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| Deafness_IsolatedAndComplex v0.45 | DCDC2 | Zornitza Stark Marked gene: DCDC2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.45 | DCDC2 | Zornitza Stark Gene: dcdc2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.45 | DCDC2 |
Zornitza Stark gene: DCDC2 was added gene: DCDC2 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert list Mode of inheritance for gene: DCDC2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DCDC2 were set to 25601850; 22558177; 25130614 Phenotypes for gene: DCDC2 were set to Deafness, autosomal recessive 66, MIM# 610212 Review for gene: DCDC2 was set to RED Added comment: Single family reported with deafness, some supportive functional data. Rated as LIMITED by ClinGen. Sources: Expert list |
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