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Defects of innate immunity v0.132 | HMOX1 | Zornitza Stark Publications for gene: HMOX1 were set to 21088618; 9884342; 20844238 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.131 | HMOX1 | Zornitza Stark Classified gene: HMOX1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.131 | HMOX1 | Zornitza Stark Gene: hmox1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.130 | HMOX1 | Achchuthan Shanmugasundram reviewed gene: HMOX1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33066778; Phenotypes: Heme oxygenase-1 deficiency, OMIM:614034; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.18 | HMOX1 | Zornitza Stark Marked gene: HMOX1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.18 | HMOX1 | Zornitza Stark Gene: hmox1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.18 | HMOX1 | Zornitza Stark Classified gene: HMOX1 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.18 | HMOX1 | Zornitza Stark Gene: hmox1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Defects of innate immunity v0.17 | HMOX1 |
Zornitza Stark gene: HMOX1 was added gene: HMOX1 was added to Defects of innate immunity. Sources: Expert list Mode of inheritance for gene: HMOX1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: HMOX1 were set to 21088618; 9884342; 20844238 Phenotypes for gene: HMOX1 were set to Heme oxygenase-1 deficiency, MIM# 614034; Asplenia Review for gene: HMOX1 was set to AMBER Added comment: Two families reported, functional data. Sources: Expert list |