ANO5
HGNC:27337 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in ANO5 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| congenital myopathy | — | 2 | 2 |
| Duchenne muscular dystrophy | — | 1 | 1 |
| Pompe disease | — | 1 | 1 |
Linked variants
Variants normalized to ANO5| 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 · Riyadh | — | 2 | 1 |
Supporting publications
2 records- 2017The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.Journal of human genetics1 mentions
- 2015Clinical and genetic features of anoctaminopathy in Saudi Arabia.Neurosciences (Riyadh, Saudi Arabia)1 mentions