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    LOC100129687 C-x9-C motif containing 2 pseudogene [ Homo sapiens (human) ]

    Gene ID: 100129687, updated on 29-Mar-2018

    Summary

    Gene symbol
    LOC100129687
    Gene description
    C-x9-C motif containing 2 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

    Genomic context

    See LOC100129687 in Genome Data Viewer
    Location:
    15q13.1
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 15 NC_000015.10 (28830966..28831182, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (29076112..29076328, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene zinc finger FYVE-type containing 9 pseudogene Neighboring gene Dexi homolog (mouse) pseudogene Neighboring gene PDCD6IP pseudogene 2 Neighboring gene golgin A6 family like 7 Neighboring gene ferritin light chain pseudogene 11

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    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_030229.1 

      Range
      101..317
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

    Reference GRCh38.p12 Primary Assembly

    Genomic

    1. NC_000015.10 Reference GRCh38.p12 Primary Assembly

      Range
      28830966..28831182 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p12 PATCHES

    Genomic

    1. NW_011332701.1 Reference GRCh38.p12 PATCHES

      Range
      992969..993185 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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