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Hypertrophic cardiomyopathy_HCM v0.183 UQCRFS1 Bryony Thompson Classified gene: UQCRFS1 as Red List (low evidence)
Hypertrophic cardiomyopathy_HCM v0.183 UQCRFS1 Bryony Thompson Added comment: Comment on list classification: Paediatric onset condition. This gene is on the paediatric cardiomyopathy panel. Not one of the 29 genes recommended for HCM testing by the ClinGen HCVD GCEP.
Hypertrophic cardiomyopathy_HCM v0.183 UQCRFS1 Bryony Thompson Gene: uqcrfs1 has been classified as Red List (Low Evidence).
Hypertrophic cardiomyopathy_HCM v0.4 UQCRFS1 Zornitza Stark Marked gene: UQCRFS1 as ready
Hypertrophic cardiomyopathy_HCM v0.4 UQCRFS1 Zornitza Stark Gene: uqcrfs1 has been classified as Green List (High Evidence).
Hypertrophic cardiomyopathy_HCM v0.4 UQCRFS1 Zornitza Stark Classified gene: UQCRFS1 as Green List (high evidence)
Hypertrophic cardiomyopathy_HCM v0.4 UQCRFS1 Zornitza Stark Gene: uqcrfs1 has been classified as Green List (High Evidence).
Hypertrophic cardiomyopathy_HCM v0.3 UQCRFS1 Zornitza Stark gene: UQCRFS1 was added
gene: UQCRFS1 was added to Hypertrophic cardiomyopathy_VCGS. Sources: Literature
Mode of inheritance for gene: UQCRFS1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: UQCRFS1 were set to 31883641
Phenotypes for gene: UQCRFS1 were set to Mitochondrial Complex III deficiency; lactic acidosis; fetal bradycardia; hypertrophic cardiomyopathy; alopecia totalis
Review for gene: UQCRFS1 was set to GREEN
Added comment: Two unrelated families reported plus functional evidence.
Sources: Literature