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| Deafness_IsolatedAndComplex v1.311 | PBXIP1 | Zornitza Stark Marked gene: PBXIP1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.311 | PBXIP1 | Zornitza Stark Gene: pbxip1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.311 | Zornitza Stark Copied gene PBXIP1 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.311 | PBXIP1 |
Zornitza Stark gene: PBXIP1 was added gene: PBXIP1 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Red,Literature Mode of inheritance for gene: PBXIP1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PBXIP1 were set to 39786576; 38947059 Phenotypes for gene: PBXIP1 were set to non-syndromic genetic hearing loss, MONDO:0019497, PBXIP1-related |
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