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Gene: GMPS (guanine monophosphate synthase) Homo sapiens

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Symbol:

GMPS

Name:

guanine monophosphate synthase

RGD ID:

1320749

HGNC Page

HGNC:4378

Description:

Enables GMP synthase activity. Acts upstream of or within GMP biosynthetic process. Located in cytosol. Implicated in acute myelomonocytic leukemia.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

GATD7; glutamine amidotransferase; GMP synthase; GMP synthase [glutamine-hydrolyzing]; GMP synthetase; guanine monophosphate synthetase; guanine monphosphate synthetase; guanosine 5'-monophosphate synthase; MLL/GMPS fusion protein; testicular tissue protein Li 82

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):	Gmps (guanine monophosphate synthetase)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Gmps (guanine monophosphate synthase)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Gmps (guanine monophosphate synthase)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	GMPS (guanine monophosphate synthase)	NCBI	Ortholog
Canis lupus familiaris (dog):	GMPS (guanine monophosphate synthase)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Gmps (guanine monophosphate synthase)	NCBI	Ortholog
Sus scrofa (pig):	GMPS (guanine monophosphate synthase)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	GMPS (guanine monophosphate synthase)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Gmps (guanine monophosphate synthase)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Gmps (guanine monophosphate synthase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Gmps (guanine monophosphate synthetase)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	gmps (guanine monophosphate synthase)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	GUA1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	bur	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	gmps-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	gmps	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	gmps.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	gmps.L	Alliance	DIOPT (Xenbase)

Related Pseudogenes:

GMPSP1

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	3	155,869,430 - 155,944,020 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	155,870,650 - 155,944,020 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	155,588,439 - 155,661,809 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	157,071,019 - 157,138,215 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	157,071,026 - 157,138,223	NCBI
Celera	3	154,009,947 - 154,077,188 (+)	NCBI		Celera
Cytogenetic Map	3	q25.31	NCBI
HuRef	3	152,982,759 - 153,049,917 (+)	NCBI		HuRef
CHM1_1	3	155,551,614 - 155,618,831 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	158,644,070 - 158,718,668 (+)	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

acute myelomonocytic leukemia (IAGP)

Experimental Diabetes Mellitus (ISO)

hepatocellular carcinoma (ISO)

Neoplasms, Second Primary (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

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

1,2-dichloroethane (ISO)

1-chloro-2,4-dinitrobenzene (EXP)

17beta-estradiol (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)

2,6-dinitrotoluene (ISO)

4,4'-sulfonyldiphenol (EXP,ISO)

all-trans-retinoic acid (EXP)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

Aroclor 1254 (ISO)

arsane (ISO)

arsenic atom (ISO)

arsenous acid (EXP)

atrazine (EXP)

benzo[a]pyrene (EXP,ISO)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP,ISO)

bisphenol AF (EXP)

Bisphenol B (EXP)

bisphenol F (EXP,ISO)

Brodifacoum (ISO)

cadmium dichloride (EXP)

caffeine (EXP)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

chromium(6+) (ISO)

cisplatin (EXP)

copper atom (EXP)

copper(0) (EXP)

coumarin (EXP)

coumestrol (EXP)

diarsenic trioxide (EXP)

Dibutyl phosphate (EXP)

dibutyl phthalate (ISO)

diethylstilbestrol (EXP)

disodium selenite (EXP)

Enterolactone (EXP)

enzyme inhibitor (EXP)

fenvalerate (ISO)

flutamide (ISO)

folic acid (ISO)

FR900359 (EXP)

gentamycin (ISO)

gold atom (ISO)

gold(0) (ISO)

ivermectin (EXP)

lovastatin (ISO)

methyl methanesulfonate (EXP)

methylmercury chloride (EXP)

nefazodone (ISO)

nimesulide (ISO)

oxaliplatin (ISO)

PCB138 (ISO)

perfluorooctane-1-sulfonic acid (EXP)

perfluorooctanoic acid (EXP)

phenobarbital (ISO)

poly(propylene imine) macromolecule (EXP)

sodium arsenite (EXP)

Soman (ISO)

succimer (ISO)

tetrachloromethane (ISO)

titanium dioxide (ISO)

topotecan (ISO)

trimellitic anhydride (ISO)

triphenyl phosphate (EXP)

troglitazone (ISO)

tunicamycin (EXP)

valproic acid (EXP,ISO)

vinclozolin (ISO)

warfarin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

GMP biosynthetic process (IBA,IDA,IEA,ISO)

GMP metabolic process (IEA)

GMP salvage (ISO)

purine nucleobase biosynthetic process (TAS)

purine nucleotide biosynthetic process (IEA)

purine ribonucleoside monophosphate biosynthetic process (TAS)

response to L-cysteine (ISO)

response to xenobiotic stimulus (ISO)

Cellular Component

cytoplasm (IEA)

cytosol (IBA,IDA,IEA,TAS)

Molecular Function

ATP binding (IEA)

enzyme binding (ISO)

GMP synthase (glutamine-hydrolyzing) activity (EXP,IDA,IEA,ISO)

GMP synthase activity (IBA,IDA,IEA,ISO,TAS)

ligase activity (IEA)

nucleotide binding (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

2-hydroxyglutaric aciduria pathway (EXP)

adenine phoshoribosyltransferase deficiency pathway (EXP)

adenosine monophosphate deaminase deficiency pathway (EXP)

adenylosuccinate lyase deficiency pathway (EXP)

AICA-ribosuria pathway (EXP)

azathioprine pharmacodynamics pathway (EXP)

de novo purine biosynthetic pathway (TAS)

glutamic acid/glutamate metabolic pathway (EXP)

homocarnosinosis pathway (EXP)

Kelley-Seegmiller syndrome pathway (EXP)

Lesch-Nyhan syndrome pathway (EXP)

mercaptopurine pharmacodynamics pathway (EXP)

mercaptopurine pharmacokinetics pathway (EXP)

molybdenum cofactor deficiency pathway (EXP)

purine metabolic pathway (EXP,IEA)

purine nucleoside phosphorylase deficiency pathway (EXP)

succinic semialdehyde dehydrogenase deficiency pathway (EXP)

tioguanine pharmacodynamics pathway (EXP)

xanthinuria type I pathway (EXP)

xanthinuria pathway (EXP)

xanthinuria type II pathway (EXP)

References

References - curated

#	Reference Title	Reference Citation
1.	Pediatric neurological syndromes and inborn errors of purine metabolism.	Camici M, etal., Neurochem Int. 2010 Feb;56(3):367-78. Epub 2009 Dec 11.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	OMIM Disease Annotation Pipeline	OMIM Disease Annotation Pipeline
4.	t(3;11) translocation in treatment-related acute myeloid leukemia fuses MLL with the GMPS (GUANOSINE 5' MONOPHOSPHATE SYNTHETASE) gene.	Pegram LD, etal., Blood. 2000 Dec 15;96(13):4360-2.
5.	Insulin regulatory effects on purine- and pyrimidine metabolism in alloxan diabetic rat liver.	Pillwein K, etal., Padiatr Padol. 1988;23(2):135-44.
6.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
7.	SMPDB Annotation Import Pipeline	Pipeline to import SMPDB annotations from SMPDB into RGD
8.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
9.	RGD HPO Phenotype Annotation Pipeline	RGD automated import pipeline for human HPO-to-gene-to-disease annotations
10.	Enzymes of purine metabolism in cancer.	Weber G Clin Biochem. 1983 Feb;16(1):57-63.

Additional References at PubMed

PMID:1574589	PMID:6698284	PMID:7559506	PMID:7706277	PMID:8081953	PMID:8089153	PMID:8125298	PMID:9195163	PMID:12477932	PMID:14744259	PMID:15489334	PMID:15749019
PMID:16236267	PMID:16712791	PMID:19615732	PMID:19738201	PMID:19834552	PMID:20045992	PMID:20201926	PMID:20467437	PMID:20562859	PMID:20659789	PMID:21145461	PMID:21873635
PMID:21981925	PMID:21988832	PMID:22268729	PMID:22586326	PMID:22623428	PMID:22863883	PMID:22939629	PMID:24462112	PMID:24778252	PMID:25756610	PMID:25921289	PMID:25963833
PMID:26046769	PMID:26344197	PMID:26496610	PMID:26831064	PMID:26890086	PMID:26972000	PMID:27114453	PMID:27684187	PMID:27880917	PMID:27926873	PMID:28302793	PMID:28319085
PMID:28514442	PMID:28515276	PMID:28533407	PMID:28581483	PMID:28611215	PMID:28675297	PMID:28700943	PMID:28978906	PMID:29142217	PMID:29229926	PMID:29467282	PMID:29564676
PMID:29676528	PMID:29788244	PMID:29844126	PMID:30110629	PMID:30224337	PMID:30367141	PMID:30425250	PMID:30463901	PMID:30711629	PMID:30804394	PMID:30884312	PMID:31091453
PMID:31239290	PMID:31300519	PMID:31536960	PMID:31586073	PMID:31839598	PMID:32005234	PMID:32414791	PMID:32416067	PMID:32513696	PMID:32552912	PMID:32687490	PMID:32694731
PMID:32807901	PMID:32850835	PMID:32929329	PMID:32989298	PMID:33144569	PMID:33226137	PMID:33239621	PMID:33545068	PMID:33567341	PMID:33649833	PMID:33660365	PMID:33742136
PMID:33916271	PMID:33961781	PMID:34189442	PMID:34373451	PMID:34428256	PMID:34445801	PMID:34520390	PMID:34709727	PMID:35013556	PMID:35016035	PMID:35256949	PMID:35271311
PMID:35446349	PMID:35509820	PMID:35546148	PMID:35687106	PMID:35785414	PMID:35831314	PMID:35906200	PMID:35944360	PMID:35987950	PMID:36057605	PMID:36114006	PMID:36215168
PMID:36243803	PMID:36261009	PMID:36517590	PMID:36634849	PMID:36688959	PMID:37059091	PMID:37167062	PMID:37223481	PMID:37317656	PMID:37448957	PMID:37536630	PMID:37827155
PMID:38113892	PMID:38569033	PMID:39147351	PMID:39231216

Genomics

Comparative Map Data

GMPS
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	155,869,430 - 155,944,020 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	155,870,650 - 155,944,020 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	155,588,439 - 155,661,809 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	157,071,019 - 157,138,215 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	157,071,026 - 157,138,223	NCBI
Celera	3	154,009,947 - 154,077,188 (+)	NCBI		Celera
Cytogenetic Map	3	q25.31	NCBI
HuRef	3	152,982,759 - 153,049,917 (+)	NCBI		HuRef
CHM1_1	3	155,551,614 - 155,618,831 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	158,644,070 - 158,718,668 (+)	NCBI		T2T-CHM13v2.0

Gmps
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	3	63,871,054 - 63,928,975 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	3	63,883,527 - 63,930,000 (+)	Ensembl		GRCm39 Ensembl
GRCm38	3	63,963,633 - 64,021,554 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	3	63,976,106 - 64,022,579 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	3	63,780,065 - 63,823,000 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	3	64,064,072 - 64,107,007 (+)	NCBI		MGSCv36	mm8
Celera	3	63,647,946 - 63,691,053 (+)	NCBI		Celera
Cytogenetic Map	3	E1	NCBI
cM Map	3	30.08	NCBI

Gmps
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	2	150,587,824 - 150,641,564 (+)	NCBI		GRCr8
mRatBN7.2	2	148,441,369 - 148,491,908 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	148,435,643 - 148,485,875 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	2	155,179,955 - 155,214,681 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	2	153,229,417 - 153,264,155 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	2	147,862,091 - 147,896,832 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	2	154,555,967 - 154,590,662 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	2	154,555,871 - 154,590,662 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	2	173,939,844 - 173,974,539 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	2	153,804,512 - 153,840,009 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	2	153,754,474 - 153,789,970 (+)	NCBI
Celera	2	142,726,833 - 142,761,299 (+)	NCBI		Celera
Cytogenetic Map	2	q31	NCBI

Gmps
(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_004955448	6,932,926 - 6,984,662 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955448	6,931,891 - 6,984,662 (+)	NCBI	ChiLan1.0	ChiLan1.0

