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Heterotaxy v1.31 DAW1 Zornitza Stark Phenotypes for gene: DAW1 were changed from Primary ciliary dyskinesia, MONDO:0016575; Visceral heterotaxy, MONDO:0018677 to Primary ciliary dyskinesia, with or without heterotaxy, MIM#620570
Heterotaxy v1.30 DAW1 Zornitza Stark reviewed gene: DAW1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Primary ciliary dyskinesia, with or without heterotaxy, MIM#620570; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Heterotaxy v1.25 DAW1 Alison Yeung Marked gene: DAW1 as ready
Heterotaxy v1.25 DAW1 Alison Yeung Gene: daw1 has been classified as Green List (High Evidence).
Heterotaxy v1.25 DAW1 Alison Yeung Classified gene: DAW1 as Green List (high evidence)
Heterotaxy v1.25 DAW1 Alison Yeung Gene: daw1 has been classified as Green List (High Evidence).
Heterotaxy v1.25 DAW1 Alison Yeung Classified gene: DAW1 as Green List (high evidence)
Heterotaxy v1.25 DAW1 Alison Yeung Gene: daw1 has been classified as Green List (High Evidence).
Heterotaxy v1.24 DAW1 Alison Yeung gene: DAW1 was added
gene: DAW1 was added to Heterotaxy. Sources: Literature
Mode of inheritance for gene: DAW1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DAW1 were set to 36074124
Phenotypes for gene: DAW1 were set to Primary ciliary dyskinesia, MONDO:0016575; Visceral heterotaxy, MONDO:0018677
Review for gene: DAW1 was set to GREEN
Added comment: Biallelic variants identified in two unrelated families. Zebrafish model recapitulates PCD and heterotaxy phenotype
Sources: Literature
Heterotaxy v1.24 DAW1 Alison Yeung gene: DAW1 was added
gene: DAW1 was added to Heterotaxy. Sources: Literature
Mode of inheritance for gene: DAW1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DAW1 were set to 36074124
Phenotypes for gene: DAW1 were set to Primary ciliary dyskinesia, MONDO:0016575; Visceral heterotaxy, MONDO:0018677
Review for gene: DAW1 was set to GREEN
Added comment: Biallelic variants identified in two unrelated families. Zebrafish model recapitulates PCD and heterotaxy phenotype
Sources: Literature