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Deafness_IsolatedAndComplex v0.365 SOX10 Zornitza Stark Marked gene: SOX10 as ready
Deafness_IsolatedAndComplex v0.365 SOX10 Zornitza Stark Gene: sox10 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.365 SOX10 Zornitza Stark Phenotypes for gene: SOX10 were changed from to PCWH syndrome (MIM#609136); Waardenburg syndrome, type 2E, with or without neurologic involvement (MIM#611584); Waardenburg syndrome, type 4C (MIM#613266)
Deafness_IsolatedAndComplex v0.364 SOX10 Zornitza Stark Publications for gene: SOX10 were set to
Deafness_IsolatedAndComplex v0.363 SOX10 Zornitza Stark Mode of inheritance for gene: SOX10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Deafness_IsolatedAndComplex v0.362 SOX10 Crystle Lee reviewed gene: SOX10: Rating: GREEN; Mode of pathogenicity: None; Publications: 23643381, 24845202; Phenotypes: PCWH syndrome (MIM#609136), Waardenburg syndrome, type 2E, with or without neurologic involvement (MIM#611584), Waardenburg syndrome, type 4C (MIM#613266); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Deafness_IsolatedAndComplex v0.0 SOX10 Zornitza Stark gene: SOX10 was added
gene: SOX10 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Deafness Flagship
Mode of inheritance for gene: SOX10 was set to Unknown