GMPS
(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	2	153,783,747 - 153,852,239 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	3	153,788,477 - 153,862,949 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	3	152,925,905 - 152,999,180 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	3	160,977,222 - 161,045,214 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	3	160,977,222 - 161,045,214 (+)	Ensembl	panpan1.1		panPan2

GMPS
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	23	49,569,571 - 49,645,999 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	23	49,569,531 - 49,699,199 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	23	49,445,713 - 49,522,068 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	23	50,203,908 - 50,286,767 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	23	50,203,868 - 50,333,624 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	23	49,789,609 - 49,866,167 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	23	49,838,479 - 49,915,927 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	23	50,126,162 - 50,202,992 (+)	NCBI		UU_Cfam_GSD_1.0

Gmps
(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_024405602	86,587,606 - 86,639,212 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936519	3,104,701 - 3,141,549 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936519	3,094,763 - 3,143,322 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

GMPS
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	13	95,738,659 - 95,819,759 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	95,742,342 - 95,820,903 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	13	103,766,547 - 103,819,693 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

GMPS
(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	15	34,817,603 - 34,885,363 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	15	34,815,066 - 34,885,228 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	7,450,006 - 7,520,263 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Gmps
(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_004624730	33,460,566 - 33,535,593 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624730	33,459,059 - 33,535,593 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in GMPS
39 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3q24-26.32(chr3:147442566-178522531)x3	copy number gain	See cases [RCV000051724]	Chr3:147442566..178522531 [GRCh38] Chr3:147160353..178240319 [GRCh37] Chr3:148643043..179723013 [NCBI36] Chr3:3q24-26.32	pathogenic
GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	copy number gain	See cases [RCV000051725]	Chr3:147521892..198096565 [GRCh38] Chr3:147239679..197823436 [GRCh37] Chr3:148722369..199307833 [NCBI36] Chr3:3q24-29	pathogenic
GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	copy number gain	See cases [RCV000139435]	Chr3:152100512..198118383 [GRCh38] Chr3:151818301..197845254 [GRCh37] Chr3:153300991..199329651 [NCBI36] Chr3:3q25.1-29	pathogenic
GRCh37/hg19 3q24-29(chr3:142995020-192997215)x4	copy number gain	See cases [RCV000240256]	Chr3:142995020..192997215 [GRCh37] Chr3:3q24-29	pathogenic
GRCh37/hg19 3q24-26.2(chr3:147180945-168415875)x1	copy number loss	See cases [RCV000448130]	Chr3:147180945..168415875 [GRCh37] Chr3:3q24-26.2	pathogenic
GRCh37/hg19 3q25.2-29(chr3:152356847-197851986)x3	copy number gain	See cases [RCV000448608]	Chr3:152356847..197851986 [GRCh37] Chr3:3q25.2-29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	copy number gain	See cases [RCV000512358]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	copy number gain	See cases [RCV000511055]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh38/hg38 3q22.3-29(chr3:137126982-198110178)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051723]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051723]\|See cases [RCV000051723]	Chr3:137126982..198110178 [GRCh38] Chr3:136845824..197837049 [GRCh37] Chr3:138328514..199321446 [NCBI36] Chr3:3q22.3-29	pathogenic
GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	copy number gain	See cases [RCV000134948]	Chr3:103426882..198110178 [GRCh38] Chr3:103145726..197837049 [GRCh37] Chr3:104628416..199321446 [NCBI36] Chr3:3q13.11-29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3	copy number gain	not provided [RCV000742138]	Chr3:61495..197838262 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3	copy number gain	not provided [RCV000742133]	Chr3:60174..197948027 [GRCh37] Chr3:3p26.3-q29	pathogenic
NM_003875.3(GMPS):c.708G>A (p.Thr236=)	single nucleotide variant	not provided [RCV000880375]	Chr3:155910873 [GRCh38] Chr3:155628662 [GRCh37] Chr3:3q25.31	benign
NM_003875.3(GMPS):c.1017C>T (p.Ile339=)	single nucleotide variant	not provided [RCV000923742]	Chr3:155914549 [GRCh38] Chr3:155632338 [GRCh37] Chr3:3q25.31	benign
GRCh37/hg19 3q22.3-26.1(chr3:138145289-162275610)x3	copy number gain	See cases [RCV001194586]	Chr3:138145289..162275610 [GRCh37] Chr3:3q22.3-26.1	pathogenic
GRCh37/hg19 3q22.3-26.1(chr3:138173683-162494699)	copy number gain	Global developmental delay [RCV001352648]	Chr3:138173683..162494699 [GRCh37] Chr3:3q22.3-26.1	pathogenic
GRCh37/hg19 3q24-26.1(chr3:143439359-165252122)x1	copy number loss	not provided [RCV001795847]	Chr3:143439359..165252122 [GRCh37] Chr3:3q24-26.1	pathogenic
GRCh37/hg19 3q23-25.32(chr3:142729607-157921084)x3	copy number gain	Brachycephaly [RCV001801182]	Chr3:142729607..157921084 [GRCh37] Chr3:3q23-25.32	pathogenic
GRCh37/hg19 3q24-25.33(chr3:145486960-160504834)	copy number gain	not specified [RCV002053375]	Chr3:145486960..160504834 [GRCh37] Chr3:3q24-25.33	pathogenic
GRCh37/hg19 3q25.31(chr3:155464751-155599910)	copy number gain	not specified [RCV002053378]	Chr3:155464751..155599910 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.217A>G (p.Ile73Val)	single nucleotide variant	not specified [RCV004137078]	Chr3:155897934 [GRCh38] Chr3:155615723 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1028C>A (p.Thr343Asn)	single nucleotide variant	not specified [RCV004206703]	Chr3:155914560 [GRCh38] Chr3:155632349 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1814C>T (p.Ala605Val)	single nucleotide variant	not specified [RCV004079832]	Chr3:155936344 [GRCh38] Chr3:155654133 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1786C>T (p.His596Tyr)	single nucleotide variant	not specified [RCV004168208]	Chr3:155935025 [GRCh38] Chr3:155652814 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.977C>T (p.Thr326Met)	single nucleotide variant	not specified [RCV004157747]	Chr3:155914509 [GRCh38] Chr3:155632298 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1583A>C (p.Tyr528Ser)	single nucleotide variant	not provided [RCV000948270]	Chr3:155931787 [GRCh38] Chr3:155931787..155931788 [GRCh38] Chr3:155649576 [GRCh37] Chr3:155649576..155649577 [GRCh37] Chr3:3q25.31	benign
NM_003875.3(GMPS):c.209+5A>G	single nucleotide variant	not provided [RCV000958079]	Chr3:155893704 [GRCh38] Chr3:155611493 [GRCh37] Chr3:3q25.31	benign
NM_003875.3(GMPS):c.27+9G>T	single nucleotide variant	not provided [RCV000956149]	Chr3:155870906 [GRCh38] Chr3:155588695 [GRCh37] Chr3:3q25.31	benign
NM_003875.3(GMPS):c.1779T>C (p.Phe593=)	single nucleotide variant	not provided [RCV000956150]	Chr3:155935018 [GRCh38] Chr3:155652807 [GRCh37] Chr3:3q25.31	benign
GRCh37/hg19 3q13.31-26.31(chr3:116620308-172042292)x3	copy number gain	not provided [RCV002472621]	Chr3:116620308..172042292 [GRCh37] Chr3:3q13.31-26.31	pathogenic
NM_003875.3(GMPS):c.208C>T (p.Arg70Cys)	single nucleotide variant	not specified [RCV004224371]	Chr3:155893698 [GRCh38] Chr3:155611487 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1689A>G (p.Ile563Met)	single nucleotide variant	not specified [RCV004182108]	Chr3:155934928 [GRCh38] Chr3:155652717 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1655G>A (p.Arg552His)	single nucleotide variant	not specified [RCV004151483]	Chr3:155931859 [GRCh38] Chr3:155649648 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.863A>G (p.Lys288Arg)	single nucleotide variant	not specified [RCV004084217]	Chr3:155911256 [GRCh38] Chr3:155629045 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.403A>G (p.Asn135Asp)	single nucleotide variant	not specified [RCV004323180]	Chr3:155903941 [GRCh38] Chr3:155621730 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.583C>T (p.Leu195Phe)	single nucleotide variant	not specified [RCV004252477]	Chr3:155910748 [GRCh38] Chr3:155628537 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.74A>T (p.Glu25Val)	single nucleotide variant	not specified [RCV004362078]	Chr3:155893564 [GRCh38] Chr3:155611353 [GRCh37] Chr3:3q25.31	uncertain significance
NC_000003.11:g.(?_154834637)_(156272878_?)del	deletion	not provided [RCV004582258]	Chr3:154834637..156272878 [GRCh37] Chr3:3q25.2-25.31	uncertain significance
NM_003875.3(GMPS):c.1585G>A (p.Val529Met)	single nucleotide variant	not specified [RCV004919796]	Chr3:155931789 [GRCh38] Chr3:155649578 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.905C>G (p.Ser302Cys)	single nucleotide variant	not specified [RCV004932724]	Chr3:155914437 [GRCh38] Chr3:155632226 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1696C>T (p.Pro566Ser)	single nucleotide variant	not specified [RCV004155337]	Chr3:155934935 [GRCh38] Chr3:155652724 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1559A>G (p.Gln520Arg)	single nucleotide variant	not specified [RCV004147269]	Chr3:155925365 [GRCh38] Chr3:155643154 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1200G>T (p.Lys400Asn)	single nucleotide variant	not specified [RCV004167502]	Chr3:155916180 [GRCh38] Chr3:155633969 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.524C>A (p.Ala175Glu)	single nucleotide variant	not specified [RCV004314444]	Chr3:155906261 [GRCh38] Chr3:155624050 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.653C>T (p.Thr218Ile)	single nucleotide variant	not specified [RCV004356896]	Chr3:155910818 [GRCh38] Chr3:155628607 [GRCh37] Chr3:3q25.31	uncertain significance
Single allele	duplication	not provided [RCV003448680]	Chr3:140154329..197847235 [GRCh37] Chr3:3q23-29	pathogenic
NM_003875.3(GMPS):c.1586T>C (p.Val529Ala)	single nucleotide variant	not specified [RCV004395411]	Chr3:155931790 [GRCh38] Chr3:155649579 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1570C>T (p.Arg524Cys)	single nucleotide variant	not specified [RCV004395410]	Chr3:155931774 [GRCh38] Chr3:155649563 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.25A>C (p.Lys9Gln)	single nucleotide variant	not specified [RCV004395415]	Chr3:155870895 [GRCh38] Chr3:155588684 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1373A>C (p.Asp458Ala)	single nucleotide variant	not specified [RCV004395408]	Chr3:155922241 [GRCh38] Chr3:155640030 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1765C>T (p.Arg589Cys)	single nucleotide variant	not specified [RCV004395412]	Chr3:155935004 [GRCh38] Chr3:155652793 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1451A>G (p.Gln484Arg)	single nucleotide variant	not specified [RCV004395409]	Chr3:155925257 [GRCh38] Chr3:155643046 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1789A>G (p.Asn597Asp)	single nucleotide variant	not specified [RCV004395414]	Chr3:155935028 [GRCh38] Chr3:155652817 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1778T>C (p.Phe593Ser)	single nucleotide variant	not specified [RCV004395413]	Chr3:155935017 [GRCh38] Chr3:155652806 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.505C>T (p.Arg169Cys)	single nucleotide variant	not specified [RCV004395417]	Chr3:155906242 [GRCh38] Chr3:155624031 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.872G>A (p.Gly291Glu)	single nucleotide variant	not specified [RCV004629858]	Chr3:155911265 [GRCh38] Chr3:155629054 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1873C>T (p.Leu625Phe)	single nucleotide variant	not specified [RCV004629859]	Chr3:155936403 [GRCh38] Chr3:155654192 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1184C>G (p.Thr395Arg)	single nucleotide variant	not specified [RCV004919795]	Chr3:155916164 [GRCh38] Chr3:155633953 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.71A>G (p.Tyr24Cys)	single nucleotide variant	not specified [RCV004919793]	Chr3:155893561 [GRCh38] Chr3:155611350 [GRCh37] Chr3:3q25.31	uncertain significance
NM_003875.3(GMPS):c.1643G>C (p.Arg548Thr)	single nucleotide variant	not specified [RCV004932725]	Chr3:155931847 [GRCh38] Chr3:155649636 [GRCh37] Chr3:3q25.31	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	2122
Count of miRNA genes:	935
Interacting mature miRNAs:	1109
Transcripts:	ENST00000295920, ENST00000476145, ENST00000496455
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

