCTCACAGTTTCTGAAAATGTATAAAAGAATCTATAATCTAGTACTGAAATTACTAAATTGGG
TAAGATGATTTAAATGATTTTAATTTTAACATTTTATTTCTAGAATATATGGCTCCATTTTATT
TTATAGTGTAAAGTTGTATTTCCTAAAGTTTGTGTTTTGTCGACAGTATCTTTTAAATGAGTCT
TAAAAATAAAGGCATATTGTTCATGTT

hide sequence

RefSeq Acc Id:

NM_001354211 ⟹ NP_001341140

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI
T2T-CHM13v2.0	4	117,209,000 - 117,288,314 (-)	NCBI

Sequence:

show sequence

AGTTTGCAGCGCCTGCGCCGGGTGCGCCAACTACGCAAAGACCAAGCGGGCTCCGCGCGGACCG
GCCGCGGGGCTAGGGACCCGGCTTTGGCCTTCAGGCTCCCTAGCAGCGGGGAAAAGGAATTGCT
GCCCGGAGTTTCTGCGGAGGTGGAGGGAGATCAGGAAACGGCTTCTTCCTCACTTCGCCGCCTG
GTGAGTGTCGGGGAGATTGGCAAACGCCTAGGAAAGGACTGGGGAAAATAGCCCTGGGAAAGTG
GAGAAGGTGATCAGGAGGCCGGTCCACTACGGCAGTTTATCTGTCTGATCAGAGCCAGACGCGA
CGCGTCCACTTCGCAGTTCTTTCCAGGTGTGGGGACCGCAGGACAGACGGCCGATCCCGCCGCC
CTCCGTACCAGCACTCCCAGGAGAGTCAGCCTCGCTCCCCAACGTCGAGGGCGCTCTGGCCACG
AAAAGTTCCTGTCCACTGTGATTCTCAATTCCTTGCTTGGTTTTTTTCTCCAGAGAACTTTTGG
GTGGAGATATTAACTTTTTTCTTTTTTTTTTCCTTGGTGGAAGCTGCTCTAGGGAGGGGGGAGG
AGGAGGAGAAAGTGAAATGTGCTGGAGAAGAGCGAGCCCTCCTTGTTCTTCCGGAGTCCCATCC
ATTAAGCCATCACTTCTGGAAGATTAAAGTTGTCGGACATGGTGACAGCTGAGAGGAGAGGAGG
ATTTCTTGCCAGGTGGAGAGTCTTCACCGTCTGTTGGGTGCATGTGTGCGCCCGCAGCGGCGCG
GGGCGCGTGGTTCTCCGCGTGGAGTCTCACCTGGGACCTGAGTGAATGGCTCCCAGGGGCTGTG
CGGGGCATCCGCCTCCGCCTTCTCCACAGGCCTGTGTCTGTCCTGGAAAGATGCTAGCAATGGG
GGCGCTGGCAGGATTCTGGATCCTCTGCCTCCTCACTTATGGTTACCTGTCCTGGGGCCAGGCC
TTAGAAGAGGAGGAAGAAGGGGCCTTACTAGCTCAAGCTGGAGAGAAACTAGAGCCCAGCACAA
CTTCCACCTCCCAGCCCCATCTCATTTTCATCCTAGCGGATGATCAGGGATTTAGAGATGTGGG
TTACCACGGATCTGAGATTAAAACACCTACTCTTGACAAGCTCGCTGCCGAAGGAGTTAAACTG
GAGAACTACTATGTCCAGCCTATTTGCACACCATCCAGGAGTCAGTTTATTACTGGAAAGAAAG
AAGAGAGAGTATAGATGTACAGATGCAAATAGCTTGGAAGATTTGGTTTTGGGACTCTGAAGTA
ATTCTCTTCTGAATTATCCTACAGGGTCCTGCTGTGTCGCCCAGGCTGGAGTGCAGCGGCATAA
TCATGGCTCACTGCAGCCTCAACCTCCCAGGCTCAAGTCATCCTCCTGCTTCAGCCTCCCAAGT
ACCTAGGACTACAGACATCCTGTTATTTGATCTTCACATTCACGCTGAAGATGAGGAAACTGAG
GATCAGAGGGATTAAGTACTTCCCAAAACCATACAGGTATCAGATACACACCGGACTTCAACAT
TCTATCATAAGACCTACCCAACCCAACTGTTTACCTCTGGACAATGCCACCCTACCTCAGAAAC
TGAAGGAGGTTGGATATTCAACGCATATGGTCGGAAAATGGCACTTGGGTTTTTACAGAAAAGA
ATGCATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTTCCCTTTTGGGAAGTGGGGATTAC
TATACACACTACAAATGTGACAGTCCTGGGATGTGTGGCTATGACTTGTATGAAAACGACAATG
CTGCCTGGGACTATGACAATGGCATATACTCCACACAGATGTACACTCAGAGAGTACAGCAAAT
CTTAGCTTCCCATAACCCCACAAAGCCTATATTTTTATATATTGCCTATCAAGCTGTTCATTCA
CCACTGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATCCATTATCAACATAAACAGGAGGA
GATATGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAACAACGTGACATTGGCTCTAAAGAC
TTATGGTTTCTATAACAACAGCATTATCATTTACTCTTCAGATAATGGTGGCCAGCCTACGGCA
GGAGGGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATATTGGGAAGGAGGGATCCGGGCTG
TAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACAGTGTGTAAGGAACTTGTGCACAT
CACTGACTGGTACCCCACTCTCATTTCACTGGCTGAAGGACAGATTGATGAGGACATTCAACTA
GATGGCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCGCTCACCCCGAGTAGATATTTTGC
ATAACATTGACCCCATATACACCAAGGCAAAAAATGGCTCCTGGGCAGCAGGCTATGGGATCTG
GAACACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGAAATTGCTTACAGGAAATCCTGGC
TACAGCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGGACCGAACCGGTGGCACAATGAAC
GGATCACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAACATCACAGCCGACCCATATGAGAG
GGTGGACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGCTCCTACGGAGGCTCTCACAGTTC
AACAAAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCCCAGAAGTAACCCTAGGCTCAATG
GAGGGGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAAAAGAAGCCAAGCAAAAATCAGGC
TGAGAAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAACAGCAGAAAGCAGTCTCAGGTAAA
CCAGCAAATTTGGCTCGATAATATCGCTGGCCTAAGCGTCAGGCTTGTTTTCATGCTGTGCCAC
TCCAGAGACTTCTGCCACCTGGCCGCCACACTGAAAACTGTCCTGCTCAGTGCCAAGGTGCTAC
TCTTGCAAGCCACACTTAGAGAGAGTGGAGATGTTTATTTCTCTTGCTCCTTTAGAAAACGTGG
TGAGTCCTGAGTTCCACTGCTGTGCTTCAGTCAACTGACCAAACACTGCTTTGAATTATAGGAG
GAGAACAATAACCTACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTATACCATCCG
CAAGCATGCTAATTTGATGGAAGTTACAGGGTAGCATGATTAAAACTACCTTTGATAAATTACA
GTCAAAGATTGTGTCACCTCAAAGGCCTTGAAGAATATATTTTCTTGGTGAATTTTTGTATGTC
TGTCATATGACACTTGGGTTTTTTAATTAATTCTATTTTATATATATATATATGTTTCTTTTCC
TGTGAAAAGCTGTTTTTCTCACATGTGAACAGCTTGCACCTCATTTTACCATGCGTGAGGGAAT
GGCAAATAAGAATGTTTGAGCACACTGCCCACAATGAATGTAACTATTTTCTAAACACTTTACT
AGAAGAACATTTCAGTATAAAAAACCTAATTTATTTTTACAGAAAAATATTTTGTTGTTTTTAT
AAAAAGTTATGCAAATGACTTTATTTTATTTTTATTTCCTGCATACCATTAGAATAATTTTATT
TCATTTCTTCAAATTACCAAGCACTGTAATACTATAAATTAATGTAATACTGTGTGAATTCAGA
CTATAAAAAACATCATTCAGAAAACTTTATAATCGTCATTGTTCAACCAAGATTTTGAATGTAA
TAAGATGAATATATTCCTTACAAATTACTTGGAAATTCAATGTTTGTGCAGAGTTGAGACAACT
TTATTGTTTCTATCATAAACTATTTATGTATCTTAATTATTAAAATGATTTACTTTATGGCACT
AGAAAATTTACTGTGGCTTTTCTGATCTAACTTCTAGCTAAAATTGTATCATTGGTCCTAAAAA
ATAAAAATCTTTACTAATAGGCAATTGAAGGAATGGTTTGCTAACAACCACAGTAATATAATAT
GATTTTACAGATAGATGCTTCCCCTTGGCTATGACATGGAGAAAGATTTTCCCATAATAATAAC
TAACATTTATATTAGGTTGGTGCAAAACTAGTTGCGGTTTTTCCCATTAAAAGTAATAAACTTA
CTCTTATACAAAGTGGACACTGTGGGGAGATACAGAGAAATGGAAGATACGGATCCTGCCTGGA
GTAGGTAACCTTGCTTGGAAACCCCACATGCAAACGTCATGAGGAGAATTAAAGGAGTATTATC
AGTAATGAAGTTTATCATGGGTCATCAATGAGCATAGATTGGTGTGGATCCTGTAGACCCTGGT
GTTTTCTTTGAAGTGCCCTCTCCTAATGCAGAGGCCTTGAAGCTTACAGTATACACTTGAAAAG
TCACAGATAGCTAGAATTATGATCTTTGAAGTTATAACTGTGATCTGAAAATGTGTGTGGTGGT
ATGACAGCATACCATTAAATACATTTACATCACAGCTCAAAGGACTGTGATATAATCCATTTAT
ATCACAACTCAAAGGACTGTGATATAATCCATTTATATCACAGCTCACAGTTTCTGAAAATGTA
TAAAAGAATCTATAATCTAGTACTGAAATTACTAAATTGGGTAAGATGATTTAAATGATTTTAA
TTTTAACATTTTATTTCTAGAATATATGGCTCCATTTTATTTTATAGTGTAAAGTTGTATTTCC
TAAAGTTTGTGTTTTGTCGACAGTATCTTTTAAATGAGTCTTAAAAATAAAGGCATATTGTTCA
TGTT

hide sequence

RefSeq Acc Id:

