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Gene: QRFPR (pyroglutamylated RFamide peptide receptor) Homo sapiens

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Symbol:

QRFPR

Name:

pyroglutamylated RFamide peptide receptor

RGD ID:

1351393

HGNC Page

HGNC:15565

Description:

Enables G protein-coupled receptor activity. Involved in G protein-coupled receptor signaling pathway. Predicted to be located in non-motile cilium. Predicted to be active in plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

AQ27; G protein-coupled receptor 103; G-protein coupled receptor 103; GPR103; MGC149217; orexigenic neuropeptide QRFP receptor; peptide P518 receptor; pyroglutamylated RF-amide peptide receptor; QRFP receptor; SP9155

RGD Orthologs

Alliance Orthologs

More Info

more info ...

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	121,328,642 - 121,381,018 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	121,328,642 - 121,381,059 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	122,249,797 - 122,302,173 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	122,469,247 - 122,521,631 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	122,608,073 - 122,659,407	NCBI
Celera	4	119,634,941 - 119,687,269 (-)	NCBI		Celera
Cytogenetic Map	4	q27	NCBI
HuRef	4	117,976,714 - 118,029,012 (-)	NCBI		HuRef
CHM1_1	4	122,226,355 - 122,271,006 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	124,632,974 - 124,685,273 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS more ...	ClinVar	PMID:28492532
QRFPR	Human	Neurodevelopmental Disorders		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Neurodevelopmental disorder	ClinVar	PMID:25741868

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	bone structure disease		ISS	Qrfpr (Mus musculus)	13592920		MouseDO

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	1,2,4-trichloro-5-(2,5-dichlorophenyl)benzene	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
QRFPR	Human	1,2-dichloroethane	affects expression	ISO	Qrfpr (Mus musculus)	6480464	ethylene dichloride affects the expression of QRFPR mRNA	CTD	PMID:28960355
QRFPR	Human	2,2',4,4',5,5'-hexachlorobiphenyl	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
QRFPR	Human	2,2',5,5'-tetrachlorobiphenyl	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
QRFPR	Human	2,4,4'-trichlorobiphenyl	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
QRFPR	Human	6-propyl-2-thiouracil	increases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	Propylthiouracil results in increased expression of QRFPR mRNA	CTD	PMID:24780913
QRFPR	Human	amphetamine	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	Amphetamine results in decreased expression of QRFPR mRNA	CTD	PMID:30779732
QRFPR	Human	arsenite(3-)	decreases expression	EXP		6480464	arsenite results in decreased expression of QRFPR mRNA	CTD	PMID:23974009
QRFPR	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of QRFPR promoter	CTD	PMID:27901495
QRFPR	Human	benzo[a]pyrene	increases expression	EXP		6480464	Benzo(a)pyrene results in increased expression of QRFPR mRNA	CTD	PMID:32234424
QRFPR	Human	bisphenol A	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of QRFPR mRNA	CTD	PMID:25181051 and PMID:34947998
QRFPR	Human	bisphenol A	increases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	bisphenol A results in increased expression of QRFPR mRNA	CTD	PMID:30816183 and PMID:32528016
QRFPR	Human	bromobenzene	increases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	bromobenzene results in increased expression of QRFPR mRNA	CTD	PMID:32479839
QRFPR	Human	cadmium dichloride	decreases expression	EXP		6480464	Cadmium Chloride results in decreased expression of QRFPR mRNA	CTD	PMID:38568856
QRFPR	Human	caffeine	increases phosphorylation	EXP		6480464	Caffeine results in increased phosphorylation of QRFPR protein	CTD	PMID:35688186
QRFPR	Human	chloropicrin	increases expression	EXP		6480464	chloropicrin results in increased expression of QRFPR mRNA	CTD	PMID:26352163
QRFPR	Human	copper atom	increases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of QRFPR mRNA	CTD	PMID:26033743
QRFPR	Human	copper(0)	increases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of QRFPR mRNA	CTD	PMID:26033743
QRFPR	Human	crocidolite asbestos	decreases expression	EXP		6480464	Asbestos and Crocidolite results in decreased expression of QRFPR mRNA	CTD	PMID:29523930
QRFPR	Human	dimethylarsinic acid	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in increased expression of QRFPR mRNA	CTD	PMID:34876320
QRFPR	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
QRFPR	Human	ethylparaben	increases expression	EXP		6480464	ethyl-p-hydroxybenzoate results in increased expression of QRFPR mRNA	CTD	PMID:37690743
QRFPR	Human	fluoxetine	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	Fluoxetine results in decreased expression of QRFPR mRNA	CTD	PMID:21820738
QRFPR	Human	fonofos	increases methylation	EXP		6480464	Fonofos results in increased methylation of QRFPR promoter	CTD	PMID:22847954
QRFPR	Human	FR900359	increases phosphorylation	EXP		6480464	FR900359 results in increased phosphorylation of QRFPR protein	CTD	PMID:37730182
QRFPR	Human	methylarsonic acid	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in increased expression of QRFPR mRNA	CTD	PMID:34876320
QRFPR	Human	Muraglitazar	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	muraglitazar results in decreased expression of QRFPR mRNA	CTD	PMID:21515302
QRFPR	Human	N,N-diethyl-m-toluamide	multiple interactions	ISO	Qrfpr (Rattus norvegicus)	6480464	[Permethrin co-treated with DEET] results in decreased methylation of QRFPR gene	CTD	PMID:33148267
QRFPR	Human	okadaic acid	increases expression	EXP		6480464	Okadaic Acid results in increased expression of QRFPR mRNA	CTD	PMID:38832940
QRFPR	Human	organophosphorus compound	multiple interactions	ISO	Qrfpr (Rattus norvegicus)	6480464	[Dust results in increased abundance of Organophosphorus Compounds] which results in increased expression of QRFPR mRNA	CTD	PMID:39658253
QRFPR	Human	parathion	increases methylation	EXP		6480464	Parathion results in increased methylation of QRFPR promoter	CTD	PMID:22847954
QRFPR	Human	PCB138	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[2 more ...	CTD	PMID:25510870
QRFPR	Human	permethrin	multiple interactions	ISO	Qrfpr (Rattus norvegicus)	6480464	[Permethrin co-treated with DEET] results in decreased methylation of QRFPR gene	CTD	PMID:33148267
QRFPR	Human	phenylmercury acetate	increases expression	EXP		6480464	Phenylmercuric Acetate results in increased expression of QRFPR mRNA	CTD	PMID:26272509
QRFPR	Human	phenylmercury acetate	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased expression of QRFPR mRNA	CTD	PMID:27188386
QRFPR	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
QRFPR	Human	sodium arsenate	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in increased expression of QRFPR mRNA	CTD	PMID:34876320
QRFPR	Human	sodium arsenite	decreases expression	EXP		6480464	sodium arsenite results in decreased expression of QRFPR mRNA	CTD	PMID:38568856
QRFPR	Human	sodium arsenite	multiple interactions	ISO	Qrfpr (Mus musculus)	6480464	[sodium arsenate co-treated with sodium arsenite co-treated with monomethylarsonic acid co-treated with Cacodylic Acid] results in increased expression of QRFPR mRNA	CTD	PMID:34876320
QRFPR	Human	temozolomide	decreases expression	EXP		6480464	Temozolomide results in decreased expression of QRFPR mRNA	CTD	PMID:31758290
QRFPR	Human	terbufos	increases methylation	EXP		6480464	terbufos results in increased methylation of QRFPR promoter	CTD	PMID:22847954
QRFPR	Human	Tesaglitazar	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	tesaglitazar results in decreased expression of QRFPR mRNA	CTD	PMID:21515302
QRFPR	Human	thiram	decreases expression	EXP		6480464	Thiram results in decreased expression of QRFPR mRNA	CTD	PMID:38568856
QRFPR	Human	triclosan	decreases expression	EXP		6480464	Triclosan results in decreased expression of QRFPR mRNA	CTD	PMID:30510588
QRFPR	Human	triptonide	increases expression	ISO	Qrfpr (Mus musculus)	6480464	triptonide results in increased expression of QRFPR mRNA	CTD	PMID:33045310
QRFPR	Human	troglitazone	decreases expression	ISO	Qrfpr (Rattus norvegicus)	6480464	troglitazone results in decreased expression of QRFPR mRNA	CTD	PMID:21515302
QRFPR	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of QRFPR mRNA	CTD	PMID:25979313
QRFPR	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of QRFPR mRNA	CTD	PMID:26272509
QRFPR	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased expression of QRFPR mRNA	CTD	PMID:27188386

