Aliases for CPXM1 Gene
External Ids for CPXM1 Gene
Previous HGNC Symbols for CPXM1 Gene
This gene likely encodes a member of the carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a carboxypeptidase domain, but the protein appears to lack residues necessary for carboxypeptidase activity.[provided by RefSeq, May 2010]
GeneCards Summary for CPXM1 Gene
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.
UniProtKB/Swiss-Prot for CPXM1 Gene
May be involved in cell-cell interactions. No carboxypeptidase activity was found yet (By similarity).