Inactivating FANCL Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A mutation in the FANCL gene that either inhibits the expression of or results in the translation of an inactive Fanconi anemia group L protein.

**Synonyms:** - FANCL Gene Inactivation - FANCL Inactivating Gene Mutation - FANCL Inactivating Mutation - FANCL Inactivation - FANCL Loss of Function Gene Mutation - FANCL Loss of Function Mutation - Inactivating FAAP43 Gene Mutation - Inactivating FANCL Mutation - Inactivating Fanconi Anemia Complementation Group L Gene Mutation - Inactivating Fanconi Anemia, Complementation Group L Gene Mutation - Inactivating PHD Finger Protein 9 Gene Mutation - Inactivating PHF9 Gene Mutation - Inactivating POG Gene Mutation - Loss of Function FANCL Gene Mutation - Loss of Function FANCL Mutation