Biological Process

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	cellular response to hormone stimulus	involved_in	IBA	PANTHER:PTN001202348 and Cckar (Rattus norvegicus)	150520179		GO_Central	GO_REF:0000033
QRFPR	Human	G protein-coupled receptor signaling pathway	involved_in	IDA		150520179	PMID:12960173	UniProt	PMID:12960173
QRFPR	Human	G protein-coupled receptor signaling pathway	involved_in	IBA	FB:FBgn0025595 more ...	150520179		GO_Central	GO_REF:0000033
QRFPR	Human	G protein-coupled receptor signaling pathway	involved_in	IEA	UniProtKB-KW:KW-0297	150520179		UniProt	GO_REF:0000043
QRFPR	Human	G protein-coupled receptor signaling pathway	involved_in	IEA	InterPro:IPR000276 and InterPro:IPR000611	150520179		InterPro	GO_REF:0000002
QRFPR	Human	neuropeptide signaling pathway	involved_in	IEA	GO:0004983	150520179		GOC	GO_REF:0000108
QRFPR	Human	signal transduction	involved_in	IEA	UniProtKB-KW:KW-0807	150520179		UniProt	GO_REF:0000043

Cellular Component

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
QRFPR	Human	membrane	located_in	IEA	UniProtKB-SubCell:SL-0162	150520179		UniProt	GO_REF:0000044
QRFPR	Human	membrane	located_in	IC	GO:0004930	150520179	PMID:12960173	UniProt	PMID:12960173
QRFPR	Human	membrane	located_in	IEA	InterPro:IPR000276 more ...	150520179		InterPro	GO_REF:0000002
QRFPR	Human	non-motile cilium	located_in	ISO	Qrfpr (Mus musculus)	9068941	PMID:24316073	MGI	PMID:24316073
QRFPR	Human	plasma membrane	located_in	IEA	UniProtKB-SubCell:SL-0039	150520179		UniProt	GO_REF:0000044
QRFPR	Human	plasma membrane	is_active_in	IBA	FB:FBgn0038880 more ...	150520179		GO_Central	GO_REF:0000033
QRFPR	Human	plasma membrane	located_in	TAS		150520179		Reactome	Reactome:R-HSA-379048 more ...
QRFPR	Human	plasma membrane	located_in	IEA	UniProtKB-KW:KW-1003	150520179		UniProt	GO_REF:0000043

Molecular Function

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
QRFPR	Human	G protein-coupled receptor activity	enables	IDA		150520179	PMID:12960173	UniProt	PMID:12960173
QRFPR	Human	G protein-coupled receptor activity	enables	IEA	InterPro:IPR000276	150520179		InterPro	GO_REF:0000002
QRFPR	Human	G protein-coupled receptor activity	enables	IBA	FB:FBgn0038880 more ...	150520179		GO_Central	GO_REF:0000033
QRFPR	Human	G protein-coupled receptor activity	enables	IEA	UniProtKB-KW:KW-0297	150520179		UniProt	GO_REF:0000043
QRFPR	Human	neuropeptide Y receptor activity	enables	IEA	InterPro:IPR000611	150520179		InterPro	GO_REF:0000002
QRFPR	Human	protein binding	enables	IPI	UniProtKB:P48165 and UniProtKB:Q9P121-3	150520179	PMID:32296183	IntAct	PMID:32296183

