KEGG   Homo sapiens (human): 10002
Entry
10002             CDS       T01001                                 
Symbol
NR2E3, ESCS, PNR, RNR, RP37, rd7
Name
(RefSeq) nuclear receptor subfamily 2 group E member 3
  KO
K08546  nuclear receptor subfamily 2 group E member 3
Organism
hsa  Homo sapiens (human)
Disease
H00527  Retinitis pigmentosa
H00805  Vitreoretinal degeneration
H02075  Enhanced S-cone syndrome
H02341  Goldmann-Favre syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    10002 (NR2E3)
  09183 Protein families: signaling and cellular processes
   03310 Nuclear receptors [BR:hsa03310]
    10002 (NR2E3)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Zinc finger
   Cys4 hepatocyte nuclear factor 4-like
    10002 (NR2E3)
Nuclear receptors [BR:hsa03310]
 2. Hepatocyte nuclear factor 4 like
  2E. Tailless like receptor
   10002 (NR2E3)
SSDB
Motif
Pfam: Hormone_recep zf-C4 C1_2
Other DBs
NCBI-GeneID: 10002
NCBI-ProteinID: NP_055064
OMIM: 604485
HGNC: 7974
Ensembl: ENSG00000278570
UniProt: Q9Y5X4
Structure
Position
15:71810554..71818253
AA seq 410 aa
METRPTALMSSTVAAAAPAAGAASRKESPGRWGLGEDPTGVSPSLQCRVCGDSSSGKHYG
IYACNGCSGFFKRSVRRRLIYRCQVGAGMCPVDKAHRNQCQACRLKKCLQAGMNQDAVQN
ERQPRSTAQVHLDSMESNTESRPESLVAPPAPAGRSPRGPTPMSAARALGHHFMASLITA
ETCAKLEPEDADENIDVTSNDPEFPSSPYSSSSPCGLDSIHETSARLLFMAVKWAKNLPV
FSSLPFRDQVILLEEAWSELFLLGAIQWSLPLDSCPLLAPPEASAAGGAQGRLTLASMET
RVLQETISRFRALAVDPTEFACMKALVLFKPETRGLKDPEHVEALQDQSQVMLSQHSKAH
HPSQPVRFGKLLLLLPSLRFITAERIELLFFRKTIGNTPMEKLLCDMFKN
NT seq 1233 nt   +upstreamnt  +downstreamnt
atggagaccagaccaacagctctgatgagctccacagtggctgcagctgcgcctgcagct
ggggctgcctccaggaaggagtctccaggcagatggggcctgggggaggatcccacaggc
gtgagcccctcgctccagtgccgcgtgtgcggagacagcagcagcgggaagcactatggc
atctatgcctgcaacggctgcagcggcttcttcaagaggagcgtacggcggaggctcatc
tacaggtgccaggtgggggcagggatgtgccccgtggacaaggcccaccgcaaccagtgc
caggcctgccggctgaagaagtgcctgcaggcggggatgaaccaggacgccgtgcagaac
gagcgccagccgcgaagcacagcccaggtccacctggacagcatggagtccaacactgag
tcccggccggagtccctggtggctcccccggccccggcagggcgcagcccacggggcccc
acacccatgtctgcagccagagccctgggccaccacttcatggccagccttataacagct
gaaacctgtgctaagctggagccagaggatgctgatgagaatattgatgtcaccagcaat
gaccctgagttcccctcctctccatactcctcttcctccccctgcggcctggacagcatc
catgagacctcggctcgcctactcttcatggccgtcaagtgggccaagaacctgcctgtg
ttctccagcctgcccttccgggatcaggtgatcctgctggaagaggcgtggagtgaactc
tttctcctcggggccatccagtggtctctgcctctggacagctgtcctctgctggcaccg
cccgaggcctctgctgccggtggtgcccagggccggctcacgctggccagcatggagacg
cgtgtcctgcaggaaactatctctcggttccgggcattggcggtggaccccacggagttt
gcctgcatgaaggccttggtcctcttcaagccagagacgcggggcctgaaggatcctgag
cacgtagaggccttgcaggaccagtcccaagtgatgctgagccagcacagcaaggcccac
caccccagccagcccgtgaggtttgggaaattgctcctgctcctcccgtctttgaggttt
atcactgcggaacgcatcgagctcctctttttccgcaagaccatagggaatactccaatg
gagaagctcctttgtgatatgttcaaaaactag

  All links  
Disease (3)   
   OMIM (3)   
Gene (11)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (19)   
   RefSeq(nuc) (3)   
   GenBank (8)   
   EMBL (8)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (41)   

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