TTC26

tetratricopeptide repeat domain 26
OMIM: 617453, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Amber TTC26 in Pituitary hormone deficiency Level 2: Endocrinology Version 4.7 Latest signed off version: v4.6 (6 May 2026)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags new-gene-name Q2_26_promote_green
No list TTC26 in Limb disorders Level 2: Musculoskeletal Version 8.6 Latest signed off version: v8.0 (6 May 2026) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Removed Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags curated_removed new-gene-name
Amber TTC26 in Cholestasis Level 2: Gastrohepatology Version 4.3 Latest signed off version: v4.0 (6 May 2026)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags new-gene-name Q2_26_promote_green
Green TTC26 in Fetal anomalies Level 2: Fetal (including NIPD) Version 7.5 Latest signed off version: v7.0 (6 May 2026)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 Tags new-gene-name
Green TTC26 in Rare multisystem ciliopathy disorders Level 3: Congenital malformations caused by ciliopathies Level 2: Ciliopathies Version 1.182	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags new-gene-name
Amber TTC26 in Neurological ciliopathies Level 2: Neurology Version 7.1 Latest signed off version: v7.0 (6 May 2026) Component of the following Super Panels: Hereditary ataxia and cerebellar anomalies - childhood onset Paediatric disorders Rare multisystem ciliopathy Super panel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags Q2_26_promote_green new-gene-name
Amber TTC26 in Renal ciliopathies Level 2: Renal Version 5.1 Latest signed off version: v5.0 (6 May 2026) Component of the following Super Panels: Cystic renal disease Paediatric disorders Rare multisystem ciliopathy Super panel Unexplained young onset end-stage renal disease	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Biliary, renal, neurologic, and skeletal syndrome, OMIM:619534 biliary, renal, neurologic, and skeletal syndrome, MONDO:0859191 Tags Q2_26_promote_green new-gene-name