Rare multisystem ciliopathy disorders
Gene: TTC26

TTC26 (tetratricopeptide repeat domain 26)
EnsemblGeneIds (GRCh38): ENSG00000105948
EnsemblGeneIds (GRCh37): ENSG00000105948
OMIM: 617453, Gene2Phenotype
TTC26 is in 1 panel

1 review

Zornitza Stark (Australian Genomics)

Green List (high evidence)

9 families and functional data including zebrafish model.
Sources: Literature
Created: 8 Jul 2021, 8:39 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations

Publications

Created: 8 Jul 2021, 8:39 a.m.

Panel version: 1.142

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

Phenotypes

Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations

OMIM

617453

Clinvar variants

Variants in TTC26

Penetrance

None

Publications

Panels with this gene

Rare multisystem ciliopathy disorders

History Filter Activity

8 Jul 2021, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Australian Genomics)

gene: TTC26 was added gene: TTC26 was added to Rare multisystem ciliopathy disorders. Sources: Literature Mode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903 Phenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations Review for gene: TTC26 was set to GREEN

Rare multisystem ciliopathy disorders Gene: TTC26