OR5H15 (olfactory receptor family 5 subfamily H member 15)

Advanced Search (OLGA)

Gene: OR5H15 (olfactory receptor family 5 subfamily H member 15) Homo sapiens

Analyze

Symbol:

OR5H15

Name:

olfactory receptor family 5 subfamily H member 15

RGD ID:

1344642

HGNC Page

HGNC:31287

Description:

Predicted to enable odorant binding activity and olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and detection of chemical stimulus involved in sensory perception of smell. Predicted to be located in plasma membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

olfactory receptor 5H15; olfactory receptor, family 5, subfamily H, member 15

RGD Orthologs

Mouse

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	3	98,166,696 - 98,169,774 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	98,166,696 - 98,169,774 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	97,885,540 - 97,888,618 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	99,370,234 - 99,371,175 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	99,370,233 - 99,371,175	NCBI
Celera	3	96,277,330 - 96,278,271 (+)	NCBI		Celera
Cytogenetic Map	3	q11.2	NCBI
HuRef	3	95,257,464 - 95,258,405 (+)	NCBI		HuRef
CHM1_1	3	97,850,566 - 97,851,507 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	100,870,429 - 100,873,507 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dichloroethane (ISO)

benzo[a]pyrene (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

detection of chemical stimulus involved in sensory perception of smell (IEA)

G protein-coupled receptor signaling pathway (IEA)

sensory perception of smell (IEA)

Cellular Component

membrane (IEA)

plasma membrane (IEA)

Molecular Function

G protein-coupled receptor activity (IEA)

odorant binding (IBA)

olfactory receptor activity (IBA,IEA)

References

References - curated

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

Additional References at PubMed

PMID:21873635	PMID:32126975

Genomics

Comparative Map Data

OR5H15
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	98,166,696 - 98,169,774 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	98,166,696 - 98,169,774 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	97,885,540 - 97,888,618 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	99,370,234 - 99,371,175 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	99,370,233 - 99,371,175	NCBI
Celera	3	96,277,330 - 96,278,271 (+)	NCBI		Celera
Cytogenetic Map	3	q11.2	NCBI
HuRef	3	95,257,464 - 95,258,405 (+)	NCBI		HuRef
CHM1_1	3	97,850,566 - 97,851,507 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	100,870,429 - 100,873,507 (+)	NCBI		T2T-CHM13v2.0

Or5h17
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	16	58,749,781 - 58,820,979 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	16	58,815,720 - 58,821,804 (+)	Ensembl		GRCm39 Ensembl
GRCm38	16	58,929,418 - 59,000,616 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	16	58,995,357 - 59,001,441 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	16	58,995,230 - 59,000,442 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	16	58,941,943 - 58,942,872 (+)	NCBI		MGSCv36	mm8
Celera	16	59,346,271 - 59,351,476 (+)	NCBI		Celera
Cytogenetic Map	16	C1.2- C1.3	NCBI
cM Map	16	34.83	NCBI

