Short QT syndrome

Gene: ALG10

Red List (low evidence)

ALG10 (ALG10, alpha-1,2-glucosyltransferase)
EnsemblGeneIds (GRCh38): ENSG00000139133
EnsemblGeneIds (GRCh37): ENSG00000139133
OMIM: 603313, Gene2Phenotype
ALG10 is in 2 panels

2 reviews

Ivone Leong (Genomics England Curator)

Comment on list classification: TEST
Created: 29 Mar 2021, 2:52 p.m. | Last Modified: 29 Mar 2021, 2:52 p.m.
Panel Version: 2.13
Comment on list classification: TEST
Created: 29 Mar 2021, 2:52 p.m. | Last Modified: 29 Mar 2021, 2:52 p.m.
Panel Version: 2.12

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Not associated with Short QT phenotype in OMIM or in Gen2Phen.
Created: 15 Nov 2018, 12:10 p.m.

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

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Long QT syndrome (Version 1.5)
Phenotypes
  • {Long QT syndrome, acquired, reduced susceptibility to} 613688
OMIM
603313
Clinvar variants
Variants in ALG10
Penetrance
None
Panels with this gene

History Filter Activity

29 Mar 2021, Gel status: 1

Entity classified by Genomics England curator

Ivone Leong (Genomics England Curator)

Gene: alg10 has been classified as Red List (Low Evidence).

29 Mar 2021, Gel status: 2

Entity classified by Genomics England curator

Ivone Leong (Genomics England Curator)

Gene: alg10 has been classified as Amber List (Moderate Evidence).

20 Nov 2018, Gel status: 1

Panel promoted to version 1.0

Sarah Leigh (Genomics England Curator)

Sarah Leigh: Not associated with Short QT p

15 Nov 2018, Gel status: 1

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

Sarah Leigh (Genomics England Curator)

gene: ALG10 was added gene: ALG10 was added to Short QT syndrome. Sources: Long QT syndrome (Version 1.5) Mode of inheritance for gene: ALG10 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: ALG10 were set to {Long QT syndrome, acquired, reduced susceptibility to} 613688