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Renal Macrocystic Disease v0.42 | DZIP1L | Yu Leng Phua Deleted their review | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.42 | DZIP1L | Yu Leng Phua Deleted their comment | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.42 | DZIP1L | Yu Leng Phua reviewed gene: DZIP1L: Rating: GREEN; Mode of pathogenicity: None; Publications: 35211789; Phenotypes: Polycystic kidney disease 5, MIM#617610; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.6 | DZIP1L | Zornitza Stark Marked gene: DZIP1L as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.6 | DZIP1L | Zornitza Stark Gene: dzip1l has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.6 | DZIP1L | Zornitza Stark Classified gene: DZIP1L as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.6 | DZIP1L | Zornitza Stark Gene: dzip1l has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Renal Macrocystic Disease v0.5 | DZIP1L |
Zornitza Stark gene: DZIP1L was added gene: DZIP1L was added to Renal cystic disease_KidGen. Sources: Expert list Mode of inheritance for gene: DZIP1L was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DZIP1L were set to 28530676 Phenotypes for gene: DZIP1L were set to Polycystic kidney disease 5, MIM#617610 Review for gene: DZIP1L was set to GREEN gene: DZIP1L was marked as current diagnostic Added comment: 7 individuals from 4 unrelated families with bi-allelic variants in this gene. Sources: Expert list |