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:11574155	PMID:12477932	PMID:12714592	PMID:12960173	PMID:15717329	PMID:16344560	PMID:16648250	PMID:16754659	PMID:20534693	PMID:21873635	PMID:26211894	PMID:30483810
PMID:30633125	PMID:32296183	PMID:33655503	PMID:33872671	PMID:34018631

QRFPR
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	121,328,642 - 121,381,018 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	121,328,642 - 121,381,059 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	122,249,797 - 122,302,173 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	122,469,247 - 122,521,631 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	122,608,073 - 122,659,407	NCBI
Celera	4	119,634,941 - 119,687,269 (-)	NCBI		Celera
Cytogenetic Map	4	q27	NCBI
HuRef	4	117,976,714 - 118,029,012 (-)	NCBI		HuRef
CHM1_1	4	122,226,355 - 122,271,006 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	124,632,974 - 124,685,273 (-)	NCBI		T2T-CHM13v2.0

Qrfpr
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	3	36,233,575 - 36,276,462 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	3	36,233,573 - 36,276,462 (-)	Ensembl		GRCm39 Ensembl
GRCm38	3	36,179,426 - 36,222,275 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	3	36,179,424 - 36,222,313 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	3	36,078,348 - 36,121,197 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	3	36,370,975 - 36,413,824 (-)	NCBI		MGSCv36	mm8
Celera	3	36,062,081 - 36,104,668 (-)	NCBI		Celera
Cytogenetic Map	3	B	NCBI
cM Map	3	17.41	NCBI

Qrfpr
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	2	120,981,235 - 121,025,020 (-)	NCBI		GRCr8
mRatBN7.2	2	119,053,083 - 119,096,864 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	119,053,511 - 119,096,792 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	2	125,606,352 - 125,649,723 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	2	123,719,044 - 123,762,423 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	2	118,347,801 - 118,391,177 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	2	122,891,321 - 122,949,241 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	2	122,891,321 - 122,949,241 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	2	142,517,181 - 142,568,697 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	2	122,677,072 - 122,719,991 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	2	122,622,033 - 122,664,953 (-)	NCBI
Celera	2	114,013,952 - 114,057,159 (-)	NCBI		Celera
Cytogenetic Map	2	q25	NCBI

Qrfpr
(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	19,238,448 - 19,290,657 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955428	19,238,479 - 19,290,510 (+)	NCBI	ChiLan1.0	ChiLan1.0

QRFPR
(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	119,116,985 - 119,171,604 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	4	119,401,416 - 119,455,948 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	4	113,537,723 - 113,591,507 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	4	124,676,059 - 124,729,754 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	4	124,676,059 - 124,729,754 (-)	Ensembl	panpan1.1		panPan2

QRFPR
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	19	18,717,060 - 18,769,733 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	19	18,717,339 - 18,767,061 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	19	18,940,022 - 18,993,469 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	19	18,843,015 - 18,894,469 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	19	18,843,251 - 18,894,525 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	19	18,803,353 - 18,856,710 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	19	19,074,287 - 19,127,802 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	19	19,553,129 - 19,603,173 (+)	NCBI		UU_Cfam_GSD_1.0

Qrfpr
(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	66,283,441 - 66,321,512 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936662	797,281 - 825,194 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936662	797,533 - 861,989 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

QRFPR
(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	102,745,450 - 102,794,896 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	8	102,745,001 - 102,791,366 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	8	110,011,558 - 110,021,885 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

