Homo sapiens (human): 79600 Help Entry 79600             CDS       T01001                                  Symbol TCTN1, JBTS13, TECT1 Name (RefSeq) tectonic family member 1   KO K19382   tectonic-1/3 Organism hsa  Homo sapiens (human) Disease H00530   Joubert syndrome and related disorders Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     79600 (TCTN1) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   MKS complex    79600 (TCTN1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TCTN_DUF1619 Motif Other DBs NCBI-GeneID:  79600 NCBI-ProteinID:  NP_001076006 OMIM:  609863 HGNC:  26113 Ensembl:  ENSG00000204852 UniProt:  Q2MV58 B4DIB9 LinkDB All DBs Position 12:110614129..110649430 Genome browser AA seq 587 aa AA seqDB search MRPRGLPPLLVVLLGCWASVSAQTDATPAVTTEGLNSTEAALATFGTFPSTRPPGTPRAP GPSSGPRPTPVTDVAVLCVCDLSPAQCDINCCCDPDCSSVDFSVFSACSVPVVTGDSQFC SQKAVIYSLNFTANPPQRVFELVDQINPSIFCIHITNYKPALSFINPEVPDENNFDTLMK TSDGFTLNAESYVSFTTKLDIPTAAKYEYGVPLQTSDSFLRFPSSLTSSLCTDNNPAAFL VNQAVKCTRKINLEQCEEIEALSMAFYSSPEILRVPDSRKKVPITVQSIVIQSLNKTLTR REDTDVLQPTLVNAGHFSLCVNVVLEVKYSLTYTDAGEVTKADLSFVLGTVSSVVVPLQQ KFEIHFLQENTQPVPLSGNPGYVVGLPLAAGFQPHKGSGIIQTTNRYGQLTILHSTTEQD CLALEGVRTPVLFGYTMQSGCKLRLTGALPCQLVAQKVKSLLWGQGFPDYVAPFGNSQAQ DMLDWVPIHFITQSFNRKDSCQLPGALVIEVKWTKYGSLLNPQAKIVNVTANLISSSFPE ANSGNERTILISTAVTFVDVSAPAEAGFRAPPAINARLPFNFFFPFV NT seq 1764 nt NT seq  +upstreamnt  +downstreamnt atgaggccgcgaggtctcccgccgctcctggtggtgctcctgggctgctgggcctccgtg agcgcccagaccgatgccaccccggcggtgacgacagagggcctcaactccaccgaggca gccctggccaccttcggaactttcccgtcgaccaggccccccgggactcccagggctcca gggccctcctccggccccaggcctaccccagtcacggacgttgctgttctctgtgtctgt gacttatccccagcacagtgtgacatcaactgctgctgtgatcccgactgcagctccgtg gatttcagtgtcttttctgcctgctcagttccagttgtcacgggcgacagccagttttgt agtcaaaaagcagtcatctattcattgaattttacagcaaacccacctcaaagagtattt gaacttgttgaccagattaatccatctattttctgcattcatattacaaactataaacct gcattatcctttattaatccagaagtacctgatgaaaacaattttgatacattgatgaaa acatctgatggttttacattgaatgctgaatcatatgtttccttcacaaccaaactggat attcctactgctgctaaatatgagtatggggttcctctgcagacttcagattcgtttctg agatttccttcgtccctgacatcatctctgtgcactgataataaccctgcagcgtttctg gtgaaccaggctgttaagtgcaccagaaaaataaatttagaacagtgtgaagaaattgaa gccctcagcatggctttttacagcagcccggaaattctgagggtacctgattcaagaaaa aaggtccctatcactgttcagtccatcgtcattcagtctctaaataaaacgctcacccga cgggaggacactgatgtgctgcagccgactctcgtcaacgctggacactttagcctttgc gtgaatgttgttcttgaggtaaagtacagcctcacatacacagatgcaggtgaagtcacc aaagctgatctctcattcgttctggggacagttagcagcgtagtggtcccactgcagcaa aagtttgaaattcattttcttcaggaaaatacccagccagtccctctcagtggaaaccct ggttatgtcgtggggctcccattagctgctggattccagcctcataaggggtctgggatt attcagaccacaaatagatatggacagcttactattcttcatagcacaactgagcaagac tgcttagcactggagggggtccggaccccagtattatttggttacactatgcaatctggc tgtaaactaagactgactggagctctcccgtgtcagctcgtagcacagaaggtgaagagc ctgctgtggggccagggcttcccagattacgtggccccttttggaaattcccaggcccag gacatgctggactgggtgcccatccacttcatcacccagtcattcaacaggaaggattcc tgccagctcccaggggctttggttatagaagtgaagtggactaaatacggatccctgctg aatccacaggccaaaatagtcaatgtaactgcaaatctaatttcatcctcctttcctgag gccaactcaggaaatgaaaggacgattcttatttccactgcggttacttttgtggatgtg tctgcacctgcagaggcaggcttcagagctccaccagccatcaatgccaggctgcccttt aacttcttcttcccgtttgtttga

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