Variants

Variants in OR5H15
29 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3q11.1-21.1(chr3:93886671-123216683)x1	copy number loss	See cases [RCV000051543]	Chr3:93886671..123216683 [GRCh38] Chr3:93605515..122935530 [GRCh37] Chr3:95088205..124418220 [NCBI36] Chr3:3q11.1-21.1	pathogenic
NM_001005515.1(OR5H15):c.69G>A (p.Trp23Ter)	single nucleotide variant	Malignant melanoma [RCV000066217]	Chr3:98168768 [GRCh38] Chr3:97887612 [GRCh37] Chr3:99370302 [NCBI36] Chr3:3q11.2	not provided
NM_001005515.1(OR5H15):c.691G>A (p.Asp231Asn)	single nucleotide variant	Malignant melanoma [RCV000066219]	Chr3:98169390 [GRCh38] Chr3:97888234 [GRCh37] Chr3:99370924 [NCBI36] Chr3:3q11.2	not provided
NM_001005515.1(OR5H15):c.548C>T (p.Pro183Leu)	single nucleotide variant	Malignant melanoma [RCV000060881]	Chr3:98169247 [GRCh38] Chr3:97888091 [GRCh37] Chr3:99370781 [NCBI36] Chr3:3q11.2	not provided
GRCh38/hg38 3q11.1-13.31(chr3:93819623-116887056)x1	copy number loss	See cases [RCV000135320]	Chr3:93819623..116887056 [GRCh38] Chr3:93538467..116605903 [GRCh37] Chr3:95021157..118088593 [NCBI36] Chr3:3q11.1-13.31	pathogenic
GRCh38/hg38 3q11.2-13.31(chr3:97795369-115663349)x1	copy number loss	See cases [RCV000138186]	Chr3:97795369..115663349 [GRCh38] Chr3:97514213..115382196 [GRCh37] Chr3:98996903..116864886 [NCBI36] Chr3:3q11.2-13.31	pathogenic\|uncertain significance
GRCh38/hg38 3q11.2(chr3:98023760-98332789)x1	copy number loss	See cases [RCV000138146]	Chr3:98023760..98332789 [GRCh38] Chr3:97742604..98051633 [GRCh37] Chr3:99225294..99534323 [NCBI36] Chr3:3q11.2	likely benign
GRCh38/hg38 3q11.1-24(chr3:93800620-145695381)x3	copy number gain	See cases [RCV000142340]	Chr3:93800620..145695381 [GRCh38] Chr3:93519464..145413168 [GRCh37] Chr3:95002154..146895858 [NCBI36] Chr3:3q11.1-24	pathogenic
GRCh38/hg38 3q11.1-13.11(chr3:93819623-103888749)x3	copy number gain	See cases [RCV000143259]	Chr3:93819623..103888749 [GRCh38] Chr3:93538467..103607593 [GRCh37] Chr3:95021157..105090283 [NCBI36] Chr3:3q11.1-13.11	likely pathogenic\|uncertain significance
GRCh37/hg19 3q11.2(chr3:96575117-98212517)x3	copy number gain	See cases [RCV000448437]	Chr3:96575117..98212517 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh37/hg19 3q11.2(chr3:96579273-98216225)x3	copy number gain	See cases [RCV000510411]	Chr3:96579273..98216225 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	copy number gain	See cases [RCV000511055]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	copy number gain	See cases [RCV000512358]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
NM_001005515.2(OR5H15):c.898T>G (p.Ser300Ala)	single nucleotide variant	not specified [RCV004298593]	Chr3:98169597 [GRCh38] Chr3:97888441 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh37/hg19 3q11.2(chr3:97650137-98174233)x3	copy number gain	See cases [RCV000512476]	Chr3:97650137..98174233 [GRCh37] Chr3:3q11.2	uncertain significance
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
GRCh37/hg19 3q11.2(chr3:97866177-97888337)x3	copy number gain	not provided [RCV000742636]	Chr3:97866177..97888337 [GRCh37] Chr3:3q11.2	benign
GRCh37/hg19 3q11.2(chr3:96850456-97974150)x3	copy number gain	not provided [RCV001005454]	Chr3:96850456..97974150 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh37/hg19 3q11.2-12.1(chr3:97606054-98499715)x3	copy number gain	not provided [RCV001005456]	Chr3:97606054..98499715 [GRCh37] Chr3:3q11.2-12.1	uncertain significance
GRCh37/hg19 3q11.2-12.3(chr3:95563096-102371126)x1	copy number loss	not provided [RCV001259224]	Chr3:95563096..102371126 [GRCh37] Chr3:3q11.2-12.3	likely pathogenic
GRCh37/hg19 3p13-q12.1(chr3:72488757-99614758)x3	copy number gain	not provided [RCV002221455]	Chr3:72488757..99614758 [GRCh37] Chr3:3p13-q12.1	likely pathogenic
GRCh37/hg19 3q11.2(chr3:97283117-98218677)x3	copy number gain	not provided [RCV002475836]	Chr3:97283117..98218677 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.410C>T (p.Thr137Ile)	single nucleotide variant	not provided [RCV004695337]\|not specified [RCV004079266]	Chr3:98169109 [GRCh38] Chr3:97887953 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.931G>C (p.Val311Leu)	single nucleotide variant	not specified [RCV004235852]	Chr3:98169630 [GRCh38] Chr3:97888474 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.314C>T (p.Ala105Val)	single nucleotide variant	not specified [RCV004239504]	Chr3:98169013 [GRCh38] Chr3:97887857 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.98T>C (p.Val33Ala)	single nucleotide variant	not specified [RCV004157127]	Chr3:98168797 [GRCh38] Chr3:97887641 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.17C>A (p.Ala6Glu)	single nucleotide