QRFPR
(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	68,617,661 - 68,672,874 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	7	68,615,807 - 68,672,477 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666037	47,581,339 - 47,639,032 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Qrfpr
(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_004624777	1,419,637 - 1,484,608 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624777	1,420,050 - 1,484,518 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in QRFPR
35 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 4q26-35.2(chr4:118065569-190042639)x3	copy number gain	See cases [RCV000051785]	Chr4:118065569..190042639 [GRCh38] Chr4:118986724..190828225 [GRCh37] Chr4:119206172..191200788 [NCBI36] Chr4:4q26-35.2	pathogenic
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
GRCh38/hg38 4q26-31.21(chr4:116630862-145429900)x1	copy number loss	See cases [RCV000053321]	Chr4:116630862..145429900 [GRCh38] Chr4:117552018..146351052 [GRCh37] Chr4:117771466..146570502 [NCBI36] Chr4:4q26-31.21	pathogenic
NM_198179.2(QRFPR):c.773G>A (p.Gly258Glu)	single nucleotide variant	Malignant melanoma [RCV000066265]	Chr4:121332845 [GRCh38] Chr4:122254000 [GRCh37] Chr4:122473450 [NCBI36] Chr4:4q27	not provided
GRCh38/hg38 4q27(chr4:121164018-122098913)x1	copy number loss	See cases [RCV000137335]	Chr4:121164018..122098913 [GRCh38] Chr4:122085173..123020068 [GRCh37] Chr4:122304623..123239518 [NCBI36] Chr4:4q27	uncertain significance
GRCh38/hg38 4q26-28.3(chr4:117351881-133565667)x1	copy number loss	See cases [RCV000143207]	Chr4:117351881..133565667 [GRCh38] Chr4:118273037..134486822 [GRCh37] Chr4:118492485..134706272 [NCBI36] Chr4:4q26-28.3	pathogenic
NM_198179.3(QRFPR):c.340+11600_340+16200del	deletion	Gestational diabetes mellitus uncontrolled [RCV000161357]	Chr4:121364108..121368708 [GRCh38] Chr4:122285263..122289863 [GRCh37] Chr4:4q27	not provided
GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3	copy number gain	See cases [RCV000240392]	Chr4:119437495..190904301 [GRCh37] Chr4:4q26-35.2	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
NM_198179.3(QRFPR):c.1025del (p.Asn342fs)	deletion	not provided [RCV000509431]	Chr4:121329585 [GRCh38] Chr4:122250740 [GRCh37] Chr4:4q27	not provided
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_198179.3(QRFPR):c.101T>C (p.Leu34Pro)	single nucleotide variant	not specified [RCV004326714]	Chr4:121380547 [GRCh38] Chr4:122301702 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.767T>G (p.Ile256Ser)	single nucleotide variant	not provided [RCV000585250]	Chr4:121332851 [GRCh38] Chr4:122254006 [GRCh37] Chr4:4q27	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 4q26-28.2(chr4:116307857-129302960)x1	copy number loss	not provided [RCV000682448]	Chr4:116307857..129302960 [GRCh37] Chr4:4q26-28.2	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 4q27(chr4:122283523-122288886)x1	copy number loss	not provided [RCV000743940]	Chr4:122283523..122288886 [GRCh37] Chr4:4q27	benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3	copy number gain	not provided [RCV000743156]	Chr4:49450..190963766 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3	copy number gain	not provided [RCV000743147]	Chr4:11525..191028879 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
Single allele	deletion	Neurodevelopmental disorder [RCV000787448]	Chr4:116624547..126168646 [GRCh37] Chr4:4q26-28.1	likely pathogenic
NM_198179.3(QRFPR):c.361G>T (p.Val121Leu)	single nucleotide variant	not specified [RCV004296424]	Chr4:121340590 [GRCh38] Chr4:122261745 [GRCh37] Chr4:4q27	uncertain significance
GRCh37/hg19 4q27(chr4:121183810-122428870)x3	copy number gain	not provided [RCV001259311]	Chr4:121183810..122428870 [GRCh37] Chr4:4q27	uncertain significance
GRCh37/hg19 4q26-28.2(chr4:116833638-130232122)	copy number loss	Atypical behavior [RCV001352657]	Chr4:116833638..130232122 [GRCh37] Chr4:4q26-28.2	pathogenic
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 4q26-28.2(chr4:116888785-129649979)	copy number loss	not specified [RCV002053451]	Chr4:116888785..129649979 [GRCh37] Chr4:4q26-28.2	pathogenic
GRCh37/hg19 4q24-31.21(chr4:104715235-145252595)	copy number gain	not specified [RCV002053446]	Chr4:104715235..145252595 [GRCh37] Chr4:4q24-31.21	pathogenic
NM_198179.3(QRFPR):c.1217A>T (p.Glu406Val)	single nucleotide variant	not specified [RCV004096198]	Chr4:121329393 [GRCh38] Chr4:122250548 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.157G>A (p.Val53Met)	single nucleotide variant	not specified [RCV004231055]	Chr4:121380491 [GRCh38] Chr4:122301646 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.820A>G (p.Met274Val)	single nucleotide variant	not specified [RCV004207490]	Chr4:121330501 [GRCh38] Chr4:122251656 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.631C>G (p.Gln211Glu)	single nucleotide variant	not specified [RCV004211474]	Chr4:121332987 [GRCh38] Chr4:122254142 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.701A>G (p.Tyr234Cys)	single nucleotide variant	not specified [RCV004093341]	Chr4:121332917 [GRCh38] Chr4:122254072 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.134A>C (p.Lys45Thr)	single nucleotide variant	not specified [RCV004111488]	Chr4:121380514 [GRCh38] Chr4:122301669 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.695T>G (p.Ile232Ser)	single nucleotide variant	not specified [RCV004186790]	Chr4:121332923 [GRCh38] Chr4:122254078 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.1238A>G (p.His413Arg)	single nucleotide variant	not specified [RCV004186338]	Chr4:121329372 [GRCh38] Chr4:122250527 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.222G>T (p.Lys74Asn)	single nucleotide variant	not specified [RCV004092161]	Chr4:121380426 [GRCh38] Chr4:122301581 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.887T>C (p.Ile296Thr)	single nucleotide variant	not provided [RCV002598581]\|not specified [RCV004847947]	Chr4:121330434 [GRCh38] Chr4:122251589 [GRCh37] Chr4:4q27	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_198179.3(QRFPR):c.47G>C (p.Arg16Pro)	single nucleotide variant	not specified [RCV004440755]	Chr4:121380601 [GRCh38] Chr4:122301756 [GRCh37] Chr4:4q27	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_198179.3(QRFPR):c.406A>G (p.Met136Val)	single nucleotide variant	not specified [RCV004851913]	Chr4:121340545 [GRCh38] Chr4:122261700 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.56A>G (p.Asn19Ser)	single nucleotide variant	not specified [RCV004851914]	Chr4:121380592 [GRCh38] Chr4:122301747 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.907A>G (p.Lys303Glu)	single nucleotide variant	not specified [RCV004851912]	Chr4:121329703 [GRCh38] Chr4:122250858 [GRCh37] Chr4:4q27	uncertain significance
NC_000004.11:g.(?_121616266)_(124323706_?)dup	duplication	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome [RCV003113657]	Chr4:121616266..124323706 [GRCh37] Chr4:4q27-28.1	uncertain significance
NM_198179.3(QRFPR):c.34T>C (p.Ser12Pro)	single nucleotide variant	not specified [RCV004114638]	Chr4:121380614 [GRCh38] Chr4:122301769 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.493A>G (p.Met165Val)	single nucleotide variant	not specified [RCV004249005]	Chr4:121340458 [GRCh38] Chr4:122261613 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.1054G>A (p.Val352Ile)	single nucleotide variant	not specified [RCV004363846]	Chr4:121329556 [GRCh38] Chr4:122250711 [GRCh37] Chr4:4q27	uncertain significance
GRCh37/hg19 4q26-32.3(chr4:117518683-168174703)x3	copy number gain	not provided [RCV003484198]	Chr4:117518683..168174703 [GRCh37] Chr4:4q26-32.3	pathogenic
NM_198179.3(QRFPR):c.115G>C (p.Glu39Gln)	single nucleotide variant	not specified [RCV004440751]	Chr4:121380533 [GRCh38] Chr4:122301688 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.67G>C (p.Glu23Gln)	single nucleotide variant	not specified [RCV004440756]	Chr4:121380581 [GRCh38] Chr4:122301736 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.983A>T (p.Asn328Ile)	single nucleotide variant	not specified [RCV004440758]	Chr4:121329627 [GRCh38] Chr4:122250782 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.1105A>G (p.Met369Val)	single nucleotide variant	not specified [RCV004440749]	Chr4:121329505 [GRCh38] Chr4:122250660 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.779A>T (p.Glu260Val)	single nucleotide variant	not specified [RCV004440757]	Chr4:121332839 [GRCh38] Chr4:122253994 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.248T>G (p.Phe83Cys)	single nucleotide variant	not specified [RCV004440752]	Chr4:121380400 [GRCh38] Chr4:122301555 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.328A>G (p.Asn110Asp)	single nucleotide variant	not specified [RCV004440753]	Chr4:121380320 [GRCh38] Chr4:122301475 [GRCh37] Chr4:4q27	uncertain significance
NC_000004.11:g.(?_121616266)_(124323706_?)del	deletion	not provided [RCV004580860]	Chr4:121616266..124323706 [GRCh37] Chr4:4q27-28.1	uncertain significance
NM_198179.3(QRFPR):c.349A>G (p.Ile117Val)	single nucleotide variant	not specified [RCV004669348]	Chr4:121340602 [GRCh38] Chr4:122261757 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.653T>C (p.Ile218Thr)	single nucleotide variant	not specified [RCV004662893]	Chr4:121332965 [GRCh38] Chr4:122254120 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.546C>G (p.His182Gln)	single nucleotide variant	not specified [RCV004662894]	Chr4:121336822 [GRCh38] Chr4:122257977 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.479G>A (p.Arg160Gln)	single nucleotide variant	not specified [RCV004851910]	Chr4:121340472 [GRCh38] Chr4:122261627 [GRCh37] Chr4:4q27	uncertain significance
NM_198179.3(QRFPR):c.37C>T (p.Arg13Trp)	single nucleotide variant	not specified [RCV004851911]	Chr4:121380611 [GRCh38] Chr4:122301766 [GRCh37] Chr4:4q27	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	687
Count of miRNA genes:	437
Interacting mature miRNAs:	471
Transcripts:	ENST00000334383, ENST00000394427, ENST00000507331, ENST00000512235
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1643256	BW127_H	Body Weight QTL 127 (human)	1.31	0.007	Body weight	body mass index	4	106319694	132319694	Human
597249907	GWAS1345981_H	body weight QTL GWAS1345981 (human)		5e-08	body mass (VT:0001259)	body weight (CMO:0000012)	4	121338887	121338888	Human

RH41058

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	175,773,100 - 175,773,199	UniSTS	GRCh37
GRCh37	4	122,289,085 - 122,289,181	UniSTS	GRCh37
Build 36	4	122,508,535 - 122,508,631	RGD	NCBI36
Celera	5	172,729,256 - 172,729,355	UniSTS
Celera	4	119,674,173 - 119,674,269	RGD
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	4	q27	UniSTS
HuRef	5	170,697,611 - 170,697,710	UniSTS
HuRef	4	118,015,929 - 118,016,025	UniSTS

SHGC-148097

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	122,300,125 - 122,300,447	UniSTS	GRCh37
Build 36	4	122,519,575 - 122,519,897	RGD	NCBI36
Celera	4	119,685,213 - 119,685,535	RGD
Cytogenetic Map	4	q27	UniSTS
HuRef	4	118,026,964 - 118,027,286	UniSTS
TNG Radiation Hybrid Map	4	76138.0	UniSTS

G20706

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	5	175,773,100 - 175,773,199	UniSTS	GRCh37
GRCh37	4	122,289,085 - 122,289,181	UniSTS	GRCh37
Build 36	4	122,508,535 - 122,508,631	RGD	NCBI36
Celera	5	172,729,256 - 172,729,355	UniSTS
Celera	4	119,674,173 - 119,674,269	RGD
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	4	q27	UniSTS
HuRef	5	170,697,611 - 170,697,710	UniSTS
HuRef	4	118,015,929 - 118,016,025	UniSTS

sY3084

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	21	q22.12	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	6	q22.33	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	7	q11.2	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	18	q22.1	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	3	q25	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	4	q27	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	18	q12.1-q21.1	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	14	q22	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	1	p35.3-p33	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	5	q15	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	18	p11.3-p11.2	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	X	q13.2	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	7	q31	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	17	q24.1	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	13	q13.3	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	19	p13.1	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	1	q25.3	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	X	q12	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	4	p16	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	18	p11.22	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	13	q32.1	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	7	p15	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	8	q13	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	2	q12	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	14	q32.1	UniSTS
Cytogenetic Map	1	p33-p32	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	7	p21.3	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	4	q32	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	9	p12	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	3	q12.3	UniSTS

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

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
693	1523	1439	1718	3697	1339	1372	267	312	155	1010	4033	3416	33	2944	615	1311	1013	120


RefSeq Transcripts	NM_198179	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017008693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054350983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB109629	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC093816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC093867	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309337	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC128132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC128133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG169612	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471056	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA461055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	JF810892	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000334383 ⟹ ENSP00000335610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	121,329,314 - 121,380,679 (-)	Ensembl