NM_024590 ⟹ NP_078866

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI
GRCh37	4	114,821,432 - 114,901,281 (-)	NCBI
Build 36	4	115,040,889 - 115,120,327 (-)	NCBI Archive
Celera	4	112,113,187 - 112,192,557 (-)	RGD
HuRef	4	110,549,726 - 110,629,095 (-)	RGD
CHM1_1	4	114,797,941 - 114,877,327 (-)	NCBI
T2T-CHM13v2.0	4	117,209,000 - 117,288,314 (-)	NCBI

Sequence:

show sequence

AGTTTGCAGCGCCTGCGCCGGGTGCGCCAACTACGCAAAGACCAAGCGGGCTCCGCGCGGACCG
GCCGCGGGGCTAGGGACCCGGCTTTGGCCTTCAGGCTCCCTAGCAGCGGGGAAAAGGAATTGCT
GCCCGGAGTTTCTGCGGAGGTGGAGGGAGATCAGGAAACGGCTTCTTCCTCACTTCGCCGCCTG
GTGAGTGTCGGGGAGATTGGCAAACGCCTAGGAAAGGACTGGGGAAAATAGCCCTGGGAAAGTG
GAGAAGGTGATCAGGAGGCCGGTCCACTACGGCAGTTTATCTGTCTGATCAGAGCCAGACGCGA
CGCGTCCACTTCGCAGTTCTTTCCAGGTGTGGGGACCGCAGGACAGACGGCCGATCCCGCCGCC
CTCCGTACCAGCACTCCCAGGAGAGTCAGCCTCGCTCCCCAACGTCGAGGGCGCTCTGGCCACG
AAAAGTTCCTGTCCACTGTGATTCTCAATTCCTTGCTTGGTTTTTTTCTCCAGAGAACTTTTGG
GTGGAGATATTAACTTTTTTCTTTTTTTTTTCCTTGGTGGAAGCTGCTCTAGGGAGGGGGGAGG
AGGAGGAGAAAGTGAAATGTGCTGGAGAAGAGCGAGCCCTCCTTGTTCTTCCGGAGTCCCATCC
ATTAAGCCATCACTTCTGGAAGATTAAAGTTGTCGGACATGGTGACAGCTGAGAGGAGAGGAGG
ATTTCTTGCCAGGTGGAGAGTCTTCACCGTCTGTTGGGTGCATGTGTGCGCCCGCAGCGGCGCG
GGGCGCGTGGTTCTCCGCGTGGAGTCTCACCTGGGACCTGAGTGAATGGCTCCCAGGGGCTGTG
CGGGGCATCCGCCTCCGCCTTCTCCACAGGCCTGTGTCTGTCCTGGAAAGATGCTAGCAATGGG
GGCGCTGGCAGGATTCTGGATCCTCTGCCTCCTCACTTATGGTTACCTGTCCTGGGGCCAGGCC
TTAGAAGAGGAGGAAGAAGGGGCCTTACTAGCTCAAGCTGGAGAGAAACTAGAGCCCAGCACAA
CTTCCACCTCCCAGCCCCATCTCATTTTCATCCTAGCGGATGATCAGGGATTTAGAGATGTGGG
TTACCACGGATCTGAGATTAAAACACCTACTCTTGACAAGCTCGCTGCCGAAGGAGTTAAACTG
GAGAACTACTATGTCCAGCCTATTTGCACACCATCCAGGAGTCAGTTTATTACTGGAAAGTATC
AGATACACACCGGACTTCAACATTCTATCATAAGACCTACCCAACCCAACTGTTTACCTCTGGA
CAATGCCACCCTACCTCAGAAACTGAAGGAGGTTGGATATTCAACGCATATGGTCGGAAAATGG
CACTTGGGTTTTTACAGAAAAGAATGCATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTT
CCCTTTTGGGAAGTGGGGATTACTATACACACTACAAATGTGACAGTCCTGGGATGTGTGGCTA
TGACTTGTATGAAAACGACAATGCTGCCTGGGACTATGACAATGGCATATACTCCACACAGATG
TACACTCAGAGAGTACAGCAAATCTTAGCTTCCCATAACCCCACAAAGCCTATATTTTTATATA
TTGCCTATCAAGCTGTTCATTCACCACTGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATC
CATTATCAACATAAACAGGAGGAGATATGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAAC
AACGTGACATTGGCTCTAAAGACTTATGGTTTCTATAACAACAGCATTATCATTTACTCTTCAG
ATAATGGTGGCCAGCCTACGGCAGGAGGGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATA
TTGGGAAGGAGGGATCCGGGCTGTAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACA
GTGTGTAAGGAACTTGTGCACATCACTGACTGGTACCCCACTCTCATTTCACTGGCTGAAGGAC
AGATTGATGAGGACATTCAACTAGATGGCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCG
CTCACCCCGAGTAGATATTTTGCATAACATTGACCCCATATACACCAAGGCAAAAAATGGCTCC
TGGGCAGCAGGCTATGGGATCTGGAACACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGA
AATTGCTTACAGGAAATCCTGGCTACAGCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGG
ACCGAACCGGTGGCACAATGAACGGATCACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAAC
ATCACAGCCGACCCATATGAGAGGGTGGACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGC
TCCTACGGAGGCTCTCACAGTTCAACAAAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCC
CAGAAGTAACCCTAGGCTCAATGGAGGGGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAA
AAGAAGCCAAGCAAAAATCAGGCTGAGAAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAAC
AGCAGAAAGCAGTCTCAGGTTCAACTTGCCATTCAGGTGTTACTTGTGGATAAGCACAAATATT
TCCTGTTTGGTTAAACTTTAATCAGTTCTTATCTTTCATCTGTTTCCTAGGTAAACCAGCAAAT
TTGGCTCGATAATATCGCTGGCCTAAGCGTCAGGCTTGTTTTCATGCTGTGCCACTCCAGAGAC
TTCTGCCACCTGGCCGCCACACTGAAAACTGTCCTGCTCAGTGCCAAGGTGCTACTCTTGCAAG
CCACACTTAGAGAGAGTGGAGATGTTTATTTCTCTTGCTCCTTTAGAAAACGTGGTGAGTCCTG
AGTTCCACTGCTGTGCTTCAGTCAACTGACCAAACACTGCTTTGAATTATAGGAGGAGAACAAT
AACCTACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTATACCATCCGCAAGCATGC
TAATTTGATGGAAGTTACAGGGTAGCATGATTAAAACTACCTTTGATAAATTACAGTCAAAGAT
TGTGTCACCTCAAAGGCCTTGAAGAATATATTTTCTTGGTGAATTTTTGTATGTCTGTCATATG
ACACTTGGGTTTTTTAATTAATTCTATTTTATATATATATATATGTTTCTTTTCCTGTGAAAAG
CTGTTTTTCTCACATGTGAACAGCTTGCACCTCATTTTACCATGCGTGAGGGAATGGCAAATAA
GAATGTTTGAGCACACTGCCCACAATGAATGTAACTATTTTCTAAACACTTTACTAGAAGAACA
TTTCAGTATAAAAAACCTAATTTATTTTTACAGAAAAATATTTTGTTGTTTTTATAAAAAGTTA
TGCAAATGACTTTATTTTATTTTTATTTCCTGCATACCATTAGAATAATTTTATTTCATTTCTT
CAAATTACCAAGCACTGTAATACTATAAATTAATGTAATACTGTGTGAATTCAGACTATAAAAA
ACATCATTCAGAAAACTTTATAATCGTCATTGTTCAACCAAGATTTTGAATGTAATAAGATGAA
TATATTCCTTACAAATTACTTGGAAATTCAATGTTTGTGCAGAGTTGAGACAACTTTATTGTTT
CTATCATAAACTATTTATGTATCTTAATTATTAAAATGATTTACTTTATGGCACTAGAAAATTT
ACTGTGGCTTTTCTGATCTAACTTCTAGCTAAAATTGTATCATTGGTCCTAAAAAATAAAAATC
TTTACTAATAGGCAATTGAAGGAATGGTTTGCTAACAACCACAGTAATATAATATGATTTTACA
GATAGATGCTTCCCCTTGGCTATGACATGGAGAAAGATTTTCCCATAATAATAACTAACATTTA
TATTAGGTTGGTGCAAAACTAGTTGCGGTTTTTCCCATTAAAAGTAATAAACTTACTCTTATAC
AAAGTGGACACTGTGGGGAGATACAGAGAAATGGAAGATACGGATCCTGCCTGGAGTAGGTAAC
CTTGCTTGGAAACCCCACATGCAAACGTCATGAGGAGAATTAAAGGAGTATTATCAGTAATGAA
GTTTATCATGGGTCATCAATGAGCATAGATTGGTGTGGATCCTGTAGACCCTGGTGTTTTCTTT
GAAGTGCCCTCTCCTAATGCAGAGGCCTTGAAGCTTACAGTATACACTTGAAAAGTCACAGATA
GCTAGAATTATGATCTTTGAAGTTATAACTGTGATCTGAAAATGTGTGTGGTGGTATGACAGCA
TACCATTAAATACATTTACATCACAGCTCAAAGGACTGTGATATAATCCATTTATATCACAACT
CAAAGGACTGTGATATAATCCATTTATATCACAGCTCACAGTTTCTGAAAATGTATAAAAGAAT
CTATAATCTAGTACTGAAATTACTAAATTGGGTAAGATGATTTAAATGATTTTAATTTTAACAT
TTTATTTCTAGAATATATGGCTCCATTTTATTTTATAGTGTAAAGTTGTATTTCCTAAAGTTTG
TGTTTTGTCGACAGTATCTTTTAAATGAGTCTTAAAAATAAAGGCATATTGTTCATGTT

