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    EPS15P1 epidermal growth factor receptor pathway substrate 15 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 55380, updated on 10-Oct-2023

    Summary

    Official Symbol
    EPS15P1provided by HGNC
    Official Full Name
    epidermal growth factor receptor pathway substrate 15 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:18166
    See related
    AllianceGenome:HGNC:18166
    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
    EPS15L2; PRO1866
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    Genomic context

    Location:
    7p12.3
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (46781990..46783420)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (46943391..46944820)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (46821588..46823018)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:46690590-46691789 Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 19 Neighboring gene uncharacterized LOC730338 Neighboring gene uncharacterized LOC124901626 Neighboring gene uncharacterized LOC105375267

    Genomic regions, transcripts, and products

    Phenotypes

    EBI GWAS Catalog

    Description
    Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    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_008280.3 

      Range
      101..1531
      Download
      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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      46781990..46783420
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      46943391..46944820
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_018510.1: Suppressed sequence

      Description
      NM_018510.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.