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Fetal anomalies

Gene: TTC26

Green List (high evidence)

TTC26 (tetratricopeptide repeat domain 26)
EnsemblGeneIds (GRCh38): ENSG00000105948
EnsemblGeneIds (GRCh37): ENSG00000105948
OMIM: 617453, Gene2Phenotype
TTC26 is in 4 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

9 families and functional data including zebrafish model. Multiple congenital anomalies likely identifiable by US.
Sources: Literature
Created: 21 May 2025, 11:58 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Biliary, renal, neurologic, and skeletal syndrome, MIM# 619534

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Biliary, renal, neurologic, and skeletal syndrome, MIM# 619534
OMIM
617453
Clinvar variants
Variants in TTC26
Penetrance
None
Publications
Panels with this gene

History Filter Activity

21 May 2025, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ttc26 has been classified as Green List (High Evidence).

21 May 2025, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ttc26 has been classified as Green List (High Evidence).

21 May 2025, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: TTC26 was added gene: TTC26 was added to Fetal anomalies. 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 Biliary, renal, neurologic, and skeletal syndrome, MIM# 619534 Review for gene: TTC26 was set to GREEN