hide sequence

RefSeq Acc Id:

XM_011532238 ⟹ XP_011530540

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,918,300 (-)	NCBI

Sequence:

show sequence

ATTTTTTCAAATCTCTTTAATGTCTGCTCTAATAGAAGATAGCTGGATTTCTTGTTGCTAGTTA
TTGTTTCTGTTGAAGTGTGTGAGGACAATTCAGCCTCGTGGATATATGTAGCTGGAAAAGGAAG
ATGTGCCTGAGTCATGTTTTCTGATAATTGTGATATTCTTCTTTGTTACTGCATCAAGAGTTGA
CCAAAAGTGGTAGTTTATTAGAGATTCTTATTACTCATTGGTTAGGTAAGAGCAGACAATAACC
AATAGGTTGGGAAATGTAAGGCTGATAAAATTCTAACAACCATATTGAACTCCGTAATTTCTTA
AATATTGTGTTTCTATGTGCTAGGCATTATGTTGCGTACCTCACATTTATAAGCTCATTTAATC
TTCATGGTAACTCAGTGAGAAAAGTGTTATTATTAATCCCATTTCATGCAAATTAGGAAACTGA
GGCATAGAAATTCTTTGAAATGGATTTGCCATTTTGATTTTCAGCTATATTGTTTTACAGGATA
ACAATTCAAAGTAAAATAAACCTAATATAAAGGATGCATAATAGAACTTCAGAATTATTGATGA
GGAAACTGAGGATCAGAGGGATTAAGTACTTCCCAAAACCATACAGGTATCAGATACACACCGG
ACTTCAACATTCTATCATAAGACCTACCCAACCCAACTGTTTACCTCTGGACAATGCCACCCTA
CCTCAGAAACTGAAGGAGGTTGGATATTCAACGCATATGGTCGGAAAATGGCACTTGGGTTTTT
ACAGAAAAGAATGCATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTTCCCTTTTGGGAAG
TGGGGATTACTATACACACTACAAATGTGACAGTCCTGGGATGTGTGGCTATGACTTGTATGAA
AACGACAATGCTGCCTGGGACTATGACAATGGCATATACTCCACACAGATGTACACTCAGAGAG
TACAGCAAATCTTAGCTTCCCATAACCCCACAAAGCCTATATTTTTATATATTGCCTATCAAGC
TGTTCATTCACCACTGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATCCATTATCAACATA
AACAGGAGGAGATATGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAACAACGTGACATTGG
CTCTAAAGACTTATGGTTTCTATAACAACAGCATTATCATTTACTCTTCAGATAATGGTGGCCA
GCCTACGGCAGGAGGGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATATTGGGAAGGAGGG
ATCCGGGCTGTAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACAGTGTGTAAGGAAC
TTGTGCACATCACTGACTGGTACCCCACTCTCATTTCACTGGCTGAAGGACAGATTGATGAGGA
CATTCAACTAGATGGCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCGCTCACCCCGAGTA
GATATTTTGCATAACATTGACCCCATATACACCAAGGCAAAAAATGGCTCCTGGGCAGCAGGCT
ATGGGATCTGGAACACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGAAATTGCTTACAGG
AAATCCTGGCTACAGCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGGACCGAACCGGTGG
CACAATGAACGGATCACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAACATCACAGCCGACC
CATATGAGAGGGTGGACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGCTCCTACGGAGGCT
CTCACAGTTCAACAAAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCCCAGAAGTAACCCT
AGGCTCAATGGAGGGGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAAAAGAAGCCAAGCA
AAAATCAGGCTGAGAAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAACAGCAGAAAGCAGT
CTCAGGTTCAACTTGCCATTCAGGTGTTACTTGTGGATAAGCACAAATATTTCCTGTTTGGTTA
AACTTTAATCAGTTCTTATCTTTCATCTGTTTCCTAGGTAAACCAGCAAATTTGGCTCGATAAT
ATCGCTGGCCTAAGCGTCAGGCTTGTTTTCATGCTGTGCCACTCCAGAGACTTCTGCCACCTGG
CCGCCACACTGAAAACTGTCCTGCTCAGTGCCAAGGTGCTACTCTTGCAAGCCACACTTAGAGA
GAGTGGAGATGTTTATTTCTCTTGCTCCTTTAGAAAACGTGGTGAGTCCTGAGTTCCACTGCTG
TGCTTCAGTCAACTGACCAAACACTGCTTTGAATTATAGGAGGAGAACAATAACCTACCATCCG
CAAGCATGCTAATTTGATGGAAGTTACAGGGTATACCATCCGCAAGCATGCTAATTTGATGGAA
GTTACAGGGTAGCATGATTAAAACTACCTTTGATAAATTACAGTCAAAGATTGTGTCACCTCAA
AGGCCTTGAAGAATATATTTTCTTGGTGAATTTTTGTATGTCTGTCATATGACACTTGGGTTTT
TTAATTAATTCTATTTTATATATATATATATGTTTCTTTTCCTGTGAAAAGCTGTTTTTCTCAC
ATGTGAACAGCTTGCACCTCATTTTACCATGCGTGAGGGAATGGCAAATAAGAATGTTTGAGCA
CACTGCCCACAATGAATGTAACTATTTTCTAAACACTTTACTAGAAGAACATTTCAGTATAAAA
AACCTAATTTATTTTTACAGAAAAATATTTTGTTGTTTTTATAAAAAGTTATGCAAATGACTTT
ATTTTATTTTTATTTCCTGCATACCATTAGAATAATTTTATTTCATTTCTTCAAATTACCAAGC
ACTGTAATACTATAAATTAATGTAATACTGTGTGAATTCAGACTATAAAAAACATCATTCAGAA
AACTTTATAATCGTCATTGTTCAACCAAGATTTTGAATGTAATAAGATGAATATATTCCTTACA
AATTACTTGGAAATTCAATGTTTGTGCAGAGTTGAGACAACTTTATTGTTTCTATCATAAACTA
TTTATGTATCTTAATTATTAAAATGATTTACTTTATGGCACTAGAAAATTTACTGTGGCTTTTC
TGATCTAACTTCTAGCTAAAATTGTATCATTGGTCCTAAAAAATAAAAATCTTTACTAATAGGC
AATTGAAGGAATGGTTTGCTAACAACCACAGTAATATAATATGATTTTACAGATAGATGCTTCC
CCTTGGCTATGACATGGAGAAAGATTTTCCCATAATAATAACTAACATTTATATTAGGTTGGTG
CAAAACTAGTTGCGGTTTTTCCCATTAAAAGTAATAAACTTACTCTTATACAAAGTGGACACTG
TGGGGAGATACAGAGAAATGGAAGATACGGATCCTGCCTGGAGTAGGTAACCTTGCTTGGAAAC
CCCACATGCAAACGTCATGAGGAGAATTAAAGGAGTATTATCAGTAATGAAGTTTATCATGGGT
CATCAATGAGCATAGATTGGTGTGGATCCTGTAGACCCTGGTGTTTTCTTTGAAGTGCCCTCTC
CTAATGCAGAGGCCTTGAAGCTTACAGTATACACTTGAAAAGTCACAGATAGCTAGAATTATGA
TCTTTGAAGTTATAACTGTGATCTGAAAATGTGTGTGGTGGTATGACAGCATACCATTAAATAC
ATTTACATCACAGCTCAAAGGACTGTGATATAATCCATTTATATCACAACTCAAAGGACTGTGA
TATAATCCATTTATATCACAGCTCACAGTTTCTGAAAATGTATAAAAGAATCTATAATCTAGTA
CTGAAATTACTAAATTGGGTAAGATGATTTAAATGATTTTAATTTTAACATTTTATTTCTAGAA
TATATGGCTCCATTTTATTTTATAGTGTAAAGTTGTATTTCCTAAAGTTTGTGTTTTGTCGACA
GTATCTTTTAAATGAGTCTTAAAAATAAAGGCATATTGTTCATGTTTTTCTTTCCTGGTGGCAC
ATAAATGACATGTCTTAAAATAGATGGCATCTTATACATTTTTTAAAAATAGACATCTTTACAC
TAAAAAAGAGTTCTGAAGAAAGTAAGTTTGGGAGATGCTGGGTTAAAGAACGTCAAAGGAGTCA
CTTTAATGCAGGTTTTTCTTTTAGAGGAGTTTTTAAAATCTTAGCTTGTATTGTAACCCTGACA
GAAGGAAAATGTTATACAGTATTTCATAATTTCACCACAAAACTGCTGTCTGTGGCACAATGCA
CAGGACTAGGGTTCTGAGGAACTATACTGTTATTGGAAACATAGTGTAAACATAGAATCTTCTA
GAAGTTCCTAGAAAGAC

