KEGG ORTHOLOGY: K08546

ORTHOLOGY: K08546

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

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:	100365683
CGE:	100752298(Nr2e3)
HGL:	101724001(Nr2e3)
TUP:	102497265(NR2E3)
CFA:	487629(NR2E3)
AML:	100478490
FCA:	101093940(NR2E3)
BTA:	281944(NR2E3)
BOM:	102282114(NR2E3)
PHD:	102324907(NR2E3)
CHX:	102177064(NR2E3)
SSC:	102159757(NR2E3)
CFR:	102521893(NR2E3)
ECB:	100063879(NR2E3)
MYB:	102252756(NR2E3)
MDO:	100018049
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
PSS:	102459248(NR2E3)
ACS:	100565262
XTR:	100036597(nr2e3)
DRE:	492496(nr2e3)
TRU:	101065759
MZE:	101475152
OLA:	101156874
XMA:	102220885
LCM:	102356760(NR2E3)
BFO:	BRAFLDRAFT_235500
SPU:	575196
DME:	Dmel_CG16801(Hr51)
DPO:	Dpse_GA30480
DAN:	Dana_GF13031
DER:	Dere_GG20513
DPE:	Dper_GL17753
DSE:	Dsec_GM21604
DSI:	Dsim_GD11109
DWI:	Dwil_GK20892
DYA:	Dyak_GE13645
DGR:	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
HMG:	100204761

» show all

Reference

PMID:12963616

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)

All links

Ontology (3)   
   KEGG BRITE (3)   
Disease (2)   
   KEGG DISEASE (2)   
Gene (87)   
   KEGG GENES (74)   
   KEGG DGENES (7)   
   KEGG EGENES (1)   
   KEGG MGENES (3)   
   OC (2)   
Protein sequence (38)   
   UniProt (36)   
   SWISS-PROT (2)   
Literature (1)   
   PubMed (1)   
All databases (131)   

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