UTRN Chromosome 6
Utrophin
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What This Gene Does
This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Zinc fingers ZZ-type|Spectrin repeat containing"
Locus Type
gene with protein product
Location
6q24.2
Ensembl
ENSG00000152818
Associated Conditions (1)
Duchenne muscular dystrophy
Key Variants
RS115230292
Conflicting classifications of pathogenicity
Health Risk
RS142621533
Conflicting classifications of pathogenicity
Health Risk
RS148685925
Conflicting classifications of pathogenicity
Health Risk
RS61738782
Conflicting classifications of pathogenicity
Health Risk
RS766709360
Likely pathogenic
Duchenne muscular dystrophy, Duchenne muscular dystrophy
Health Risk
All Variants (5)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS115230292 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS142621533 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS148685925 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS61738782 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS766709360 | Health Risk | Likely pathogenic | Duchenne muscular dystrophy, Duchenne muscular dystrophy |