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Mendeliome

Gene: ALOX5AP

Red List (low evidence)

ALOX5AP (arachidonate 5-lipoxygenase activating protein)
EnsemblGeneIds (GRCh38): ENSG00000132965
EnsemblGeneIds (GRCh37): ENSG00000132965
OMIM: 603700, Gene2Phenotype
ALOX5AP is in 1 panel

1 review

Bryony Thompson (Royal Melbourne Hospital)

Red List (low evidence)

I cannot find any eividence of an association with Mendelian disease. Multifactorial susceptibility to stroke reported in OMIM.
Created: 22 Jun 2020, 11:56 p.m. | Last Modified: 22 Jun 2020, 11:56 p.m.
Panel Version: 0.3147

Mode of inheritance
Unknown

Phenotypes
{Stroke, susceptibility to} MIM#601367

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
603700
Clinvar variants
Variants in ALOX5AP
Penetrance
None
Panels with this gene

History Filter Activity

22 Jun 2020, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: alox5ap has been classified as Red List (Low Evidence).

22 Jun 2020, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: alox5ap 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: ALOX5AP was added gene: ALOX5AP was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ALOX5AP was set to Unknown