hide sequence

RefSeq Acc Id:

XM_017008592 ⟹ XP_016864081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI

Sequence:

show sequence

AGTTTGCAGCGCCTGCGCCGGGTGCGCCAACTACGCAAAGACCAAGCGGGCTCCGCGCGGACCG
GCCGCGGGGCTAGGGACCCGGCTTTGGCCTTCAGGCTCCCTAGCAGCGGGGAAAAGGAATTGCT
GCCCGGAGTTTCTGCGGAGGTGGAGGGAGATCAGGAAACGGCTTCTTCCTCACTTCGCCGCCTG
CTGCTCTAGGGAGGGGGGAGGAGGAGGAGAAAGTGAAATGTGCTGGAGAAGAGCGAGCCCTCCT
TGTTCTTCCGGAGTCCCATCCATTAAGCCATCACTTCTGGAAGATTAAAGTTGTCGGACATGGT
GACAGCTGAGAGGAGAGGAGGATTTCTTGCCAGGTGGAGAGTCTTCACCGTCTGTTGGGTGCAT
GTGTGCGCCCGCAGCGGCGCGGGGCGCGTGGTTCTCCGCGTGGAGTCTCACCTGGGACCTGAGT
GAATGGCTCCCAGGGGCTGTGCGGGGCATCCGCCTCCGCCTTCTCCACAGGCCTGTGTCTGTCC
TGGAAAGATGCTAGCAATGGGGGCGCTGGCAGGATTCTGGATCCTCTGCCTCCTCACTTATGGT
TACCTGTCCTGGGGCCAGGCCTTAGAAGAGGAGGAAGAAGGGGCCTTACTAGCTCAAGCTGGAG
AGAAACTAGAGCCCAGCACAACTTCCACCTCCCAGCCCCATCTCATTTTCATCCTAGCGGATGA
TCAGGGATTTAGAGATGTGGGTTACCACGGATCTGAGATTAAAACACCTACTCTTGACAAGCTC
GCTGCCGAAGGAGTTAAACTGGAGAACTACTATGTCCAGCCTATTTGCACACCATCCAGGAGTC
AGTTTATTACTGGAAAGTATCAGATACACACCGGACTTCAACATTCTATCATAAGACCTACCCA
ACCCAACTGTTTACCTCTGGACAATGCCACCCTACCTCAGAAACTGAAGGAGGTTGGATATTCA
ACGCATATGGTCGGAAAATGGCACTTGGGTTTTTACAGAAAAGAATGCATGCCCACCAGAAGAG
GATTTGATACCTTTTTTGGTTCCCTTTTGGGAAGTGGGGATTACTATACACACTACAAATGTGA
CAGTCCTGGGATGTGTGGCTATGACTTGTATGAAAACGACAATGCTGCCTGGGACTATGACAAT
GGCATATACTCCACACAGATGTACACTCAGAGAGTACAGCAAATCTTAGCTTCCCATAACCCCA
CAAAGCCTATATTTTTATATATTGCCTATCAAGCTGTTCATTCACCACTGCAAGCTCCTGGCAG
GTATTTCGAACACTACCGATCCATTATCAACATAAACAGGAGGAGATATGCTGCCATGCTTTCC
TGCTTAGATGAAGCAATCAACAACGTGACATTGGCTCTAAAGACTTATGGTTTCTATAACAACA
GCATTATCATTTACTCTTCAGATAATGGTGGCCAGCCTACGGCAGGAGGGAGTAACTGGCCTCT
CAGAGGTAGCAAAGGAACATATTGGGAAGGAGGGATCCGGGCTGTAGGCTTTGTGCATAGCCCA
CTTCTGAAAAACAAGGGAACAGTGTGTAAGGAACTTGTGCACATCACTGACTGGTACCCCACTC
TCATTTCACTGGCTGAAGGACAGATTGATGAGGACATTCAACTAGATGGCTATGATATCTGGGA
GACCATAAGTGAGGGTCTTCGCTCACCCCGAGTAGATATTTTGCATAACATTGACCCCATATAC
ACCAAGGCAAAAAATGGCTCCTGGGCAGCAGGCTATGGGATCTGGAACACTGCAATCCAGTCAG
CCATCAGAGTGCAGCACTGGAAATTGCTTACAGGAAATCCTGGCTACAGCGACTGGGTCCCCCC
TCAGTCTTTCAGCAACCTGGGACCGAACCGGTGGCACAATGAACGGATCACCTTGTCAACTGGC
AAAAGTGTATGGCTTTTCAACATCACAGCCGACCCATATGAGAGGGTGGACCTATCTAACAGGT
ATCCAGGAATCGTGAAGAAGCTCCTACGGAGGCTCTCACAGTTCAACAAAACTGCAGTGCCGGT
CAGGTATCCCCCCAAAGACCCCAGAAGTAACCCTAGGCTCAATGGAGGGGTCTGGGGACCATGG
TATAAAGAGGAAACCAAGAAAAAGAAGCCAAGCAAAAATCAGGCTGAGAAAAAGCAAAAGAAAA
GCAAAAAAAAGAAGAAGAAACAGCAGAAAGCAGTCTCAGGTTCAACTTGCCATTCAGGTGTTAC
TTGTGGATAAGCACAAATATTTCCTGTTTGGTTAAACTTTAATCAGTTCTTATCTTTCATCTGT
TTCCTAGGTAAACCAGCAAATTTGGCTCGATAATATCGCTGGCCTAAGCGTCAGGCTTGTTTTC
ATGCTGTGCCACTCCAGAGACTTCTGCCACCTGGCCGCCACACTGAAAACTGTCCTGCTCAGTG
CCAAGGTGCTACTCTTGCAAGCCACACTTAGAGAGAGTGGAGATGTTTATTTCTCTTGCTCCTT
TAGAAAACGTGGTGAGTCCTGAGTTCCACTGCTGTGCTTCAGTCAACTGACCAAACACTGCTTT
GAATTATAGGAGGAGAACAATAACCTACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGG
GTATACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTAGCATGATTAAAACTACCTT
TGATAAATTACAGTCAAAGATTGTGTCACCTCAAAGGCCTTGAAGAATATATTTTCTTGGTGAA
TTTTTGTATGTCTGTCATATGACACTTGGGTTTTTTAATTAATTCTATTTTATATATATATATA
TGTTTCTTTTCCTGTGAAAAGCTGTTTTTCTCACATGTGAACAGCTTGCACCTCATTTTACCAT
GCGTGAGGGAATGGCAAATAAGAATGTTTGAGCACACTGCCCACAATGAATGTAACTATTTTCT
AAACACTTTACTAGAAGAACATTTCAGTATAAAAAACCTAATTTATTTTTACAGAAAAATATTT
TGTTGTTTTTATAAAAAGTTATGCAAATGACTTTATTTTATTTTTATTTCCTGCATACCATTAG
AATAATTTTATTTCATTTCTTCAAATTACCAAGCACTGTAATACTATAAATTAATGTAATACTG
TGTGAATTCAGACTATAAAAAACATCATTCAGAAAACTTTATAATCGTCATTGTTCAACCAAGA
TTTTGAATGTAATAAGATGAATATATTCCTTACAAATTACTTGGAAATTCAATGTTTGTGCAGA
GTTGAGACAACTTTATTGTTTCTATCATAAACTATTTATGTATCTTAATTATTAAAATGATTTA
CTTTATGGCACTAGAAAATTTACTGTGGCTTTTCTGATCTAACTTCTAGCTAAAATTGTATCAT
TGGTCCTAAAAAATAAAAATCTTTACTAATAGGCAATTGAAGGAATGGTTTGCTAACAACCACA
GTAATATAATATGATTTTACAGATAGATGCTTCCCCTTGGCTATGACATGGAGAAAGATTTTCC
CATAATAATAACTAACATTTATATTAGGTTGGTGCAAAACTAGTTGCGGTTTTTCCCATTAAAA
GTAATAAACTTACTCTTATACAAAGTGGACACTGTGGGGAGATACAGAGAAATGGAAGATACGG
ATCCTGCCTGGAGTAGGTAACCTTGCTTGGAAACCCCACATGCAAACGTCATGAGGAGAATTAA
AGGAGTATTATCAGTAATGAAGTTTATCATGGGTCATCAATGAGCATAGATTGGTGTGGATCCT
GTAGACCCTGGTGTTTTCTTTGAAGTGCCCTCTCCTAATGCAGAGGCCTTGAAGCTTACAGTAT
ACACTTGAAAAGTCACAGATAGCTAGAATTATGATCTTTGAAGTTATAACTGTGATCTGAAAAT
GTGTGTGGTGGTATGACAGCATACCATTAAATACATTTACATCACAGCTCAAAGGACTGTGATA
TAATCCATTTATATCACAACTCAAAGGACTGTGATATAATCCATTTATATCACAGCTCACAGTT
TCTGAAAATGTATAAAAGAATCTATAATCTAGTACTGAAATTACTAAATTGGGTAAGATGATTT
AAATGATTTTAATTTTAACATTTTATTTCTAGAATATATGGCTCCATTTTATTTTATAGTGTAA
AGTTGTATTTCCTAAAGTTTGTGTTTTGTCGACAGTATCTTTTAAATGAGTCTTAAAAATAAAG
GCATATTGTTCATGTTTTTCTTTCCTGGTGGCACATAAATGACATGTCTTAAAATAGATGGCAT
CTTATACATTTTTTAAAAATAGACATCTTTACACTAAAAAAGAGTTCTGAAGAAAGTAAGTTTG
GGAGATGCTGGGTTAAAGAACGTCAAAGGAGTCACTTTAATGCAGGTTTTTCTTTTAGAGGAGT
TTTTAAAATCTTAGCTTGTATTGTAACCCTGACAGAAGGAAAATGTTATACAGTATTTCATAAT
TTCACCACAAAACTGCTGTCTGTGGCACAATGCACAGGACTAGGGTTCTGAGGAACTATACTGT
TATTGGAAACATAGTGTAAACATAGAATCTTCTAGAAGTTCCTAGAAAGAC

