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C179352Level 6

Inactivating ERCC5 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the ERCC5 gene that either inhibits expression or results in the translation of an inactive DNA repair protein complementing XP-G cells protein.

**Synonyms:** - ERCC5 Gene Inactivation - ERCC5 Inactivating Gene Mutation - ERCC5 Inactivating Mutation - ERCC5 Loss of Function Gene Mutation - ERCC5 Loss of Function Mutation - Inactivating COFS3 Gene Mutation - Inactivating ERCC Excision Repair 5, Endonuclease Gene Mutation - Inactivating ERCC5 Mutation - Inactivating ERCM2 Gene Mutation - Inactivating Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 5 Gene Mutation - Inactivating Excision-Repair, Complementing Defective, In Chinese Hamster, 5 Gene Mutation - Inactivating UVDR Gene Mutation - Inactivating XPG Gene Mutation - Inactivating XPGC Gene Mutation

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