variant	not specified [RCV004160861]	Chr3:98168716 [GRCh38] Chr3:97887560 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.364C>T (p.Arg122Cys)	single nucleotide variant	not specified [RCV004124884]	Chr3:98169063 [GRCh38] Chr3:97887907 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.320G>C (p.Gly107Ala)	single nucleotide variant	not specified [RCV004092968]	Chr3:98169019 [GRCh38] Chr3:97887863 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.774G>A (p.Met258Ile)	single nucleotide variant	not specified [RCV004262879]	Chr3:98169473 [GRCh38] Chr3:97888317 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.457A>C (p.Ile153Leu)	single nucleotide variant	not specified [RCV004258125]	Chr3:98169156 [GRCh38] Chr3:97888000 [GRCh37] Chr3:3q11.2	likely benign
NM_001005515.2(OR5H15):c.740C>G (p.Ser247Cys)	single nucleotide variant	not specified [RCV004297084]	Chr3:98169439 [GRCh38] Chr3:97888283 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.209A>G (p.Asp70Gly)	single nucleotide variant	not specified [RCV004327725]	Chr3:98168908 [GRCh38] Chr3:97887752 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh38/hg38 3q11.1-21.2(chr3:93979547-124774010)x1	copy number loss	Chromosome 3q13.31 deletion syndrome [RCV003327614]	Chr3:93979547..124774010 [GRCh38] Chr3:3q11.1-21.2	pathogenic
NM_001005515.2(OR5H15):c.335G>A (p.Cys112Tyr)	single nucleotide variant	not specified [RCV004355706]	Chr3:98169034 [GRCh38] Chr3:97887878 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.286G>C (p.Glu96Gln)	single nucleotide variant	not specified [RCV004339343]	Chr3:98168985 [GRCh38] Chr3:97887829 [GRCh37] Chr3:3q11.2	uncertain significance
GRCh37/hg19 3q11.2(chr3:97542156-98076080)x1	copy number loss	not provided [RCV003485395]	Chr3:97542156..98076080 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.598T>C (p.Phe200Leu)	single nucleotide variant	not provided [RCV003437927]	Chr3:98169297 [GRCh38] Chr3:97888141 [GRCh37] Chr3:3q11.2	likely benign
GRCh37/hg19 3q11.1-12.3(chr3:93519465-101464485)x3	copy number gain	not specified [RCV003986472]	Chr3:93519465..101464485 [GRCh37] Chr3:3q11.1-12.3	uncertain significance
GRCh37/hg19 3q11.2(chr3:96308168-98033912)x1	copy number loss	See cases [RCV004442802]	Chr3:96308168..98033912 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.700G>A (p.Val234Ile)	single nucleotide variant	not specified [RCV004499628]	Chr3:98169399 [GRCh38] Chr3:97888243 [GRCh37] Chr3:3q11.2	likely benign
NM_001005515.2(OR5H15):c.235C>T (p.Pro79Ser)	single nucleotide variant	not specified [RCV004499621]	Chr3:98168934 [GRCh38] Chr3:97887778 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.649T>C (p.Ser217Pro)	single nucleotide variant	not specified [RCV004499626]	Chr3:98169348 [GRCh38] Chr3:97888192 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.899C>T (p.Ser300Leu)	single nucleotide variant	not specified [RCV004499630]	Chr3:98169598 [GRCh38] Chr3:97888442 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.521T>C (p.Val174Ala)	single nucleotide variant	not specified [RCV004499624]	Chr3:98169220 [GRCh38] Chr3:97888064 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.589C>G (p.Leu197Val)	single nucleotide variant	not specified [RCV004499625]	Chr3:98169288 [GRCh38] Chr3:97888132 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.658T>C (p.Phe220Leu)	single nucleotide variant	not specified [RCV004499627]	Chr3:98169357 [GRCh38] Chr3:97888201 [GRCh37] Chr3:3q11.2	likely benign
NM_001005515.2(OR5H15):c.82T>C (p.Phe28Leu)	single nucleotide variant	not specified [RCV004499629]	Chr3:98168781 [GRCh38] Chr3:97887625 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.508A>G (p.Asn170Asp)	single nucleotide variant	not specified [RCV004499623]	Chr3:98169207 [GRCh38] Chr3:97888051 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.905T>C (p.Ile302Thr)	single nucleotide variant	not specified [RCV004499631]	Chr3:98169604 [GRCh38] Chr3:97888448 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.480A>T (p.Glu160Asp)	single nucleotide variant	not specified [RCV004499622]	Chr3:98169179 [GRCh38] Chr3:97888023 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.115A>G (p.Ile39Val)	single nucleotide variant	not specified [RCV004647789]	Chr3:98168814 [GRCh38] Chr3:97887658 [GRCh37] Chr3:3q11.2	uncertain significance
NM_001005515.2(OR5H15):c.689C>G (p.Ser230Cys)	single nucleotide variant	not specified [RCV004646517]	Chr3:98169388 [GRCh38] Chr3:97888232 [GRCh37] Chr3:3q11.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	61
Count of miRNA genes:	61
Interacting mature miRNAs:	61
Transcripts:	ENST00000356526
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.

