Type | Description |
---|---|
Definition | pannier |
Date | Results | Publications |
---|---|---|
2016-05-07 10:20:00 | Overexpression of Tinman and Pannier resulted in 20% of embryos with ectopic Hand and Sur expression. By adding MEF2 alongside Tinman and Pannier, an expansion in expression of Hand and Sur was observed. | 26225919 |
2013-08-10 11:47:00 | A second 20E-mediated mechanism, which robustly affects only a subset of AMP genes, is uniquely controlled by BR-C, SRP and PNR. | 23652443 |
2012-07-21 11:07:00 | pnr appears to be highly regulated by Dpp and Brk on both the DV and AP axes during embryo patterning. | 22513375 |
2012-06-09 10:54:00 | Genetic interaction analysis shows that spir functionally interacts with Dorsocross, tin, and pannier to properly specify the cardiac fate. | 22276214 |
2011-06-18 10:10:00 | This study uncovers complex transcriptional interactions between the pnr isoforms and the cofactor Ush that may be important for regulation of proneural expression and thorax patterning. | 20709169 |
Type | IDs |
---|---|
Synonymous | CG3978, CG3978-PA, Dmel\CG3978, GATA, GATA4, GATAa, GATAa/Pannier, PNR, Pnr, dGATAa, dGATAa/pannier, l(3)89B3, prn |
Gene |
UniProtKB-ID:
PNR_DROME,
Q9VEZ8_DROME,
A8WHL1_DROME,
A0A0B4KH81_DROME
UniprotKB:
P52168,
Q9VEZ8,
A8WHL1,
A0A0B4KH81
UniParc:
UPI0000078015,
UPI00000075A9,
UPI0002ADBDA6
EMBL:
S68798,
BT053737,
S68803,
S68909,
S68793,
S68795,
S68802,
BT031157,
AE014297
EnsemblGenome:
FBgn0003117
KO:
dme:Dmel_CG3978
|
Nucleutide sequences |
EMBL-CDS:
AAB29874.1,
AAB29876.2,
AAN13693.1,
AGB96001.1,
AAF55264.3,
ACK77655.1,
ABX00779.1,
AGB96000.1
Gene_ORFName:
CG3978,
Dmel_CG3978,
CG3978,
Dmel_CG3978,
CG3978
EnsemblGenome_TRS:
FBtr0083221,
FBtr0335427,
FBtr0083220,
FBtr0083221,
FBtr0335426
|
Protein sequencees |
EnsemblGenome_PRO:
FBpp0082675,
FBpp0307409,
FBpp0082674,
FBpp0082675,
FBpp0307408
RefSeq:
NP_476685.1,
NP_001262621.1,
NP_001262620.1,
NP_732102.1
|
Others |
UniRef100:
UniRef100_A0A0B4KH81,
UniRef100_P52168
UniRef90:
UniRef90_P52168
UniRef50:
UniRef50_P52168
UniGene:
Dm.7432
|
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