Homo sapiens (human): 343035 Help Entry 343035            CDS       T01001                                  Symbol RD3, C1orf36, LCA12 Name (RefSeq) RD3 regulator of GUCY2D   KO K25404   protein RD3 Organism hsa  Homo sapiens (human) Disease H00837   Leber congenital amaurosis Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     343035 (RD3) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   Other primary cilia associated proteins    343035 (RD3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RD3 Motif Other DBs NCBI-GeneID:  343035 NCBI-ProteinID:  NP_001158160 OMIM:  180040 HGNC:  19689 Ensembl:  ENSG00000198570 UniProt:  Q7Z3Z2 Structure PDBPDBj LinkDB All DBs Position 1:complement(211476522..211492162) Genome browser AA seq 195 aa AA seqDB search MSLISWLRWNEAPSRLSTRSPAEMVLETLMMELTGQMREAERQQRERSNAVRKVCTGVDY SWLASTPRSTYDLSPIERLQLEDVCVKIHPSYCGPAILRFRQLLAEQEPEVQEVSQLFRS VLQEVLERMKQEEEAHKLTRQWSLRPRGSLATFKTRARISPFASDIRTISEDVERDTPPP LRSWSMPEFRAPKAD NT seq 588 nt NT seq  +upstreamnt  +downstreamnt atgtctctcatctcatggcttcggtggaacgaggccccatcccggctgtccaccaggagc cctgctgagatggtgctggagacgcttatgatggagctgacggggcagatgcgagaggct gagaggcagcagcgggagcgcagcaatgcggtcagaaaggtctgcaccggtgtggactac agctggctggccagcacaccccggtccacctatgacctcagccccattgagcggttgcag ctggaagatgtctgcgttaagatccacccatcctattgtgggcctgctatcctcaggttc cggcagctgctggcggagcaggagcccgaggtgcaggaggtgtcccagctcttccgctcg gtgctgcaggaggtcctggagaggatgaagcaggaagaggaggcccacaagctgacgcgc cagtggagcctgcggccccgcggcagcctggccaccttcaagacccgcgcgcgcatctcg cccttcgccagcgacatcaggaccatctccgaggacgtggagcgggacacaccgccgcca ctgcggtcctggagcatgcccgaattccgggcgcccaaagccgactga

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