Homo sapiens (human): 26123 Help Entry 26123             CDS       T01001                                  Symbol TCTN3, C10orf61, JBTS18, OFD4, TECT3 Name (RefSeq) tectonic family member 3   KO K19382   tectonic-1/3 Organism hsa  Homo sapiens (human) Disease H00454   Oral-facial-digital syndrome 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]     26123 (TCTN3) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   MKS complex    26123 (TCTN3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TCTN_DUF1619 Motif Other DBs NCBI-GeneID:  26123 NCBI-ProteinID:  NP_056446 OMIM:  613847 HGNC:  24519 Ensembl:  ENSG00000119977 UniProt:  Q6NUS6 LinkDB All DBs Position 10:complement(95663401..95693927) Genome browser AA seq 607 aa AA seqDB search MRTPQLALLQVFFLVFPDGVRPQPSSSPSGAVPTSLELQRGTDGGTLQSPSEATATRPAV PGLPTVVPTLVTPSAPGNRTVDLFPVLPICVCDLTPGACDINCCCDRDCYLLHPRTVFSF CLPGSVRSSSWVCVDNSVIFRSNSPFPSRVFMDSNGIRQFCVHVNNSNLNYFQKLQKVNA TNFQALAAEFGGESFTSTFQTQSPPSFYRAGDPILTYFPKWSVISLLRQPAGVGAGGLCA ESNPAGFLESKSTTCTRFFKNLASSCTLDSALNAASYYNFTVLKVPRSMTDPQNMEFQVP VILTSQANAPLLAGNTCQNVVSQVTYEIETNGTFGIQKVSVSLGQTNLTVEPGASLQQHF ILRFRAFQQSTAASLTSPRSGNPGYIVGKPLLALTDDISYSMTLLQSQGNGSCSVKRHEV QFGVNAISGCKLRLKKADCSHLQQEIYQTLHGRPRPEYVAIFGNADPAQKGGWTRILNRH CSISAINCTSCCLIPVSLEIQVLWAYVGLLSNPQAHVSGVRFLYQCQSIQDSQQVTEVSL TTLVNFVDITQKPQPPRGQPKMDWKWPFDFFPFKVAFSRGVFSQKCSVSPILILCLLLLG VLNLETM NT seq 1824 nt NT seq  +upstreamnt  +downstreamnt atgcgcaccccacagctcgcgctcctgcaagtgttctttctggtgttccccgatggcgtc cggcctcagccctcttcctccccatcaggggcagtgcccacgtctttggagctgcagcga gggacggatggcggaaccctccagtccccttcagaggcgactgcaactcgcccggccgtg cctggactccctacagtggtccctactctcgtgactccctcggcccctgggaataggact gtggacctcttcccagtcttaccgatctgtgtctgtgacttgactcctggagcctgcgat ataaattgctgctgcgacagggactgctatcttctccatccgaggacagttttctccttc tgccttccaggcagcgtaaggtcttcaagctgggtttgtgtagacaactctgttatcttc aggagtaattccccgtttccttcaagagttttcatggattctaatggaatcaggcagttt tgtgtccatgtgaacaactcaaacttaaactatttccagaagcttcaaaaggtcaatgca accaacttccaggccctggctgcagagtttggaggcgaatcattcacttcaacattccaa actcaatcaccaccatctttttacagggctggggaccccattcttacttacttccccaag tggtctgtaataagcttgctgagacaacctgcaggagttggagctgggggactctgtgct gaaagcaatcctgcaggtttcctagagagtaaaagtacaacttgcactcgttttttcaag aacctggctagtagctgtaccttggattcagccctcaatgctgcctcttactataacttc acagtcttaaaggttccaagaagcatgactgatccacagaatatggagttccaggttcct gtaatacttacctcacaggctaatgctcctctgttggctggaaacacttgtcagaatgta gtttctcaggtcacctatgagatagagaccaatgggacttttggaatccagaaagtttct gtcagtttgggacaaaccaacctgactgttgagccaggcgcttccttacagcaacacttc atccttcgcttcagggcttttcaacagagcacagctgcttctctcaccagtcctagaagt gggaatcctggctatatagttgggaagccactcttggctctgactgatgatataagttac tcaatgaccctcttacagagccagggtaatggaagttgctctgttaaaagacatgaagtg cagtttggagtgaatgcaatatctggatgcaagctcaggttgaagaaggcagactgcagc cacttgcagcaggagatttatcagactcttcatggaaggcccagaccagagtatgttgcc atctttggtaatgctgacccagcccagaaaggagggtggaccaggatcctcaacaggcac tgcagcatttcagctataaactgtacttcctgctgtctcataccagtttccctggagatc caggtattgtgggcatatgtaggtctcctgtccaacccgcaagctcatgtatcaggagtt cgattcctataccagtgccagtctatacaggattctcagcaagttacagaagtatctttg acaactcttgtgaactttgtggacattacccagaagccacagcctccaaggggccaaccc aaaatggactggaaatggccattcgacttctttcccttcaaagtggcattcagcagagga gtattctctcaaaaatgctcagtctctcccatccttatcctgtgcctcttactacttgga gttctcaacctagagactatgtga

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