Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51181
Gene name Gene Name - the full gene name approved by the HGNC.
Dicarbonyl and L-xylulose reductase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DCXR
Synonyms (NCBI Gene) Gene synonyms aliases
DCR, HCR2, HCRII, KIDCR, P34H, PNTSU, SDR20C1, XR
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q25.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene acts as a homotetramer to catalyze diacetyl reductase and L-xylulose reductase reactions. The encoded protein may play a role in the uronate cycle of glucose metabolism and in the cellular osmoregulation in the proximal re
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT037386 hsa-miR-744-5p CLASH 23622248
MIRT928393 hsa-miR-1255b CLIP-seq
MIRT928394 hsa-miR-3622b-5p CLIP-seq
MIRT928395 hsa-miR-3675-5p CLIP-seq
MIRT928396 hsa-miR-4283 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004090 Function Carbonyl reductase (NADPH) activity IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus HDA 21630459
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005829 Component Cytosol IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608347 18985 ENSG00000169738
Protein
UniProt ID Q7Z4W1
Protein name L-xylulose reductase (XR) (EC 1.1.1.10) (Carbonyl reductase II) (Dicarbonyl/L-xylulose reductase) (Kidney dicarbonyl reductase) (kiDCR) (Short chain dehydrogenase/reductase family 20C member 1) (Sperm surface protein P34H)
Protein function Catalyzes the NADPH-dependent reduction of several pentoses, tetroses, trioses, alpha-dicarbonyl compounds and L-xylulose. Participates in the uronate cycle of glucose metabolism. May play a role in the water absorption and cellular osmoregulati
PDB 1PR9 , 1WNT , 3D3W
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13561 adh_short_C2 14 242 Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in kidney, liver and epididymis. In the epididymis, it is mainly expressed in the proximal and distal sections of the corpus region. Weakly or not expressed in brain, lung, heart, spleen and testis. {ECO:0000269|PubMed
Sequence
Sequence length 244
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Pentose and glucuronate interconversions
Metabolic pathways
  Formation of xylulose-5-phosphate
Essential pentosuria
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Pentosuria pentosuria N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 36077333
Carcinogenesis Associate 16847567
Carcinoma Hepatocellular Inhibit 16847567
Carcinoma Hepatocellular Associate 27658779
Diabetes Mellitus Associate 31217356
Infertility Associate 24882558
Neoplasms Inhibit 16847567
Nephrotic Syndrome Inhibit 31217356
Pentosuria Associate 22042873
Renal Insufficiency Chronic Associate 31217356