About: HNRNPA2B1 wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • HNRNPA2B1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 600124
GenBank_Accession_Number
  • D28877
Semantic_Type
  • Gene or Genome
Preferred_Name
  • HNRNPA2B1 wt Allele
NCI_META_CUI
  • CL430247
EntrezGene_ID
  • 3181
HGNC_ID
  • HGNC:5033
FULL_SYN
  • DKFZp779B0244SYNCI
  • Heterogeneous Nuclear Ribonucleoprotein A2/B1 wt AlleleSYNCI
  • RNPA2SYNCI
  • HNRPA2SYNCI
  • HNRPB1SYNCI
  • SNRPB1SYNCI
  • HNRNPA2SYNCI
  • HNRNPB1SYNCI
  • HNRNPA2B1 wt AllelePTNCI
  • FLJ22720SYNCI
  • HNRPA2B1SYNCI
DEFINITION
  • Human HNRNPA2B1 wild-type allele is located in the vicinity of 7p15 and is approximately 12 kb in length. This allele, which encodes heterogeneous nuclear ribonucleoproteins A2/B1, plays a role in both the processing and transport of mRNA. Point mutations in the gene have been associated with ovarian serous carcinoma and medulloblastoma.NCICOSMIC
DesignNote
  • The HNRNPA2B1 gene has been described to generate two alternatively spliced transcript variants which encode different isoforms.
code
  • C97497
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