SLC37A4 Loss of Function Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the SLC37A4 gene that either inhibits expression or results in the translation of an inactive glucose-6-phosphate exchanger SLC37A4 protein.

**Synonyms:** - G6PT Loss of Function Gene Mutation - Inactivating SLC37A4 Gene Mutation - Inactivating SLC37A4 Mutation - SLC37A4 Inactivating Gene Mutation - SLC37A4 Inactivating Mutation - SLC37A4 Loss of Function Mutation - Solute Carrier Family 37 Member 4 Loss of Function Gene Mutation - TRG-19 Loss of Function Gene Mutation - TRG19 Loss of Function Gene Mutation