UBQLN2
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | ubiquilin 2 |
| EntrezGene | 29978 |
| PheGenI | 29978 |
| VariationViewer | 29978 |
| ClinVar | UBQLN2 |
| GeneCards | UBQLN2 |
| dbSNP | 29978 |
| Diseases | UBQLN2 |
| SADR | 29978 |
| HugeNav | 29978 |
| wikipedia | UBQLN2 |
| UBQLN2 | |
| gopubmed | UBQLN2 |
| EVS | UBQLN2 |
| HEFalMp | UBQLN2 |
| MyGene2 | UBQLN2 |
| 23andMe | UBQLN2 |
| UniProt | Q9UHD9 |
| OMIM | 300264 |
| # SNPs | 5 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs369947678 | 0 | 56,565,446 | |
| rs387906709 | 7.9 | 56,565,363 | |
| rs387906710 | 0 | 56,565,362 | |
| rs387906711 | 0 | 56,565,389 | |
| rs387906712 | 0 | 56,565,398 |
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. [PMID 21857683]
