| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Deafness_Isolated v0.11 | CEACAM16 | Zornitza Stark Marked gene: CEACAM16 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.11 | CEACAM16 | Zornitza Stark Gene: ceacam16 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.11 | CEACAM16 | Zornitza Stark Classified gene: CEACAM16 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.11 | CEACAM16 | Zornitza Stark Gene: ceacam16 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.3 | CEACAM16 | Lilian Downie reviewed gene: CEACAM16: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: AD and AR deafness: adult onset; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | CEACAM16 |
Zornitza Stark gene: CEACAM16 was added gene: CEACAM16 was added to DeafnessIsolated. Sources: Melbourne Genomics Health Alliance Deafness Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CEACAM16 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: CEACAM16 were set to 25589040; 21368133; 22544735; 31249509; 29703829; 30514912 Phenotypes for gene: CEACAM16 were set to Deafness, autosomal dominant 4B, MIM# 614614; Deafness, autosomal recessive 113, MIM# 618410 |
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