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Additional findings_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
Unknown
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Cardiomyopathy, dilated
OMIM
600435
Clinvar variants
Variants in CTF1
Penetrance
None
Panels with this gene

History Filter Activity

27 Aug 2020, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CTF1 was added gene: CTF1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: CTF1 was set to Unknown Phenotypes for gene: CTF1 were set to Cardiomyopathy, dilated