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