Format

Send to:

Choose Destination
    • Showing Current items.

    TAGLN2P2 transgelin 2 pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 642319, updated on 17-Jun-2019

    Summary

    Official Symbol
    TAGLN2P2provided by HGNC
    Official Full Name
    transgelin 2 pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:31039
    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 TAGLN2P2 in Genome Data Viewer
    Location:
    8p12
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 8 NC_000008.11 (30249500..30250169, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (30107021..30107635, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene dynactin subunit 6 Neighboring gene heat shock protein family A (Hsp70) member 8 pseudogene 11 Neighboring gene VISTA enhancer hs1962 Neighboring gene general transcription factor IIA subunit 2 pseudogene

    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_022383.2 

      Range
      101..770
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000008.11 Reference GRCh38.p13 Primary Assembly

      Range
      30249500..30250169 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Support Center