Gene Gene information from NCBI Gene database.
Entrez ID 51181
Gene name Dicarbonyl and L-xylulose reductase
Gene symbol DCXR
Synonyms (NCBI Gene)
DCRHCR2HCRIIKIDCRP34HPNTSUSDR20C1XR
Chromosome 17
Chromosome location 17q25.3
Summary 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.
11
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608347 18985 ENSG00000169738
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
DCXR-related disorder Pathogenic rs747887427 RCV004758639
Essential pentosuria Pathogenic rs747887427 RCV000087312
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs113680823 RCV005935579
Cholangiocarcinoma Benign rs113680823 RCV005935585
Colon adenocarcinoma Uncertain significance rs375243154 RCV005887808
Gastric cancer Benign rs113680823 RCV005935583
Associations from Text MiningDisease 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