Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10202
Gene name Gene Name - the full gene name approved by the HGNC.
Dehydrogenase/reductase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DHRS2
Synonyms (NCBI Gene) Gene synonyms aliases
HEP27, SDR25C1
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family, which has over 46,000 members. Members of this family are enzymes that metabolize many different compounds, such as steroid hormones, prostaglandins, retinoids, lipids a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT934930 hsa-miR-1226 CLIP-seq
MIRT934931 hsa-miR-29a CLIP-seq
MIRT934932 hsa-miR-29b CLIP-seq
MIRT934933 hsa-miR-29c CLIP-seq
MIRT934934 hsa-miR-330-3p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
MYB Unknown 15105423
MYBL1 Unknown 15105423
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 IDA 16685466
GO:0005515 Function Protein binding IPI 25416956
GO:0005634 Component Nucleus IDA 1847869
GO:0005635 Component Nuclear envelope IDA 11997086
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615194 18349 ENSG00000100867
Protein
UniProt ID Q13268
Protein name Dehydrogenase/reductase SDR family member 2, mitochondrial (EC 1.1.1.-) (Dicarbonyl reductase HEP27) (Protein D) (Short chain dehydrogenase/reductase family 25C member 1) (Protein SDR25C1)
Protein function NADPH-dependent oxidoreductase which catalyzes the reduction of dicarbonyl compounds. Displays reductase activity in vitro with 3,4-hexanedione, 2,3-heptanedione and 1-phenyl-1,2-propanedione as substrates (PubMed:16685466). May function as a di
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13561 adh_short_C2 43 277 Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, with highest levels in liver and kidney, followed by heart, spleen, skeletal muscle and placenta. In hemopoietic cells, expressed in dendritic cells, but not in monocytes, macrophages, granulocytes, nor in B and T lym
Sequence
Sequence length 280
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
Dementia Dementia GWAS
Alzheimer disease Alzheimer disease GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 20547751, 36594618
Carcinoma Hepatocellular Associate 33667649
Carcinoma Renal Cell Associate 37119764
Colorectal Neoplasms Associate 31436301
Endometrial Neoplasms Associate 35401936
Hepatoblastoma Associate 7556196
Leukemia Myeloid Acute Associate 32586085
Neoplasm Metastasis Inhibit 36192391
Neoplasms Inhibit 32586085, 36192391
Neoplasms Associate 36594618