Activity

Filter

Cancel
Date Panel Item Activity
15 actions
Cataract v0.143 COG4 Zornitza Stark Marked gene: COG4 as ready
Cataract v0.143 COG4 Zornitza Stark Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.143 COG4 Zornitza Stark Publications for gene: COG4 were set to Saul-Wilson syndrome, OMIM #618150; Congenital disorder of glycosylation, type IIj, OMIM #613489
Cataract v0.142 COG4 Zornitza Stark Phenotypes for gene: COG4 were changed from PMID: 31949312; 30290151 to Saul-Wilson syndrome, OMIM #618150; Congenital disorder of glycosylation, type IIj, OMIM #613489
Cataract v0.141 COG4 Chirag Patel Classified gene: COG4 as Green List (high evidence)
Cataract v0.141 COG4 Chirag Patel Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.140 COG4 Chirag Patel Classified gene: COG4 as Green List (high evidence)
Cataract v0.140 COG4 Chirag Patel Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.140 COG4 Chirag Patel Classified gene: COG4 as Green List (high evidence)
Cataract v0.140 COG4 Chirag Patel Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.140 COG4 Chirag Patel Classified gene: COG4 as Green List (high evidence)
Cataract v0.140 COG4 Chirag Patel Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.140 COG4 Chirag Patel Classified gene: COG4 as Green List (high evidence)
Cataract v0.140 COG4 Chirag Patel Gene: cog4 has been classified as Green List (High Evidence).
Cataract v0.139 COG4 Chirag Patel gene: COG4 was added
gene: COG4 was added to Cataract. Sources: Literature
Mode of inheritance for gene: COG4 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: COG4 were set to Saul-Wilson syndrome, OMIM #618150; Congenital disorder of glycosylation, type IIj, OMIM #613489
Phenotypes for gene: COG4 were set to PMID: 31949312; 30290151
Review for gene: COG4 was set to GREEN
Added comment: Saul-Wilson syndrome (AD)
14 patients reported with DD, skeletal changes, cataracts, and growth retardation (progeriod like)
All have a recurrent de novo heterozygous missense variant (p.Gly516Arg)

Congenital disorder of glycosylation, type IIj (AR)
Sources: Literature