MYOF Chromosome 10

Myoferlin
7 variants 7 Health Risk

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What This Gene Does
Mutations in dysferlin, a protein associated with the plasma membrane, can cause muscle weakness that affects both proximal and distal muscles. The protein encoded by this gene is a type II membrane protein that is structurally similar to dysferlin. It is a member of the ferlin family and associates with both plasma and nuclear membranes. The protein contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. Two transcript variants encoding different isoforms have been found for this gene. Other possible variants have been detected, but their full-length nature has not been determined. [provided by RefSeq, Dec 2008]
Gene Info
Gene Group
Ferlin family
Locus Type
gene with protein product
Location
10q23.33
Ensembl
ENSG00000138119
Associated Conditions (3)
Angioedema
hereditary
7
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS200722080 Health Risk Conflicting classifications of pathogenicity
RS202041377 Health Risk Conflicting classifications of pathogenicity
RS529445117 Health Risk Conflicting classifications of pathogenicity
RS563338043 Health Risk Conflicting classifications of pathogenicity Angioedema, hereditary, 7
RS764965243 Health Risk Conflicting classifications of pathogenicity Angioedema, hereditary, 7
RS776610506 Health Risk Conflicting classifications of pathogenicity
RS1256778304 Health Risk Pathogenic Angioedema, hereditary, 7
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