Insufficient scRNA-seq data for expression of DHRS2 at single-cell level.
Insufficient scRNA-seq data for expression of DHRS2 at tissue level.
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
bladder | 95% | 34358.00 | 20 / 21 | 61% | 291.01 | 306 / 504 |
pancreas | 98% | 575.09 | 322 / 328 | 52% | 48.16 | 93 / 178 |
liver | 95% | 1151.81 | 214 / 226 | 54% | 26.76 | 220 / 406 |
adrenal gland | 56% | 75.35 | 144 / 258 | 63% | 27.03 | 146 / 230 |
breast | 58% | 3621.68 | 265 / 459 | 56% | 79.11 | 626 / 1118 |
ovary | 97% | 1617.31 | 174 / 180 | 15% | 2.55 | 64 / 430 |
kidney | 89% | 111.74 | 79 / 89 | 12% | 12.95 | 109 / 901 |
spleen | 100% | 1998.29 | 241 / 241 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 100% | 252.11 | 1 / 1 |
prostate | 89% | 257.55 | 218 / 245 | 10% | 1.86 | 49 / 502 |
stomach | 72% | 276.33 | 260 / 359 | 21% | 3.89 | 59 / 286 |
brain | 50% | 46.50 | 1318 / 2642 | 21% | 1.65 | 149 / 705 |
uterus | 25% | 27.36 | 43 / 170 | 33% | 39.06 | 150 / 459 |
skin | 24% | 122.56 | 441 / 1809 | 31% | 3.10 | 148 / 472 |
lung | 30% | 12.34 | 176 / 578 | 16% | 6.06 | 189 / 1155 |
esophagus | 7% | 3.06 | 95 / 1445 | 22% | 17.14 | 41 / 183 |
intestine | 7% | 2.85 | 68 / 966 | 17% | 3.28 | 91 / 527 |
peripheral blood | 19% | 17.62 | 177 / 929 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 18% | 6.87 | 8 / 45 |
thymus | 4% | 4.54 | 26 / 653 | 7% | 6.35 | 41 / 605 |
adipose | 10% | 5.82 | 120 / 1204 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 9% | 1.14 | 7 / 80 |
blood vessel | 2% | 5.68 | 27 / 1335 | 0% | 0 | 0 / 0 |
muscle | 1% | 0.31 | 7 / 803 | 0% | 0 | 0 / 0 |
heart | 1% | 0.34 | 6 / 861 | 0% | 0 | 0 / 0 |
abdomen | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
bone marrow | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
diaphragm | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
gingiva | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 29 |
nasal cavity | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasopharynx | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nose | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
placenta | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spinal column | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
GO_0022900 | Biological process | electron transport chain |
GO_0008285 | Biological process | negative regulation of cell population proliferation |
GO_0034599 | Biological process | cellular response to oxidative stress |
GO_0008207 | Biological process | C21-steroid hormone metabolic process |
GO_0009636 | Biological process | response to toxic substance |
GO_0043066 | Biological process | negative regulation of apoptotic process |
GO_0043011 | Biological process | myeloid dendritic cell differentiation |
GO_0005654 | Cellular component | nucleoplasm |
GO_0005759 | Cellular component | mitochondrial matrix |
GO_0005635 | Cellular component | nuclear envelope |
GO_0005737 | Cellular component | cytoplasm |
GO_0005739 | Cellular component | mitochondrion |
GO_0005634 | Cellular component | nucleus |
GO_0004090 | Molecular function | carbonyl reductase (NADPH) activity |
GO_0005515 | Molecular function | protein binding |
GO_0016616 | Molecular function | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor |
Gene name | DHRS2 |
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) Dehydrogenase/reductase 2 |
Synonyms | SDR25C1 |
Description | 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 . 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 . . |
Accessions | ENST00000611765.4 [Q13268-2] ENST00000250383.11 [Q13268-1] ENST00000557535.5 ENST00000553600.1 Q13268 H0YJG9 C9JZP6 H0YJP4 ENST00000344777.11 [Q13268-2] ENST00000432832.6 |