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| Deafness_Isolated v0.182 | MIR96 | Zornitza Stark Marked gene: MIR96 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | MIR96 | Zornitza Stark Gene: mir96 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | MIR96 |
Zornitza Stark gene: MIR96 was added gene: MIR96 was added to DeafnessIsolated. Sources: Expert Review Amber,Melbourne Genomics Health Alliance Deafness Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: MIR96 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MIR96 were set to 19363479; 29325119 Phenotypes for gene: MIR96 were set to Deafness, autosomal dominant 50, MIM# 613074 |
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