Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Deafness_Isolated v1.74 | TECTB | Zornitza Stark Marked gene: TECTB as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Deafness_Isolated v1.74 | TECTB | Zornitza Stark Gene: tectb has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Deafness_Isolated v1.74 | TECTB |
Zornitza Stark gene: TECTB was added gene: TECTB was added to Deafness_Isolated. Sources: Literature Mode of inheritance for gene: TECTB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TECTB were set to 40832383 Phenotypes for gene: TECTB were set to Hearing loss disorder, MONDO:0005365, TECTB-related Review for gene: TECTB was set to RED Added comment: Single multigenerational family segregating a missense variant and a mouse model. Sources: Literature |