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    GCOM2 GRINL1B complex locus 2 (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 339970, updated on 5-Nov-2017
    Official Symbol
    GCOM2provided by HGNC
    Official Full Name
    GRINL1B complex locus 2 (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:15712
    See related
    MIM:608311
    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
    GLURR2; GRINL1B
    Location:
    4q13.2
    Annotation release Status Assembly Chr Location
    108 current GRCh38.p7 (GCF_000001405.33) 4 NC_000004.12 (68038416..68042511)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (68904134..68908238)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene transmembrane protease, serine 11G, pseudogene Neighboring gene RNA, U6 small nuclear 95, pseudogene Neighboring gene transmembrane protease, serine 11F Neighboring gene uncharacterized LOC550113 Neighboring gene synaptotagmin 14 pseudogene 1 Neighboring gene solute carrier family 47 member 2 pseudogene

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Products Interactant Other Gene Complex Source Pubs Description

    Markers

    Other Names

    • glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    molecular_function ND
    No biological Data available
    more info
     
    Process Evidence Code Pubs
    biological_process ND
    No biological Data available
    more info
     
    maintenance of ER location IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    DNA-directed RNA polymerase II, holoenzyme IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    cellular_component ND
    No biological Data available
    more info
     

    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_009901.2 

      Range
      101..4196
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108

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

    Reference GRCh38.p7 Primary Assembly

    Genomic

    1. NC_000004.12 Reference GRCh38.p7 Primary Assembly

      Range
      68038416..68042511
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.1

    Genomic

    1. NC_018915.2 Alternate CHM1_1.1

      Range
      68941140..68945235
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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