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Mendeliome

Gene: ALDH2

Red List (low evidence)

ALDH2 (aldehyde dehydrogenase 2 family (mitochondrial))
EnsemblGeneIds (GRCh38): ENSG00000111275
EnsemblGeneIds (GRCh37): ENSG00000111275
OMIM: 100650, Gene2Phenotype
ALDH2 is in 1 panel

1 review

Ain Roesley (Victorian Clinical Genetics Services)

Red List (low evidence)

no mendelian disease association.

PMID: 31368097 is a review the function of ALDH2 in various pathological conditions of the heart in relation to aldehyde toxicity
Created: 11 Feb 2022, 5:42 a.m. | Last Modified: 11 Feb 2022, 5:42 a.m.
Panel Version: 0.10945

Publications

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
100650
Clinvar variants
Variants in ALDH2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

11 Feb 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: aldh2 has been classified as Red List (Low Evidence).

11 Feb 2022, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: ALDH2 were set to

11 Feb 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: aldh2 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ALDH2 was added gene: ALDH2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ALDH2 was set to Unknown