Aliases for TMEM38A Gene
External Ids for TMEM38A Gene
Previous GeneCards Identifiers for TMEM38A Gene
GeneCards Summary for TMEM38A Gene
TMEM38A (Transmembrane Protein 38A) is a Protein Coding gene. Diseases associated with TMEM38A include Hyperalphalipoproteinemia 1 and Myopathy, X-Linked, With Postural Muscle Atrophy. Gene Ontology (GO) annotations related to this gene include potassium channel activity and cation channel activity. An important paralog of this gene is TMEM38B.
UniProtKB/Swiss-Prot Summary for TMEM38A Gene
Monovalent cation channel required for maintenance of rapid intracellular calcium release. May act as a potassium counter-ion channel that functions in synchronization with calcium release from intracellular stores.