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Cardiac arrhythmias - previous panel

Gene: SNTA1

Green List (high evidence)
SNTA1 (syntrophin alpha 1)
EnsemblGeneIds (GRCh38): ENSG00000101400
EnsemblGeneIds (GRCh37): ENSG00000101400
OMIM: 601017, Gene2Phenotype
SNTA1 is in 2 panels

1 review

Eleanor Williams (Genomics England Curator)

Comment on phenotypes: Added phenotype from OMIM that was missing from source panels
Created: 16 Jan 2019, 11:51 a.m.
Created: 16 Jan 2019, 11:51 a.m.

Panel version: 0.9

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
Phenotypes
  • Long QT syndrome 12 612955
OMIM
601017
Clinvar variants
Variants in SNTA1
Penetrance
None
Panels with this gene

History Filter Activity

28 Jan 2019, Gel status: 4

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Eleanor Williams: Comment on phenotypes: Added p

16 Jan 2019, Gel status: 4

Set Phenotypes

Eleanor Williams (Genomics England Curator)

Phenotypes for gene: SNTA1 were changed from Long QT syndrome 12 to Long QT syndrome 12 612955

16 Jan 2019, Gel status: 4

Set Phenotypes

Eleanor Williams (Genomics England Curator)

Phenotypes for gene: SNTA1 were changed from to Long QT syndrome 12

17 Dec 2018, Gel status: 4

Created, Added New Source, Set mode of inheritance

Rebecca Foulger (Genomics England curator)

gene: SNTA1 was added gene: SNTA1 was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: SNTA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted