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    ADAM3A ADAM metallopeptidase domain 3A (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 1587, updated on 2-Apr-2017
    Official Symbol
    ADAM3Aprovided by HGNC
    Official Full Name
    ADAM metallopeptidase domain 3A (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:209
    See related
    Ensembl:ENSG00000197475
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ADAM3; CYRN1; tMDCI
    Location:
    8p11.22
    Exon count:
    22
    Annotation release Status Assembly Chr Location
    108 current GRCh38.p7 (GCF_000001405.33) 8 NC_000008.11 (39451045..39522989, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (39308564..39380508, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene lysine acetyltransferase 2B pseudogene Neighboring gene ADAM metallopeptidase domain 5 (pseudogene) Neighboring gene ADAM metallopeptidase domain 3A-like Neighboring gene ADAM metallopeptidase domain 18

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Markers

    Other Names

    • a disintegrin and metalloproteinase domain 3a (cyritestin 1)
    • cyritestin 1

    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.

    RNA

    1. NR_001569.3 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate internal exon, compared to variant 4.
      Source sequence(s)
      AC106011, AJ005372, BG717260, HY234081, X89654
      Related
      ENST00000495171.6
    2. NR_024106.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) lacks an alternate internal exon, compared to variant 4.
      Source sequence(s)
      AC106011, AK308250, BG717260, HY234081, X89655
      Related
      ENST00000481351.6
    3. NR_024107.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) uses an alternate internal splice site, compared to variant 4.
      Source sequence(s)
      AC106011, AC123767, BC025386, BG717260, HY234081, X89654
      Related
      ENST00000460383.6
    4. NR_073423.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) represents the longest variant.
      Source sequence(s)
      AC106011, AC123767, BC025386, BG717260, HY234081, X89657
      Related
      ENST00000490268.6

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108 details...Open this link in a new tab

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

    Reference GRCh38.p7 Primary Assembly

    Genomic

    1. NC_000008.11 Reference GRCh38.p7 Primary Assembly

      Range
      39451045..39522989 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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