KEGG   Homo sapiens (human): 26123
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)
SSDB
Motif
Pfam: TCTN_DUF1619
Other DBs
NCBI-GeneID: 26123
NCBI-ProteinID: NP_056446
OMIM: 613847
HGNC: 24519
Ensembl: ENSG00000119977
UniProt: Q6NUS6
Position
10:complement(95663401..95693927)
AA seq 607 aa
MRTPQLALLQVFFLVFPDGVRPQPSSSPSGAVPTSLELQRGTDGGTLQSPSEATATRPAV
PGLPTVVPTLVTPSAPGNRTVDLFPVLPICVCDLTPGACDINCCCDRDCYLLHPRTVFSF
CLPGSVRSSSWVCVDNSVIFRSNSPFPSRVFMDSNGIRQFCVHVNNSNLNYFQKLQKVNA
TNFQALAAEFGGESFTSTFQTQSPPSFYRAGDPILTYFPKWSVISLLRQPAGVGAGGLCA
ESNPAGFLESKSTTCTRFFKNLASSCTLDSALNAASYYNFTVLKVPRSMTDPQNMEFQVP
VILTSQANAPLLAGNTCQNVVSQVTYEIETNGTFGIQKVSVSLGQTNLTVEPGASLQQHF
ILRFRAFQQSTAASLTSPRSGNPGYIVGKPLLALTDDISYSMTLLQSQGNGSCSVKRHEV
QFGVNAISGCKLRLKKADCSHLQQEIYQTLHGRPRPEYVAIFGNADPAQKGGWTRILNRH
CSISAINCTSCCLIPVSLEIQVLWAYVGLLSNPQAHVSGVRFLYQCQSIQDSQQVTEVSL
TTLVNFVDITQKPQPPRGQPKMDWKWPFDFFPFKVAFSRGVFSQKCSVSPILILCLLLLG
VLNLETM
NT seq 1824 nt   +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

  All links  
Disease (3)   
   OMIM (3)   
Gene (23)   
   RefGene (12)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (15)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (13)   
DNA sequence (47)   
   RefSeq(nuc) (13)   
   GenBank (17)   
   EMBL (17)   
Protein domain (1)   
   Pfam (1)   
All databases (89)   

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