|
XB-GENEPAGE-1011097
???displayGene.symbol???:
mme
???displayGene.name???:
membrane metalloendopeptidase
???displayGene.synonyms???
Neprilysin
(
Nomenclature history )
???displayGene.geneFunction???
M13 family peptidase
AI Protein Function
:
The mme gene encodes a membrane-bound metalloendopeptidase localized to the cell surface. This protein functions as a peptidase that cleaves and inactivates specific neuropeptides including enkephalins...[+]
???displayGene.geneInteractants???
Loading ...
Diseases:
Disease Ontology:
Charcot-Marie-Tooth disease axonal type 2T
MIM:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T
External Links:
Loading gene data...
Please wait while we fetch the latest information
| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
|
|
|
|||||||||||
| More Information |
|
|||||||||||
Symbol legend:
