SIGMAR1
HGNC:8157 · SaudiVarKB evidence summary derived from retained literature mentions.
4Gene mentions
4Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in SIGMAR1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| amyotrophic lateral sclerosis | — | 1 | 1 |
| dyslipidemia | — | 1 | 1 |
Linked variants
Variants normalized to SIGMAR1| 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 |
|---|---|---|---|
| Not specified | — | — | 1 |
| Saudi Arabia | — | 41 | 1 |
Supporting publications
4 records- 2024Berberine modulates cardiovascular diseases as a multitarget-mediated alkaloid with insights into its downstream signals using in silico prospective screening approaches.Saudi journal of biological sciences1 mentions
- 2020Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.Frontiers in genetics1 mentions
- 2017Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder.Psychiatric genetics1 mentions
- 2011A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis.Annals of neurology1 mentions