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Fetal anomalies v1.358 KIF3B Zornitza Stark Marked gene: KIF3B as ready
Fetal anomalies v1.358 KIF3B Zornitza Stark Gene: kif3b has been classified as Amber List (Moderate Evidence).
Fetal anomalies v1.358 KIF3B Zornitza Stark Classified gene: KIF3B as Amber List (moderate evidence)
Fetal anomalies v1.358 KIF3B Zornitza Stark Gene: kif3b has been classified as Amber List (Moderate Evidence).
Fetal anomalies v1.357 KIF3B Zornitza Stark gene: KIF3B was added
gene: KIF3B was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: KIF3B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KIF3B were set to 32386558; 38665936
Phenotypes for gene: KIF3B were set to Retinitis pigmentosa 89, MIM#618955; polydactyly
Review for gene: KIF3B was set to AMBER
Added comment: Two families reported with supportive functional data. Predominant phenotype is RP, however polydactyly reported, which would be detectable by US.
Sources: Literature