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    WHAMMP1 WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100288615, updated on 15-Jun-2019

    Summary

    Official Symbol
    WHAMMP1provided by HGNC
    Official Full Name
    WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:32361
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    WHDC1P1
    Expression
    Ubiquitous expression in bone marrow (RPKM 17.2), lymph node (RPKM 8.4) and 24 other tissues See more

    Genomic context

    See WHAMMP1 in Genome Data Viewer
    Location:
    15q13.3
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    109 current GRCh38.p12 (GCF_000001405.38) 15 NC_000015.10 (32519848..32533741, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (32812049..32825942, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene golgin subfamily A member 6-like protein 1 Neighboring gene U3 small nucleolar ribonucleoprotein protein MPP10-like Neighboring gene uncharacterized LOC107987222 Neighboring gene long intergenic non-protein coding RNA 2256 Neighboring gene uncharacterized LOC101928042 Neighboring gene 15q13 distal microdeletion recombination region Neighboring gene golgin A8 family member N Neighboring gene RNA, 7SL, cytoplasmic 286, pseudogene

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Markers

    Other Names

    • WAS protein homology region 2 domain containing 1 pseudogene 1

    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.

    RNA

    1. NR_036650.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC135983, BC117556, BI910970, BX643549, CA841617

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

      Range
      32519848..32533741 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 PATCHES

    Genomic

    1. NW_011332701.1 Reference GRCh38.p13 PATCHES

      Range
      4571964..4585870 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 PATCHES

    Genomic

    1. NW_012132920.1 Reference GRCh38.p13 PATCHES

      Range
      2038218..2052100 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p13 ALT_REF_LOCI_2

    Genomic

    1. NT_187660.1 Reference GRCh38.p13 ALT_REF_LOCI_2

      Range
      4734416..4748322 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_022106.1: Suppressed sequence

      Description
      NG_022106.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
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