Ensembl Acc Id:

ENST00000394427 ⟹ ENSP00000377948

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	121,328,642 - 121,381,018 (-)	Ensembl

Ensembl Acc Id:

ENST00000507331 ⟹ ENSP00000423369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	121,329,312 - 121,380,647 (-)	Ensembl

Ensembl Acc Id:

ENST00000512235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	121,340,133 - 121,381,059 (-)	Ensembl

RefSeq Acc Id:

NM_198179 ⟹ NP_937822

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	121,328,642 - 121,381,018 (-)	NCBI
GRCh37	4	122,249,797 - 122,302,181 (-)	RGD
Build 36	4	122,469,247 - 122,521,631 (-)	NCBI Archive
Celera	4	119,634,941 - 119,687,269 (-)	RGD
HuRef	4	117,976,714 - 118,029,012 (-)	RGD
CHM1_1	4	122,226,355 - 122,271,006 (-)	NCBI
T2T-CHM13v2.0	4	124,632,974 - 124,685,273 (-)	NCBI

Sequence:

show sequence

ATGGCCAGAAGGCGGGGAGCCAGAGGCGCCAGGACCCTCGCGTGGCGCTCCAGCACCCCAGACCGTGGCGGCGCCTCGCCTTAGGGAAGAGCAAGGGAAGAACTTTATTTGAACCGCGAACATTTTTT
GGTCACTGAGATCGAGTCTCCCAGTGCTTTGGCTTCCCGCCTCTTTATCGTGGGTTTGATCCCTGAGCTGCTCTCCTTTCCCGAACCTCCCGGGGTGCAGCCTAGAGCCCTCCCGCGCGGCTGACTCC
AGAGTAGAGGAAGGGAGGCGGCCTCCGGCTGGTCCCCCGAAGCCCTCGCTGCCCCGCAGATGCGGATGGCCAGCCAGTAGCGGGCGGTGGCCCCGCGTCCCGGGAGCGCACAGCAATGCAGGCGCTTA
ACATTACCCCGGAGCAGTTCTCTCGGCTGCTGCGGGACCACAACCTGACGCGGGAGCAGTTCATCGCTCTGTACCGGCTGCGACCGCTCGTCTACACCCCAGAGCTGCCGGGACGCGCCAAGCTGGCC
CTCGTGCTCACCGGCGTGCTCATCTTCGCCCTGGCGCTCTTTGGCAATGCTCTGGTGTTCTACGTGGTGACCCGCAGCAAGGCCATGCGCACCGTCACCAACATCTTTATCTGCTCCTTGGCGCTCAG
TGACCTGCTCATCACCTTCTTCTGCATTCCCGTCACCATGCTCCAGAACATTTCCGACAACTGGCTGGGGGGTGCTTTCATTTGCAAGATGGTGCCATTTGTCCAGTCTACCGCTGTTGTGACAGAAA
TCCTCACTATGACCTGCATTGCTGTGGAAAGGCACCAGGGACTTGTGCATCCTTTTAAAATGAAGTGGCAATACACCAACCGAAGGGCTTTCACAATGCTAGGTGTGGTCTGGCTGGTGGCAGTCATC
GTAGGATCACCCATGTGGCACGTGCAACAACTTGAGATCAAATATGACTTCCTATATGAAAAGGAACACATCTGCTGCTTAGAAGAGTGGACCAGCCCTGTGCACCAGAAGATCTACACCACCTTCAT
CCTTGTCATCCTCTTCCTCCTGCCTCTTATGGTGATGCTTATTCTGTACAGTAAAATTGGTTATGAACTTTGGATAAAGAAAAGAGTTGGGGATGGTTCAGTGCTTCGAACTATTCATGGAAAAGAAA
TGTCCAAAATAGCCAGGAAGAAGAAACGAGCTGTCATTATGATGGTGACAGTGGTGGCTCTCTTTGCTGTGTGCTGGGCACCATTCCATGTTGTCCATATGATGATTGAATACAGTAATTTTGAAAAG
GAATATGATGATGTCACAATCAAGATGATTTTTGCTATCGTGCAAATTATTGGATTTTCCAACTCCATCTGTAATCCCATTGTCTATGCATTTATGAATGAAAACTTCAAAAAAAATGTTTTGTCTGC
AGTTTGTTATTGCATAGTAAATAAAACCTTCTCTCCAGCACAAAGGCATGGAAATTCAGGAATTACAATGATGCGGAAGAAAGCAAAGTTTTCCCTCAGAGAGAATCCAGTGGAGGAAACCAAAGGAG
AAGCATTCAGTGATGGCAACATTGAAGTCAAATTGTGTGAACAGACAGAGGAGAAGAAAAAGCTCAAACGACATCTTGCTCTCTTTAGGTCTGAACTGGCTGAGAATTCTCCTTTAGACAGTGGGCAT
TAATTATAACAATATCTTCATAATTAATGCCCTTCAGATTGTAACCCAAAGAGAAAATTATTTTGAGCAAAGGTCAAATACTCTTTTTATTCTTAAGATGATGACAAGAAGAAAACAAATCATGTTTC
CATTAAAAAATGACACGAGGCTAGTCCAAGTGCAGTGATGTTTACAACCAATTGATCACAATCATTTAACAGATTTCTGTGTTCCTTCTCATTCCCACTGCTTCACTTGACTAGCCTTAAAAAAGCAA
CATGGAAGGCCAGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCTAGACGGGCGGATCACGAGGTCAGGAGATCAAAACCATCCTGGCTAACACGGTGAAACCCCATCTCTGCTAAA
AATACAAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGCCTCAGGCGGGAGAATGGTGTGAACCCGGGAGGCGGAGCTTGCAGTGATCCGAGATCATGCCACTGCACTC
CAGCCTGGGCGAAAGAGCGAGACTCCCCGTCTCAAAAAAAATTTTTTTGAAAAATTCGTAAACCATACTTTTAAGATTATTTCAGTGGATTTTTAAAAATCTTGTACAGAAATCAGGGTTCTTAGCTA
GCAGTTTTTCTCCCACGCAGTCACTGTAATGTGAC

hide sequence

RefSeq Acc Id:

