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RNF43 NP_060233.3:p.A169T

MedGen UID:
1637723
•Concept ID:
C4687622
•
Cell or Molecular Dysfunction
Synonyms: E3 Ubiquitin-Protein Ligase RNF43 Protein Variant A169T; E3 Ubiquitin-Protein Ligase RNF43 Protein Variant Ala169Thr; NP_060233.3:p.A169T; NP_060233.3:p.Ala169Thr; RING Finger Protein 124 Protein Variant A169T; RING Finger Protein 124 Protein Variant Ala169Thr; Ring Finger Protein 43 Protein Variant A169T; Ring Finger Protein 43 Protein Variant Ala169Thr; RING-Type E3 Ubiquitin Transferase RNF43 Protein Variant A169T; RING-Type E3 Ubiquitin Transferase RNF43 Protein Variant Ala169Thr; RNF43 A169T; RNF43 Ala169Thr; RNF43 NP_060233.3:p.Ala169Thr; RNF43 p.A169T; RNF43 p.Ala169Thr

Definition

A change in the amino acid residue at position 169 in the E3 ubiquitin-protein ligase RNF43 protein where alanine has been replaced by threonine. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVRNF43 NP_060233.3:p.A169T

Recent clinical studies

Prognosis

Whole-exome sequencing of pancreatic neoplasms with acinar differentiation.
Jiao Y, Yonescu R, Offerhaus GJ, Klimstra DS, Maitra A, Eshleman JR, Herman JG, Poh W, Pelosof L, Wolfgang CL, Vogelstein B, Kinzler KW, Hruban RH, Papadopoulos N, Wood LD
J Pathol 2014 Mar;232(4):428-35. doi: 10.1002/path.4310. PMID: 24293293Free PMC Article

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