KEGG   Homo sapiens (human): 1406Help
Entry
1406              CDS       T01001                                 

Gene name
CRX, CORD2, CRD, LCA7, OTX3
Definition
cone-rod homeobox
Orthology
K09337  
cone-rod homeobox protein
Organism
hsa  Homo sapiens (human)
Disease
H00481  
Cone-rod dystrophy and cone dystrophy
H00837  
Leber congenital amaurosis (LCR)
Class
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
OMIM: 
HGNC: 
HPRD: 
Ensembl: 
Vega: 
UniProt: 
Position
19q13.3
AA seq 299 aa AA seqDB search
MMAYMNPGPHYSVNALALSGPSVDLMHQAVPYPSAPRKQRRERTTFTRSQLEELEALFAK
TQYPDVYAREEVALKINLPESRVQVWFKNRRAKCRQQRQQQKQQQQPPGGQAKARPAKRK
AGTSPRPSTDVCPDPLGISDSYSPPLPGPSGSPTTAVATVSIWSPASESPLPEAQRAGLV
ASGPSLTSAPYAMTYAPASAFCSSPSAYGSPSSYFSGLDPYLSPMVPQLGGPALSPLSGP
SVGPSLAQSPTSLSGQSYGAYSPVDSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL
NT seq 900 nt NT seq  +upstreamnt  +downstreamnt
atgatggcgtatatgaacccggggccccactattctgtcaacgccttggccctaagtggc
cccagtgtggatctgatgcaccaggctgtgccctacccaagcgcccccaggaagcagcgg
cgggagcgcaccaccttcacccggagccaactggaggagctggaggcactgtttgccaag
acccagtacccagacgtctatgcccgtgaggaggtggctctgaagatcaatctgcctgag
tccagggttcaggtttggttcaagaaccggagggctaaatgcaggcagcagcgacagcag
cagaaacagcagcagcagcccccagggggccaggccaaggcccggcctgccaagaggaag
gcgggcacgtccccaagaccctccacagatgtgtgtccagaccctctgggcatctcagat
tcctacagtccccctctgcccggcccctcaggctccccaaccacggcagtggccactgtg
tccatctggagcccagcctcagagtcccctttgcctgaggcgcagcgggctgggctggtg
gcctcagggccgtctctgacctccgccccctatgccatgacctacgccccggcctccgct
ttctgctcttccccctccgcctatgggtctccgagctcctatttcagcggcctagacccc
tacctttctcccatggtgccccagctagggggcccggctcttagccccctctctggcccc
tccgtgggaccttccctggcccagtcccccacctccctatcaggccagagctatggcgcc
tacagccccgtggatagcttggaattcaaggaccccacgggcacctggaaattcacctac
aatcccatggaccctctggactacaaggatcagagtgcctggaagtttcagatcttgtag

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