CPXM1 (Carboxypeptidase X, M14 Family Member 1) is a Protein Coding gene. Diseases associated with CPXM1 include Simpson-Golabi-Behmel Syndrome. Gene Ontology (GO) annotations related to this gene include metallocarboxypeptidase activity. An important paralog of this gene is CPXM2.
Carboxypeptidase X, M14 Family Member 1; Carboxypeptidase X (M14 Family), Member 1; Carboxypeptidase-Like Protein X1; Metallocarboxypeptidase CPX-1; CPX1; CPXM;