XM_017008693 ⟹ XP_016864182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	121,333,066 - 121,381,018 (-)	NCBI

Sequence:

show sequence

CCACCGCTCCCCAAGCGGGTCCGGCGTCCGCATCGCATGGCCAGAAGGCGGGGAGCCAGAGGCG
CCAGGACCCTCGCGTGGCGCTCCAGCACCCCAGACCGTGGCGGCGCCTCGCCTTAGGGAAGAGCAAGGGAAGAACTTTATTTGAACCGCGAACATTTTTTGGTCACTGAGATCGAGTCTCCCAGTGCT
TTGGCTTCCCGCCTCTTTATCGTGGGTTTGATCCCTGAGCTGCTCTCCTTTCCCGAACCTCCCGGGGTGCAGCCTAGAGCCCTCCCGCGCGGCTGACTCCAGAGTAGAGGAAGGGAGGCGGCCTCCGG
CTGGTCCCCCGAAGCCCTCGCTGCCCCGCAGATGCGGATGGCCAGCCAGTAGCGGGCGGTGGCCCCGCGTCCCGGGAGCGCACAGCAATGCAGGCGCTTAACATTACCCCGGAGCAGTTCTCTCGGCT
GCTGCGGGACCACAACCTGACGCGGGAGCAGTTCATCGCTCTGTACCGGCTGCGACCGCTCGTCTACACCCCAGAGCTGCCGGGACGCGCCAAGCTGGCCCTCGTGCTCACCGGCGTGCTCATCTTCG
CCCTGGCGCTCTTTGGCAATGCTCTGGTGTTCTACGTGGTGACCCGCAGCAAGGCCATGCGCACCGTCACCAACATCTTTATCTGCTCCTTGGCGCTCAGTGACCTGCTCATCACCTTCTTCTGCATT
CCCGTCACCATGCTCCAGAACATTTCCGACAACTGGCTGGGGGGTGCTTTCATTTGCAAGATGGTGCCATTTGTCCAGTCTACCGCTGTTGTGACAGAAATCCTCACTATGACCTGCATTGCTGTGGA
AAGGCACCAGGGACTTGTGCATCCTTTTAAAATGAAGTGGCAATACACCAACCGAAGGGCTTTCACAATGCTAGGTGTGGTCTGGCTGGTGGCAGTCATCGTAGGATCACCCATGTGGCACGTGCAAC
AACTTGAGGCTTTACCCTGAATAGAAATATATTTAAGAGAGAGAAGAGCACAAAGCCCTGCCATGTGTTTATGATGCCTTGATCAATGTGGCTTCACTGACATCAGTCATTGAATTATGTCTTGTTTT
GGTGCCCCGTGGTAAGATTCATTATGGGTGAGAGATGTGATTTCTGTAACTTGGGAAAAGGGTGATTATGAAACAGGAAGTGGGAATTTAGACCCAGCGTGACACTTCAAACTTGGGGACGATATTAG
GCAGTGGAATTTTAGAGAAGTGTATGTTTGGAAATAGAAGATCTGAAATTGAAGATCAAAGATCTGAAATTTTCCATAAAACCATCTGAGCATACCCTCAGGAAGTCTTTGCTGAAGTCCACAGTCAG
GACTTTGCTGAAGTCAGGAAGTCCGTAGTCCCTAGGGCTATGTGAACCTGATCCAAGACTTCCAGTTCAGCATGCTCTTAGATGTGTCAGTCCATACCCCCTGGTCATTGGCCTTTGCATGCTTTGCT
TCCATGGAGTTGGAATGAATTTCATTTTAACATCCTATTTCCAGAGAGTTTGAATCTTGAGATTATTTTTCAGTGAGTGTTATTCCTAGTTGCATCTGTAAGTAACACCTAGGTCAGAACTTGAATTT
TCTTACCTTTGATGAGTAACCAAAAAGTTGCTGTCCCTCATTCAATTCACATTGAAGACTGGTGATAAAATTTCCTGGGAATGTAGGCAGAAATATGTCTGAGACCCAAGTATTCAGCTCCACAGTAA
CTAAAATAACAATGGTTTTGATAAATATTCTCGTTTTTATTCCTATTACCCAAAAAAGTGACTTCTGAATATGCTTTAAATATTTAGTTTGTTCTTGAACTAGCCCTTAAAGCACTCTCTATTATTTA
TTATTGTTGTTAATAATACTTTTGAGCTTATAAGATGAGTCTACCAGAAATAGTACGAATAAACCAGCAGGTACAATCTGAATATTTGTATATTGGCAATAGTTTGAATCCCAATTTCTCATTCATCT
CAGGATAAAAGCTGCCAGTTGCCTCTTTAATATCTTTCTAAGCAATCTGATCATTGCAATATATGAAGTAGCAGTAACAAAACGCAGCTTTCAGTACTTTTCAATTGAAAGATGTCTCATGCCTTGTC
AAAAATCTGTCTCAACAATTGAAGAAGCAAAATAATTTAATATTAGACTACCTAGCATGTATTGCAAAATATTTTTCAGTATATACTTTGGCAAATATAGTGCTCTTTCAGTCGATTGAAAACTTGTG
ACTAGTGGAAATAGAAGTTGAGAAAGACAATAAATGAAAGTAAACAGGCTATGGACCTGAATTCCATTTAGAATAGAAAAGCTGGTATAAAACTCTTAAGAACTTAAGCAGTGAAGTGGAAAAACTAT
GCTTCACAACAAAAGAACAATTAAAAATGTATCTCATTTGAAATACGTGCTGGGGACAAATTTGAAAGAACTTAAAAAATGTTGTGTTGCAATAATACTTGGCTGATTTCTGTTTTTTGATGCTGACT
ACTGGTTCTTTTAATGAATTATTCTT

hide sequence

RefSeq Acc Id:

