Sudden death in young people

Gene: MAOA

Red List (low evidence)

MAOA (monoamine oxidase A)
EnsemblGeneIds (GRCh38): ENSG00000189221
EnsemblGeneIds (GRCh37): ENSG00000189221
OMIM: 309850, Gene2Phenotype
MAOA is in 10 panels

1 review

Rebecca Foulger (Genomics England curator)

PMID:22351881 (2012) report an association between MAOA promoter length and SIDS (sudden infant death syndrome) cases.
Created: 29 Nov 2016, 10:11 a.m.

Mode of pathogenicity
Other

Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Literature
Phenotypes
  • sudden infant death syndrome
Tags
promoter
OMIM
309850
Clinvar variants
Variants in MAOA
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

19 Dec 2016, Gel status: 0

panel promoted to version 1

Ellen Thomas (Genomics England Curator)

This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.

29 Nov 2016, Gel status: 0

Added New Source

Rebecca Foulger (Genomics England curator)

MAOA was added to Sudden death in young peoplepanel. Sources: Literature

29 Nov 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

MAOA was created by rfoulger