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    OR6C76 olfactory receptor family 6 subfamily C member 76 [ Homo sapiens (human) ]

    Gene ID: 390326, updated on 27-Nov-2024

    Summary

    Official Symbol
    OR6C76provided by HGNC
    Official Full Name
    olfactory receptor family 6 subfamily C member 76provided by HGNC
    Primary source
    HGNC:HGNC:31305
    See related
    Ensembl:ENSG00000185821 AllianceGenome:HGNC:31305
    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. [provided by RefSeq, Jul 2008]
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    Genomic context

    See OR6C76 in Genome Data Viewer
    Location:
    12q13.2
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (55426254..55427192)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (55392802..55393761)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (55820038..55820976)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 6 subfamily C member 65 Neighboring gene polyhomeotic homolog 1 pseudogene 1 Neighboring gene uncharacterized LOC124902940 Neighboring gene olfactory receptor family 6 subfamily C member 2 Neighboring gene olfactory receptor family 6 subfamily C member 70

    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

    General gene information

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables G protein-coupled receptor activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables olfactory receptor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    located_in plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     

    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_001005183.1NP_001005183.1  olfactory receptor 6C76 isoform 1

      See identical proteins and their annotated locations for NP_001005183.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the allele encoded by the GRCh38 reference genome and encodes isoform (1).
      Source sequence(s)
      AC125816
      Consensus CDS
      CCDS31823.1
      UniProtKB/Swiss-Prot
      A6NM76
      UniProtKB/TrEMBL
      A0A126GW16
      Related
      ENSP00000328402.3, ENST00000328314.3
      Conserved Domains (2) summary
      pfam00001
      Location:39287
      7tm_1; 7 transmembrane receptor (rhodopsin family)
      cl21561
      Location:31302
      7tm_4; Olfactory receptor
    2. NM_001412214.1NP_001399143.1  olfactory receptor 6C76 isoform 2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) represents the allele encoded by the T2T-CHM13v2.0 genome assembly. The encoded isoform (2) has a frameshifted C-terminus compared to isoform 1.
      Source sequence(s)
      CP068266

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    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
      55426254..55427192
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      55392802..55393761
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)