hide sequence

RefSeq Acc Id:

XM_017008594 ⟹ XP_016864083

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI

Sequence:

show sequence

AGACACCCTGTGGGTAAGTTAGGGGAGAGGTAAGAGGGAGCGGGCAATTCCAGTATTTTCACAT
AGGGAAAGGGTAACGAAGAATCAGGCTGTAAAAGCCAGCTATTGGGAGAGGAAATAAAACTTAA
AAATTTGTCATCGTTACTGAAAAAAAAAAAAAAAAAGGTAGGGACAAAAGGAATAGGAAAATGA
TGGGGGTGGGGGGACTAGTAAAGGAAAACCTGCAAAGGAAGTTGGAAAGAGGAAAGAGTGTCAT
ACGCATTTTGTTTTTATTCCTGCTCCTTCTCTCTCACTCCCTCCAGAAGCTAGAAAAAGTTTGC
AAGCGCAACTTTAGGGATGGGAGACGGGGCTCTTCACCAACAGCCCCACGAAAAGAAGTGCCCG
CTTTACCCTTCCCCATTCGCGCCGCCGTCCTTTCCCTCTAGCGGGGTGATGGGCAGGAGGCGAC
ACTCTTGGGACGCGGTAGCCCAGGCGGATCCCCCGGAATCCCGCTGGGCTGGAGCAGCACGCAG
CTCTCTCTCTGGCAAAGCCTCCTCTGCCTTGGCCATCCACCTCCCGGAAAAGAAAAAGGAAAGA
TCGAGCCTCTAAACAGTCCTTTTCCCCCACCCCCTCTTCCCGGGGGAGCTCAGGAAGAAAGTAC
CGTTCTGTGATTCACTGGAGAGAAAAGAGGGAGGAGGCAAAAGAACTCGGAGTGCCAAAGCTAA
ATAAGTTAGCTGAGAAAACGCACGCAGTTTGCAGCGCCTGCGCCGGGTGCGCCAACTACGCAAA
GACCAAGCGGGCTCCGCGCGGACCGGCCGCGGGGCTAGGGACCCGGCTTTGGCCTTCAGGCTCC
CTAGCAGCGGGGAAAAGGAATTGCTGCCCGGAGTTTCTGCGGAGGTGGAGGGAGATCAGGAAAC
GGCTTCTTCCTCACTTCGCCGCCTGGTGAGTGTCGGGGAGATTGGCAAACGCCTAGGAAAGGAC
TGGGGAAAATAGCCCTGGGAAAGTGGAGAAGGTGATCAGGAGGCCGGTCCACTACGGCAGTTTA
TCTGTCTGATCAGAGCCAGACGCGACGCGTCCACTTCGCAGTTCTTTCCAGGTGTGGGGACCGC
AGGACAGACGGCCGATCCCGCCGCCCTCCGTACCAGCACTCCCAGGAGAGTCAGCCTCGCTCCC
CAACGTCGAGGGCGCTCTGGCCACGAAAAGTTCCTGTCCACTGTGATTCTCAATTCCTTGCTTG
GTTTTTTTCTCCAGAGAACTTTTGGGTGGAGATATTAACTTTTTTCTTTTTTTTTTCCTTGGTG
GAAGCTGCTCTAGGGAGGGGGGAGGAGGAGGAGAAAGTGAAATGTGCTGGAGAAGAGCGAGCCC
TCCTTGTTCTTCCGGAGTCCCATCCATTAAGCCATCACTTCTGGAAGATTAAAGTTGTCGGACA
TGGTGACAGCTGAGAGGAGAGGAGGATTTCTTGCCAGGTGGAGAGTCTTCACCGTCTGTTGGGT
GCATGTGTGCGCCCGCAGCGGCGCGGGGCGCGTGGTTCTCCGCGTGGAGTCTCACCTGGGACCT
GAGTGAATGGCTCCCAGGGGCTGTGCGGGGCATCCGCCTCCGCCTTCTCCACAGGCCTGTGTCT
GTCCTGGAAAGATGCTAGCAATGGGGGCGCTGGCAGGATTCTGGATCCTCTGCCTCCTCACTTA
TGGTTACCTGTCCTGGGGCCAGGCCTTAGAAGAGGAGGAAGAAGGGGCCTTACTAGCTCAAGCT
GGAGAGAAACTAGAGCCCAGCACAACTTCCACCTCCCAGCCCCATCTCATTTTCATCCTAGCGG
ATGATCAGGGATTTAGAGATGTGGGTTACCACGGATCTGAGATTAAAACACCTACTCTTGACAA
GCTCGCTGCCGAAGGAGTTAAACTGGAGAACTACTATGTCCAGCCTATTTGCACACCATCCAGG
AGTCAGTTTATTACTGGAAAGGTCCTGCTGTGTCGCCCAGGCTGGAGTGCAGCGGCATAATCAT
GGCTCACTGCAGCCTCAACCTCCCAGGCTCAAGTCATCCTCCTGCTTCAGCCTCCCAAGTACCT
AGGACTACAGACATCCTGTTATTTGATCTTCACATTCACGCTGAAGATGAGGAAACTGAGGATC
AGAGGGATTAAGTACTTCCCAAAACCATACAGGTATCAGATACACACCGGACTTCAACATTCTA
TCATAAGACCTACCCAACCCAACTGTTTACCTCTGGACAATGCCACCCTACCTCAGAAACTGAA
GGAGGTTGGATATTCAACGCATATGGTCGGAAAATGGCACTTGGGTTTTTACAGAAAAGAATGC
ATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTTCCCTTTTGGGAAGTGGGGATTACTATA
CACACTACAAATGTGACAGTCCTGGGATGTGTGGCTATGACTTGTATGAAAACGACAATGCTGC
CTGGGACTATGACAATGGCATATACTCCACACAGATGTACACTCAGAGAGTACAGCAAATCTTA
GCTTCCCATAACCCCACAAAGCCTATATTTTTATATATTGCCTATCAAGCTGTTCATTCACCAC
TGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATCCATTATCAACATAAACAGGAGGAGATA
TGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAACAACGTGACATTGGCTCTAAAGACTTAT
GGTTTCTATAACAACAGCATTATCATTTACTCTTCAGATAATGGTGGCCAGCCTACGGCAGGAG
GGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATATTGGGAAGGAGGGATCCGGGCTGTAGG
CTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACAGTGTGTAAGGAACTTGTGCACATCACT
GACTGGTACCCCACTCTCATTTCACTGGCTGAAGGACAGATTGATGAGGACATTCAACTAGATG
GCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCGCTCACCCCGAGTAGATATTTTGCATAA
CATTGACCCCATATACACCAAGGCAAAAAATGGCTCCTGGGCAGCAGGCTATGGGATCTGGAAC
ACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGAAATTGCTTACAGGAAATCCTGGCTACA
GCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGGACCGAACCGGTGGCACAATGAACGGAT
CACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAACATCACAGCCGACCCATATGAGAGGGTG
GACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGCTCCTACGGAGGCTCTCACAGTTCAACA
AAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCCCAGAAGTAACCCTAGGCTCAATGGAGG
GGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAAAAGAAGCCAAGCAAAAATCAGGCTGAG
AAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAACAGCAGAAAGCAGTCTCAGGTTCAACTT
GCCATTCAGGTGTTACTTGTGGATAAGCACAAATATTTCCTGTTTGGTTAAACTTTAATCAGTT
CTTATCTTTCATCTGTTTCCTAGGTAAACCAGCAAATTTGGCTCGATAATATCGCTGGCCTAAG
CGTCAGGCTTGTTTTCATGCTGTGCCACTCCAGAGACTTCTGCCACCTGGCCGCCACACTGAAA
ACTGTCCTGCTCAGTGCCAAGGTGCTACTCTTGCAAGCCACACTTAGAGAGAGTGGAGATGTTT
ATTTCTCTTGCTCCTTTAGAAAACGTGGTGAGTCCTGAGTTCCACTGCTGTGCTTCAGTCAACT
GACCAAACACTGCTTTGAATTATAGGAGGAGAACAATAACCTACCATCCGCAAGCATGCTAATT
TGATGGAAGTTACAGGGTATACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTAGCA
TGATTAAAACTACCTTTGATAAATTACAGTCAAAGATTGTGTCACCTCAAAGGCCTTGAAGAAT
ATATTTTCTTGGTGAATTTTTGTATGTCTGTCATATGACACTTGGGTTTTTTAATTAATTCTAT
TTTATATATATATATATGTTTCTTTTCCTGTGAAAAGCTGTTTTTCTCACATGTGAACAGCTTG
CACCTCATTTTACCATGCGTGAGGGAATGGCAAATAAGAATGTTTGAGCACACTGCCCACAATG
AATGTAACTATTTTCTAAACACTTTACTAGAAGAACATTTCAGTATAAAAAACCTAATTTATTT
TTACAGAAAAATATTTTGTTGTTTTTATAAAAAGTTATGCAAATGACTTTATTTTATTTTTATT
TCCTGCATACCATTAGAATAATTTTATTTCATTTCTTCAAATTACCAAGCACTGTAATACTATA
AATTAATGTAATACTGTGTGAATTCAGACTATAAAAAACATCATTCAGAAAACTTTATAATCGT
CATTGTTCAACCAAGATTTTGAATGTAATAAGATGAATATATTCCTTACAAATTACTTGGAAAT
TCAATGTTTGTGCAGAGTTGAGACAACTTTATTGTTTCTATCATAAACTATTTATGTATCTTAA
TTATTAAAATGATTTACTTTATGGCACTAGAAAATTTACTGTGGCTTTTCTGATCTAACTTCTA
GCTAAAATTGTATCATTGGTCCTAAAAAATAAAAATCTTTACTAATAGGCAATTGAAGGAATGG
TTTGCTAACAACCACAGTAATATAATATGATTTTACAGATAGATGCTTCCCCTTGGCTATGACA
TGGAGAAAGATTTTCCCATAATAATAACTAACATTTATATTAGGTTGGTGCAAAACTAGTTGCG
GTTTTTCCCATTAAAAGTAATAAACTTACTCTTATACAAAGTGGACACTGTGGGGAGATACAGA
GAAATGGAAGATACGGATCCTGCCTGGAGTAGGTAACCTTGCTTGGAAACCCCACATGCAAACG
TCATGAGGAGAATTAAAGGAGTATTATCAGTAATGAAGTTTATCATGGGTCATCAATGAGCATA
GATTGGTGTGGATCCTGTAGACCCTGGTGTTTTCTTTGAAGTGCCCTCTCCTAATGCAGAGGCC
TTGAAGCTTACAGTATACACTTGAAAAGTCACAGATAGCTAGAATTATGATCTTTGAAGTTATA
ACTGTGATCTGAAAATGTGTGTGGTGGTATGACAGCATACCATTAAATACATTTACATCACAGC
TCAAAGGACTGTGATATAATCCATTTATATCACAACTCAAAGGACTGTGATATAATCCATTTAT
ATCACAGCTCACAGTTTCTGAAAATGTATAAAAGAATCTATAATCTAGTACTGAAATTACTAAA
TTGGGTAAGATGATTTAAATGATTTTAATTTTAACATTTTATTTCTAGAATATATGGCTCCATT
TTATTTTATAGTGTAAAGTTGTATTTCCTAAAGTTTGTGTTTTGTCGACAGTATCTTTTAAATG
AGTCTTAAAAATAAAGGCATATTGTTCATGTTTTTCTTTCCTGGTGGCACATAAATGACATGTC
TTAAAATAGATGGCATCTTATACATTTTTTAAAAATAGACATCTTTACACTAAAAAAGAGTTCT
GAAGAAAGTAAGTTTGGGAGATGCTGGGTTAAAGAACGTCAAAGGAGTCACTTTAATGCAGGTT
TTTCTTTTAGAGGAGTTTTTAAAATCTTAGCTTGTATTGTAACCCTGACAGAAGGAAAATGTTA
TACAGTATTTCATAATTTCACCACAAAACTGCTGTCTGTGGCACAATGCACAGGACTAGGGTTC
TGAGGAACTATACTGTTATTGGAAACATAGTGTAAACATAGAATCTTCTAGAAGTTCCTAGAAA
GAC

hide sequence

RefSeq Acc Id:

XM_024454215 ⟹ XP_024309983

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,918,300 (-)	NCBI

Sequence:

show sequence

ATTTTTTCAAATCTCTTTAATGTCTGCTCTAATAGAAGATAGCTGGATTTCTTGTTGCTAGTTA
TTGTTTCTGTTGAAGTGTGTGAGGACAATTCAGCCTCGTGGATATATGTAGCTGGAAAAGGAAG
ATGTGCCTGAGTCATGTTTTCTGATAATTGTGATATTCTTCTTTGTTACTGCATCAAGAGTTGA
CCAAAAGTGGTAGTTTATTAGAGATTCTTATTACTCATTGGTTAGGTAAGAGCAGACAATAACC
AATAGGTTGGGAAATGTAAGGCTGATAAAATTCTAACAACCATATTGAACTCCGTAATTTCTTA
AATATTGTGTTTCTATGTGCTAGGCATTATGTTGCGTACCTCACATTTATAAGCTCATTTAATC
TTCATGGTAACTCAGTGAGAAAAGTGTTATTATTAATCCCATTTCATGCAAATTAGGAAACTGA
GGCATAGAAATTCTTTGAAATGGATTTGCCATTTTGATTTTCAGCTATATTGTTTTACAGGATA
ACAATTCAAAGTAAAATAAACCTAATATAAAGGATGCATAATAGAACTTCAGAATTATTGATGA
GGAAACTGAGGATCAGAGGGATTAAGTACTTCCCAAAACCATACAGGTATCAGATACACACCGG
ACTTCAACATTCTATCATAAGACCTACCCAACCCAACTGTTTACCTCTGGACAATGCCACCCTA
CCTCAGAAACTGAAGGAGGTTGGATATTCAACGCATATGGTCGGAAAATGGCACTTGGGTTTTT
ACAGAAAAGAATGCATGCCCACCAGAAGAGGATTTGATACCTTTTTTGGTTCCCTTTTGGGAAG
TGGGGATTACTATACACACTACAAATGTGACAGTCCTGGGATGTGTGGCTATGACTTGTATGAA
AACGACAATGCTGCCTGGGACTATGACAATGGCATATACTCCACACAGATGTACACTCAGAGAG
TACAGCAAATCTTAGCTTCCCATAACCCCACAAAGCCTATATTTTTATATATTGCCTATCAAGC
TGTTCATTCACCACTGCAAGCTCCTGGCAGGTATTTCGAACACTACCGATCCATTATCAACATA
AACAGGAGGAGATATGCTGCCATGCTTTCCTGCTTAGATGAAGCAATCAACAACGTGACATTGG
CTCTAAAGACTTATGGTTTCTATAACAACAGCATTATCATTTACTCTTCAGATAATGGTGGCCA
GCCTACGGCAGGAGGGAGTAACTGGCCTCTCAGAGGTAGCAAAGGAACATATTGGGAAGGAGGG
ATCCGGGCTGTAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACAGTGTGTAAGGAAC
TTGTGCACATCACTGACTGGTACCCCACTCTCATTTCACTGGCTGAAGGACAGATTGATGAGGA
CATTCAACTAGATGGCTATGATATCTGGGAGACCATAAGTGAGGGTCTTCGCTCACCCCGAGTA
GATATTTTGCATAACATTGACCCCATATACACCAAGGCAAAAAATGGCTCCTGGGCAGCAGGCT
ATGGGATCTGGAACACTGCAATCCAGTCAGCCATCAGAGTGCAGCACTGGAAATTGCTTACAGG
AAATCCTGGCTACAGCGACTGGGTCCCCCCTCAGTCTTTCAGCAACCTGGGACCGAACCGGTGG
CACAATGAACGGATCACCTTGTCAACTGGCAAAAGTGTATGGCTTTTCAACATCACAGCCGACC
CATATGAGAGGGTGGACCTATCTAACAGGTATCCAGGAATCGTGAAGAAGCTCCTACGGAGGCT
CTCACAGTTCAACAAAACTGCAGTGCCGGTCAGGTATCCCCCCAAAGACCCCAGAAGTAACCCT
AGGCTCAATGGAGGGGTCTGGGGACCATGGTATAAAGAGGAAACCAAGAAAAAGAAGCCAAGCA
AAAATCAGGCTGAGAAAAAGCAAAAGAAAAGCAAAAAAAAGAAGAAGAAACAGCAGAAAGCAGT
CTCAGGTAAACCAGCAAATTTGGCTCGATAATATCGCTGGCCTAAGCGTCAGGCTTGTTTTCAT
GCTGTGCCACTCCAGAGACTTCTGCCACCTGGCCGCCACACTGAAAACTGTCCTGCTCAGTGCC
AAGGTGCTACTCTTGCAAGCCACACTTAGAGAGAGTGGAGATGTTTATTTCTCTTGCTCCTTTA
GAAAACGTGGTGAGTCCTGAGTTCCACTGCTGTGCTTCAGTCAACTGACCAAACACTGCTTTGA
ATTATAGGAGGAGAACAATAACCTACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGT
ATACCATCCGCAAGCATGCTAATTTGATGGAAGTTACAGGGTAGCATGATTAAAACTACCTTTG
ATAAATTACAGTCAAAGATTGTGTCACCTCAAAGGCCTTGAAGAATATATTTTCTTGGTGAATT
TTTGTATGTCTGTCATATGACACTTGGGTTTTTTAATTAATTCTATTTTATATATATATATATG
TTTCTTTTCCTGTGAAAAGCTGTTTTTCTCACATGTGAACAGCTTGCACCTCATTTTACCATGC
GTGAGGGAATGGCAAATAAGAATGTTTGAGCACACTGCCCACAATGAATGTAACTATTTTCTAA
ACACTTTACTAGAAGAACATTTCAGTATAAAAAACCTAATTTATTTTTACAGAAAAATATTTTG
TTGTTTTTATAAAAAGTTATGCAAATGACTTTATTTTATTTTTATTTCCTGCATACCATTAGAA
TAATTTTATTTCATTTCTTCAAATTACCAAGCACTGTAATACTATAAATTAATGTAATACTGTG
TGAATTCAGACTATAAAAAACATCATTCAGAAAACTTTATAATCGTCATTGTTCAACCAAGATT
TTGAATGTAATAAGATGAATATATTCCTTACAAATTACTTGGAAATTCAATGTTTGTGCAGAGT
TGAGACAACTTTATTGTTTCTATCATAAACTATTTATGTATCTTAATTATTAAAATGATTTACT
TTATGGCACTAGAAAATTTACTGTGGCTTTTCTGATCTAACTTCTAGCTAAAATTGTATCATTG
GTCCTAAAAAATAAAAATCTTTACTAATAGGCAATTGAAGGAATGGTTTGCTAACAACCACAGT
AATATAATATGATTTTACAGATAGATGCTTCCCCTTGGCTATGACATGGAGAAAGATTTTCCCA
TAATAATAACTAACATTTATATTAGGTTGGTGCAAAACTAGTTGCGGTTTTTCCCATTAAAAGT
AATAAACTTACTCTTATACAAAGTGGACACTGTGGGGAGATACAGAGAAATGGAAGATACGGAT
CCTGCCTGGAGTAGGTAACCTTGCTTGGAAACCCCACATGCAAACGTCATGAGGAGAATTAAAG
GAGTATTATCAGTAATGAAGTTTATCATGGGTCATCAATGAGCATAGATTGGTGTGGATCCTGT
AGACCCTGGTGTTTTCTTTGAAGTGCCCTCTCCTAATGCAGAGGCCTTGAAGCTTACAGTATAC
ACTTGAAAAGTCACAGATAGCTAGAATTATGATCTTTGAAGTTATAACTGTGATCTGAAAATGT
GTGTGGTGGTATGACAGCATACCATTAAATACATTTACATCACAGCTCAAAGGACTGTGATATA
ATCCATTTATATCACAACTCAAAGGACTGTGATATAATCCATTTATATCACAGCTCACAGTTTC
TGAAAATGTATAAAAGAATCTATAATCTAGTACTGAAATTACTAAATTGGGTAAGATGATTTAA
ATGATTTTAATTTTAACATTTTATTTCTAGAATATATGGCTCCATTTTATTTTATAGTGTAAAG
TTGTATTTCCTAAAGTTTGTGTTTTGTCGACAGTATCTTTTAAATGAGTCTTAAAAATAAAGGC
ATATTGTTCATGTTTTTCTTTCCTGGTGGCACATAAATGACATGTCTTAAAATAGATGGCATCT
TATACATTTTTTAAAAATAGACATCTTTACACTAAAAAAGAGTTCTGAAGAAAGTAAGTTTGGG
AGATGCTGGGTTAAAGAACGTCAAAGGAGTCACTTTAATGCAGGTTTTTCTTTTAGAGGAGTTT
TTAAAATCTTAGCTTGTATTGTAACCCTGACAGAAGGAAAATGTTATACAGTATTTCATAATTT
CACCACAAAACTGCTGTCTGTGGCACAATGCACAGGACTAGGGTTCTGAGGAACTATACTGTTA
TTGGAAACATAGTGTAAACATAGAATCTTCTAGAAGTTCCTAGAAAGAC

hide sequence

RefSeq Acc Id:

XM_047416154 ⟹ XP_047272110

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI

RefSeq Acc Id:

XM_047416155 ⟹ XP_047272111

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI

RefSeq Acc Id:

XM_047416157 ⟹ XP_047272113

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,900,284 - 113,979,647 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001341139	(Get FASTA)	NCBI Sequence Viewer
	NP_001341140	(Get FASTA)	NCBI Sequence Viewer
	NP_078866	(Get FASTA)	NCBI Sequence Viewer
	XP_011530540	(Get FASTA)	NCBI Sequence Viewer
	XP_016864081	(Get FASTA)	NCBI Sequence Viewer
	XP_016864083	(Get FASTA)	NCBI Sequence Viewer
	XP_024309983	(Get FASTA)	NCBI Sequence Viewer
	XP_047272110	(Get FASTA)	NCBI Sequence Viewer
	XP_047272111	(Get FASTA)	NCBI Sequence Viewer
	XP_047272113	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH32010	(Get FASTA)	NCBI Sequence Viewer
	AAH89445	(Get FASTA)	NCBI Sequence Viewer
	AAI32880	(Get FASTA)	NCBI Sequence Viewer
	AAI32882	(Get FASTA)	NCBI Sequence Viewer
	AAI44266	(Get FASTA)	NCBI Sequence Viewer
	AAQ89010	(Get FASTA)	NCBI Sequence Viewer
	AAW66666	(Get FASTA)	NCBI Sequence Viewer
	BAB15689	(Get FASTA)	NCBI Sequence Viewer
	CAC60191	(Get FASTA)	NCBI Sequence Viewer
	CAJ18095	(Get FASTA)	NCBI Sequence Viewer
	EAX06303	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000320219
	ENSP00000320219.7
GenBank Protein	Q5FYB0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_078866 ⟸ NM_024590
- Peptide Label:	isoform 1 precursor
- UniProtKB:	Q5FWE4 (UniProtKB/Swiss-Prot), Q1HA39 (UniProtKB/Swiss-Prot), B7ZM45 (UniProtKB/Swiss-Prot), A2RUG0 (UniProtKB/Swiss-Prot), Q6UWT9 (UniProtKB/Swiss-Prot), Q5FYB0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAPRGCAGHPPPPSPQACVCPGKMLAMGALAGFWILCLLTYGYLSWGQALEEEEEGALLAQAGE KLEPSTTSTSQPHLIFILADDQGFRDVGYHGSEIKTPTLDKLAAEGVKLENYYVQPICTPSRSQ FITGKYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYSTHMVGKWHLGFYRKECMPTRRG FDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNGIYSTQMYTQRVQQILASHNPT KPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSCLDEAINNVTLALKTYGFYNNS IIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPLLKNKGTVCKELVHITDWYPTL ISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYTKAKNGSWAAGYGIWNTAIQSA IRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGKSVWLFNITADPYERVDLSNRY PGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWYKEETKKKKPSKNQAEKKQKKS KKKKKKQQKAVSGSTCHSGVTCG hide sequence

