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Intellectual disability syndromic and non-syndromic v0.1261 STT3B Zornitza Stark Marked gene: STT3B as ready
Intellectual disability syndromic and non-syndromic v0.1261 STT3B Zornitza Stark Gene: stt3b has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.1180 STT3B Chirag Patel Classified gene: STT3B as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.1180 STT3B Chirag Patel Gene: stt3b has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.1179 STT3B Chirag Patel Source Genetic Health Queensland was removed from STT3B.
Source Expert list was added to STT3B.
Mode of inheritance for gene STT3B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: STT3B were changed from to ?Congenital disorder of glycosylation, type Ix; OMIM #615597
Publications for gene STT3B were changed from PMID: 23842455 to PMID: 23842455
Intellectual disability syndromic and non-syndromic v0.1178 STT3B Chirag Patel reviewed gene: STT3B: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 23842455; Phenotypes: ?Congenital disorder of glycosylation, type Ix, OMIM #615597; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.0 STT3B Zornitza Stark gene: STT3B was added
gene: STT3B was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: STT3B was set to Unknown