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	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system
9	43	38	31	42	14	20	5	28	5	23	110	92	1	30	9	89	12

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001005515	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC117460	(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

Ensembl Acc Id:

ENST00000383696 ⟹ ENSP00000373196

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	98,168,700 - 98,169,733 (+)	Ensembl

Ensembl Acc Id:

ENST00000641450 ⟹ ENSP00000493082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	98,166,696 - 98,169,774 (+)	Ensembl

RefSeq Acc Id:

NM_001005515 ⟹ NP_001005515

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	98,166,696 - 98,169,774 (+)	NCBI
GRCh37	3	97,887,544 - 97,888,485 (+)	RGD
Build 36	3	99,370,234 - 99,371,175 (+)	NCBI Archive
Celera	3	96,277,330 - 96,278,271 (+)	RGD
HuRef	3	95,257,464 - 95,258,405 (+)	ENTREZGENE
CHM1_1	3	97,850,566 - 97,851,507 (+)	NCBI
T2T-CHM13v2.0	3	100,870,429 - 100,873,507 (+)	NCBI

Sequence:

show sequence

AATGAAACCTTCAAAAAGCATGAGTACGTAATGAATGGCTACCTGTGTTATTGACATTGCTGTG
CTACTGTATGTATTTCGGTTTTAGAAGGCGTAACACATTTAAAGGATATCCACAATTTCCTTCA
AAATATAGAGGACATGCAGTGAGGACATGGAAGAGGAAAATGCAACATTGCTGACAGAGTTTGT
TCTCACAGGATTTTTATATCAACCACAGTGGAAAATACCCCTGTTCTTGGCATTCTTGGTAATA
TATCTCATCACCATCATGGGGAATCTTGGTCTGATTGCTGTCATCTGGAAAGACCCTCACCTTC
ATATCCCAATGTACTTACTCCTTGGGAATTTAGCTTTTGTGGATGCTTGGATATCATCCACAGT
GACCCCAAAGATGCTGAATAACTTCTTAGCTAAGAGTAAGATGATATCTCTCTCTGAATGCAAG
ATACAATTTTTTTCCATTGCAATTGGCGTAACCACAGAATGTTTTCTCTTGGCAACAATGGCAT
ATGATCGCTATGTAGCCATATGCAAACCTTTACTTTATCCAGCCATTATGACCAATGGACTGTG
CATCCGGCTATTAATCTTGTCATATATAGCTGGTATTCTTCATGCTTTAATCCATGAAGGATTT
TTATTCAGACTAACCTTCTGTAACTCCAACATAGTACATCACATTTACTGTGACACTATCCCAT
TGTCTAAGATTTCTTGTACTGATTCTTCTATTAATTTTCTAATGGTTTTTATTTTCTCAGGTTC
AATTCAGGTATTCAGCATTGTGACTATTCTTATATCTTACACATTTGTTCTCTTCACAGTCTTA
GAAAAGAAATCTGATAAGGGTGTAAGGAAAGCCTTTTCCACCTGTGGAGCCCATCTCTTCTCTG
TCTGTTTATACTATGGCCCCCTTCTCTTAATGTATGTGGGCCCTGCATCTCCGCAAGCAGATGG
TCAAAATATGGTGGAGCCTCTATTCTACACTGTCATCATTCCTTTGTTAAATCCTATCATCTAC
AGTCTGAGAAATAAGCAAGTCATAGTTTCATTCATAAAAATGTTAAAAAGAAATGTTAAGGTTT
CATACTAATATCCTTTTTCTATTTACTAAAATAGTCACAAAATTACGCAAGTTAGAGGTACCTA
TGTTGTTTCCAGTGTTCAAACATTTTTGCAAGTATAACTGTCCTAGCACTTTAATGACCTAACA
TTTTAGTACCTAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001005515	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	A6NDH6	(Get FASTA)	NCBI Sequence Viewer
	EAW79867	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000493082
	ENSP00000493082.1

