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| Deafness_Isolated v0.29 | CABP2 | Zornitza Stark Marked gene: CABP2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.29 | CABP2 | Zornitza Stark Gene: cabp2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | CABP2 |
Zornitza Stark gene: CABP2 was added gene: CABP2 was added to DeafnessIsolated. Sources: Melbourne Genomics Health Alliance Deafness Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CABP2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CABP2 were set to 22981119; 28183797; 31661684 Phenotypes for gene: CABP2 were set to Deafness, autosomal recessive 93, MIM# 614899 |
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