MeSH Browser

MeSH Supplementary: Fcmd protein, mouse
Unique ID: C491879
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C491879
Entry Term(s): Fukuyama type congenital muscular dystrophy homolog (human) protein, mouse; fukutin protein, mouse
Registry Numbers: EC 2.-
Previous Indexing: *Proteins (2005-2020)
Heading Mapped to: *Transferases
Frequency: 26
Note: FCMD - Fukuyama-type congenital muscular dystrophy; not expressed in individuals with FCMD due to ancient retrotransposal integration; RefSeq NM_139309
Indexing Information: Muscular Dystrophies
Date of Entry: 2004/11/02
Revision Date: 2019/11/07

Fcmd protein, mouse MeSH Supplementary Concept Data 2025