RefSeq Acc Id:

NP_001005515 ⟸ NM_001005515

- UniProtKB:

A6NDH6 (UniProtKB/Swiss-Prot), A0A126GW64 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MEEENATLLTEFVLTGFLYQPQWKIPLFLAFLVIYLITIMGNLGLIAVIWKDPHLHIPMYLLLG
NLAFVDAWISSTVTPKMLNNFLAKSKMISLSECKIQFFSIAIGVTTECFLLATMAYDRYVAICK
PLLYPAIMTNGLCIRLLILSYIAGILHALIHEGFLFRLTFCNSNIVHHIYCDTIPLSKISCTDS
SINFLMVFIFSGSIQVFSIVTILISYTFVLFTVLEKKSDKGVRKAFSTCGAHLFSVCLYYGPLL
LMYVGPASPQADGQNMVEPLFYTVIIPLLNPIIYSLRNKQVIVSFIKMLKRNVKVSY

hide sequence

Ensembl Acc Id:

ENSP00000493082 ⟸ ENST00000641450

Ensembl Acc Id:

ENSP00000373196 ⟸ ENST00000383696

Protein Domains

G-protein coupled receptors family 1 profile

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-A6NDH6-F1-model_v2	AlphaFold	A6NDH6	1-313	view protein structure

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:31287	AgrOrtholog
COSMIC	OR5H15	COSMIC
Ensembl Genes	ENSG00000233412	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000641450	ENTREZGENE
	ENST00000641450.1	UniProtKB/Swiss-Prot
Gene3D-CATH	Rhodopsin 7-helix transmembrane proteins	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000233412	GTEx
HGNC ID	HGNC:31287	ENTREZGENE
Human Proteome Map	OR5H15	Human Proteome Map
InterPro	GPCR_Rhodpsn	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	GPCR_Rhodpsn_7TM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Olfact_rcpt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Olfactory_GPCR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:403274	UniProtKB/Swiss-Prot
NCBI Gene	403274	ENTREZGENE
PANTHER	OLFACTORY RECEPTOR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	OLFACTORY RECEPTOR 5H1	UniProtKB/TrEMBL
	OLFACTORY RECEPTOR 5H15	UniProtKB/Swiss-Prot
Pfam	7tm_4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134956122	PharmGKB
PRINTS	GPCRRHODOPSN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	OLFACTORYR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	G_PROTEIN_RECEP_F1_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	G_PROTEIN_RECEP_F1_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Family A G protein-coupled receptor-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A126GW64	ENTREZGENE, UniProtKB/TrEMBL
	A6NDH6	ENTREZGENE, UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-12-15	OR5H15	olfactory receptor family 5 subfamily H member 15		olfactory receptor, family 5, subfamily H, member 15	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)

Send us a Message