Homo sapiens (human): 100996631
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Entry
100996631 CDS
T01001
Symbol
TCP11X1
Name
(RefSeq) t-complex 11 family, X-linked 1
KO
K25628
T-complex protein 11
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
100996631 (TCP11X1)
Cilium and associated proteins [BR:
hsa03037
]
Motile cilia and associated proteins
Sperm associated proteins
100996631 (TCP11X1)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tcp11
Motif
Other DBs
NCBI-GeneID:
100996631
NCBI-ProteinID:
NP_001355087
HGNC:
48369
Ensembl:
ENSG00000268235
LinkDB
All DBs
Position
X:102215301..102226795
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AA seq
407 aa
AA seq
DB search
MYNAFWNHLKEQLLSTPPDFTCALELLKDVKENRLRNEIEEALDTDLLKQEAEHGALDVP
HLSNYILNLMALLCAPVRDEAIQKLETIRDPVQLLRGILRVLGLMKMDMVNYTIQSFRPY
LQEHSIQYEQAKFQELLDKQPSLLDYTTKWLTKAATDITTLCPSSPDSPSSSCSMVCSLP
SGAGNNSEPPSPTMVLYQGYLNLLLWDLENVEFPETLLMDRIRLQELAFQLHQLTVLASV
LLVARSFSGEVLFRSPEFVDRLKCTTKALTEEFISRPEETMLSVSEQVSQEVHQGLKDMG
LTTLSSENTASLLGQLQNITKKENCIRSIVDQWIRFFLKCCLLHGMQESLLHFPGGLILI
EKELAELGWKFLNLMHHNQQVFGPYYAEILKHIIHPAQAQETDVEPN
NT seq
1224 nt
NT seq
+upstream
nt +downstream
nt
atgtacaatgctttttggaaccatctgaaagaacagctattgagtactcctcctgacttc
acttgtgcccttgaacttctaaaagatgttaaggagaaccgcctaagaaatgagatagaa
gaagctctggacacagatctcctcaagcaggaagcagaacatggggccctggatgtccct
catctttctaactacattctcaatttgatggctctgctatgtgcaccggttcgagatgaa
gcgatacagaaactagagaccataagagatccagtgcagttactgaggggcatcctccgt
gttctgggcctaatgaaaatggacatggtgaactataccatccagagctttcgaccctac
ctgcaggaacattccatccagtatgaacaagctaaattccaggaactccttgataaacag
cccagtctcctcgattataccacaaaatggctaaccaaagcagccacagacatcactaca
ctatgtccgagttctcctgactcacctagctcctcctgcagcatggtgtgttcacttcca
agcggggcaggtaacaattcagagccccccagtccaacaatggtgctataccaaggttac
ctgaacctcctcctctgggatcttgaaaacgtagaattcccagagactctgctgatggac
agaatccggctccaggaactggcattccagttgcaccagttaactgtcctggcctcagtc
ttgctagtggccagaagcttctctggtgaagttttattcagatcacctgaatttgtggat
agactgaaatgcaccaccaaggccctaactgaggaatttatctccaggcctgaagagact
atgctgagtgtgagtgaacaggtgtctcaggaagtccatcaaggccttaaggacatgggc
ctcactactctgagcagtgaaaacacagcatctcttctaggccaactccagaacatcacc
aagaaagagaactgcattcgtagcattgttgatcagtggatccgtttttttctcaaatgc
tgtttgcttcatggcatgcaggagtctctgctacactttcctggaggcctcattctcatt
gaaaaggagttggcagaactgggctggaagtttctcaatctgatgcatcataatcagcag
gtatttggcccatactatgctgagatcctaaaacacatcatccatccagctcaagcacaa
gaaacagatgtggagcctaactga
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