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    ADAM1A ADAM metallopeptidase domain 1A (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 8759, updated on 23-Nov-2021

    Summary

    Official Symbol
    ADAM1Aprovided by HGNC
    Official Full Name
    ADAM metallopeptidase domain 1A (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:187
    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
    Ftna; ADAM1; FTNAP; ADAM1P; PH-30a
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    Genomic context

    See ADAM1A in Genome Data Viewer
    Location:
    12q24.12-q24.13
    Annotation release Status Assembly Chr Location
    109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (111899063..111901902)
    105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (112336867..112339706)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene MAPKAPK5 antisense RNA 1 Neighboring gene MAPK activated protein kinase 5 Neighboring gene ribosomal protein S2 pseudogene 41 Neighboring gene transmembrane protein 116 Neighboring gene ADAM metallopeptidase domain 1B (pseudogene) Neighboring gene solute carrier family 25 member 3 pseudogene 2

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Other Names

    • ADAM metallopeptidase domain 1 (fertilin alpha) pseudogene
    • ADAM metallopeptidase domain 1, pseudogene
    • a disintegrin and metalloproteinase domain 1 ( fertilin alpha)
    • a disintegrin and metalloproteinase domain 1 (fertilin alpha) pseudogene
    • fertilin alpha

    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.

    Genomic

    1. NG_065830.1 

      Range
      101..2940
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

      Range
      111899063..111901902
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_001216.2: Suppressed sequence

      Description
      NG_001216.2: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene rather than a non-transcribed pseudogene and should be represented by an NR_ accession prefix rather than an NG_ accession prefix.
    2. NG_024128.1: Suppressed sequence

      Description
      NG_024128.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
    3. NR_036636.1: Suppressed sequence

      Description
      NR_036636.1: This RefSeq was removed because there is insufficient evidence that this locus is transcribed.
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