Homo sapiens (human): 6010 Help 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) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  7tm_1 Rhodopsin_N 7TM_GPCR_Srv 7TM_GPCR_Srw 7TM_GPCR_Srsx TAS2R Motif Other DBs NCBI-GeneID:  6010 NCBI-ProteinID:  NP_000530 OMIM:  180380 HGNC:  10012 Ensembl:  ENSG00000163914 UniProt:  P08100 Structure PDBPDBj LinkDB All DBs Position 3:129528639..129535344 Genome browser AA seq 348 aa AA seqDB search MNGTEGPNFYVPFSNATGVVRSPFEYPQYYLAEPWQFSMLAAYMFLLIVLGFPINFLTLY VTVQHKKLRTPLNYILLNLAVADLFMVLGGFTSTLYTSLHGYFVFGPTGCNLEGFFATLG GEIALWSLVVLAIERYVVVCKPMSNFRFGENHAIMGVAFTWVMALACAAPPLAGWSRYIP EGLQCSCGIDYYTLKPEVNNESFVIYMFVVHFTIPMIIIFFCYGQLVFTVKEAAAQQQES ATTQKAEKEVTRMVIIMVIAFLICWVPYASVAFYIFTHQGSNFGPIFMTIPAFFAKSAAI YNPVIYIMMNKQFRNCMLTTICCGKNPLGDDEASATVSKTETSQVAPA NT seq 1047 nt NT seq  +upstreamnt  +downstreamnt atgaatggcacagaaggccctaacttctacgtgcccttctccaatgcgacgggtgtggta cgcagccccttcgagtacccacagtactacctggctgagccatggcagttctccatgctg gccgcctacatgtttctgctgatcgtgctgggcttccccatcaacttcctcacgctctac gtcaccgtccagcacaagaagctgcgcacgcctctcaactacatcctgctcaacctagcc gtggctgacctcttcatggtcctaggtggcttcaccagcaccctctacacctctctgcat ggatacttcgtcttcgggcccacaggatgcaatttggagggcttctttgccaccctgggc ggtgaaattgccctgtggtccttggtggtcctggccatcgagcggtacgtggtggtgtgt aagcccatgagcaacttccgcttcggggagaaccatgccatcatgggcgttgccttcacc tgggtcatggcgctggcctgcgccgcacccccactcgccggctggtccaggtacatcccc gagggcctgcagtgctcgtgtggaatcgactactacacgctcaagccggaggtcaacaac gagtcttttgtcatctacatgttcgtggtccacttcaccatccccatgattatcatcttt ttctgctatgggcagctcgtcttcaccgtcaaggaggccgctgcccagcagcaggagtca gccaccacacagaaggcagagaaggaggtcacccgcatggtcatcatcatggtcatcgct ttcctgatctgctgggtgccctacgccagcgtggcattctacatcttcacccaccagggc tccaacttcggtcccatcttcatgaccatcccagcgttctttgccaagagcgccgccatc tacaaccctgtcatctatatcatgatgaacaagcagttccggaactgcatgctcaccacc atctgctgcggcaagaacccactgggtgacgatgaggcctctgctaccgtgtccaagacg gagacgagccaggtggccccggcctaa

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