KDM5B
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | lysine (K)-specific demethylase 5B |
| EntrezGene | 10765 |
| PheGenI | 10765 |
| VariationViewer | 10765 |
| ClinVar | KDM5B |
| GeneCards | KDM5B |
| dbSNP | 10765 |
| Diseases | KDM5B |
| SADR | 10765 |
| HugeNav | 10765 |
| wikipedia | KDM5B |
| KDM5B | |
| gopubmed | KDM5B |
| EVS | KDM5B |
| HEFalMp | KDM5B |
| MyGene2 | KDM5B |
| 23andMe | KDM5B |
| UniProt | Q9UGL1 |
| Ensembl | ENSG00000117139 |
| OMIM | 605393 |
| # SNPs | 1 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs10494836 | 0 | 202,727,750 |
https://www.genomicseducation.hee.nhs.uk/news/item/167-answers-for-100-000-genomes-project-participants a spontaneous mutation in this gene is the source of http://ghr.nlm.nih.gov/condition/glut1-deficiency-syndrome
