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  3. ALG10B
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Short QT syndrome

Gene: ALG10B

Red List (low evidence)
ALG10B (ALG10B, alpha-1,2-glucosyltransferase)
EnsemblGeneIds (GRCh38): ENSG00000175548
EnsemblGeneIds (GRCh37): ENSG00000175548
ALG10B is in 2 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Sources: Other
Created: 28 Oct 2021, 1:15 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
{Acquired long QT syndrome, reduced susceptibility to} OMIM:613688

Publications

Created: 28 Oct 2021, 1:15 p.m.

Copied from panel: Cardiac arrhythmias - previous panel v1.5

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Other
Phenotypes
  • {Acquired long QT syndrome, reduced susceptibility to} OMIM:613688
Clinvar variants
Variants in ALG10B
Penetrance
None
Publications
Panels with this gene

History Filter Activity

28 Oct 2021, Gel status: 1

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

Sarah Leigh (Genomics England Curator)

gene: ALG10B was added gene: ALG10B was added to Short QT syndrome. Sources: Other Mode of inheritance for gene: ALG10B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ALG10B were set to 15280551 Phenotypes for gene: ALG10B were set to {Acquired long QT syndrome, reduced susceptibility to} OMIM:613688