KEGG   Homo sapiens (human): 5015
Entry
5015              CDS       T01001                                 
Symbol
OTX2, CPHD6, MCOPS5
Name
(RefSeq) orthodenticle homeobox 2
  KO
K18490  homeobox protein OTX2
Organism
hsa  Homo sapiens (human)
Disease
H00254  Growth hormone deficiency
H00544  Septo-optic dysplasia
H01667  Medulloblastoma
H02036  Combined pituitary hormone deficiency
H02170  Microphthalmia, syndromic
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5015 (OTX2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    5015 (OTX2)
SSDB
Motif
Pfam: TF_Otx Homeodomain Homeobox_KN NUDE_C SatD
Other DBs
NCBI-GeneID: 5015
NCBI-ProteinID: NP_001257452
OMIM: 600037
HGNC: 8522
Ensembl: ENSG00000165588
UniProt: P32243 F1T0D1
Position
14:complement(56799905..56810479)
AA seq 289 aa
MMSYLKQPPYAVNGLSLTTSGMDLLHPSVGYPATPRKQRRERTTFTRAQLDVLEALFAKT
RYPDIFMREEVALKINLPESRVQVWFKNRRAKCRQQQQQQQNGGQNKVRPAKKKTSPARE
VSSESGTSGQFTPPSSTSVPTIASSSAPVSIWSPASISPLSDPLSTSSSCMQRSYPMTYT
QASGYSQGYAGSTSYFGGMDCGSYLTPMHHQLPGPGATLSPMGTNAVTSHLNQSPASLST
QGYGASSLGFNSTTDCLDYKDQTASWKLNFNADCLDYKDQTSSWKFQVL
NT seq 870 nt   +upstreamnt  +downstreamnt
atgatgtcttatcttaagcaaccgccttacgcagtcaatgggctgagtctgaccacttcg
ggtatggacttgctgcacccctccgtgggctacccggccaccccccggaaacagcgccgg
gagaggacgacgttcactcgggcgcagctagatgtgctggaagcactgtttgccaagacc
cggtacccagacatcttcatgcgagaggaggtggcactgaaaatcaacttgcccgagtcg
agggtgcaggtatggtttaagaatcgaagagctaagtgccgccaacaacagcaacaacag
cagaatggaggtcaaaacaaagtgagacctgccaaaaagaagacatctccagctcgggaa
gtgagttcagagagtggaacaagtggccaattcactcccccctctagcacctcagtcccg
accattgccagcagcagtgctcctgtgtctatctggagcccagcttccatctccccactg
tcagatcccttgtccacctcctcttcctgcatgcagaggtcctatcccatgacctatact
caggcttcaggttatagtcaaggatatgctggctcaacttcctactttgggggcatggac
tgtggatcatatttgacccctatgcatcaccagcttcccggaccaggggccacactcagt
cccatgggtaccaatgcagtcaccagccatctcaatcagtccccagcttctctttccacc
cagggatatggagcttcaagcttgggttttaactcaaccactgattgcttggattataag
gaccaaactgcctcctggaagcttaacttcaatgctgactgcttggattataaagatcag
acatcctcgtggaaattccaggttttgtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (8)   
   KEGG DISEASE (5)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (27)   
   RefSeq(nuc) (7)   
   GenBank (10)   
   EMBL (10)   
Protein domain (5)   
   Pfam (5)   
All databases (63)   

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