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| Deafness_Isolated v0.115 | OSBPL2 | Zornitza Stark Marked gene: OSBPL2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.115 | OSBPL2 | Zornitza Stark Gene: osbpl2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | OSBPL2 |
Zornitza Stark gene: OSBPL2 was added gene: OSBPL2 was added to DeafnessIsolated. Sources: Melbourne Genomics Health Alliance Deafness Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: OSBPL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: OSBPL2 were set to 30894143; 31451425; 25759012; 25077649 Phenotypes for gene: OSBPL2 were set to Deafness, autosomal dominant 67, MIM# 616340 |
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