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Protein Coding Gene : Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1
Primary Identifier  MGI:104819 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  53379
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables pre-mRNA intronic binding activity. Acts upstream of or within negative regulation of mRNA splicing, via spliceosome and negative regulation of transcription by RNA polymerase II. Located in nucleus. Is expressed in several structures, including brain; genitourinary system; liver; lung; and spleen. Human ortholog(s) of this gene implicated in inclusion body myopathy with Paget disease of bone and frontotemporal dementia and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2. Orthologous to human HNRNPA2B1 (heterogeneous nuclear ribonucleoprotein A2/B1).
  • synonyms:
  • heterogeneous nuclear ribonucleoprotein A2,
  • heterogeneous nuclear ribonucleoprotein A2/B1,
  • MGI:1918855,
  • Hnrpa2,
  • MGD-MRK-28113,
  • 9130414A06Rik,
  • Hnrnpa2b1,
  • Hnrpa2b1,
  • RIKEN cDNA 9130414A06 gene
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