DCXR
From SNPedia
is a | gene |
is | mentioned by |
Full name | dicarbonyl/L-xylulose reductase |
EntrezGene | 51181 |
PheGenI | 51181 |
VariationViewer | 51181 |
ClinVar | DCXR |
GeneCards | DCXR |
dbSNP | 51181 |
Diseases | DCXR |
SADR | 51181 |
HugeNav | 51181 |
wikipedia | DCXR |
DCXR | |
gopubmed | DCXR |
EVS | DCXR |
HEFalMp | DCXR |
MyGene2 | DCXR |
23andMe | DCXR |
UniProt | Q7Z4W1 |
Ensembl | ENSG00000169738 |
OMIM | 608347 |
# SNPs | 0 |
[PMID 22042873] Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria. News article reports on how a genetic disorder known about since 1908 has finally been associated with causative gene variants through exome sequencing.