About: PRKAR1A wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • PRKAR1A wt Allele
equivalentClass
OMIM_Number
  • 188830
GenBank_Accession_Number
  • NM_002734
Semantic_Type
  • Gene or Genome
Preferred_Name
  • PRKAR1A wt Allele
NCI_META_CUI
  • CL430404
EntrezGene_ID
  • 5573
HGNC_ID
  • HGNC:9388
FULL_SYN
  • CARSYNCI
  • DKFZp779L0468SYNCI
  • CNCSYNCI
  • CNC1SYNCI
  • TSE1SYNCI
  • PKR1SYNCI
  • ADOHRSYNCI
  • PRKAR1A wt AllelePTNCI
  • Protein Kinase A Type 1a Regulatory Subunit GeneSYNCI
  • PPNAD1SYNCI
  • PRKAR1SYNCI
  • MGC17251SYNCI
  • Protein Kinase, cAMP-Dependent, Regulatory, Type I, Alpha (Tissue Specific Extinguisher 1) wt AlleleSYNCI
DEFINITION
  • Human PRKAR1A wild-type allele is located within 17q23-q24 and is approximately 21 kb in length. This allele, which encodes cAMP-dependent protein kinase type I-alpha regulatory subunit protein, is involved in the modulation of protein kinase A activation. Mutation of the gene is associated with Carney complex type 1, intracardiac myxoma, and primary pigmented nodular adrenocortical disease type 1. Papillary thyroid carcinoma is associated with a chromosomal translocation of this gene and the RET gene. A chromosomal aberration affecting this gene and the RARA gene is associated with acute promyelocytic leukemia.NCIOMIM
code
  • C97743
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