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BabyScreen+ newborn screening

Gene: DTNA

Red List (low evidence)

DTNA (dystrobrevin alpha)
EnsemblGeneIds (GRCh38): ENSG00000134769
EnsemblGeneIds (GRCh37): ENSG00000134769
OMIM: 601239, Gene2Phenotype
DTNA is in 6 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Left ventricular noncompaction 1
OMIM
601239
Clinvar variants
Variants in DTNA
Penetrance
None
Panels with this gene

History Filter Activity

18 Sep 2022, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DTNA was added gene: DTNA was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: DTNA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: DTNA were set to Left ventricular noncompaction 1