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Ciliary Dyskinesia v1.35 AKNA Zornitza Stark Phenotypes for gene: AKNA were changed from Primary ciliary dyskinesia to Primary ciliary dyskinesia, MONDO:0016575, AKNA-related
Ciliary Dyskinesia v1.34 AKNA Zornitza Stark edited their review of gene: AKNA: Changed phenotypes: Primary ciliary dyskinesia, MONDO:0016575, AKNA-related
Ciliary Dyskinesia v0.131 AKNA Zornitza Stark reviewed gene: AKNA: Rating: RED; Mode of pathogenicity: None; Publications: 32367404; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ciliary Dyskinesia v0.128 AKNA Seb Lunke Marked gene: AKNA as ready
Ciliary Dyskinesia v0.128 AKNA Seb Lunke Gene: akna has been classified as Red List (Low Evidence).
Ciliary Dyskinesia v0.128 AKNA Seb Lunke Classified gene: AKNA as Red List (low evidence)
Ciliary Dyskinesia v0.128 AKNA Seb Lunke Gene: akna has been classified as Red List (Low Evidence).
Ciliary Dyskinesia v0.125 AKNA Elena Savva gene: AKNA was added
gene: AKNA was added to Ciliary Dyskinesia. Sources: Literature
Mode of inheritance for gene: AKNA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AKNA were set to PMID: 21606955
Phenotypes for gene: AKNA were set to Primary ciliary dyskinesia
Review for gene: AKNA was set to RED
Added comment: https://link.springer.com/article/10.1007/s00439-020-02170-2
Two siblings with homozygous PTCs with PCD. Carrier parents and mutation negative siblings (5) was normal.

PMID: 21606955: Null mice have neonatal death with systemic inflammation and alveolar loss
Sources: Literature