Type | Description |
---|---|
Definition | PBX homeobox 2 |
Date | Results | Publications |
---|---|---|
2017-11-11 12:04:00 | The findings from the present study that a SNP of the PBX2 gene in the MHC region (at 6p21.3) was associated with allergic rhinitis (AR) in allele and genotypic analysis suggests a new susceptibility gene for AR in the MHC region and another gene associated with both asthma and AR in Chinese subjects. | 26852910 |
2016-10-01 12:33:00 | miR19153p functions as a silencer of apoptosis, which regulates lung cancer apoptosis via targeting DRG2/PBX2. | 26572100 |
2013-08-31 10:14:00 | findings suggest the disruption of the HOXB7/PBX2 complexes, miR-221&222 inhibition or even better their combination, as innovative therapeutic approaches | 23400877 |
2012-07-14 10:33:00 | a high level of PBX2 is a poor prognosticator for disease-free survival and overall survival in gingival squamous cell carcinoma | 22374608 |
2010-10-23 11:10:00 | Pre B cell leukemia homeobox 2 has a role in poor prognosis of gastric adenocarcinoma and esophageal squamous cell carcinoma | 20126986 |
Type | IDs |
---|---|
Synonymous | G17, HOX12, PBX2MHC |
Gene |
UniProtKB-ID:
PBX2_HUMAN,
A0A024RCR3_HUMAN
UniprotKB:
P40425,
A0A024RCR3
UniParc:
UPI00001313B2
EMBL:
CH471081,
BC082261,
X59842,
D28769,
BX284686,
KY500544,
KY500545,
X80700,
CR812478,
CR933878,
AL662884,
AL845464,
AL662830,
KY500548,
U89336,
KY500549,
BX927239
Ensembl:
ENSG00000204304,
ENSG00000232005,
ENSG00000206315,
ENSG00000236353,
ENSG00000224952,
ENSG00000237344,
ENSG00000225987
KO:
hsa:5089
|
Nucleutide sequences |
EMBL-CDS:
AAB47490.1,
CAA56717.1,
BAA05957.1,
AAH82261.1,
CAA42503.1,
EAX03613.1,
EAX03622.1,
AQY77017.1,
AQY77021.1,
AQY77020.1,
AQY77016.1
Gene_ORFName:
hCG_2039588
Ensembl_TRS:
ENST00000383270,
ENST00000375050,
ENST00000431537,
ENST00000453487,
ENST00000453961,
ENST00000420432,
ENST00000433552
|
Protein sequencees |
Ensembl_PRO:
ENSP00000403948,
ENSP00000410710,
ENSP00000372757,
ENSP00000391745,
ENSP00000397177,
ENSP00000390009,
ENSP00000364190
RefSeq:
NP_002577.2
|
Others |
UniRef100:
UniRef100_P40425
UniRef90:
UniRef90_P40425
UniRef50:
UniRef50_P40425
UniGene:
Hs.509545,
Hs.718462
CCDS:
CCDS4748.1
|
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Refseq |
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