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Interstitial Lung Disease v0.331 | KCNK3 | Zornitza Stark Marked gene: KCNK3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.331 | KCNK3 | Zornitza Stark Gene: kcnk3 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.331 | KCNK3 | Zornitza Stark Phenotypes for gene: KCNK3 were changed from to Pulmonary hypertension, primary, 4 MIM#615344 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.330 | KCNK3 | Zornitza Stark Publications for gene: KCNK3 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.329 | KCNK3 | Zornitza Stark Classified gene: KCNK3 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.329 | KCNK3 | Zornitza Stark Gene: kcnk3 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.183 | KCNK3 | Suzanna Lindsey-Temple reviewed gene: KCNK3: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 23883380, 27649371; Phenotypes: Pulmonary arterial hypertension.; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Interstitial Lung Disease v0.183 | KCNK3 |
Suzanna Lindsey-Temple gene: KCNK3 was added gene: KCNK3 was added to Interstitial Lung Disease. Sources: Expert list Mode of inheritance for gene: KCNK3 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |