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QuickView for FSHD (gene)


Gene Symbol:
FSHMD1A Homo sapiens Homo sapiens
Full name:
facioscapulohumeral muscular dystrophy 1A
Synonyms:
FMD, FSHD, FSHD1A, FSHMD
Genomic Location:
N/A
Description:
Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary disease of muscle. Patients with FSHD have a chromosomal rearrangement within the subtelomeric region of chromosome 4 (4q35). This region is composed mainly of a polymorphic repeat structure consisting of 3.3 kb repeat units, designated D4Z4. The number of repeat units varies from...
External Links:
Entrez Gene


Transcripts Names
No transcripts found.
Protein Names
No proteins found.



GO Molecular Function

No molecular functions found.

GO Biological Process

No biological processes found.

GO Cellular Component

No cellular components found.