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
1300026	BP36_H	Blood pressure QTL 36 (human)	4.04		Blood pressure	hypertension susceptibility	3	135720453	161720453	Human
406997145	GWAS646121_H	intelligence QTL GWAS646121 (human)		0.000007	intelligence		3	155933374	155933375	Human
1298415	BP24_H	Blood pressure QTL 24 (human)	2.9		Blood pressure	hypertension susceptibility	3	135720453	161720453	Human
597100714	GWAS1196788_H	blood metabolite measurement QTL GWAS1196788 (human)		9e-10	blood metabolite measurement	blood metabolite measurement (CMO:0003699)	3	155931787	155931788	Human

Markers in Region

D3S3587

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	155,650,005 - 155,650,153	UniSTS	GRCh37
Build 36	3	157,132,699 - 157,132,847	RGD	NCBI36
Celera	3	154,071,672 - 154,071,820	RGD
Cytogenetic Map	3	q24	UniSTS
HuRef	3	153,044,403 - 153,044,549	UniSTS
Marshfield Genetic Map	3	170.14	RGD
Marshfield Genetic Map	3	170.14	UniSTS
Genethon Genetic Map	3	177.6	UniSTS
TNG Radiation Hybrid Map	3	87694.0	UniSTS
deCODE Assembly Map	3	164.05	UniSTS
Whitehead-YAC Contig Map	3		UniSTS

RH93796

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	8,176,336 - 8,176,466	UniSTS	GRCh37
Build 36	4	8,227,236 - 8,227,366	RGD	NCBI36
Celera	4	8,068,247 - 8,068,377	RGD
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	3	q24	UniSTS
HuRef	4	8,095,756 - 8,095,886	UniSTS
GeneMap99-GB4 RH Map	4	53.86	UniSTS

SHGC-84195

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	155,620,924 - 155,621,207	UniSTS	GRCh37
Build 36	3	157,103,618 - 157,103,901	RGD	NCBI36
Celera	3	154,042,587 - 154,042,870	RGD
Cytogenetic Map	3	q24	UniSTS
HuRef	3	153,015,307 - 153,015,590	UniSTS
TNG Radiation Hybrid Map	3	87685.0	UniSTS

RH121689

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	155,630,574 - 155,630,910	UniSTS	GRCh37
Build 36	3	157,113,268 - 157,113,604	RGD	NCBI36
Celera	3	154,052,240 - 154,052,576	RGD
Cytogenetic Map	3	q24	UniSTS
HuRef	3	153,024,967 - 153,025,303	UniSTS
TNG Radiation Hybrid Map	3	87685.0	UniSTS

SHGC-50194

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	8,176,514 - 8,176,666	UniSTS	GRCh37
GRCh37	3	155,654,189 - 155,655,421	UniSTS	GRCh37
Build 36	4	8,227,414 - 8,227,566	RGD	NCBI36
Celera	3	154,075,856 - 154,077,088	UniSTS
Celera	4	8,068,425 - 8,068,577	RGD
Cytogenetic Map	3	q24	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
HuRef	4	8,095,934 - 8,096,086	UniSTS
HuRef	3	153,048,585 - 153,049,817	UniSTS
TNG Radiation Hybrid Map	4	4958.0	UniSTS

D3S4088

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	155,588,660 - 155,588,915	UniSTS	GRCh37
Build 36	3	157,071,354 - 157,071,609	RGD	NCBI36
Celera	3	154,010,282 - 154,010,537	RGD
Cytogenetic Map	3	q24	UniSTS
HuRef	3	152,983,094 - 152,983,349	UniSTS

SHGC-16466

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	8,176,514 - 8,176,648	UniSTS	GRCh37
GRCh37	3	155,654,189 - 155,655,403	UniSTS	GRCh37
Build 36	4	8,227,414 - 8,227,548	RGD	NCBI36
Celera	4	8,068,425 - 8,068,559	RGD
Celera	3	154,075,856 - 154,077,070	UniSTS
Cytogenetic Map	3	q24	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
HuRef	3	153,048,585 - 153,049,799	UniSTS
HuRef	4	8,095,934 - 8,096,068	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	visual system
1204	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_023247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003875	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011513263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017007422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047449144	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047449145	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047449146	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054348272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054348273	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054348274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054348275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054348276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC067721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC140753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK223399	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK291504	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300787	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302148	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK315832	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC012178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG721087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CB159072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HB946314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HD003724	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HM005395	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U10860	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000295920 ⟹ ENSP00000295920

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	155,870,650 - 155,937,710 (+)	Ensembl

Ensembl Acc Id:

ENST00000476145

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	155,895,413 - 155,910,810 (+)	Ensembl

Ensembl Acc Id:

ENST00000496455 ⟹ ENSP00000419851

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	155,870,650 - 155,944,020 (+)	Ensembl

RefSeq Acc Id:

NM_003875 ⟹ NP_003866

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,870,650 - 155,944,020 (+)	NCBI
GRCh37	3	155,588,325 - 155,657,150 (+)	NCBI
Build 36	3	157,071,019 - 157,138,215 (+)	NCBI Archive
HuRef	3	152,982,759 - 153,049,917 (+)	ENTREZGENE
CHM1_1	3	155,551,614 - 155,618,831 (+)	NCBI
T2T-CHM13v2.0	3	158,645,288 - 158,718,668 (+)	NCBI

Sequence:

show sequence

AGCGTGCGCGCTGCTGGTCTTCTCTCCCGCGGCGCTGGGGCCCGCGCTCCGCTGCTGTTGCTCC
ATTCGGCGCTTTTCTGGCGGCTGGCTCCTCTCCGCTGCCGGCTGCTCCTCGACCAGGCCTCCTT
CTCAACCTCAGCCCGCGGCGCCGACCCTTCCGGCACCCTCCCGCCCCGTCTCGTACTGTCGCCG
TCACCGCCGCGGCTCCGGCCCTGGCCCCGATGGCTCTGTGCAACGGAGACTCCAAGCTGGAGAA
TGCTGGAGGAGACCTTAAGGATGGCCACCACCACTATGAAGGAGCTGTTGTCATTCTGGATGCT
GGTGCTCAGTACGGGAAAGTCATAGACCGAAGAGTGAGGGAACTGTTCGTGCAGTCTGAAATTT
TCCCCTTGGAAACACCAGCATTTGCTATAAAGGAACAAGGATTCCGTGCTATTATCATCTCTGG
AGGACCTAATTCTGTGTATGCTGAAGATGCTCCCTGGTTTGATCCAGCAATATTCACTATTGGC
AAGCCTGTTCTTGGAATTTGCTATGGTATGCAGATGATGAATAAGGTATTTGGAGGTACTGTGC
ACAAAAAAAGTGTCAGAGAAGATGGAGTTTTCAACATTAGTGTGGATAATACATGTTCATTATT
CAGGGGCCTTCAGAAGGAAGAAGTTGTTTTGCTTACACATGGAGATAGTGTAGACAAAGTAGCT
GATGGATTCAAGGTTGTGGCACGTTCTGGAAACATAGTAGCAGGCATAGCAAATGAATCTAAAA
AGTTATATGGAGCACAGTTCCACCCTGAAGTTGGCCTTACAGAAAATGGAAAAGTAATACTGAA
GAATTTCCTTTATGATATAGCTGGATGCAGTGGAACCTTCACCGTGCAGAACAGAGAACTTGAG
TGTATTCGAGAGATCAAAGAGAGAGTAGGCACGTCAAAAGTTTTGGTTTTACTCAGTGGTGGAG
TAGACTCAACAGTTTGTACAGCTTTGCTAAATCGTGCTTTGAACCAAGAACAAGTCATTGCTGT
GCACATTGATAATGGCTTTATGAGAAAACGAGAAAGCCAGTCTGTTGAAGAGGCCCTCAAAAAG
CTTGGAATTCAGGTCAAAGTGATAAATGCTGCTCATTCTTTCTACAATGGAACAACAACCCTAC
CAATATCAGATGAAGATAGAACCCCACGGAAAAGAATTAGCAAAACGTTAAATATGACCACAAG
TCCTGAAGAGAAAAGAAAAATCATTGGGGATACTTTTGTTAAGATTGCCAATGAAGTAATTGGA
GAAATGAACTTGAAACCAGAGGAGGTTTTCCTTGCCCAAGGTACTTTACGGCCTGATCTAATTG
AAAGTGCATCCCTTGTTGCAAGTGGCAAAGCTGAACTCATCAAAACCCATCACAATGACACAGA
GCTCATCAGAAAGTTGAGAGAGGAGGGAAAAGTAATAGAACCTCTGAAAGATTTTCATAAAGAT
GAAGTGAGAATTTTGGGCAGAGAACTTGGACTTCCAGAAGAGTTAGTTTCCAGGCATCCATTTC
CAGGTCCTGGCCTGGCAATCAGAGTAATATGTGCTGAAGAACCTTATATTTGTAAGGACTTTCC
TGAAACCAACAATATTTTGAAAATAGTAGCTGATTTTTCTGCAAGTGTTAAAAAGCCACATACC
CTATTACAGAGAGTCAAAGCCTGCACAACAGAAGAGGATCAGGAGAAGCTGATGCAAATTACCA
GTCTGCATTCACTGAATGCCTTCTTGCTGCCAATTAAAACTGTAGGTGTGCAGGGTGACTGTCG
TTCCTACAGTTACGTGTGTGGAATCTCCAGTAAAGATGAACCTGACTGGGAATCACTTATTTTT
CTGGCTAGGCTTATACCTCGCATGTGTCACAACGTTAACAGAGTTGTTTATATATTTGGCCCAC
CAGTTAAAGAACCTCCTACAGATGTTACTCCCACTTTCTTGACAACAGGGGTGCTCAGTACTTT
ACGCCAAGCTGATTTTGAGGCCCATAACATTCTCAGGGAGTCTGGGTATGCTGGGAAAATCAGC
CAGATGCCGGTGATTTTGACACCATTACATTTTGATCGGGACCCACTTCAAAAGCAGCCTTCAT
GCCAGAGATCTGTGGTTATTCGAACCTTTATTACTAGTGACTTCATGACTGGTATACCTGCAAC
ACCTGGCAATGAGATCCCTGTAGAGGTGGTATTAAAGATGGTCACTGAGATTAAGAAGATTCCT
GGTATTTCTCGAATTATGTATGACTTAACATCAAAGCCCCCAGGAACTACTGAGTGGGAGTAAT
AAACTTCTTGTTCTATTAAAGTACCGTGTGCAGTTTAAATTGATTAGAAATCATTCCCATTATT
GACATGCAGTACTGTGAAAAGAGTTACTGGAGCAGCTACATCACATCTGAGTTCTCCACAGCAA
AAATCTACGGCTTAAGAGCTGAGTTGGGGATAACCAAAAGGGACTGAAGAGTTTGTACGGGTAA
ATAATCAAAGCACCATTGCCTACACTCAGACAGATTGATACTGCTTTTGCCTTTGCCTCACTTA
TTCTTTATGTATAAATTCACTGTTGATGTCTCTGTGAATATGTATGAAGGTGGGTGAATTTGGG
GGTAATTATGGGCTTCTGTCTCCTTACCAGTTTCTAAGAACTGTTAGAAACGCCCATTATTTAC
CAGTGTTACTTACTACTTATATATACTTTTTGGAGAATCAGTTTTCTTATAAGTAATCTTATTT
CTCCAAAGGGTGAAAAAGAGATGAACATATCAGATAAAGGTATAGGTGGGCTATTCCAGCCACT
TTTGAAGGACACTGAGGGTATAAAATGTAAGCTACCATAAGATGGAAAAGCACCAGGAATTTGT
TGATGTACTTTTGAATTTTATTTCACAGCCTTGGGAGGAAGAAACTATGAGTGGTCTCAGATGT
CTATGAATGGTCTTAAAATGTTTTCAAACCATGTTCCACATAGATGCCATGTTATTCAATGTCA
GCTTGTTTATTAGTAAGGAGCTTTATCCTCCTAGCCTTATATTACCAGCCCCCCACAGCCTTGC
ATAGAAAGTTTCTGTTATCTCCTTAGAAGAAACTGGCTCAATGACGTTTCTGGTGTAGTGCAGA
TAGAGGTCAAGAGGAGCATTTTCATCTCTTCTTTTGCTGGTCAGAGAAACGGTTCTGAGATCAC
AGAAGCTATGATGCATACCTACAGCTTACAAAAGGGAGAGGAAAAATGTTTATATCATCTAGTA
AACAGTTGTAAAATGAGCTTTTAAATCTAATCTATAGACATATTATTCATTGCTCAGACACCTG
TGAACAGTCTTGATACATGCAAGATGTTTGCCAAACTTTGTAATCCTTTCTACTAGCTATAAGA
GAGGATTTAAGAACTGGTGTAGGACTTGTTGCCATCACCACCAGTTTCTAACAGATCTTTTATA
ACATTCACATAAGTACTGTAGACAGTAGTAGACTTAAACTCTCCGTTTCTCTCAGTATTTTAGC
TAAGAATGTTACCATATTTTTCTCTTAACAATTCCATCTCAGGTTGCTGCTGCTTGTCTAGTTT
AAAAGGTCAGATCTATTAATCAGGAATGAAATTTTATTTGGGATTCAGTGTTAGACAAACAACA
AAATGATGCGTGGCAGAAGTCATCTTTTTATTCTGGCTGGTCCAGGGAACAAGAAAACTGCTGC
TGGACCAGCAAGGGAAGAGTTTCTGTCTGTCTTAACAGAAATCTGTCCCCAAGACAAAGGGGTA
CTTGACTCCTACAAAACTTAAAGGGTACATTCTCTATCTGATGAGGAGGTACTCATTATGGCCT
TCTGGAAAGAGGCTATGTTAGTGATCTGGTCTTTACAGATTTAGAGTCATGTTATTTGAAAGCT
AGAATAGACAACCTATAAAATGCTTACCAACATGTGTCAGTACACGTTTATGTTTATATGAAAA
AAAATTTCTAGCCACAGTGTCTTATGATTTTGTATTGAAGCAAACAGTAGGAATTTTGGAAAAA
TAGAGAGTAAGAATGTGTGTTCTATGGAACACTGCTCCACTGAGAAGGTCCATGTAAAAAGGAT
TAGGTGGTCATATAAGTTTGGGGAACATAAGCTCACTTGTCCTTTCCTGGAGATTCATGGTATA
TAATATTCAAAGCTCTGAGAAATTCTGAAGTTAAAAACAATTGTTAAATTCTGCTTAAATTAGT
GTTTTCCTGATATTTGTTTTTTGAACACCTTTTATATAATCCCTTCTAATATATACTTAGTATA
TACTTAATATAATATTGGGAAAATTGTTACTCCAAAGCACATCTTGACATGACATAGTTTCTTA
AAAATCCAAATTTTCTGGAACTCAGAAATTTCCTAATATTTAGCACACTGTCTTCTTTTGCACA
GCACTTTTTGCTTTGTGCCATATAGCATTACTCTGTACCTTCACAGTATTTCATCTGAGCCACT
GAGGAAAGTTAAAGGTTGCACTTCCATTTTACAGTTAAGAAAACAAGCTCACCTTAGGCATGGT
TACTTAATTAATTTCAGAATTAAATTTCAGGTTTCCTTAGTCCAGATTGTCCTGATGTGTATTC
TGACACCTAAAATTATATAAACATTTATGGGATGCTTATTTTACTAAGACTAGAATGGTGGCTA
CCTGGCTAATAACATTCATCATTGGTTATTCTGGGCATATCATGACTTTATTCCCGTTGCTTAC
CATCTACCTGGGACACATCTCTCTTTGATTAAATATATTCTTTTTCTTTGTACTTTTTAGGTAG
ACAGAGAATGTAGATCATTGAAAGCATTATTTATTCCTAAGATTGGCAGGCACAGAATCATTTT
TAAGAACCAAATACCCAGTCCTGCCTTAAAGGCCACATCTATGATCATCAGCTCTGTTAGAAAT
AACAGCCTGGCATAATTCCTAAATACAAGTCTGTAGATATATCCAGGAGATAGGGTTACACTGT
TTTCTAACCTTTTTTAAATCCCTTAATCTTGAGGTAAACTGCATGCATTTAGTCAAACAAGCAT
CATAAAATTTGTTTCCTCACTGTTTGGGCTTAACCTCCTGATAGCCTGTTTTACTGAATAACTT
GACCCTAACCTGTAGAGAATAAGAGCATTCAAATTAGGAAGGCAGGACTATCCATCTTTAGTGC
TTTTCCTGCCGTTAAACAACAATGTGAACTTGGTCAAGTCATTTCTGTTCTTTATCTGTGACAT
GAGGTAACTGTATTAAATTTTCAGCATCAAATCCAGCTATAAATTTGTATTTTGTAAACAAGAG
AAAGTAAAGCAGGAGACAGAATGGAGAAGCTGGATAGTGTTTTTTTTTTTTTTTTTTAAGGTTC
TTTTATCATCAGATATGACACAAAGGGAAACATCAAAATGCACCGTAAAGTTAAATCCTAGTTA
CCTTTTTTTGAAGCTGTTGGCAAGGTTTGACCACTTGGGGCATCTTCTGCTGTGAGATGACACT
TGAAAAACACCCATCAAAGTTTTCCTGGTAGGAATCTCTCTTTACTGCGTGTTTTTTTGAAAAG
CTGACAGAGAATATGCTTTGGCTTTGACACTAATGAAGTCACCCATCATCAATTACATACAGCT
AATTGTTGGGAGCTAGAGCTAGAATCCAAGCTTTCTGATTCTCTGCATGGAAGAGGAAATGCTC
TAGGGCCCTTCAGGGCAAATCTTAAAAGGAAGTTCTTGGCCGGGCGCGGTGGCTCATGCCTGTA
ATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAGATCAGGAGATCGAGACCATCTTGG
CTAACACGGTGAAACCCCATCTCTACTAAAAATACAACAAATTAGCTGGGCGCGGTGGCGGGTG
CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCCTGAACCCAGGAGGCGGAGCT
TGCAGTGAGCTGAGATAGTGCCACTGCACTCCGGCCTGGTGAAAGAGCGAGACTCAGTCTCAAA
AAAAAAAAAAAAAGGAAGTTCTTAGTGTGTAATTGACCATCAGGGATAAATGGGCTTCAAAAGT
GTTAATTGTCTCCTTACTTACAGTGAGTTTCTAGAGATAGCCCTGTCTTTCAGAAATTCTCTGA
CATCTGCTTGCGCAATGTTATAACCACTTTCCCACACTACTCCCCTCCAGAAATCTCATTGATA
TGTGGCGAGGACACGCCTTAGCTATCACCCCAATGGATGCTTCTTTCATTGACCCAAATCCAGA
ATGTAATGGGGAACTGAATACAAGTTGGATGTCTCCACCCTTGGAAAGCACATCTTTTGTTCTT
ACTGAAGTAGTTTAACACCACCAGATGATCAAGGGATCAGGGTATCTTTCTGGTATCTTTTTAA
TCACTGAAGGACTTTGACAGCAGTAATGGTGGCATTGTTGACTCTTAAATTTCTGAACGTTTCA
CTTAATGGCAAGTGAAGAGATATAGAATCCCCCAAAGAGTGTCAAGATGCTAACTTCCAACCCT
ATTTTTATGTACTGAAGAGGCCTCAGTGTCTCACTGAACTCTAACCTTTTTGTCAGTGTTCCTC
AACACTGGATGCGTATTATTACATAACCTGAGGAGTTAAAAAATACAATAACCAGATGTCCAAT
TAAATAAAATTAGAATCTGGAGGAGGTAGAACTCAAGCATTTACAGTTTTGTTTTGTTTTTTTT
TTAAGACAGAGTCTCGCTCTGTCCCCAAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCCG
CTTCGTGGGTTCACGCCATTCTCCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGGCGCCCGC
CACTACGCCCGGCTAATTTTTTTGTACTTTTTAGTAGAGACAGGGTTTCACTGTGTTATACAGG
ATGGTCTCGATCTCCCGACCTCATGATCCGCCCGCCTCGGCCTCTCAGAGTGCTGGGATTACAG
GCGTGAGCCACCACGCCCGGCAAGCATTTACAGTTTTAAATCTCCCAGTCAGAATAAATTCTTA
TTGAGGGCCATACCTAGCCTGTCTTCATCAAACTCATAGGTGAATCTTTGTCAAACCTATAGGA
GAGAGATGCAGGCCATAGAGATGGTCTTGCTGAAGGTCTTATAGCTAAATTAGTTCAGATCCAG
GAACCAGATTCTGGAACTGATTGCACCTATATTATGTTGTGTGTCAGACACTCCCAGGACCTGT
TTGGTAATAATTAGGACAGCTGACATACTTGTTGCTAATTTTGAGATCTGGGCAACAACTGTGT
AGGCTGTTCTTTCAACCTCTTTCTTCTTACTTCTTTACTTTTCCTTCAGAGAGGAGAAAGCCAC
CCCTGTGCTATAGCCACCGCTCCAATTCTGACTCTAGCTAGGTCATGAAACAGACTGAGCTATT
ATTGCATCAACACATAAATCCTGTCATTTGGGTATTATTCTTTAGAGAACTAGAGATTACCTAG
CTGCAACCTAAGTTTCCTGAATTAGAATCATTTGAGCAGCACCATCTTAATTGGCTCATTAACA
TATTTGTGACCAGGCACAGTGGCGCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC
GGATCTCTTGAGGTCAGGAGTTTGAGACCAGCGTGGCCAACATGGTGAAACCCCATTTCTACTA
AAAATGTAAAAATTAGCTGGGCTTGGTGGCGCGCGCCTGTAATCCCAGCTACTCGGAAGGCTGA
GGTGTGAGAATCACTTAAACCCGGGAGATGGAGGTTGCAGTGAGCAGAGATTGCGCCACTGCAC
TCCAGCCTAGGTGACAAGAATGAGACTCCGTCTTAAAACAAAAACAACATATTTGTTCACTTTT
GAACCCTGTGGTGTCTTTTAACTTTGTTAAGGGCCCTTGGTTAGCAAAATTATGAAAGTTTAGG
AAATTTGGCTATTGAGTATATTAAGTACAACTACAAAATCCTCTGAGTTCTCCAGGAAGCCTAA
ACCTTGAGCAGTATCTTATTCAAGTGGAGTATATATCTTCAAGAATACAGATTTTTAAGGTAAG
TAGTTTTTCGTCTTTGCATCTCCTAAGACCATTGTTAACAACCTTGATATTAAACGAAGAAGTG
AATGTAAACCTCCTTTTGAACATATTTTTTATAAAGAAATATTTTGTTAATTGGAGTAAGTAGT
ATTGTTATGAAATCACTGTGTAATTGTTAATTGTAAACTGCAATGTCTATTTTGTGTTGTAACA
ATGTTGCCATAAAATAGCTTTGCTAAATGTGAAATGACTTTAATCCCTTTTGTCTTCAATATAC
TTCATAAAGGAGGAAATGATGATTTACACAATTTGTCATGAAGCTTCCGTGTTTATGAGAAATT
CCAAGAAGTAAGAGCCAAGAGGACAGATATTATCAGAATATGGGACATAAGAAATTGCATATAG
TGTCAAGGGTTTCTATATAACAACTTAATTTATTTCCCTTGCATATATAGTAGGGGTTAACATT
TTGCTCAATGTTAACGGGGGACATAATGGACATAAAACATTGGATAGCTTTTTATTTAAATGAG
CTAAAGGTGTGCGTATACACATGCACTTATAAAATTAAAGTCATATATGTATATA

hide sequence

RefSeq Acc Id:

XM_011513263 ⟹ XP_011511565

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,869,430 - 155,944,020 (+)	NCBI

