Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
282763
Gene name Gene Name - the full gene name approved by the HGNC.
Olfactory receptor family 51 subfamily B member 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OR51B5
Synonyms (NCBI Gene) Gene synonyms aliases
HOR5'Beta5, OR11-37
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.4
Summary Summary of gene provided in NCBI Entrez Gene.
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from sing
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018015 hsa-miR-335-5p Microarray 18185580
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004984 Function Olfactory receptor activity IBA 21873635
GO:0004984 Function Olfactory receptor activity NAS 11121057
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q9H339
Protein name Olfactory receptor 51B5 (Odorant receptor HOR5'beta5) (Olfactory receptor OR11-37)
Protein function Odorant receptor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13853 7tm_4 29 308 Olfactory receptor Family
Sequence
Sequence length 312
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Olfactory transduction   Olfactory Signaling Pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia, Sickle Cell rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
23406172
Unknown
Disease term Disease name Evidence References Source
Mastocytosis Mastocytosis GWAS
Cutaneous mastocytosis Cutaneous mastocytosis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Age Related Hearing Impairment 1 Associate 34337005
Anemia Sickle Cell Associate 37895268