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Deafness_IsolatedAndComplex v1.265 TRPV4 Chirag Patel Phenotypes for gene: TRPV4 were changed from Auditory neuropathy spectrum disorder; Peripheral neuropathy; Hearing loss to Auditory neuropathy spectrum disorder; Charcot-Marie-Tooth disease axonal type 2C, MONDO:0011633; Hearing loss
Deafness_IsolatedAndComplex v1.264 TRPV4 Chirag Patel reviewed gene: TRPV4: Rating: GREEN; Mode of pathogenicity: None; Publications: 20037586; Phenotypes: Charcot-Marie-Tooth disease axonal type 2C, MONDO:0011633; Mode of inheritance: None
Deafness_IsolatedAndComplex v1.27 TRPV4 Bryony Thompson Marked gene: TRPV4 as ready
Deafness_IsolatedAndComplex v1.27 TRPV4 Bryony Thompson Gene: trpv4 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v1.26 TRPV4 Bryony Thompson Publications for gene: TRPV4 were set to
Deafness_IsolatedAndComplex v1.25 TRPV4 Bryony Thompson Phenotypes for gene: TRPV4 were changed from to Auditory neuropathy spectrum disorder; Peripheral neuropathy; Hearing loss
Deafness_IsolatedAndComplex v1.24 TRPV4 Bryony Thompson Classified gene: TRPV4 as Green List (high evidence)
Deafness_IsolatedAndComplex v1.24 TRPV4 Bryony Thompson Gene: trpv4 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v1.23 TRPV4 Bryony Thompson Classified gene: TRPV4 as Amber List (moderate evidence)
Deafness_IsolatedAndComplex v1.23 TRPV4 Bryony Thompson Gene: trpv4 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v1.21 TRPV4 Bryony Thompson gene: TRPV4 was added
gene: TRPV4 was added to Deafness_IsolatedAndComplex. Sources: Literature
Mode of inheritance for gene: TRPV4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted