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DCXR

From SNPedia

is agene
is mentioned by
Full namedicarbonyl/L-xylulose reductase
EntrezGene51181
PheGenI51181
VariationViewer51181
ClinVarDCXR
GeneCardsDCXR
dbSNP51181
SADR51181
HugeNav51181
wikipediaDCXR
googleDCXR
gopubmedDCXR
EVSDCXR
HEFalMpDCXR
MyGene2DCXR
23andMeDCXR
UniProtQ7Z4W1
EnsemblENSG00000169738
OMIM608347
# SNPs0

[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.