LCAT
HGNC:6522 · SaudiVarKB evidence summary derived from retained literature mentions.
4Gene mentions
4Publications
0Linked variants
6Associated phenotypes
Associated phenotypes
Co-mentioned in LCAT publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| renal failure | — | 2 | 2 |
| diabetes mellitus | — | 1 | 1 |
| nephrotic syndrome | — | 1 | 1 |
| dyslipidemia | — | 1 | 1 |
| hepatitis C | — | 1 | 1 |
| hepatitis B | — | 1 | 1 |
Linked variants
Variants normalized to LCAT| 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 |
|---|
No structured population context is available.
Supporting publications
4 records- 2025Diagnostic significance of clinical scoring system and serum lipid profiles as recovery indicators in ketotic dairy cattle using hormonal-steroids-carbohydrates therapeutic protocol.Open veterinary journalPubMed ↗
- 2023Metabolomics Analysis and Biochemical Profiling of Arsenic-Induced Metabolic Impairment and Disease Susceptibility.BiomoleculesPubMed ↗
- 2022Clinical Dilemma of Corneal Opacity, Very Low High-density Lipoprotein, and Nephrotic Syndrome: Mystery Revealed.Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi ArabiaPubMed ↗
- 2015Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria.Journal of nephropathologyPubMed ↗