ALDH4A1
HGNC:406 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
9Associated phenotypes
Associated phenotypes
Co-mentioned in ALDH4A1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| obesity | HP:0001513 | 1 | 1 |
| cardiomyopathy | HP:0001638 | 1 | 1 |
| Alzheimer disease | — | 1 | 1 |
| diabetes mellitus | — | 1 | 1 |
| developmental delay | HP:0001263 | 1 | 1 |
| autism spectrum disorder | HP:0000729 | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
| inborn error of metabolism | HP:0001939 | 1 | 1 |
| metabolic syndrome | — | 1 | 1 |
Linked variants
Variants normalized to ALDH4A1| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Saudi Arabia · Jeddah | — | — | 1 |
Supporting publications
3 records- 2025Case Report: Hyperprolinemia type II in a child with autism spectrum disorder and ALDH4A1 gene variant in a consanguineous family.Frontiers in pediatricsPubMed ↗
- 2016Integrated Left Ventricular Global Transcriptome and Proteome Profiling in Human End-Stage Dilated Cardiomyopathy.PloS onePubMed ↗
- 2015In Vivo Exposures to Particulate Matter Collected from Saudi Arabia or Nickel Chloride Display Similar Dysregulation of Metabolic Syndrome Genes.Journal of toxicology and environmental health. Part APubMed ↗