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    HTR5BP 5-hydroxytryptamine receptor 5B, pseudogene [ Homo sapiens (human) ]

    Gene ID: 645694, updated on 17-Jun-2019

    Summary

    Official Symbol
    HTR5BPprovided by HGNC
    Official Full Name
    5-hydroxytryptamine receptor 5B, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:16291
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HTR5B; 5-HT5B; GPR134

    Genomic context

    See HTR5BP in Genome Data Viewer
    Location:
    2q14.1
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (117859427..117903680)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (118617003..118661256)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 195 Neighboring gene uncharacterized LOC107985939 Neighboring gene DEAD-box helicase 18 Neighboring gene uncharacterized LOC101929908 Neighboring gene coiled-coil domain containing 93 Neighboring gene RNA, 7SL, cytoplasmic 111, pseudogene

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Pathways from BioSystems

    General gene information

    Markers

    Other Names

    • 5-hydroxytryptamine (serotonin) receptor 5 pseudogene
    • 5-hydroxytryptamine (serotonin) receptor 5A pseudogene
    • 5-hydroxytryptamine (serotonin) receptor 5B, pseudogene
    • G protein-coupled receptor 134

    NCBI Reference Sequences (RefSeq)

    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.

    Genomic

    1. NG_008325.1 

      Range
      101..44354
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

      Range
      117859427..117903680
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NR_003947.1: Suppressed sequence

      Description
      NR_003947.1: This RefSeq was permanently suppressed because there is insufficient evidence that this locus is transcribed.
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