XM_054350983 ⟹ XP_054206958

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	4	124,637,391 - 124,685,273 (-)	NCBI


Protein RefSeqs	NP_937822	(Get FASTA)	NCBI Sequence Viewer
	XP_016864182	(Get FASTA)	NCBI Sequence Viewer
	XP_054206958	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAI28134	(Get FASTA)	NCBI Sequence Viewer
	AEP43759	(Get FASTA)	NCBI Sequence Viewer
	BAC98938	(Get FASTA)	NCBI Sequence Viewer
	EAX05261	(Get FASTA)	NCBI Sequence Viewer
	EAX05262	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000377948
	ENSP00000377948.2
	ENSP00000423369
GenBank Protein	Q96P65	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_937822 ⟸ NM_198179

- UniProtKB:

Q96P65 (UniProtKB/Swiss-Prot), G4XH69 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MQALNITPEQFSRLLRDHNLTREQFIALYRLRPLVYTPELPGRAKLALVLTGVLIFALALFGNALVFYVVTRSKAMRTVTNIFICSLALSDLLITFFCIPVTMLQNISDNWLGGAFICKMVPFVQSTA
VVTEILTMTCIAVERHQGLVHPFKMKWQYTNRRAFTMLGVVWLVAVIVGSPMWHVQQLEIKYDFLYEKEHICCLEEWTSPVHQKIYTTFILVILFLLPLMVMLILYSKIGYELWIKKRVGDGSVLRTI
HGKEMSKIARKKKRAVIMMVTVVALFAVCWAPFHVVHMMIEYSNFEKEYDDVTIKMIFAIVQIIGFSNSICNPIVYAFMNENFKKNVLSAVCYCIVNKTFSPAQRHGNSGITMMRKKAKFSLRENPVE
ETKGEAFSDGNIEVKLCEQTEEKKKLKRHLALFRSELAENSPLDSGH

hide sequence

RefSeq Acc Id:	XP_016864182 ⟸ XM_017008693
- Peptide Label:	isoform X1
- UniProtKB:	F2Z3L3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQALNITPEQFSRLLRDHNLTREQFIALYRLRPLVYTPELPGRAKLALVLTGVLIFALALFGNA LVFYVVTRSKAMRTVTNIFICSLALSDLLITFFCIPVTMLQNISDNWLGGAFICKMVPFVQSTAVVTEILTMTCIAVERHQGLVHPFKMKWQYTNRRAFTMLGVVWLVAVIVGSPMWHVQQLEALP hide sequence

Ensembl Acc Id:

ENSP00000335610 ⟸ ENST00000334383

Ensembl Acc Id:

ENSP00000423369 ⟸ ENST00000507331

Ensembl Acc Id:

ENSP00000377948 ⟸ ENST00000394427

Protein Domains

G-protein coupled receptors family 1 profile

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96P65-F1-model_v2	AlphaFold	Q96P65	1-431	view protein structure

RGD ID:

6868394

Promoter ID:

EPDNEW_H7362

Type:

initiation region

Name:

QRFPR_1

Description:

pyroglutamylated RFamide peptide receptor

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	121,381,052 - 121,381,112	EPDNEW

Database	Acc Id	Source(s)
COSMIC	QRFPR	COSMIC
Ensembl Genes	ENSG00000186867	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000394427	ENTREZGENE
	ENST00000394427.3	UniProtKB/Swiss-Prot
	ENST00000507331	ENTREZGENE
Gene3D-CATH	Rhodopsin 7-helix transmembrane proteins	UniProtKB/Swiss-Prot
GTEx	ENSG00000186867	GTEx
HGNC ID	HGNC:15565	ENTREZGENE
Human Proteome Map	QRFPR	Human Proteome Map
InterPro	GPCR_Rhodpsn	UniProtKB/Swiss-Prot
	GPCR_Rhodpsn_7TM	UniProtKB/Swiss-Prot
	NPY_rcpt	UniProtKB/Swiss-Prot
KEGG Report	hsa:84109	UniProtKB/Swiss-Prot
NCBI Gene	84109	ENTREZGENE
OMIM	606925	OMIM
PANTHER	LEUCOKININ RECEPTOR-RELATED	UniProtKB/Swiss-Prot
	PYROGLUTAMYLATED RFAMIDE PEPTIDE RECEPTOR	UniProtKB/Swiss-Prot
Pfam	7tm_1	UniProtKB/Swiss-Prot
PharmGKB	PA164725243	PharmGKB
PRINTS	GPCRRHODOPSN	UniProtKB/Swiss-Prot
	NRPEPTIDEYR	UniProtKB/Swiss-Prot
PROSITE	G_PROTEIN_RECEP_F1_1	UniProtKB/Swiss-Prot
	G_PROTEIN_RECEP_F1_2	UniProtKB/Swiss-Prot
Superfamily-SCOP	Family A G protein-coupled receptor-like	UniProtKB/Swiss-Prot
UniProt	A1A4W1_HUMAN	UniProtKB/TrEMBL
	F2Z3L3	ENTREZGENE, UniProtKB/TrEMBL
	G4XH69	ENTREZGENE, UniProtKB/TrEMBL
	J3KNR3_HUMAN	UniProtKB/TrEMBL
	Q96P65	ENTREZGENE, UniProtKB/Swiss-Prot

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


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


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