Sequence:

show sequence

GAGAAGCCAGTATCCATGGCTTTGGAGAGTTCAAATATTCAATTTTCCGTTCAAAAAAAGCTGG
AGAATGCTGGAGGAGACCTTAAGGATGGCCACCACCACTATGAAGGAGCTGTTGTCATTCTGGA
TGCTGGTGCTCAGTACGGGAAAGTCATAGACCGAAGAGTGAGGGAACTGTTCGTGCAGTCTGAA
ATTTTCCCCTTGGAAACACCAGCATTTGCTATAAAGGAACAAGGATTCCGTGCTATTATCATCT
CTGGAGGACCTAATTCTGTGTATGCTGAAGATGCTCCCTGGTTTGATCCAGCAATATTCACTAT
TGGCAAGCCTGTTCTTGGAATTTGCTATGGTATGCAGATGATGAATAAGGTATTTGGAGGTACT
GTGCACAAAAAAAGTGTCAGAGAAGATGGAGTTTTCAACATTAGTGTGGATAATACATGTTCAT
TATTCAGGGGCCTTCAGAAGGAAGAAGTTGTTTTGCTTACACATGGAGATAGTGTAGACAAAGT
AGCTGATGGATTCAAGGTTGTGGCACGTTCTGGAAACATAGTAGCAGGCATAGCAAATGAATCT
AAAAAGTTATATGGAGCACAGTTCCACCCTGAAGTTGGCCTTACAGAAAATGGAAAAGTAATAC
TGAAGAATTTCCTTTATGATATAGCTGGATGCAGTGGAACCTTCACCGTGCAGAACAGAGAACT
TGAGTGTATTCGAGAGATCAAAGAGAGAGTAGGCACGTCAAAAGTTTTGGTTTTACTCAGTGGT
GGAGTAGACTCAACAGTTTGTACAGCTTTGCTAAATCGTGCTTTGAACCAAGAACAAGTCATTG
CTGTGCACATTGATAATGGCTTTATGAGAAAACGAGAAAGCCAGTCTGTTGAAGAGGCCCTCAA
AAAGCTTGGAATTCAGGTCAAAGTGATAAATGCTGCTCATTCTTTCTACAATGGAACAACAACC
CTACCAATATCAGATGAAGATAGAACCCCACGGAAAAGAATTAGCAAAACGTTAAATATGACCA
CAAGTCCTGAAGAGAAAAGAAAAATCATTGGGGATACTTTTGTTAAGATTGCCAATGAAGTAAT
TGGAGAAATGAACTTGAAACCAGAGGAGGTTTTCCTTGCCCAAGGTACTTTACGGCCTGATCTA
ATTGAAAGTGCATCCCTTGTTGCAAGTGGCAAAGCTGAACTCATCAAAACCCATCACAATGACA
CAGAGCTCATCAGAAAGTTGAGAGAGGAGGGAAAAGTAATAGAACCTCTGAAAGATTTTCATAA
AGATGAAGTGAGAATTTTGGGCAGAGAACTTGGACTTCCAGAAGAGTTAGTTTCCAGGCATCCA
TTTCCAGGTCCTGGCCTGGCAATCAGAGTAATATGTGCTGAAGAACCTTATATTTGTAAGGACT
TTCCTGAAACCAACAATATTTTGAAAATAGTAGCTGATTTTTCTGCAAGTGTTAAAAAGCCACA
TACCCTATTACAGAGAGTCAAAGCCTGCACAACAGAAGAGGATCAGGAGAAGCTGATGCAAATT
ACCAGTCTGCATTCACTGAATGCCTTCTTGCTGCCAATTAAAACTGTAGGTGTGCAGGGTGACT
GTCGTTCCTACAGTTACGTGTGTGGAATCTCCAGTAAAGATGAACCTGACTGGGAATCACTTAT
TTTTCTGGCTAGGCTTATACCTCGCATGTGTCACAACGTTAACAGAGTTGTTTATATATTTGGC
CCACCAGTTAAAGAACCTCCTACAGATGTTACTCCCACTTTCTTGACAACAGGGGTGCTCAGTA
CTTTACGCCAAGCTGATTTTGAGGCCCATAACATTCTCAGGGAGTCTGGGTATGCTGGGAAAAT
CAGCCAGATGCCGGTGATTTTGACACCATTACATTTTGATCGGGACCCACTTCAAAAGCAGCCT
TCATGCCAGAGATCTGTGGTTATTCGAACCTTTATTACTAGTGACTTCATGACTGGTATACCTG
CAACACCTGGCAATGAGATCCCTGTAGAGGTGGTATTAAAGATGGTCACTGAGATTAAGAAGAT
TCCTGGTATTTCTCGAATTATGTATGACTTAACATCAAAGCCCCCAGGAACTACTGAGTGGGAG
TAATAAACTTCTTGTTCTATTAAAGTACCGTGTGCAGTTTAAATTGATTAGAAATCATTCCCAT
TATTGACATGCAGTACTGTGAAAAGAGTTACTGGAGCAGCTACATCACATCTGAGTTCTCCACA
GCAAAAATCTACGGCTTAAGAGCTGAGTTGGGGATAACCAAAAGGGACTGAAGAGTTTGTACGG
GTAAATAATCAAAGCACCATTGCCTACACTCAGACAGATTGATACTGCTTTTGCCTTTGCCTCA
CTTATTCTTTATGTATAAATTCACTGTTGATGTCTCTGTGAATATGTATGAAGGTGGGTGAATT
TGGGGGTAATTATGGGCTTCTGTCTCCTTACCAGTTTCTAAGAACTGTTAGAAACGCCCATTAT
TTACCAGTGTTACTTACTACTTATATATACTTTTTGGAGAATCAGTTTTCTTATAAGTAATCTT
ATTTCTCCAAAGGGTGAAAAAGAGATGAACATATCAGATAAAGGTATAGGTGGGCTATTCCAGC
CACTTTTGAAGGACACTGAGGGTATAAAATGTAAGCTACCATAAGATGGAAAAGCACCAGGAAT
TTGTTGATGTACTTTTGAATTTTATTTCACAGCCTTGGGAGGAAGAAACTATGAGTGGTCTCAG
ATGTCTATGAATGGTCTTAAAATGTTTTCAAACCATGTTCCACATAGATGCCATGTTATTCAAT
GTCAGCTTGTTTATTAGTAAGGAGCTTTATCCTCCTAGCCTTATATTACCAGCCCCCCACAGCC
TTGCATAGAAAGTTTCTGTTATCTCCTTAGAAGAAACTGGCTCAATGACGTTTCTGGTGTAGTG
CAGATAGAGGTCAAGAGGAGCATTTTCATCTCTTCTTTTGCTGGTCAGAGAAACGGTTCTGAGA
TCACAGAAGCTATGATGCATACCTACAGCTTACAAAAGGGAGAGGAAAAATGTTTATATCATCT
AGTAAACAGTTGTAAAATGAGCTTTTAAATCTAATCTATAGACATATTATTCATTGCTCAGACA
CCTGTGAACAGTCTTGATACATGCAAGATGTTTGCCAAACTTTGTAATCCTTTCTACTAGCTAT
AAGAGAGGATTTAAGAACTGGTGTAGGACTTGTTGCCATCACCACCAGTTTCTAACAGATCTTT
TATAACATTCACATAAGTACTGTAGACAGTAGTAGACTTAAACTCTCCGTTTCTCTCAGTATTT
TAGCTAAGAATGTTACCATATTTTTCTCTTAACAATTCCATCTCAGGTTGCTGCTGCTTGTCTA
GTTTAAAAGGTCAGATCTATTAATCAGGAATGAAATTTTATTTGGGATTCAGTGTTAGACAAAC
AACAAAATGATGCGTGGCAGAAGTCATCTTTTTATTCTGGCTGGTCCAGGGAACAAGAAAACTG
CTGCTGGACCAGCAAGGGAAGAGTTTCTGTCTGTCTTAACAGAAATCTGTCCCCAAGACAAAGG
GGTACTTGACTCCTACAAAACTTAAAGGGTACATTCTCTATCTGATGAGGAGGTACTCATTATG
GCCTTCTGGAAAGAGGCTATGTTAGTGATCTGGTCTTTACAGATTTAGAGTCATGTTATTTGAA
AGCTAGAATAGACAACCTATAAAATGCTTACCAACATGTGTCAGTACACGTTTATGTTTATATG
AAAAAAAATTTCTAGCCACAGTGTCTTATGATTTTGTATTGAAGCAAACAGTAGGAATTTTGGA
AAAATAGAGAGTAAGAATGTGTGTTCTATGGAACACTGCTCCACTGAGAAGGTCCATGTAAAAA
GGATTAGGTGGTCATATAAGTTTGGGGAACATAAGCTCACTTGTCCTTTCCTGGAGATTCATGG
TATATAATATTCAAAGCTCTGAGAAATTCTGAAGTTAAAAACAATTGTTAAATTCTGCTTAAAT
TAGTGTTTTCCTGATATTTGTTTTTTGAACACCTTTTATATAATCCCTTCTAATATATACTTAG
TATATACTTAATATAATATTGGGAAAATTGTTACTCCAAAGCACATCTTGACATGACATAGTTT
CTTAAAAATCCAAATTTTCTGGAACTCAGAAATTTCCTAATATTTAGCACACTGTCTTCTTTTG
CACAGCACTTTTTGCTTTGTGCCATATAGCATTACTCTGTACCTTCACAGTATTTCATCTGAGC
CACTGAGGAAAGTTAAAGGTTGCACTTCCATTTTACAGTTAAGAAAACAAGCTCACCTTAGGCA
TGGTTACTTAATTAATTTCAGAATTAAATTTCAGGTTTCCTTAGTCCAGATTGTCCTGATGTGT
ATTCTGACACCTAAAATTATATAAACATTTATGGGATGCTTATTTTACTAAGACTAGAATGGTG
GCTACCTGGCTAATAACATTCATCATTGGTTATTCTGGGCATATCATGACTTTATTCCCGTTGC
TTACCATCTACCTGGGACACATCTCTCTTTGATTAAATATATTCTTTTTCTTTGTACTTTTTAG
GTAGACAGAGAATGTAGATCATTGAAAGCATTATTTATTCCTAAGATTGGCAGGCACAGAATCA
TTTTTAAGAACCAAATACCCAGTCCTGCCTTAAAGGCCACATCTATGATCATCAGCTCTGTTAG
AAATAACAGCCTGGCATAATTCCTAAATACAAGTCTGTAGATATATCCAGGAGATAGGGTTACA
CTGTTTTCTAACCTTTTTTAAATCCCTTAATCTTGAGGTAAACTGCATGCATTTAGTCAAACAA
GCATCATAAAATTTGTTTCCTCACTGTTTGGGCTTAACCTCCTGATAGCCTGTTTTACTGAATA
ACTTGACCCTAACCTGTAGAGAATAAGAGCATTCAAATTAGGAAGGCAGGACTATCCATCTTTA
GTGCTTTTCCTGCCGTTAAACAACAATGTGAACTTGGTCAAGTCATTTCTGTTCTTTATCTGTG
ACATGAGGTAACTGTATTAAATTTTCAGCATCAAATCCAGCTATAAATTTGTATTTTGTAAACA
AGAGAAAGTAAAGCAGGAGACAGAATGGAGAAGCTGGATAGTGTTTTTTTTTTTTTTTTTTAAG
GTTCTTTTATCATCAGATATGACACAAAGGGAAACATCAAAATGCACCGTAAAGTTAAATCCTA
GTTACCTTTTTTTGAAGCTGTTGGCAAGGTTTGACCACTTGGGGCATCTTCTGCTGTGAGATGA
CACTTGAAAAACACCCATCAAAGTTTTCCTGGTAGGAATCTCTCTTTACTGCGTGTTTTTTTGA
AAAGCTGACAGAGAATATGCTTTGGCTTTGACACTAATGAAGTCACCCATCATCAATTACATAC
AGCTAATTGTTGGGAGCTAGAGCTAGAATCCAAGCTTTCTGATTCTCTGCATGGAAGAGGAAAT
GCTCTAGGGCCCTTCAGGGCAAATCTTAAAAGGAAGTTCTTGGCCGGGCGCGGTGGCTCATGCC
TGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAGATCAGGAGATCGAGACCATC
TTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAACAAATTAGCTGGGCGCGGTGGCG
GGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCCTGAACCCAGGAGGCGG
AGCTTGCAGTGAGCTGAGATAGTGCCACTGCACTCCGGCCTGGTGAAAGAGCGAGACTCAGTCT
CAAAAAAAAAAAAAAAAGGAAGTTCTTAGTGTGTAATTGACCATCAGGGATAAATGGGCTTCAA
AAGTGTTAATTGTCTCCTTACTTACAGTGAGTTTCTAGAGATAGCCCTGTCTTTCAGAAATTCT
CTGACATCTGCTTGCGCAATGTTATAACCACTTTCCCACACTACTCCCCTCCAGAAATCTCATT
GATATGTGGCGAGGACACGCCTTAGCTATCACCCCAATGGATGCTTCTTTCATTGACCCAAATC
CAGAATGTAATGGGGAACTGAATACAAGTTGGATGTCTCCACCCTTGGAAAGCACATCTTTTGT
TCTTACTGAAGTAGTTTAACACCACCAGATGATCAAGGGATCAGGGTATCTTTCTGGTATCTTT
TTAATCACTGAAGGACTTTGACAGCAGTAATGGTGGCATTGTTGACTCTTAAATTTCTGAACGT
TTCACTTAATGGCAAGTGAAGAGATATAGAATCCCCCAAAGAGTGTCAAGATGCTAACTTCCAA
CCCTATTTTTATGTACTGAAGAGGCCTCAGTGTCTCACTGAACTCTAACCTTTTTGTCAGTGTT
CCTCAACACTGGATGCGTATTATTACATAACCTGAGGAGTTAAAAAATACAATAACCAGATGTC
CAATTAAATAAAATTAGAATCTGGAGGAGGTAGAACTCAAGCATTTACAGTTTTGTTTTGTTTT
TTTTTTAAGACAGAGTCTCGCTCTGTCCCCAAGTGCAGTGGCACAATCTCGGCTCACTGCAAGC
TCCGCTTCGTGGGTTCACGCCATTCTCCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGGCGC
CCGCCACTACGCCCGGCTAATTTTTTTGTACTTTTTAGTAGAGACAGGGTTTCACTGTGTTATA
CAGGATGGTCTCGATCTCCCGACCTCATGATCCGCCCGCCTCGGCCTCTCAGAGTGCTGGGATT
ACAGGCGTGAGCCACCACGCCCGGCAAGCATTTACAGTTTTAAATCTCCCAGTCAGAATAAATT
CTTATTGAGGGCCATACCTAGCCTGTCTTCATCAAACTCATAGGTGAATCTTTGTCAAACCTAT
AGGAGAGAGATGCAGGCCATAGAGATGGTCTTGCTGAAGGTCTTATAGCTAAATTAGTTCAGAT
CCAGGAACCAGATTCTGGAACTGATTGCACCTATATTATGTTGTGTGTCAGACACTCCCAGGAC
CTGTTTGGTAATAATTAGGACAGCTGACATACTTGTTGCTAATTTTGAGATCTGGGCAACAACT
GTGTAGGCTGTTCTTTCAACCTCTTTCTTCTTACTTCTTTACTTTTCCTTCAGAGAGGAGAAAG
CCACCCCTGTGCTATAGCCACCGCTCCAATTCTGACTCTAGCTAGGTCATGAAACAGACTGAGC
TATTATTGCATCAACACATAAATCCTGTCATTTGGGTATTATTCTTTAGAGAACTAGAGATTAC
CTAGCTGCAACCTAAGTTTCCTGAATTAGAATCATTTGAGCAGCACCATCTTAATTGGCTCATT
AACATATTTGTGACCAGGCACAGTGGCGCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC
GGGCGGATCTCTTGAGGTCAGGAGTTTGAGACCAGCGTGGCCAACATGGTGAAACCCCATTTCT
ACTAAAAATGTAAAAATTAGCTGGGCTTGGTGGCGCGCGCCTGTAATCCCAGCTACTCGGAAGG
CTGAGGTGTGAGAATCACTTAAACCCGGGAGATGGAGGTTGCAGTGAGCAGAGATTGCGCCACT
GCACTCCAGCCTAGGTGACAAGAATGAGACTCCGTCTTAAAACAAAAACAACATATTTGTTCAC
TTTTGAACCCTGTGGTGTCTTTTAACTTTGTTAAGGGCCCTTGGTTAGCAAAATTATGAAAGTT
TAGGAAATTTGGCTATTGAGTATATTAAGTACAACTACAAAATCCTCTGAGTTCTCCAGGAAGC
CTAAACCTTGAGCAGTATCTTATTCAAGTGGAGTATATATCTTCAAGAATACAGATTTTTAAGG
TAAGTAGTTTTTCGTCTTTGCATCTCCTAAGACCATTGTTAACAACCTTGATATTAAACGAAGA
AGTGAATGTAAACCTCCTTTTGAACATATTTTTTATAAAGAAATATTTTGTTAATTGGAGTAAG
TAGTATTGTTATGAAATCACTGTGTAATTGTTAATTGTAAACTGCAATGTCTATTTTGTGTTGT
AACAATGTTGCCATAAAATAGCTTTGCTAAATGTGAAA

