KEGG   Homo sapiens (human): 1406
Entry
1406              CDS       T01001                                 
Symbol
CRX, CORD2, CRD, LCA7, OTX3
Name
(RefSeq) cone-rod homeobox
  KO
K09337  cone-rod homeobox protein
Organism
hsa  Homo sapiens (human)
Disease
H00481  Cone-rod dystrophy and cone dystrophy
H00837  Leber congenital amaurosis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    1406 (CRX)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    1406 (CRX)
SSDB
Motif
Pfam: Homeodomain TF_Otx Homeobox_KN MRP-L20
Other DBs
NCBI-GeneID: 1406
NCBI-ProteinID: NP_000545
OMIM: 602225
HGNC: 2383
Ensembl: ENSG00000105392
UniProt: O43186
Structure
Position
19:47821937..47843324
AA seq 299 aa
MMAYMNPGPHYSVNALALSGPSVDLMHQAVPYPSAPRKQRRERTTFTRSQLEELEALFAK
TQYPDVYAREEVALKINLPESRVQVWFKNRRAKCRQQRQQQKQQQQPPGGQAKARPAKRK
AGTSPRPSTDVCPDPLGISDSYSPPLPGPSGSPTTAVATVSIWSPASESPLPEAQRAGLV
ASGPSLTSAPYAMTYAPASAFCSSPSAYGSPSSYFSGLDPYLSPMVPQLGGPALSPLSGP
SVGPSLAQSPTSLSGQSYGAYSPVDSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL
NT seq 900 nt   +upstreamnt  +downstreamnt
atgatggcgtatatgaacccggggccccactattctgtcaacgccttggccctaagtggc
cccagtgtggatctgatgcaccaggctgtgccctacccaagcgcccccaggaagcagcgg
cgggagcgcaccaccttcacccggagccaactggaggagctggaggcactgtttgccaag
acccagtacccagacgtctatgcccgtgaggaggtggctctgaagatcaatctgcctgag
tccagggttcaggtttggttcaagaaccggagggctaaatgcaggcagcagcgacagcag
cagaaacagcagcagcagcccccagggggccaggccaaggcccggcctgccaagaggaag
gcgggcacgtccccaagaccctccacagatgtgtgtccagaccctctgggcatctcagat
tcctacagtccccctctgcccggcccctcaggctccccaaccacggcagtggccactgtg
tccatctggagcccagcctcagagtcccctttgcctgaggcgcagcgggctgggctggtg
gcctcagggccgtctctgacctccgccccctatgccatgacctacgccccggcctccgct
ttctgctcttccccctccgcctatgggtctccgagctcctatttcagcggcctagacccc
tacctttctcccatggtgccccagctagggggcccggctcttagccccctctctggcccc
tccgtgggaccttccctggcccagtcccccacctccctatcaggccagagctatggcgcc
tacagccccgtggatagcttggaattcaaggaccccacgggcacctggaaattcacctac
aatcccatggaccctctggactacaaggatcagagtgcctggaagtttcagatcttgtag

  All links  
Disease (4)   
   OMIM (4)   
Gene (13)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (37)   
   RefSeq(nuc) (1)   
   GenBank (18)   
   EMBL (18)   
3D Structure (1)   
   PDB (1)   
Protein domain (4)   
   Pfam (4)   
All databases (62)   

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