G1135T
G1135T · SaudiVarKB evidence summary derived from retained literature mentions.
1Variant mentions
1Publications
1Associated gene records
2Associated phenotype records
Associated gene records
Co-mentioned in the same publications| Gene | Identifier / context | Articles | Mentions |
|---|---|---|---|
| SORL1 | HGNC:11185 | 1 | 1 |
Associated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Alzheimer disease | — | 1 | 1 |
| Parkinson disease | — | 1 | 1 |
Associated population records
Co-mentioned in the same publicationsNo retained population associations.
Supporting publications
1 records- 2021SORL1 mutation in a Greek family with Parkinson's disease and dementia.Annals of clinical and translational neurologyPubMed ↗