RefSeq Acc Id:

XP_011530540 ⟸ XM_011532238

- Peptide Label:

isoform X3

- Sequence:

show sequence

MHNRTSELLMRKLRIRGIKYFPKPYRYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYST
HMVGKWHLGFYRKECMPTRRGFDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNG
IYSTQMYTQRVQQILASHNPTKPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSC
LDEAINNVTLALKTYGFYNNSIIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPL
LKNKGTVCKELVHITDWYPTLISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYT
KAKNGSWAAGYGIWNTAIQSAIRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGK
SVWLFNITADPYERVDLSNRYPGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWY
KEETKKKKPSKNQAEKKQKKSKKKKKKQQKAVSGSTCHSGVTCG

hide sequence

RefSeq Acc Id:	XP_016864081 ⟸ XM_017008592
- Peptide Label:	isoform X1
- UniProtKB:	Q5FWE4 (UniProtKB/Swiss-Prot), Q1HA39 (UniProtKB/Swiss-Prot), B7ZM45 (UniProtKB/Swiss-Prot), A2RUG0 (UniProtKB/Swiss-Prot), Q6UWT9 (UniProtKB/Swiss-Prot), Q5FYB0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAPRGCAGHPPPPSPQACVCPGKMLAMGALAGFWILCLLTYGYLSWGQALEEEEEGALLAQAGE KLEPSTTSTSQPHLIFILADDQGFRDVGYHGSEIKTPTLDKLAAEGVKLENYYVQPICTPSRSQ FITGKYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYSTHMVGKWHLGFYRKECMPTRRG FDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNGIYSTQMYTQRVQQILASHNPT KPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSCLDEAINNVTLALKTYGFYNNS IIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPLLKNKGTVCKELVHITDWYPTL ISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYTKAKNGSWAAGYGIWNTAIQSA IRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGKSVWLFNITADPYERVDLSNRY PGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWYKEETKKKKPSKNQAEKKQKKS KKKKKKQQKAVSGSTCHSGVTCG hide sequence

RefSeq Acc Id:

XP_016864083 ⟸ XM_017008594

- Peptide Label:

isoform X5

- Sequence:

show sequence

MRKLRIRGIKYFPKPYRYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYSTHMVGKWHLG
FYRKECMPTRRGFDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNGIYSTQMYTQ
RVQQILASHNPTKPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSCLDEAINNVT
LALKTYGFYNNSIIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPLLKNKGTVCK
ELVHITDWYPTLISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYTKAKNGSWAA
GYGIWNTAIQSAIRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGKSVWLFNITA
DPYERVDLSNRYPGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWYKEETKKKKP
SKNQAEKKQKKSKKKKKKQQKAVSGSTCHSGVTCG

hide sequence

RefSeq Acc Id:

XP_024309983 ⟸ XM_024454215

- Peptide Label:

isoform X4

- Sequence:

show sequence

MHNRTSELLMRKLRIRGIKYFPKPYRYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYST
HMVGKWHLGFYRKECMPTRRGFDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNG
IYSTQMYTQRVQQILASHNPTKPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSC
LDEAINNVTLALKTYGFYNNSIIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPL
LKNKGTVCKELVHITDWYPTLISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYT
KAKNGSWAAGYGIWNTAIQSAIRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGK
SVWLFNITADPYERVDLSNRYPGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWY
KEETKKKKPSKNQAEKKQKKSKKKKKKQQKAVSGKPANLAR

hide sequence

RefSeq Acc Id:

NP_001341139 ⟸ NM_001354210

- Peptide Label:

isoform 2 precursor

- Sequence:

show sequence

MAPRGCAGHPPPPSPQACVCPGKMLAMGALAGFWILCLLTYGYLSWGQALEEEEEGALLAQAGE
KLEPSTTSTSQPHLIFILADDQGFRDVGYHGSEIKTPTLDKLAAEGVKLENYYVQPICTPSRSQ
FITGKYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYSTHMVGKWHLGFYRKECMPTRRG
FDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNGIYSTQMYTQRVQQILASHNPT
KPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSCLDEAINNVTLALKTYGFYNNS
IIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPLLKNKGTVCKELVHITDWYPTL
ISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYTKAKNGSWAAGYGIWNTAIQSA
IRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGKSVWLFNITADPYERVDLSNRY
PGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWYKEETKKKKPSKNQAEKKQKKS
KKKKKKQQKAVSGKPANLAR

hide sequence

RefSeq Acc Id:

NP_001341140 ⟸ NM_001354211

- Peptide Label:

isoform 3

- Sequence:

show sequence

MRKLRIRGIKYFPKPYRYQIHTGLQHSIIRPTQPNCLPLDNATLPQKLKEVGYSTHMVGKWHLG
FYRKECMPTRRGFDTFFGSLLGSGDYYTHYKCDSPGMCGYDLYENDNAAWDYDNGIYSTQMYTQ
RVQQILASHNPTKPIFLYIAYQAVHSPLQAPGRYFEHYRSIININRRRYAAMLSCLDEAINNVT
LALKTYGFYNNSIIIYSSDNGGQPTAGGSNWPLRGSKGTYWEGGIRAVGFVHSPLLKNKGTVCK
ELVHITDWYPTLISLAEGQIDEDIQLDGYDIWETISEGLRSPRVDILHNIDPIYTKAKNGSWAA
GYGIWNTAIQSAIRVQHWKLLTGNPGYSDWVPPQSFSNLGPNRWHNERITLSTGKSVWLFNITA
DPYERVDLSNRYPGIVKKLLRRLSQFNKTAVPVRYPPKDPRSNPRLNGGVWGPWYKEETKKKKP
SKNQAEKKQKKSKKKKKKQQKAVSGKPANLAR

hide sequence

Ensembl Acc Id:

ENSP00000421327 ⟸ ENST00000509829

Ensembl Acc Id:

ENSP00000320219 ⟸ ENST00000315366

RefSeq Acc Id:	XP_047272113 ⟸ XM_047416157
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047272111 ⟸ XM_047416155
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047272110 ⟸ XM_047416154
- Peptide Label:	isoform X2

Protein Domains

Sulfatase N-terminal

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q5FYB0-F1-model_v2	AlphaFold	Q5FYB0	1-599	view protein structure

Promoters

RGD ID:

6868342

Promoter ID:

EPDNEW_H7324

Type:

initiation region

Name:

ARSJ_1

Description:

arylsulfatase family member J

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H7325 EPDNEW_H7326

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,979,647 - 113,979,707	EPDNEW

RGD ID:

6868320

Promoter ID:

EPDNEW_H7325

Type:

initiation region

Name:

ARSJ_3

Description:

arylsulfatase family member J

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H7326 EPDNEW_H7324

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	113,980,390 - 113,980,450	EPDNEW

RGD ID:

6802054

Promoter ID:

HG_KWN:48957

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3, Lymphoblastoid

Transcripts:

NM_024590, UC010IMU.1, UC010IMV.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	4	115,119,919 - 115,120,419 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:26286	AgrOrtholog
COSMIC	ARSJ	COSMIC
Ensembl Genes	ENSG00000180801	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000315366	ENTREZGENE
	ENST00000315366.8	UniProtKB/Swiss-Prot
Gene3D-CATH	3.30.1120.10	UniProtKB/Swiss-Prot
	3.40.720.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000180801	GTEx
HGNC ID	HGNC:26286	ENTREZGENE
Human Proteome Map	ARSJ	Human Proteome Map
InterPro	Alkaline_phosphatase_core_sf	UniProtKB/Swiss-Prot
	ARSB	UniProtKB/Swiss-Prot
	Sulfatase_CS	UniProtKB/Swiss-Prot
	Sulfatase_N	UniProtKB/Swiss-Prot
KEGG Report	hsa:79642	UniProtKB/Swiss-Prot
NCBI Gene	79642	ENTREZGENE
OMIM	610010	OMIM
PANTHER	ARYLSULFATASE	UniProtKB/Swiss-Prot
	ARYLSULFATASE J	UniProtKB/Swiss-Prot
Pfam	Sulfatase	UniProtKB/Swiss-Prot
PharmGKB	PA143485310	PharmGKB
PROSITE	SULFATASE_1	UniProtKB/Swiss-Prot
	SULFATASE_2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF53649	UniProtKB/Swiss-Prot
UniProt	A2RUG0	ENTREZGENE
	ARSJ_HUMAN	UniProtKB/Swiss-Prot
	B7ZM45	ENTREZGENE
	D6RGC1_HUMAN	UniProtKB/TrEMBL
	Q1HA39	ENTREZGENE
	Q5FWE4	ENTREZGENE
	Q5FYB0	ENTREZGENE
	Q6UWT9	ENTREZGENE
	Q8N5N6_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	A2RUG0	UniProtKB/Swiss-Prot
	B7ZM45	UniProtKB/Swiss-Prot
	Q1HA39	UniProtKB/Swiss-Prot
	Q5FWE4	UniProtKB/Swiss-Prot
	Q6UWT9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-11-24	ARSJ	arylsulfatase family member J	ARSJ	arylsulfatase family, member J	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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