KEGG   ORTHOLOGY: K08546Help
Entry
K08546                      KO                                     
Name
NR2E3, PNR
Definition
nuclear receptor subfamily 2 group E member 3
Disease
H00527  
Retinitis pigmentosa (RP)
H00805  
Vitreoretinal degeneration
Brite
Transcription factors [BR:ko03000]
 Eukaryotic Type
  Zinc finger
   Cys4 hepatocyte nuclear factor 4-like
    K08546  NR2E3, PNR; nuclear receptor subfamily 2 group E member 3
Nuclear receptors [BR:ko03310]
 2. Hepatocyte nuclear factor 4 like
  2E. Tailless like receptor
   K08546  NR2E3, PNR; nuclear receptor subfamily 2 group E member 3
BRITE hierarchy
Genes
HSA: 
10002(NR2E3)
PTR: 
748665(NR2E3)
PPS: 
100981430(NR2E3)
GGO: 
101129867(NR2E3)
PON: 
100434712(NR2E3)
MCC: 
701402(NR2E3)
MCF: 
102118891(NR2E3)
MMU: 
23958(Nr2e3)
RNO: 
CGE: 
100752298(Nr2e3)
HGL: 
101724001(Nr2e3)
TUP: 
102497265(NR2E3)
CFA: 
487629(NR2E3)
AML: 
100478490
FCA: 
101093940(NR2E3)
PTG: 
102956953(NR2E3)
BTA: 
281944(NR2E3)
BOM: 
102282114(NR2E3)
PHD: 
102324907(NR2E3)
CHX: 
102177064(NR2E3)
SSC: 
102159757(NR2E3)
CFR: 
102521893(NR2E3)
BACU: 
103002739(NR2E3)
LVE: 
103075605(NR2E3)
ECB: 
100063879(NR2E3)
MYB: 
102252756(NR2E3)
MYD: 
102754690(NR2E3)
PALE: 
102894527(NR2E3)
MDO: 
100018049(NR2E3)
SHR: 
100934552(NR2E3)
GGA: 
395289(NR2E3)
MGP: 
100540956
TGU: 
100228348(NR2E3)
FAB: 
101816771(NR2E3)
PHI: 
102106981(NR2E3)
APLA: 
101798374(NR2E3)
FPG: 
101922584(NR2E3)
FCH: 
102059347(NR2E3)
CLV: 
102084994(NR2E3)
ASN: 
102387979
AMJ: 
102564335
PSS: 
102459248(NR2E3)
CMY: 
102940731(NR2E3)
ACS: 
100565262
PBI: 
103054728(NR2E3)
XTR: 
100036597(nr2e3)
DRE: 
492496(nr2e3)
TRU: 
101065759
MZE: 
101470418 101475152
OLA: 
101156874 101157353 101164305
XMA: 
102220885 102229583
LCM: 
102356760(NR2E3)
CMK: 
103189537(nr2e3)
BFO: 
BRAFLDRAFT_235500 BRAFLDRAFT_236186
SPU: 
575196
DME: 
Dmel_CG16801(Hr51)
DPO: 
Dpse_GA30480
DAN: 
Dana_GF13031
DER: 
Dere_GG20513
DPE: 
Dper_GL17752 Dper_GL17753
DSE: 
Dsec_GM21604
DSI: 
Dsim_GD11109
DWI: 
Dwil_GK20892
DYA: 
Dyak_GE13645
DGR: 
Dgri_GH20426 Dgri_GH20427
DMO: 
Dmoj_GI19610
DVI: 
Dvir_GJ14974
AGA: 
AgaP_AGAP009890
AAG: 
AaeL_AAEL007190
CQU: 
CpipJ_CPIJ017333
AME: 
413558(Hr51)
NVI: 
100114216(Tll) 100122615(Hr51)
TCA: 
658951 661886
BMOR: 
101745996
API: 
100166752
PHU: 
Phum_PHUM039420
ISC: 
IscW_ISCW019467
BMY: 
Bm1_32150
LOA: 
LOAG_06205
TSP: 
Tsp_06560 Tsp_10966
HMG: 
100204761
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP
  Title
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
  Journal
Arch Ophthalmol 121:1316-23 (2003)
Reference
  Authors
Peng GH, Ahmad O, Ahmad F, Liu J, Chen S
  Title
The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes.
  Journal
Hum Mol Genet 14:747-64 (2005)
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