KEGG   Homo sapiens (human): 79867
Entry
79867             CDS       T01001                                 
Symbol
TCTN2, C12orf38, JBTS24, MKS8, TECT2
Name
(RefSeq) tectonic family member 2
  KO
K19361  tectonic-2
Organism
hsa  Homo sapiens (human)
Disease
H00261  Meckel 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]
    79867 (TCTN2)
Cilium and associated proteins [BR:hsa03037]
 Primary cilia and associated proteins
  MKS complex
   79867 (TCTN2)
SSDB
Motif
Pfam: TCTN_DUF1619
Other DBs
NCBI-GeneID: 79867
NCBI-ProteinID: NP_079085
OMIM: 613846
HGNC: 25774
Ensembl: ENSG00000168778
UniProt: Q96GX1
Position
12:123671113..123708399
AA seq 697 aa
MGFQPPAALLLRLFLLQGILRLLWGDLAFIPPFIRMSGPAVSASLVGDTEGVTVSLAVLQ
DEAGILPIPTCGVLNNETEDWSVTVIPGAKVLEVTVRWKRGLDWCSSNETDSFSESPCIL
QTLLVSASHNSSCSAHLLIQVEIYANSSLTHNASENVTVIPNQVYQPLGPCPCNLTAGAC
DVRCCCDQECSSNLTTLFRRSCFTGVFGGDVNPPFDQLCSAGTTTRGVPDWFPFLCVQSP
LANTPFLGYFYHGAVSPKQDSSFEVYVDTDAKDFADFGYKQGDPIMTVKKAYFTIPQVSL
AGQCMQNAPVAFLHNFDVKCVTNLELYQERDGIINAKIKNVALGGIVTPKVIYEEATDLD
KFITNTETPLNNGSTPRIVNVEEHYIFKWNNNTISEINVKIFRAEINAHQKGIMTQRFVV
KFLSYNSGNEEELSGNPGYQLGKPVRALNINRMNNVTTLHLWQSAGRGLCTSATFKPILF
GENVLSGCLLEVGINENCTQLRENAVERLDSLIQATHVAMRGNSDYADLSDGWLEIIRVD
APDPGADPLASSVNGMCLDIPAHLSIRILISDAGAVEGITQQEILGVETRFSSVNWQYQC
GLTCEHKADLLPISASVQFIKIPAQLPHPLTRFQINYTEYDCNRNEVCWPQLLYPWTQYY
QGELHSQCVAKGLLLLLFLTLALFLSNPWTRICKAYS
NT seq 2094 nt   +upstreamnt  +downstreamnt
atgggcttccagcctccggccgctcttcttttgaggcttttccttctgcagggcatcctg
aggcttctgtggggggacctggctttcatccctccttttatccgaatgtccggccctgcg
gtcagcgcgtccctggtcggagacaccgagggtgtgaccgtgtccctggcagtgctgcag
gacgaggcgggaatattgccaattccgacgtgtggagtgctgaacaatgagacggaagac
tggagcgtgactgtgatccccggtgcgaaggtgttggaagtgacagtgaggtggaagaga
ggtctggactggtgttcctccaatgagacagattccttctcagagtccccctgtatcctc
cagacccttctggtttcagcatctcataattcatcctgttcagcacatctactcattcaa
gtggaaatttatgccaactcttctctgacccataatgcctcagagaacgtgactgtcatt
cctaaccaggtgtatcagccccttggcccttgtccttgtaatttaacagctggagcctgt
gatgttcgctgctgctgtgaccaggaatgctcatcaaatttaacaacgctgttcagacgg
tcctgcttcaccggcgtgtttggaggagacgtcaatcctccttttgatcagctctgctct
gctgggacgacgacacgtggtgtccccgattggtttccctttctgtgtgtgcagtccccc
cttgccaacacacccttccttggttacttctatcatggtgctgtttcccccaaacaggac
tcttcctttgaagtatatgtggatactgacgcaaaagactttgcagactttggttacaaa
caaggagatcccattatgactgtaaagaaggcatattttactattccgcaggtgtccctg
gctgggcagtgtatgcagaacgccccagtggcatttcttcacaattttgatgttaaatgc
gttactaatttggaactataccaagaacgagatggtattatcaatgcgaagataaagaat
gttgccttaggaggcatagttacaccaaaagtgatctatgaggaagcaactgacctagac
aaattcatcaccaatacagaaactcctttaaataacggatcaacccctagaattgtgaat
gtggaagaacattatattttcaaatggaataataataccatcagtgaaataaatgttaaa
atttttagggcagagattaatgcccaccagaaagggataatgacacagagatttgtagta
aaatttttaagctataatagtggtaatgaagaagaattatctggaaatccaggttaccaa
cttggcaagcctgtccgagctctaaatatcaacaggatgaataatgtcacgactttacat
ctttggcaatcggctggaaggggtctgtgtacatcagcaactttcaaacccattttattt
ggagaaaatgtactctctggatgcctgttagaagtcgggattaatgaaaattgtactcag
ctcagggagaatgctgttgaaagacttgattcattaatacaagcgactcacgttgcaatg
agaggcaactccgattacgctgatcttagtgatggctggctcgaaataatacgtgtagat
gcccctgatccaggtgcagacccgctggctagcagtgtgaacggcatgtgcctggatatt
cctgctcacctgagcatccgcatcctcatctcggatgctggcgcggtggaagggattact
cagcaggagatactcggtgtagagacaaggttctcctcagtgaactggcagtaccagtgt
gggcttacctgtgagcacaaggccgaccttctccctatcagtgcatccgtccagtttatt
aaaattcctgcacagttaccccaccccctgacaagattccagatcaattatacagagtat
gactgcaacagaaatgaggtgtgttggccgcagcttctatatccatggactcagtattat
caaggggagctgcattctcagtgtgttgctaagggcttactgttgctgttgttcctcaca
ttggccttgttcctcagcaacccctggaccagaatatgcaaagcctatagttag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (29)   
   KEGG ORTHOLOGY (1)   
   RefGene (22)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (9)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (21)   
   RefSeq(nuc) (7)   
   GenBank (7)   
   EMBL (7)   
Protein domain (1)   
   Pfam (1)   
All databases (68)   

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