Type | Description |
---|---|
Definition | period circadian regulator 3 |
Date | Results | Publications |
---|---|---|
2020-11-28 13:10:00 | PER3 variable number tandem repeat (VNTR) polymorphism modulates the circadian variation of the descending pain modulatory system in healthy subjects. | 31249322 |
2020-10-03 12:58:00 | Clock gene PERIOD3 polymorphism is associated with susceptibility to Graves' disease but not to Hashimoto's thyroiditis. | 31328557 |
2020-06-27 11:33:00 | Enhanced expression of miR-181a in iBMSCs and PASCs produced a robust increase in adipogenesis through the direct targeting of the circadian factor period circadian regulator 3 (PER3). | 30670712 |
2020-04-18 12:20:00 | The Per3 rs228697 CC genotype was associated with a higher sleep factor score when compared with the CG genotype. In addition, the rs228729 TC genotype was associated with a greater risk of suffering from excitement/agitation, akathisia and weight loss (p = 0.041, OR = 2.287) when compared with the CC genotype. Finally, the rs10746473 AA genotype patients were more likely to suffer from dizziness | 31692380 |
2019-11-23 12:27:00 | genotype may play an important role in individual vulnerability to the different mechanisms of daytime sleep disturbance in night shift workers | 29510794 |
Type | IDs |
---|---|
Synonymous | FASPS3, GIG13 |
Gene |
UniProtKB-ID:
PER3_HUMAN,
A2I2N5_HUMAN,
A0A087WV69_HUMAN
UniprotKB:
P56645,
A2I2N5,
A0A087WV69
UniParc:
UPI00003664CA,
UPI000387D6D4,
UPI0000167B1D
EMBL:
AB047531,
AB047530,
AB047532,
AY493418,
AL157954,
EF015893,
AB047686,
AB047534,
AB047521,
Z98884,
AB047533
Ensembl:
ENSG00000049246
KO:
hsa:8863
|
Nucleutide sequences |
EMBL-CDS:
BAB63252.1,
BAB63255.1,
BAB32925.2,
BAB63251.1,
BAB63250.1,
BAB63254.1,
BAB63253.1,
CAB76084.1,
AAS72879.1,
ABM64204.1
Gene_ORFName:
GIG13
Ensembl_TRS:
ENST00000377532,
ENST00000361923,
ENST00000613533,
ENST00000614998
|
Protein sequencees |
Ensembl_PRO:
ENSP00000482093,
ENSP00000366755,
ENSP00000355031,
ENSP00000479223
RefSeq:
XP_024306358.1,
XP_016858218.1,
XP_016858216.1,
XP_024306380.1,
XP_016858222.1,
NP_001276791.1,
NP_001276790.1,
XP_016858227.1,
NP_001364204.1,
XP_016858219.1,
XP_016858212.1,
XP_016858217.1,
XP_016858213.1,
XP_016858221.1,
XP_024306354.1,
NP_001276792.1,
XP_024306355.1,
NP_058515.1,
XP_005263581.1,
XP_016858223.1,
XP_016858220.1,
NP_001276793.1,
XP_016858215.1,
XP_024306379.1,
XP_016858224.1,
XP_016858226.1,
NP_001364205.1
|
Others |
UniRef100:
UniRef100_A0A087WV69,
UniRef100_P56645
UniRef90:
UniRef90_G1RBV0,
UniRef90_P56645
UniRef50:
UniRef50_P56645
UniGene:
Hs.162200
CCDS:
CCDS89.1,
CCDS72695.1
|
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Refseq |
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