hide sequence

RefSeq Acc Id:

XM_017007422 ⟹ XP_016862911

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,870,650 - 155,944,020 (+)	NCBI

Sequence:

show sequence

CCGGCCGGTTTGGCGGCGGCTGCGGAGGGTATCTGAGGCTCGGCTGCCAAGCCGAACGGGCTCT
GGCTCCTCCCAGTGGCCGGCCGGGGCGGAAGCAGGAGGCGGGGGCAGCGTGCGCGCTGCTGGTC
TTCTCTCCCGCGGCGCTGGGGCCCGCGCTCCGCTGCTGTTGCTCCATTCGGCGCTTTTCTGGCG
GCTGGCTCCTCTCCGCTGCCGGCTGCTCCTCGACCAGGCCTCCTTCTCAACCTCAGCCCGCGGC
GCCGACCCTTCCGGCACCCTCCCGCCCCGTCTCGTACTGTCGCCGTCACCGCCGCGGCTCCGGC
CCTGGCCCCGATGGCTCTGTGCAACGGAGACTCCAAGAATCTGATCATGATACAACAAAGAGAT
CCAGTGTGGGACATTCTACAAAAAGCTGGTCTGATCTTTAAAAAAGGTCAATGCCATAAAAGAC
TATAAAAAGAGTTGCTTTAATGTGAAGTATTTTCCTGGAGTCACTTCCTTTGGGACGTTGCCAT
TCTTTCCATCACAACCAGTTTCCTCACTGATGTTGCTGGAGAATGCTGGAGGAGACCTTAAGGA
TGGCCACCACCACTATGAAGGAGCTGTTGTCATTCTGGATGCTGGTGCTCAGTACGGGAAAGTC
ATAGACCGAAGAGTGAGGGAACTGTTCGTGCAGTCTGAAATTTTCCCCTTGGAAACACCAGCAT
TTGCTATAAAGGAACAAGGATTCCGTGCTATTATCATCTCTGGAGGACCTAATTCTGTGTATGC
TGAAGATGCTCCCTGGTTTGATCCAGCAATATTCACTATTGGCAAGCCTGTTCTTGGAATTTGC
TATGGTATGCAGATGATGAATAAGGTATTTGGAGGTACTGTGCACAAAAAAAGTGTCAGAGAAG
ATGGAGTTTTCAACATTAGTGTGGATAATACATGTTCATTATTCAGGGGCCTTCAGAAGGAAGA
AGTTGTTTTGCTTACACATGGAGATAGTGTAGACAAAGTAGCTGATGGATTCAAGGTTGTGGCA
CGTTCTGGAAACATAGTAGCAGGCATAGCAAATGAATCTAAAAAGTTATATGGAGCACAGTTCC
ACCCTGAAGTTGGCCTTACAGAAAATGGAAAAGTAATACTGAAGAATTTCCTTTATGATATAGC
TGGATGCAGTGGAACCTTCACCGTGCAGAACAGAGAACTTGAGTGTATTCGAGAGATCAAAGAG
AGAGTAGGCACGTCAAAAGTTTTGGTTTTACTCAGTGGTGGAGTAGACTCAACAGTTTGTACAG
CTTTGCTAAATCGTGCTTTGAACCAAGAACAAGTCATTGCTGTGCACATTGATAATGGCTTTAT
GAGAAAACGAGAAAGCCAGTCTGTTGAAGAGGCCCTCAAAAAGCTTGGAATTCAGGTCAAAGTG
ATAAATGCTGCTCATTCTTTCTACAATGGAACAACAACCCTACCAATATCAGATGAAGATAGAA
CCCCACGGAAAAGAATTAGCAAAACGTTAAATATGACCACAAGTCCTGAAGAGAAAAGAAAAAT
CATTGGGGATACTTTTGTTAAGATTGCCAATGAAGTAATTGGAGAAATGAACTTGAAACCAGAG
GAGGTTTTCCTTGCCCAAGGTACTTTACGGCCTGATCTAATTGAAAGTGCATCCCTTGTTGCAA
GTGGCAAAGCTGAACTCATCAAAACCCATCACAATGACACAGAGCTCATCAGAAAGTTGAGAGA
GGAGGGAAAAGTAATAGAACCTCTGAAAGATTTTCATAAAGATGAAGTGAGAATTTTGGGCAGA
GAACTTGGACTTCCAGAAGAGTTAGTTTCCAGGCATCCATTTCCAGGTCCTGGCCTGGCAATCA
GAGTAATATGTGCTGAAGAACCTTATATTTGTAAGGACTTTCCTGAAACCAACAATATTTTGAA
AATAGTAGCTGATTTTTCTGCAAGTGTTAAAAAGCCACATACCCTATTACAGAGAGTCAAAGCC
TGCACAACAGAAGAGGATCAGGAGAAGCTGATGCAAATTACCAGTCTGCATTCACTGAATGCCT
TCTTGCTGCCAATTAAAACTGTAGGTGTGCAGGGTGACTGTCGTTCCTACAGTTACGTGTGTGG
AATCTCCAGTAAAGATGAACCTGACTGGGAATCACTTATTTTTCTGGCTAGGCTTATACCTCGC
ATGTGTCACAACGTTAACAGAGTTGTTTATATATTTGGCCCACCAGTTAAAGAACCTCCTACAG
ATGTTACTCCCACTTTCTTGACAACAGGGGTGCTCAGTACTTTACGCCAAGCTGATTTTGAGGC
CCATAACATTCTCAGGGAGTCTGGGTATGCTGGGAAAATCAGCCAGATGCCGGTGATTTTGACA
CCATTACATTTTGATCGGGACCCACTTCAAAAGCAGCCTTCATGCCAGAGATCTGTGGTTATTC
GAACCTTTATTACTAGTGACTTCATGACTGGTATACCTGCAACACCTGGCAATGAGATCCCTGT
AGAGGTGGTATTAAAGATGGTCACTGAGATTAAGAAGATTCCTGGTATTTCTCGAATTATGTAT
GACTTAACATCAAAGCCCCCAGGAACTACTGAGTGGGAGTAATAAACTTCTTGTTCTATTAAAG
TACCGTGTGCAGTTTAAATTGATTAGAAATCATTCCCATTATTGACATGCAGTACTGTGAAAAG
AGTTACTGGAGCAGCTACATCACATCTGAGTTCTCCACAGCAAAAATCTACGGCTTAAGAGCTG
AGTTGGGGATAACCAAAAGGGACTGAAGAGTTTGTACGGGTAAATAATCAAAGCACCATTGCCT
ACACTCAGACAGATTGATACTGCTTTTGCCTTTGCCTCACTTATTCTTTATGTATAAATTCACT
GTTGATGTCTCTGTGAATATGTATGAAGGTGGGTGAATTTGGGGGTAATTATGGGCTTCTGTCT
CCTTACCAGTTTCTAAGAACTGTTAGAAACGCCCATTATTTACCAGTGTTACTTACTACTTATA
TATACTTTTTGGAGAATCAGTTTTCTTATAAGTAATCTTATTTCTCCAAAGGGTGAAAAAGAGA
TGAACATATCAGATAAAGGTATAGGTGGGCTATTCCAGCCACTTTTGAAGGACACTGAGGGTAT
AAAATGTAAGCTACCATAAGATGGAAAAGCACCAGGAATTTGTTGATGTACTTTTGAATTTTAT
TTCACAGCCTTGGGAGGAAGAAACTATGAGTGGTCTCAGATGTCTATGAATGGTCTTAAAATGT
TTTCAAACCATGTTCCACATAGATGCCATGTTATTCAATGTCAGCTTGTTTATTAGTAAGGAGC
TTTATCCTCCTAGCCTTATATTACCAGCCCCCCACAGCCTTGCATAGAAAGTTTCTGTTATCTC
CTTAGAAGAAACTGGCTCAATGACGTTTCTGGTGTAGTGCAGATAGAGGTCAAGAGGAGCATTT
TCATCTCTTCTTTTGCTGGTCAGAGAAACGGTTCTGAGATCACAGAAGCTATGATGCATACCTA
CAGCTTACAAAAGGGAGAGGAAAAATGTTTATATCATCTAGTAAACAGTTGTAAAATGAGCTTT
TAAATCTAATCTATAGACATATTATTCATTGCTCAGACACCTGTGAACAGTCTTGATACATGCA
AGATGTTTGCCAAACTTTGTAATCCTTTCTACTAGCTATAAGAGAGGATTTAAGAACTGGTGTA
GGACTTGTTGCCATCACCACCAGTTTCTAACAGATCTTTTATAACATTCACATAAGTACTGTAG
ACAGTAGTAGACTTAAACTCTCCGTTTCTCTCAGTATTTTAGCTAAGAATGTTACCATATTTTT
CTCTTAACAATTCCATCTCAGGTTGCTGCTGCTTGTCTAGTTTAAAAGGTCAGATCTATTAATC
AGGAATGAAATTTTATTTGGGATTCAGTGTTAGACAAACAACAAAATGATGCGTGGCAGAAGTC
ATCTTTTTATTCTGGCTGGTCCAGGGAACAAGAAAACTGCTGCTGGACCAGCAAGGGAAGAGTT
TCTGTCTGTCTTAACAGAAATCTGTCCCCAAGACAAAGGGGTACTTGACTCCTACAAAACTTAA
AGGGTACATTCTCTATCTGATGAGGAGGTACTCATTATGGCCTTCTGGAAAGAGGCTATGTTAG
TGATCTGGTCTTTACAGATTTAGAGTCATGTTATTTGAAAGCTAGAATAGACAACCTATAAAAT
GCTTACCAACATGTGTCAGTACACGTTTATGTTTATATGAAAAAAAATTTCTAGCCACAGTGTC
TTATGATTTTGTATTGAAGCAAACAGTAGGAATTTTGGAAAAATAGAGAGTAAGAATGTGTGTT
CTATGGAACACTGCTCCACTGAGAAGGTCCATGTAAAAAGGATTAGGTGGTCATATAAGTTTGG
GGAACATAAGCTCACTTGTCCTTTCCTGGAGATTCATGGTATATAATATTCAAAGCTCTGAGAA
ATTCTGAAGTTAAAAACAATTGTTAAATTCTGCTTAAATTAGTGTTTTCCTGATATTTGTTTTT
TGAACACCTTTTATATAATCCCTTCTAATATATACTTAGTATATACTTAATATAATATTGGGAA
AATTGTTACTCCAAAGCACATCTTGACATGACATAGTTTCTTAAAAATCCAAATTTTCTGGAAC
