Conger conger (European conger): 133121683
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Entry
133121683 CDS
T10633
Symbol
septin9b
Name
(RefSeq) septin 9b isoform X1
KO
K16938
septin 3/9/12
Organism
ccog Conger conger (European conger)
Pathway
ccog05100
Bacterial invasion of epithelial cells
Brite
KEGG Orthology (KO) [BR:
ccog00001
]
09160 Human Diseases
09171 Infectious disease: bacterial
05100 Bacterial invasion of epithelial cells
133121683 (septin9b)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
ccog03037
]
133121683 (septin9b)
04812 Cytoskeleton proteins [BR:
ccog04812
]
133121683 (septin9b)
04147 Exosome [BR:
ccog04147
]
133121683 (septin9b)
Cilium and associated proteins [BR:
ccog03037
]
Motile cilia and associated proteins
Sperm associated proteins
133121683 (septin9b)
Cytoskeleton proteins [BR:
ccog04812
]
Eukaryotic cytoskeleton proteins
Septins
Septins
Group 1
133121683 (septin9b)
Exosome [BR:
ccog04147
]
Exosomal proteins
Exosomal proteins of haemopoietic cells (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
133121683 (septin9b)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Septin
MMR_HSR1
RsgA_GTPase
AIG1
GTP_EFTU
Roc
Dynamin_N
Ras
AAA_16
AAA_22
ABC_tran
NB-ARC
URGCP_GTPase
IIGP
AAA_29
P-loop_TraG
FtsK_SpoIIIE
GatC
Sigma54_activat
AAA_7
G-alpha
MCM
Motif
Other DBs
NCBI-GeneID:
133121683
NCBI-ProteinID:
XP_061087043
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All DBs
Position
2:71722467..71787363
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AA seq
570 aa
AA seq
DB search
MSDSTVNPHLEGIISDFEALKRSFEVEDVDPTAHPSPHGRRTPNLRAAVTSPSQRYQELG
ARNSDLSANQRSPKPSQGPGGRTPEPVSRRTEISIDISSKQVDSSPSPGISRFGLKRPEV
QGHSRAPEQAHRRPELSPNRAQEPPPVRRPDPPAASVSRIPEPIHRKAEPTNSGDVPSRR
VEITVAKAPEGPAPAKPPVNSLTPAVPSAHHPHKAQPLGSDIRIRSPDGSEVIPSYTSTM
SEPAKPAQGPQPPVRSDKPGADFSYVGIDAILEQMRRKAMKQGFELNIMVVGQSGLGKST
LMNTLFKSKVSRKSVLATGEERIPQTIEIKSISHDIEEKGVRMKLTVIDTPGFGDQINNE
NCWKPIMKFINDQYEQYLQEEINIERKKRIPDSRVHCCIYFIPATGHCLRPLDVEFMRRL
SKVVNIVPVIAKADTLTLEERDFFKKKIREELRTNGIDVYPQKEFDEDAEDRMINEKIRE
MIPFAVVGSDQEYQVNGKRLLGRKTKWGTIEVENIAHCEFAFLRDLLIRTHMQNIKDITS
NIHYEVYRVRRLNETNKQANGVSEGEVFLP
NT seq
1713 nt
NT seq
+upstream
nt +downstream
nt
atgtctgattccactgtcaatcctcacttggaaggaattatatcagattttgaagctcta
aagaggtcgtttgaggtggaggacgttgacccgacggcgcacccctccccgcacggtcgg
cgaacgcccaaccttcgcgcggccgtgacctctcccagccagcgctaccaggagctgggc
gcgcgaaactctgacctgagcgccaaccagcgctcgcccaaacccagccaagggccgggc
ggccgcacccccgagcctgtgtcccgccgcacggagatctccatcgacatctcctccaag
caggtggacagctcccccagccccggcatctcccgcttcggcctgaagaggcccgaggtc
cagggccacagcagggcccccgagcaggcccaccggcggcctgagctcagccccaaccgg
gcccaggagcccccgcccgtcaggaggcccgacccccccgccgcctccgtctccaggatc
cccgagcccatccacaggaaggcggagcccaccaactcgggagacgtcccgtcccggcgt
gttgagattaccgtcgccaaggcccctgagggcccggctcccgccaagccgccagtgaac
agcctcaccccggccgtgcccagcgcccaccaccctcacaaagcgcagccgctgggctcg
gacatccgcatccggagtcctgacgggtcagaggtcattcccagctacaccagcaccatg
tcagagcccgccaagccagcccagggcccccagccccccgtgcgcagcgacaagcccggc
gcggacttcagctacgtgggcatcgatgccatcctggagcagatgaggcggaaggccatg
aagcagggcttcgagctcaacatcatggtagtggggcagagcggtttggggaaatccacc
ctcatgaacaccctcttcaagtccaaggtgagccgcaaatctgtgctggccacgggagag
gagaggatcccccagactatcgagatcaagtccatcagtcacgacatcgaggaaaagggc
gtgaggatgaaattgacagtaatcgacactcccggttttggggatcagatcaacaatgaa
aactgctggaagcccatcatgaagttcattaatgaccagtatgagcagtaccttcaggag
gagatcaacatcgagaggaagaagagaatcccagactcgcgcgttcactgctgtatatac
ttcatccccgctaccggccactgcctcaggcccctggacgtggagttcatgagacgcctc
agtaaagtggtcaacatcgtccctgtcatcgccaaggctgacactttaactctggaagag
agagacttcttcaaaaagaagatcagggaggagttgcggaccaatgggattgatgtttac
ccgcagaaggagtttgacgaggatgcggaggacaggatgatcaatgagaagatcagagag
atgatccccttcgctgtggttgggagtgaccaggagtaccaggtcaacgggaaaaggctt
ctgggaaggaaaacaaagtggggcaccatagaagtggagaacattgcacactgtgagttc
gcttttttgcgggacctgcttattagaacccacatgcagaacatcaaggacatcaccagc
aacatccactacgaggtgtaccgcgtccgcaggctgaacgagaccaacaaacaggccaac
ggagtgtccgagggcgaagttttcctcccatga
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