Cottoperca gobio: 115014375 Help Entry 115014375         CDS       T07513                                  Symbol septin6 Name (RefSeq) septin-6 isoform X1   KO K16939   septin 6/8/11 Organism cgob  Cottoperca gobio Pathway cgob05100   Bacterial invasion of epithelial cells Brite KEGG Orthology (KO) [BR:cgob00001]  09160 Human Diseases   09171 Infectious disease: bacterial    05100 Bacterial invasion of epithelial cells     115014375 (septin6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:cgob03037]     115014375 (septin6)    04812 Cytoskeleton proteins [BR:cgob04812]     115014375 (septin6)    04147 Exosome [BR:cgob04147]     115014375 (septin6) Cilium and associated proteins [BR:cgob03037]  Motile cilia and associated proteins   Sperm associated proteins    115014375 (septin6) Cytoskeleton proteins [BR:cgob04812]  Eukaryotic cytoskeleton proteins   Septins    Septins     Group 1      115014375 (septin6) Exosome [BR:cgob04147]  Exosomal proteins   Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)    115014375 (septin6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Septin MMR_HSR1 AAA_22 FlgN AAA_16 Roc ATG14 DUF3080 AAA_29 UBA_NBR1_C AAA_7 Ras DUF4478 Fzo_mitofusin TPR_MLP1_2 ABC_tran Motif Other DBs NCBI-GeneID:  115014375 NCBI-ProteinID:  XP_029297019 Ensembl:  ENSCGOG00000014875 UniProt:  A0A6J2QGB5 LinkDB All DBs Position 10:complement(8203479..8222202) Genome browser AA seq 455 aa AA seqDB search MQLPLLTESSRCFVLQLAATTMASTEIARQAGEGARAVPLAGHVGFDSMPDQLVNKSVNH GFCFNILCVGETGLGKSTLMDTLFNTKFEGEPTQHNQPGVTLKSNTYELQESNVRLKLTV VNTVGFGDQINKEDSYKSIVEFIDAQFEAYLQEELKIKRTLHSYHDTRIHACLYFIAPTG HSLKSLDLVTMKKLDSKVNIIPIVAKSDAISKSELAKFKIKITSELVSNGVQIYQFPTDD ESVAEINSTMNSHLPFAVVGSTEEVKIGNKMVKARQYPWGTVQVENENHCDFVKLREMLI RVNMEDLREQTHTRHYELYRRCKLEEMGFKDTDPDSKPFSLQETYEAKRNEFMGELQKKE EEMRQMFVQRVKEKEAELKEAEKELHEKFDRLKKLHQDEKKKLEDKKKSLDDELNMFKQK KTAAELLYNQAQQAGGSTTLKRDKERKNNPWLCTE NT seq 1368 nt NT seq  +upstreamnt  +downstreamnt atgcagcttcctttgctaacagagagtagtagatgtttcgtcctccagctagcagctacc accatggcgtcaactgagatagcaaggcaagcgggtgaaggtgctcgtgctgtccctctg gcaggccatgtcggctttgatagcatgcctgaccagttggtcaataagtctgtcaaccac ggattctgcttcaacatcctctgtgttggtgagacgggtctggggaagtccaccctcatg gacacgttgttcaacactaagtttgagggcgagcccactcagcacaatcagccaggagtc acgctcaagtccaacacctacgagctccaggagagtaacgtacgcctcaaactcacagtc gtcaacaccgtgggcttcggagaccagataaacaaagaagacagctacaagtctatcgtg gagttcattgatgcccagtttgaagcatatctacaagaggaactgaaaatcaagcgcacg ctacacagctaccacgacacacgcatccacgcgtgtctttattttatagcacccacagga cactcgctcaaatccctggacttggtgaccatgaagaaacttgatagcaaggtcaatatt atcccaatcgttgccaagtcggacgccatctccaagagcgagctggccaagtttaaaatc aaaatcaccagtgagctggtcagcaacggagtgcagatctaccagttccccactgatgac gagtctgtggcagagatcaactccaccatgaacagccatttgccatttgccgtggtgggg agcacggaagaagtgaagattgggaacaagatggtgaaggcccggcagtacccctggggg acggtgcaggtggaaaatgagaatcactgtgacttcgtcaagctgcgagaaatgctgatc agagtgaacatggaggacctgcgagagcagactcacacccgtcattatgagctctatcgc cgctgcaaacttgaagagatgggcttcaaggacacagaccctgacagcaagccctttagc cttcaggagacgtatgaagctaagaggaatgagttcatgggtgagctccaaaagaaagaa gaagaaatgaggcaaatgtttgtccaaagagtgaaagagaaggaggcagagctcaaagaa gcagagaaagagctgcacgagaagtttgaccgtctgaagaagctccaccaggacgagaaa aagaaactggaggacaagaagaagtccctggacgacgagctcaacatgttcaaacagaaa aagactgctgcagagctcttgtacaatcaagcccagcaggcagggggctccaccacactc aagagggacaaagagaggaaaaataatccctggctctgcactgagtag

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