Inactivating TGFBR2 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the TGFBR2 gene that either inhibits expression or results in the translation of an inactive von Hippel-Lindau disease tumor suppressor protein.

**Synonyms:** - Inactivating TBR-ii Gene Mutation - Inactivating TBRII Gene Mutation - Inactivating TGFBR2 Mutation - Inactivating TGFR-2 Gene Mutation - Inactivating TGFbeta-RII Gene Mutation - Inactivating Von Hippel Lindau Tumor Suppressor Gene Mutation - Loss of Function TGFBR2 Gene Mutation - Loss of Function TGFBR2 Mutation - Loss of FunctionTransforming Growth Factor Beta Receptor 2 Gene Mutation - TGF-beta RII Tumor-Suppressor Gene Inactivation - TGF-beta Receptor Type II Tumor-Suppressor Gene Inactivation - TGFBR2 Gene Inactivation - TGFBR2 Tumor-Suppressor Gene Inactivation - TGFbetaRII Tumor-Suppressor Gene Inactivation