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OR6C65 olfactory receptor family 6 subfamily C member 65 [ Homo sapiens (human) ]

Gene ID: 403282, updated on 5-Mar-2024

Summary

Official Symbol
OR6C65provided by HGNC
Official Full Name
olfactory receptor family 6 subfamily C member 65provided by HGNC
Primary source
HGNC:HGNC:31295
See related
Ensembl:ENSG00000205328 AllianceGenome:HGNC:31295
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
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 single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
Orthologs
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Genomic context

See OR6C65 in Genome Data Viewer
Location:
12q13.2
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (55400529..55401467)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (55367089..55368027)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (55794313..55795251)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 6 subfamily C member 66 pseudogene Neighboring gene olfactory receptor family 6 subfamily C member 73 pseudogene Neighboring gene polyhomeotic homolog 1 pseudogene 1 Neighboring gene olfactory receptor family 6 subfamily C member 76

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
EBI GWAS Catalog

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001005518.1NP_001005518.1  olfactory receptor 6C65

    See identical proteins and their annotated locations for NP_001005518.1

    Status: VALIDATED

    Source sequence(s)
    AC125816
    Consensus CDS
    CCDS31821.1
    UniProtKB/Swiss-Prot
    A6NJZ3, B2RNH9
    UniProtKB/TrEMBL
    A0A126GW71
    Related
    ENSP00000368986.2, ENST00000379665.3
    Conserved Domains (2) summary
    pfam00001
    Location:39288
    7tm_1; 7 transmembrane receptor (rhodopsin family)
    cl21561
    Location:33299
    7tm_4; Olfactory receptor

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    55400529..55401467
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    55367089..55368027
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)