DHRS2 report

I. Expression across cell types

Insufficient scRNA-seq data for expression of DHRS2 at single-cell level.

II. Expression across tissues

sc-RNAseq data

Insufficient scRNA-seq data for expression of DHRS2 at tissue level.

III. Associated gene sets

GO_0022900Biological processelectron transport chain
GO_0008285Biological processnegative regulation of cell population proliferation
GO_0034599Biological processcellular response to oxidative stress
GO_0008207Biological processC21-steroid hormone metabolic process
GO_0009636Biological processresponse to toxic substance
GO_0043066Biological processnegative regulation of apoptotic process
GO_0043011Biological processmyeloid dendritic cell differentiation
GO_0005654Cellular componentnucleoplasm
GO_0005759Cellular componentmitochondrial matrix
GO_0005635Cellular componentnuclear envelope
GO_0005737Cellular componentcytoplasm
GO_0005739Cellular componentmitochondrion
GO_0005634Cellular componentnucleus
GO_0004090Molecular functioncarbonyl reductase (NADPH) activity
GO_0005515Molecular functionprotein binding
GO_0016616Molecular functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor

IV. Literature review

[source]
Gene nameDHRS2
Protein nameDehydrogenase/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)
Dehydrogenase/reductase 2
SynonymsSDR25C1
DescriptionFUNCTION: 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 . May function as a dicarbonyl reductase in the enzymatic inactivation of reactive carbonyls involved in covalent modification of cellular components . Also displays a minor hydroxysteroid dehydrogenase activity toward bile acids such as ursodeoxycholic acid (UDCA) and isoursodeoxycholic acid (isoUDCA), which makes it unlikely to control hormone levels . Doesn't show any activity in vitro with retinoids and sugars as substrates . Attenuates MDM2-mediated p53/TP53 degradation, leading to p53/TP53 stabilization and increased transcription activity, resulting in the accumulation of MDM2 and CDKN1A/p21 . Reduces proliferation, migration and invasion of cancer cells and well as the production of ROS in cancer . .

AccessionsENST00000611765.4 [Q13268-2]
ENST00000250383.11 [Q13268-1]
ENST00000557535.5
ENST00000553600.1
Q13268
H0YJG9
C9JZP6
H0YJP4
ENST00000344777.11 [Q13268-2]
ENST00000432832.6