| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Deafness_Isolated v1.78 | CLIC5 | Chirag Patel Classified gene: CLIC5 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.78 | CLIC5 | Chirag Patel Gene: clic5 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.77 | CLIC5 | Chirag Patel reviewed gene: CLIC5: Rating: GREEN; Mode of pathogenicity: None; Publications: 40957967, 40928595, 33114113; Phenotypes: Autosomal recessive nonsyndromic hearing loss 103, MONDO:0014469; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.77 | CLIC5 |
Chirag Patel Source Victorian Clinical Genetics Services was removed from CLIC5. Source Melbourne Genomics Health Alliance Deafness Flagship was removed from CLIC5. Source Melbourne Genomics Health Alliance Deafness Flagship was removed from CLIC5. Source Victorian Clinical Genetics Services was removed from CLIC5. Source Literature was added to CLIC5. Phenotypes for gene: CLIC5 were changed from Deafness, autosomal recessive 103, MIM# 616042 to Autosomal recessive nonsyndromic hearing loss 103, MONDO:0014469 |
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| Deafness_Isolated v0.182 | CLIC5 | Zornitza Stark Marked gene: CLIC5 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | CLIC5 | Zornitza Stark Gene: clic5 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | CLIC5 | Zornitza Stark Marked gene: CLIC5 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | CLIC5 | Zornitza Stark Gene: clic5 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | CLIC5 |
Zornitza Stark gene: CLIC5 was added gene: CLIC5 was added to DeafnessIsolated. Sources: Expert Review Amber,Melbourne Genomics Health Alliance Deafness Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: CLIC5 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CLIC5 were set to 24781754; 17021174 Phenotypes for gene: CLIC5 were set to Deafness, autosomal recessive 103, MIM# 616042 |
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