TCAGAAATTTCCTAATATTTAGCACACTGTCTTCTTTTGCACAGCACTTTTTGCTTTGTGCCAT
ATAGCATTACTCTGTACCTTCACAGTATTTCATCTGAGCCACTGAGGAAAGTTAAAGGTTGCAC
TTCCATTTTACAGTTAAGAAAACAAGCTCACCTTAGGCATGGTTACTTAATTAATTTCAGAATT
AAATTTCAGGTTTCCTTAGTCCAGATTGTCCTGATGTGTATTCTGACACCTAAAATTATATAAA
CATTTATGGGATGCTTATTTTACTAAGACTAGAATGGTGGCTACCTGGCTAATAACATTCATCA
TTGGTTATTCTGGGCATATCATGACTTTATTCCCGTTGCTTACCATCTACCTGGGACACATCTC
TCTTTGATTAAATATATTCTTTTTCTTTGTACTTTTTAGGTAGACAGAGAATGTAGATCATTGA
AAGCATTATTTATTCCTAAGATTGGCAGGCACAGAATCATTTTTAAGAACCAAATACCCAGTCC
TGCCTTAAAGGCCACATCTATGATCATCAGCTCTGTTAGAAATAACAGCCTGGCATAATTCCTA
AATACAAGTCTGTAGATATATCCAGGAGATAGGGTTACACTGTTTTCTAACCTTTTTTAAATCC
CTTAATCTTGAGGTAAACTGCATGCATTTAGTCAAACAAGCATCATAAAATTTGTTTCCTCACT
GTTTGGGCTTAACCTCCTGATAGCCTGTTTTACTGAATAACTTGACCCTAACCTGTAGAGAATA
AGAGCATTCAAATTAGGAAGGCAGGACTATCCATCTTTAGTGCTTTTCCTGCCGTTAAACAACA
ATGTGAACTTGGTCAAGTCATTTCTGTTCTTTATCTGTGACATGAGGTAACTGTATTAAATTTT
CAGCATCAAATCCAGCTATAAATTTGTATTTTGTAAACAAGAGAAAGTAAAGCAGGAGACAGAA
TGGAGAAGCTGGATAGTGTTTTTTTTTTTTTTTTTTAAGGTTCTTTTATCATCAGATATGACAC
AAAGGGAAACATCAAAATGCACCGTAAAGTTAAATCCTAGTTACCTTTTTTTGAAGCTGTTGGC
AAGGTTTGACCACTTGGGGCATCTTCTGCTGTGAGATGACACTTGAAAAACACCCATCAAAGTT
TTCCTGGTAGGAATCTCTCTTTACTGCGTGTTTTTTTGAAAAGCTGACAGAGAATATGCTTTGG
CTTTGACACTAATGAAGTCACCCATCATCAATTACATACAGCTAATTGTTGGGAGCTAGAGCTA
GAATCCAAGCTTTCTGATTCTCTGCATGGAAGAGGAAATGCTCTAGGGCCCTTCAGGGCAAATC
TTAAAAGGAAGTTCTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCC
GAGGTGGGTGGATCACGAGATCAGGAGATCGAGACCATCTTGGCTAACACGGTGAAACCCCATC
TCTACTAAAAATACAACAAATTAGCTGGGCGCGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGG
GAGGCTGAGGCAGGAGAATGGCCTGAACCCAGGAGGCGGAGCTTGCAGTGAGCTGAGATAGTGC
CACTGCACTCCGGCCTGGTGAAAGAGCGAGACTCAGTCTCAAAAAAAAAAAAAAAAGGAAGTTC
TTAGTGTGTAATTGACCATCAGGGATAAATGGGCTTCAAAAGTGTTAATTGTCTCCTTACTTAC
AGTGAGTTTCTAGAGATAGCCCTGTCTTTCAGAAATTCTCTGACATCTGCTTGCGCAATGTTAT
AACCACTTTCCCACACTACTCCCCTCCAGAAATCTCATTGATATGTGGCGAGGACACGCCTTAG
CTATCACCCCAATGGATGCTTCTTTCATTGACCCAAATCCAGAATGTAATGGGGAACTGAATAC
AAGTTGGATGTCTCCACCCTTGGAAAGCACATCTTTTGTTCTTACTGAAGTAGTTTAACACCAC
CAGATGATCAAGGGATCAGGGTATCTTTCTGGTATCTTTTTAATCACTGAAGGACTTTGACAGC
AGTAATGGTGGCATTGTTGACTCTTAAATTTCTGAACGTTTCACTTAATGGCAAGTGAAGAGAT
ATAGAATCCCCCAAAGAGTGTCAAGATGCTAACTTCCAACCCTATTTTTATGTACTGAAGAGGC
CTCAGTGTCTCACTGAACTCTAACCTTTTTGTCAGTGTTCCTCAACACTGGATGCGTATTATTA
CATAACCTGAGGAGTTAAAAAATACAATAACCAGATGTCCAATTAAATAAAATTAGAATCTGGA
GGAGGTAGAACTCAAGCATTTACAGTTTTGTTTTGTTTTTTTTTTAAGACAGAGTCTCGCTCTG
TCCCCAAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCCGCTTCGTGGGTTCACGCCATTC
TCCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCTAATTTTT
TTGTACTTTTTAGTAGAGACAGGGTTTCACTGTGTTATACAGGATGGTCTCGATCTCCCGACCT
CATGATCCGCCCGCCTCGGCCTCTCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGC
AAGCATTTACAGTTTTAAATCTCCCAGTCAGAATAAATTCTTATTGAGGGCCATACCTAGCCTG
TCTTCATCAAACTCATAGGTGAATCTTTGTCAAACCTATAGGAGAGAGATGCAGGCCATAGAGA
TGGTCTTGCTGAAGGTCTTATAGCTAAATTAGTTCAGATCCAGGAACCAGATTCTGGAACTGAT
TGCACCTATATTATGTTGTGTGTCAGACACTCCCAGGACCTGTTTGGTAATAATTAGGACAGCT
GACATACTTGTTGCTAATTTTGAGATCTGGGCAACAACTGTGTAGGCTGTTCTTTCAACCTCTT
TCTTCTTACTTCTTTACTTTTCCTTCAGAGAGGAGAAAGCCACCCCTGTGCTATAGCCACCGCT
CCAATTCTGACTCTAGCTAGGTCATGAAACAGACTGAGCTATTATTGCATCAACACATAAATCC
TGTCATTTGGGTATTATTCTTTAGAGAACTAGAGATTACCTAGCTGCAACCTAAGTTTCCTGAA
TTAGAATCATTTGAGCAGCACCATCTTAATTGGCTCATTAACATATTTGTGACCAGGCACAGTG
GCGCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCTCTTGAGGTCAGGAGT
TTGAGACCAGCGTGGCCAACATGGTGAAACCCCATTTCTACTAAAAATGTAAAAATTAGCTGGG
CTTGGTGGCGCGCGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGTGTGAGAATCACTTAAACC
CGGGAGATGGAGGTTGCAGTGAGCAGAGATTGCGCCACTGCACTCCAGCCTAGGTGACAAGAAT
GAGACTCCGTCTTAAAACAAAAACAACATATTTGTTCACTTTTGAACCCTGTGGTGTCTTTTAA
CTTTGTTAAGGGCCCTTGGTTAGCAAAATTATGAAAGTTTAGGAAATTTGGCTATTGAGTATAT
TAAGTACAACTACAAAATCCTCTGAGTTCTCCAGGAAGCCTAAACCTTGAGCAGTATCTTATTC
AAGTGGAGTATATATCTTCAAGAATACAGATTTTTAAGGTAAGTAGTTTTTCGTCTTTGCATCT
CCTAAGACCATTGTTAACAACCTTGATATTAAACGAAGAAGTGAATGTAAACCTCCTTTTGAAC
ATATTTTTTATAAAGAAATATTTTGTTAATTGGAGTAAGTAGTATTGTTATGAAATCACTGTGT
AATTGTTAATTGTAAACTGCAATGTCTATTTTGTGTTGTAACAATGTTGCCATAAAATAGCTTT
GCTAAATGTGAAA

hide sequence

RefSeq Acc Id:

XM_047449144 ⟹ XP_047305100

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,887,570 - 155,944,020 (+)	NCBI

RefSeq Acc Id:

XM_047449145 ⟹ XP_047305101

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,870,650 - 155,944,020 (+)	NCBI

RefSeq Acc Id:

XM_047449146 ⟹ XP_047305102

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,870,650 - 155,944,020 (+)	NCBI

RefSeq Acc Id:

XM_054348272 ⟹ XP_054204247

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	158,644,070 - 158,718,668 (+)	NCBI

RefSeq Acc Id:

XM_054348273 ⟹ XP_054204248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	158,662,214 - 158,718,668 (+)	NCBI

RefSeq Acc Id:

XM_054348274 ⟹ XP_054204249

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	158,645,288 - 158,718,668 (+)	NCBI

