Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol SGCE contributors: mct - updated : 23-05-2011
HGNC name sarcoglycan, epsilon
HGNC id 10808
ASSOCIATED DISORDERS
corresponding disease(s) DYT11 , DEL7Q21
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   LOI    
maternal chromosome 7 disomy- can cause myoclonus-dystonia
Susceptibility to obsessive-compulsive disorder, and alcohol dependence
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS