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    LOC100533628 WD repeat domain 75 pseudogene [ Homo sapiens (human) ]

    Gene ID: 100533628, updated on 10-Oct-2023

    Summary

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    Gene symbol
    LOC100533628
    Gene description
    WD repeat domain 75 pseudogene
    See related
    Ensembl:ENSG00000258385
    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 LOC100533628 in Genome Data Viewer
    Location:
    14q21.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (41296410..41298686)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (35487298..35489574)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (41765613..41767889)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370467 Neighboring gene NANOG hESC enhancer GRCh37_chr14:41328024-41328794 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr14:41423413-41423986 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:41423987-41424559 Neighboring gene long intergenic non-protein coding RNA 2315 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:41613785-41614285 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:41872411-41873214 Neighboring gene NANOG hESC enhancer GRCh37_chr14:41873331-41873866 Neighboring gene NANOG hESC enhancer GRCh37_chr14:41974655-41975156 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:41984914-41985504 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:42009653-42010250 Neighboring gene small nucleolar RNA SNORA31 Neighboring gene LRFN5 divergent transcript

    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_028872.1 

      Range
      101..2377
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      41296410..41298686
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      35487298..35489574
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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