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Joubert syndrome and other neurological ciliopathies v2.0 KIAA0586 Gene migrated from ENSG00000100578 to ENSG00000100578 (gene set migration)
Joubert syndrome and other neurological ciliopathies v1.2 KIAA0586 Zornitza Stark Marked gene: KIAA0586 as ready
Joubert syndrome and other neurological ciliopathies v1.2 KIAA0586 Zornitza Stark Added comment: Comment when marking as ready: HGNC approved name KATNIP
Joubert syndrome and other neurological ciliopathies v1.2 KIAA0586 Zornitza Stark Gene: kiaa0586 has been classified as Green List (High Evidence).
Joubert syndrome and other neurological ciliopathies v1.2 KIAA0586 Zornitza Stark Tag new gene name tag was added to gene: KIAA0586.
Joubert syndrome and other neurological ciliopathies v0.49 KIAA0586 Zornitza Stark Marked gene: KIAA0586 as ready
Joubert syndrome and other neurological ciliopathies v0.49 KIAA0586 Zornitza Stark Gene: kiaa0586 has been classified as Green List (High Evidence).
Joubert syndrome and other neurological ciliopathies v0.49 KIAA0586 Zornitza Stark Classified gene: KIAA0586 as Green List (high evidence)
Joubert syndrome and other neurological ciliopathies v0.49 KIAA0586 Zornitza Stark Gene: kiaa0586 has been classified as Green List (High Evidence).
Joubert syndrome and other neurological ciliopathies v0.48 KIAA0586 Elena Savva gene: KIAA0586 was added
gene: KIAA0586 was added to Joubert syndrome and other neurological ciliopathies. Sources: Literature
Mode of inheritance for gene: KIAA0586 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: KIAA0586 were set to PMID: 26096313
Phenotypes for gene: KIAA0586 were set to Joubert syndrome 23 616490; Short-rib thoracic dysplasia 14 with polydactyly 616546
Review for gene: KIAA0586 was set to GREEN
Added comment: PMID: 26096313 - 9 unrelated families with Joubert syndrome. MRI shows the molar tooth sign in 3/3 scanned patients. Patients tended to have biallelic PTCs, though missense also reported. p.Arg143Lysfs*4 appears to be a recurring mutation, seen in patients either as a homozygote or in chet with another unique mutation in 7/9 families. Interestingly these 7 families were of different ethnicity
Sources: Literature