| Type | Description |
|---|---|
| Definition | dehydrogenase/reductase 2 |
| Date | Results | Publications |
|---|---|---|
| 2020-04-18 12:26:00 | DHRS2 is dispensable for up-regulation of romidepsin effectors. | 30460772 |
| 2020-03-28 10:41:00 | Results show that DHRS2 is highly expressed in oxaliplatin-resistant colorectal cancer (CRC) cell line. Furthermore, DHRS2 regulates ERCC1 to promote oxaliplatin resistance through a p53dependent pathway, and mediates EMT by suppressing Ecadherin expression. | 31436301 |
| 2019-12-21 12:01:00 | Our report suggests that activating DHRS2 to reprogram lipid homeostasis may be a target for the development of targeted therapies against NPC. | 31291971 |
| 2019-04-06 10:31:00 | Among these targets, dehydrogenase/reductase member 2 DHRS2 and MYO1B were directly regulated by miR1453p in esophageal squamous cell carcinoma (ESCC) cells by dual luciferase reporter assays. Aberrantly expressed DHRS2 and MYOIB were detected in ESCC clinical specimens, and their overexpression enhanced cancer cell aggressiveness. | 30535463 |
| 2019-03-09 11:07:00 | Low DHRS2 expression promotes esophageal squamous cell carcinoma. | 29106393 |
| Type | IDs |
|---|---|
| Synonymous | HEP27, SDR25C1 |
| Gene |
UniProtKB-ID:
DHRS2_HUMAN
UniprotKB:
Q13268
UniParc:
UPI00001A3E34,
UPI000004C787
EMBL:
CH471078,
AK222857,
AF244132,
U31875,
BC002786,
AL135999,
BC007339
Ensembl:
ENSG00000100867
KO:
hsa:10202
|
| Nucleutide sequences |
EMBL-CDS:
EAW66130.1,
AAH07339.2,
EAW66131.1,
AAA82048.1,
BAD96577.1,
AAG33703.1,
AAH02786.1
Ensembl_TRS:
ENST00000250383,
ENST00000344777,
ENST00000611765
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000344674,
ENSP00000481607,
ENSP00000250383
RefSeq:
NP_005785.1,
XP_005267306.1,
NP_878912.1,
XP_011534640.1,
XP_011534641.1,
NP_001305764.1,
XP_006720064.1
|
| Others |
UniRef100:
UniRef100_Q13268
UniRef90:
UniRef90_Q13268
UniRef50:
UniRef50_Q9BTZ2
UniGene:
Hs.272499
CCDS:
CCDS41927.1,
CCDS9604.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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