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Ciliary Dyskinesia v0.90 NFKB1 Zornitza Stark Marked gene: NFKB1 as ready
Ciliary Dyskinesia v0.90 NFKB1 Zornitza Stark Added comment: Comment when marking as ready: Not a PCD, but overlapping clinical features.
Ciliary Dyskinesia v0.90 NFKB1 Zornitza Stark Gene: nfkb1 has been classified as Amber List (Moderate Evidence).
Ciliary Dyskinesia v0.90 NFKB1 Zornitza Stark Classified gene: NFKB1 as Amber List (moderate evidence)
Ciliary Dyskinesia v0.90 NFKB1 Zornitza Stark Gene: nfkb1 has been classified as Amber List (Moderate Evidence).
Ciliary Dyskinesia v0.76 NFKB1 Elena Savva gene: NFKB1 was added
gene: NFKB1 was added to Ciliary Dyskinesia. Sources: Expert list
Mode of inheritance for gene: NFKB1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: NFKB1 were set to PMID: 32278790
Phenotypes for gene: NFKB1 were set to Immunodeficiency, common variable, 12 616576
Review for gene: NFKB1 was set to AMBER
Added comment: PMID: 32278790 - review of >150 patients with heterozygous mutations found ~25% had bronchiectasis, and 83% had upper respiratory infections. Incomplete penetrance (70%) with age dependent severity well reported.

OMIM describes haploinsufficiency

Summary: really doesnt seem like a PCD gene but some features are shared.
Sources: Expert list