PRICKLE1
From SNPedia
| is a | gene |
| is | mentioned by |
| ClinVar | PRICKLE1 |
| GeneCards | PRICKLE1 |
| Diseases | PRICKLE1 |
| wikipedia | PRICKLE1 |
| PRICKLE1 | |
| gopubmed | PRICKLE1 |
| EVS | PRICKLE1 |
| HEFalMp | PRICKLE1 |
| MyGene2 | PRICKLE1 |
| 23andMe | PRICKLE1 |
| # SNPs | 8 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs113994140 | 3 | 42,469,523 | |
| rs1300341380 | 3 | 42,466,368 | |
| rs1796390 | 0 | 42,484,802 | |
| rs281865563 | 0 | 42,468,783 | |
| rs281865564 | 3 | 42,464,620 | |
| rs557205452 | 3 | 42,460,025 | |
| rs559947948 | 0 | 42,465,210 | |
| rs796052929 | 0 | 42,468,787 |
Progressive myoclonus epilepsy-ataxia syndrome (EPM5) is an autosomal recessive form of progressive myoclonus epilepsy that may be caused by homozygous or compound heterozygous mutations.
