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    LOC100420118 transmembrane protein 132C pseudogene [ Homo sapiens (human) ]

    Gene ID: 100420118, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC100420118
    Gene description
    transmembrane protein 132C pseudogene
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    See LOC100420118 in Genome Data Viewer
    Location:
    12q24.32
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (126195019..126195657)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (126203810..126204448)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (126679565..126680203)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2826 Neighboring gene uncharacterized LOC105370056 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:126535879-126537078 Neighboring gene NANOG hESC enhancer GRCh37_chr12:126592791-126593330 Neighboring gene long intergenic non-protein coding RNA 2359 Neighboring gene uncharacterized LOC107984447 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr12:126717441-126718421 Neighboring gene NANOG hESC enhancer GRCh37_chr12:126727348-126727849 Neighboring gene uncharacterized LOC105379613 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:126835877-126836032 Neighboring gene uncharacterized LOC101927531

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    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_024134.1 

      Range
      101..739
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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
      126195019..126195657
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      126203810..126204448
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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