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Repeat Disorders v0.151 OPDM4 Bryony Thompson Publications for STR: OPDM4 were set to 35148830
Repeat Disorders v0.150 OPDM4 Bryony Thompson Marked STR: OPDM4 as ready
Repeat Disorders v0.150 OPDM4 Bryony Thompson Str: opdm4 has been classified as Green List (High Evidence).
Repeat Disorders v0.150 OPDM4 Bryony Thompson Classified STR: OPDM4 as Green List (high evidence)
Repeat Disorders v0.150 OPDM4 Bryony Thompson Str: opdm4 has been classified as Green List (High Evidence).
Repeat Disorders v0.149 OPDM4 Bryony Thompson STR: OPDM4 was added
STR: OPDM4 was added to Repeat Disorders. Sources: Literature
Mode of inheritance for STR: OPDM4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for STR: OPDM4 were set to 35148830
Phenotypes for STR: OPDM4 were set to Oculopharyngodistal myopathy MONDO:0025193
Review for STR: OPDM4 was set to GREEN
STR: OPDM4 was marked as clinically relevant
Added comment: 5'UTR repeat upstream of RILPL1. Analyses suggest that toxic RNA gain-of-function is the mechanism of disease for the repeat expansion.
Distribution of CGG repeat units in RILPL1 ranged from 9 to 16 among 200 normal controls. The size of the CGG repeat ranged from 139 to 197 (169.91 ± 21.82) repeats in 11 unrelated individuals with OPDM. Segregation evidence from 1 family, with 2 affected individuals with the repeat expansion and 1 individual with essential tremor but not OPDM and 86 repeats (intermediate).
Sources: Literature