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Structural eye disease v3.75 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, IP, 308300 to Incontinentia pigmenti, OMIM:308300
Structural eye disease v0.91 IKBKG Nicola Ragge reviewed gene: IKBKG: Rating: RED; Mode of pathogenicity: ; Publications: 31119873, 20499493, 30905793 ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Structural eye disease v0.89 IKBKG Ivone Leong Source NHS GMS was added to IKBKG.
Source Expert Review Red was added to IKBKG.
Publications for gene IKBKG were changed from to 31119873; 20499493; 30905793
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Structural eye disease v0.88 IKBKG Ivone Leong Source Expert Review Amber was added to IKBKG.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Structural eye disease v0.60 IKBKG Mariya Moosajee reviewed gene: IKBKG: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Incontinentia pigmenti, IP; Mode of inheritance:
Structural eye disease v0.59 IKBKG Ivone Leong gene: IKBKG was added
gene: IKBKG was added to Structural eye disease. Sources: London North GLH
Mode of inheritance for gene: IKBKG was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: IKBKG were set to Incontinentia pigmenti, IP, 308300