Homo sapiens (human): 79867
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TCTN_DUF1619
Motif
Other DBs
NCBI-GeneID:
79867
NCBI-ProteinID:
NP_079085
OMIM:
613846
HGNC:
25774
Ensembl:
ENSG00000168778
UniProt:
Q96GX1
LinkDB
All DBs
Position
12:123671113..123708399
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AA seq
697 aa
AA seq
DB search
MGFQPPAALLLRLFLLQGILRLLWGDLAFIPPFIRMSGPAVSASLVGDTEGVTVSLAVLQ
DEAGILPIPTCGVLNNETEDWSVTVIPGAKVLEVTVRWKRGLDWCSSNETDSFSESPCIL
QTLLVSASHNSSCSAHLLIQVEIYANSSLTHNASENVTVIPNQVYQPLGPCPCNLTAGAC
DVRCCCDQECSSNLTTLFRRSCFTGVFGGDVNPPFDQLCSAGTTTRGVPDWFPFLCVQSP
LANTPFLGYFYHGAVSPKQDSSFEVYVDTDAKDFADFGYKQGDPIMTVKKAYFTIPQVSL
AGQCMQNAPVAFLHNFDVKCVTNLELYQERDGIINAKIKNVALGGIVTPKVIYEEATDLD
KFITNTETPLNNGSTPRIVNVEEHYIFKWNNNTISEINVKIFRAEINAHQKGIMTQRFVV
KFLSYNSGNEEELSGNPGYQLGKPVRALNINRMNNVTTLHLWQSAGRGLCTSATFKPILF
GENVLSGCLLEVGINENCTQLRENAVERLDSLIQATHVAMRGNSDYADLSDGWLEIIRVD
APDPGADPLASSVNGMCLDIPAHLSIRILISDAGAVEGITQQEILGVETRFSSVNWQYQC
GLTCEHKADLLPISASVQFIKIPAQLPHPLTRFQINYTEYDCNRNEVCWPQLLYPWTQYY
QGELHSQCVAKGLLLLLFLTLALFLSNPWTRICKAYS
NT seq
2094 nt
NT seq
+upstream
nt +downstream
nt
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
DBGET
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