RefSeq Acc Id:

XM_054348275 ⟹ XP_054204250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	158,645,288 - 158,718,668 (+)	NCBI

RefSeq Acc Id:

XM_054348276 ⟹ XP_054204251

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	158,645,288 - 158,718,668 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_003866	(Get FASTA)	NCBI Sequence Viewer
	XP_011511565	(Get FASTA)	NCBI Sequence Viewer
	XP_016862911	(Get FASTA)	NCBI Sequence Viewer
	XP_047305100	(Get FASTA)	NCBI Sequence Viewer
	XP_047305101	(Get FASTA)	NCBI Sequence Viewer
	XP_047305102	(Get FASTA)	NCBI Sequence Viewer
	XP_054204247	(Get FASTA)	NCBI Sequence Viewer
	XP_054204248	(Get FASTA)	NCBI Sequence Viewer
	XP_054204249	(Get FASTA)	NCBI Sequence Viewer
	XP_054204250	(Get FASTA)	NCBI Sequence Viewer
	XP_054204251	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA60331	(Get FASTA)	NCBI Sequence Viewer
	AAH12178	(Get FASTA)	NCBI Sequence Viewer
	AEE60993	(Get FASTA)	NCBI Sequence Viewer
	BAD97119	(Get FASTA)	NCBI Sequence Viewer
	BAF84193	(Get FASTA)	NCBI Sequence Viewer
	BAF98723	(Get FASTA)	NCBI Sequence Viewer
	BAG62449	(Get FASTA)	NCBI Sequence Viewer
	BAG63519	(Get FASTA)	NCBI Sequence Viewer
	CBG07889	(Get FASTA)	NCBI Sequence Viewer
	CBV21411	(Get FASTA)	NCBI Sequence Viewer
	EAW78740	(Get FASTA)	NCBI Sequence Viewer
	EAW78741	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000295920
	ENSP00000295920.7
	ENSP00000419851
	ENSP00000419851.1
GenBank Protein	P49915	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_003866 ⟸ NM_003875

- UniProtKB:

B4DXV7 (UniProtKB/Swiss-Prot), A8K639 (UniProtKB/Swiss-Prot), F8W720 (UniProtKB/Swiss-Prot), P49915 (UniProtKB/Swiss-Prot), A0A140VJK6 (UniProtKB/TrEMBL), Q53F90 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MALCNGDSKLENAGGDLKDGHHHYEGAVVILDAGAQYGKVIDRRVRELFVQSEIFPLETPAFAI
KEQGFRAIIISGGPNSVYAEDAPWFDPAIFTIGKPVLGICYGMQMMNKVFGGTVHKKSVREDGV
FNISVDNTCSLFRGLQKEEVVLLTHGDSVDKVADGFKVVARSGNIVAGIANESKKLYGAQFHPE
VGLTENGKVILKNFLYDIAGCSGTFTVQNRELECIREIKERVGTSKVLVLLSGGVDSTVCTALL
NRALNQEQVIAVHIDNGFMRKRESQSVEEALKKLGIQVKVINAAHSFYNGTTTLPISDEDRTPR
KRISKTLNMTTSPEEKRKIIGDTFVKIANEVIGEMNLKPEEVFLAQGTLRPDLIESASLVASGK
AELIKTHHNDTELIRKLREEGKVIEPLKDFHKDEVRILGRELGLPEELVSRHPFPGPGLAIRVI
CAEEPYICKDFPETNNILKIVADFSASVKKPHTLLQRVKACTTEEDQEKLMQITSLHSLNAFLL
PIKTVGVQGDCRSYSYVCGISSKDEPDWESLIFLARLIPRMCHNVNRVVYIFGPPVKEPPTDVT
PTFLTTGVLSTLRQADFEAHNILRESGYAGKISQMPVILTPLHFDRDPLQKQPSCQRSVVIRTF
ITSDFMTGIPATPGNEIPVEVVLKMVTEIKKIPGISRIMYDLTSKPPGTTEWE

hide sequence

RefSeq Acc Id:	XP_011511565 ⟸ XM_011513263
- Peptide Label:	isoform X1
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)
- Sequence:	show sequence MALESSNIQFSVQKKLENAGGDLKDGHHHYEGAVVILDAGAQYGKVIDRRVRELFVQSEIFPLE TPAFAIKEQGFRAIIISGGPNSVYAEDAPWFDPAIFTIGKPVLGICYGMQMMNKVFGGTVHKKS VREDGVFNISVDNTCSLFRGLQKEEVVLLTHGDSVDKVADGFKVVARSGNIVAGIANESKKLYG AQFHPEVGLTENGKVILKNFLYDIAGCSGTFTVQNRELECIREIKERVGTSKVLVLLSGGVDST VCTALLNRALNQEQVIAVHIDNGFMRKRESQSVEEALKKLGIQVKVINAAHSFYNGTTTLPISD EDRTPRKRISKTLNMTTSPEEKRKIIGDTFVKIANEVIGEMNLKPEEVFLAQGTLRPDLIESAS LVASGKAELIKTHHNDTELIRKLREEGKVIEPLKDFHKDEVRILGRELGLPEELVSRHPFPGPG LAIRVICAEEPYICKDFPETNNILKIVADFSASVKKPHTLLQRVKACTTEEDQEKLMQITSLHS LNAFLLPIKTVGVQGDCRSYSYVCGISSKDEPDWESLIFLARLIPRMCHNVNRVVYIFGPPVKE PPTDVTPTFLTTGVLSTLRQADFEAHNILRESGYAGKISQMPVILTPLHFDRDPLQKQPSCQRS VVIRTFITSDFMTGIPATPGNEIPVEVVLKMVTEIKKIPGISRIMYDLTSKPPGTTEWE hide sequence

RefSeq Acc Id:	XP_016862911 ⟸ XM_017007422
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLLENAGGDLKDGHHHYEGAVVILDAGAQYGKVIDRRVRELFVQSEIFPLETPAFAIKEQGFRA IIISGGPNSVYAEDAPWFDPAIFTIGKPVLGICYGMQMMNKVFGGTVHKKSVREDGVFNISVDN TCSLFRGLQKEEVVLLTHGDSVDKVADGFKVVARSGNIVAGIANESKKLYGAQFHPEVGLTENG KVILKNFLYDIAGCSGTFTVQNRELECIREIKERVGTSKVLVLLSGGVDSTVCTALLNRALNQE QVIAVHIDNGFMRKRESQSVEEALKKLGIQVKVINAAHSFYNGTTTLPISDEDRTPRKRISKTL NMTTSPEEKRKIIGDTFVKIANEVIGEMNLKPEEVFLAQGTLRPDLIESASLVASGKAELIKTH HNDTELIRKLREEGKVIEPLKDFHKDEVRILGRELGLPEELVSRHPFPGPGLAIRVICAEEPYI CKDFPETNNILKIVADFSASVKKPHTLLQRVKACTTEEDQEKLMQITSLHSLNAFLLPIKTVGV QGDCRSYSYVCGISSKDEPDWESLIFLARLIPRMCHNVNRVVYIFGPPVKEPPTDVTPTFLTTG VLSTLRQADFEAHNILRESGYAGKISQMPVILTPLHFDRDPLQKQPSCQRSVVIRTFITSDFMT GIPATPGNEIPVEVVLKMVTEIKKIPGISRIMYDLTSKPPGTTEWE hide sequence

Ensembl Acc Id:

ENSP00000295920 ⟸ ENST00000295920

Ensembl Acc Id:

ENSP00000419851 ⟸ ENST00000496455

RefSeq Acc Id:	XP_047305101 ⟸ XM_047449145
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047305102 ⟸ XM_047449146
- Peptide Label:	isoform X3
- UniProtKB:	B4DUT7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047305100 ⟸ XM_047449144
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054204247 ⟸ XM_054348272
- Peptide Label:	isoform X1
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054204250 ⟸ XM_054348275
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054204249 ⟸ XM_054348274
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054204251 ⟸ XM_054348276
- Peptide Label:	isoform X3
- UniProtKB:	B4DUT7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054204248 ⟸ XM_054348273
- Peptide Label:	isoform X2
- UniProtKB:	Q53F90 (UniProtKB/TrEMBL)

Protein Domains

Glutamine amidotransferase type-1 GMPS ATP-PPase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P49915-F1-model_v2	AlphaFold	P49915	1-693	view protein structure

Promoters

RGD ID:

6866072

Promoter ID:

EPDNEW_H6201

Type:

initiation region

Name:

GMPS_1

Description:

guanine monophosphate synthase

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H6200

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	155,870,662 - 155,870,722	EPDNEW

RGD ID:

6801081

Promoter ID:

HG_KWN:46534

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000295920, NM_003875

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	3	157,070,631 - 157,071,232 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:4378	AgrOrtholog
COSMIC	GMPS	COSMIC
Ensembl Genes	ENSG00000163655	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000295920	ENTREZGENE
	ENST00000295920.7	UniProtKB/Swiss-Prot
	ENST00000496455	ENTREZGENE
	ENST00000496455.7	UniProtKB/Swiss-Prot
Gene3D-CATH	3.30.300.10	UniProtKB/Swiss-Prot
	3.40.50.620	UniProtKB/Swiss-Prot
	3.40.50.880	UniProtKB/Swiss-Prot
GTEx	ENSG00000163655	GTEx
HGNC ID	HGNC:4378	ENTREZGENE
Human Proteome Map	GMPS	Human Proteome Map
InterPro	Class_I_gatase-like	UniProtKB/Swiss-Prot
	GATASE	UniProtKB/Swiss-Prot
	GMP_synth_C	UniProtKB/Swiss-Prot
	GMP_synth_GATase	UniProtKB/Swiss-Prot
	GMPS_ATP_PPase_dom	UniProtKB/Swiss-Prot
	NAD/GMP_synthase	UniProtKB/Swiss-Prot
	Rossmann-like_a/b/a_fold	UniProtKB/Swiss-Prot
KEGG Report	hsa:8833	UniProtKB/Swiss-Prot
NCBI Gene	8833	ENTREZGENE
OMIM	600358	OMIM
PANTHER	GMP SYNTHASE [GLUTAMINE-HYDROLYZING]	UniProtKB/Swiss-Prot
	GMP SYNTHASE-RELATED	UniProtKB/Swiss-Prot
Pfam	GATase	UniProtKB/Swiss-Prot
	GMP_synt_C	UniProtKB/Swiss-Prot
	NAD_synthase	UniProtKB/Swiss-Prot
PharmGKB	PA28763	PharmGKB
PRINTS	ANTSNTHASEII	UniProtKB/Swiss-Prot
	GATASE	UniProtKB/Swiss-Prot
PROSITE	GATASE_TYPE_1	UniProtKB/Swiss-Prot
	GMPS_ATP_PPASE	UniProtKB/Swiss-Prot
Superfamily-SCOP	Adenine nucleotide alpha hydrolases-like	UniProtKB/Swiss-Prot
	GMP synthetase C-terminal dimerisation domain	UniProtKB/Swiss-Prot
	SSF52317	UniProtKB/Swiss-Prot
UniProt	A0A140VJK6	ENTREZGENE, UniProtKB/TrEMBL
	A8K639	ENTREZGENE
	B4DUT7	ENTREZGENE, UniProtKB/TrEMBL
	B4DXV7	ENTREZGENE
	F8W720	ENTREZGENE
	GUAA_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q53F90	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	A8K639	UniProtKB/Swiss-Prot
	B4DXV7	UniProtKB/Swiss-Prot
	F8W720	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-09-08	GMPS	guanine monophosphate synthase	GMPS	guanine monphosphate synthase	Symbol and/or name change	5135510	APPROVED
2015-09-08	GMPS	guanine monophosphate synthase	GMPS	guanine monphosphate synthase	Symbol and/or name change	5135510	APPROVED
2013-06-25	GMPS	guanine monphosphate synthase	GMPS	guanine monphosphate synthetase	Symbol and/or name change	5135510	APPROVED
2013-06-25	GMPS	guanine monphosphate synthase	GMPS	guanine monphosphate synthetase	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)

RGD Manual Annotations

Imported Annotations - SMPDB

Imported Annotations - KEGG (archival)

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RGD Manual Annotations

Imported Annotations - SMPDB

Imported Annotations - KEGG (archival)