Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Cardiomyopathy_Paediatric

Gene: CTF1

Red List (low evidence)

CTF1 (cardiotrophin 1)
EnsemblGeneIds (GRCh38): ENSG00000150281
EnsemblGeneIds (GRCh37): ENSG00000150281
OMIM: 600435, Gene2Phenotype
CTF1 is in 3 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • South West GLH
  • Expert Review Red
  • NHS GMS
OMIM
600435
Clinvar variants
Variants in CTF1
Penetrance
None
Panels with this gene

History Filter Activity

28 Jul 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CTF1 was added gene: CTF1 was added to Cardiomyopathy_Paediatric. Sources: NHS GMS,Expert Review Red,South West GLH Mode of inheritance for gene: CTF1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown