| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Deafness_Isolated v1.30 | FOXI1 | Bryony Thompson Phenotypes for gene: FOXI1 were changed from Hearing loss and renal tubular acidosis to enlarged vestibular aqueduct syndrome MONDO:0023069 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.29 | FOXI1 | Bryony Thompson Classified gene: FOXI1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.29 | FOXI1 | Bryony Thompson Added comment: Comment on list classification: There is limited evidence for an association of this gene with isolated deafness. There is stronger evidence for an association with biallelic syndromic deafness (distal renal tubular acidosis with deafness), thus this gene is green on the deafness isolated and complex panel. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.29 | FOXI1 | Bryony Thompson Gene: foxi1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.28 | FOXI1 | Bryony Thompson reviewed gene: FOXI1: Rating: RED; Mode of pathogenicity: None; Publications: 17503324, 30268946, 27997596, 22285650, 23965030, 24860705, 32447495, 19204907; Phenotypes: enlarged vestibular aqueduct syndrome MONDO:0023069; Mode of inheritance: Other | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.65 | FOXI1 | Zornitza Stark Marked gene: FOXI1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.65 | FOXI1 | Zornitza Stark Gene: foxi1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | FOXI1 |
Zornitza Stark gene: FOXI1 was added gene: FOXI1 was added to DeafnessIsolated. Sources: Melbourne Genomics Health Alliance Deafness Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FOXI1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FOXI1 were set to 9843211; 29242249; 17503324 Phenotypes for gene: FOXI1 were set to Hearing loss and renal tubular acidosis |
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