KEGG   Homo sapiens (human): 6010
Entry
6010              CDS       T01001                                 
Symbol
RHO, CSNBAD1, OPN2, RP4
Name
(RefSeq) rhodopsin
  KO
K04250  rhodopsin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04744  Phototransduction
Disease
H00527  Retinitis pigmentosa
H00787  Congenital stationary night blindness
H00825  Familial flecked retina syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09157 Sensory system
   04744 Phototransduction
    6010 (RHO)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04030 G protein-coupled receptors [BR:hsa04030]
    6010 (RHO)
G protein-coupled receptors [BR:hsa04030]
 Rhodopsin family
  Vision
   Opsin
    6010 (RHO)
SSDB
Motif
Pfam: 7tm_1 Rhodopsin_N 7TM_GPCR_Srv 7TM_GPCR_Srw 7TM_GPCR_Srsx TAS2R
Other DBs
NCBI-GeneID: 6010
NCBI-ProteinID: NP_000530
OMIM: 180380
HGNC: 10012
Ensembl: ENSG00000163914
UniProt: P08100
Structure
Position
3:129528639..129535344
AA seq 348 aa
MNGTEGPNFYVPFSNATGVVRSPFEYPQYYLAEPWQFSMLAAYMFLLIVLGFPINFLTLY
VTVQHKKLRTPLNYILLNLAVADLFMVLGGFTSTLYTSLHGYFVFGPTGCNLEGFFATLG
GEIALWSLVVLAIERYVVVCKPMSNFRFGENHAIMGVAFTWVMALACAAPPLAGWSRYIP
EGLQCSCGIDYYTLKPEVNNESFVIYMFVVHFTIPMIIIFFCYGQLVFTVKEAAAQQQES
ATTQKAEKEVTRMVIIMVIAFLICWVPYASVAFYIFTHQGSNFGPIFMTIPAFFAKSAAI
YNPVIYIMMNKQFRNCMLTTICCGKNPLGDDEASATVSKTETSQVAPA
NT seq 1047 nt   +upstreamnt  +downstreamnt
atgaatggcacagaaggccctaacttctacgtgcccttctccaatgcgacgggtgtggta
cgcagccccttcgagtacccacagtactacctggctgagccatggcagttctccatgctg
gccgcctacatgtttctgctgatcgtgctgggcttccccatcaacttcctcacgctctac
gtcaccgtccagcacaagaagctgcgcacgcctctcaactacatcctgctcaacctagcc
gtggctgacctcttcatggtcctaggtggcttcaccagcaccctctacacctctctgcat
ggatacttcgtcttcgggcccacaggatgcaatttggagggcttctttgccaccctgggc
ggtgaaattgccctgtggtccttggtggtcctggccatcgagcggtacgtggtggtgtgt
aagcccatgagcaacttccgcttcggggagaaccatgccatcatgggcgttgccttcacc
tgggtcatggcgctggcctgcgccgcacccccactcgccggctggtccaggtacatcccc
gagggcctgcagtgctcgtgtggaatcgactactacacgctcaagccggaggtcaacaac
gagtcttttgtcatctacatgttcgtggtccacttcaccatccccatgattatcatcttt
ttctgctatgggcagctcgtcttcaccgtcaaggaggccgctgcccagcagcaggagtca
gccaccacacagaaggcagagaaggaggtcacccgcatggtcatcatcatggtcatcgct
ttcctgatctgctgggtgccctacgccagcgtggcattctacatcttcacccaccagggc
tccaacttcggtcccatcttcatgaccatcccagcgttctttgccaagagcgccgccatc
tacaaccctgtcatctatatcatgatgaacaagcagttccggaactgcatgctcaccacc
atctgctgcggcaagaacccactgggtgacgatgaggcctctgctaccgtgtccaagacg
gagacgagccaggtggccccggcctaa

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (7)   
   KEGG DISEASE (3)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (8)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (7)   
   RefSeq(nuc) (1)   
   GenBank (3)   
   EMBL (3)   
3D Structure (4)   
   PDB (4)   
Protein domain (6)   
   Pfam (6)   
All databases (39)   

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