Mustela nigripes (black-footed ferret): 132003122
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Entry
132003122 CDS
T09425
Symbol
SEPTIN9
Name
(RefSeq) septin-9 isoform X1
KO
K16938
septin 3/9/12
Organism
mnp
Mustela nigripes (black-footed ferret)
Pathway
mnp05100
Bacterial invasion of epithelial cells
Brite
KEGG Orthology (KO) [BR:
mnp00001
]
09160 Human Diseases
09171 Infectious disease: bacterial
05100 Bacterial invasion of epithelial cells
132003122 (SEPTIN9)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
mnp03037
]
132003122 (SEPTIN9)
04812 Cytoskeleton proteins [BR:
mnp04812
]
132003122 (SEPTIN9)
04147 Exosome [BR:
mnp04147
]
132003122 (SEPTIN9)
Cilium and associated proteins [BR:
mnp03037
]
Motile cilia and associated proteins
Sperm associated proteins
132003122 (SEPTIN9)
Cytoskeleton proteins [BR:
mnp04812
]
Eukaryotic cytoskeleton proteins
Septins
Septins
Group 1
132003122 (SEPTIN9)
Exosome [BR:
mnp04147
]
Exosomal proteins
Exosomal proteins of haemopoietic cells (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
132003122 (SEPTIN9)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Septin
MMR_HSR1
RsgA_GTPase
Dynamin_N
AIG1
GTP_EFTU
Roc
Ras
AAA_16
AAA_22
ABC_tran
FtsK_SpoIIIE
NB-ARC
IIGP
URGCP_GTPase
AAA_29
PduV-EutP
G-alpha
VapE-like_dom
AAA_7
TniB
Arf
Motif
Other DBs
NCBI-GeneID:
132003122
NCBI-ProteinID:
XP_059234397
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Position
16:complement(4091144..4235416)
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AA seq
600 aa
AA seq
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MPGGPQSRLELLSFRLLPLPPGVTRTSSNRLRKLGDPTGPALKRSFEVEEAETPNSTPHR
RVQTPVLRATVASSTQKFQDLGVKNSEPAARHVDSLSQRSPKAALRRVELSGPKAEPVSR
RTEISIDISSKQVESAGAAGPSRFGLKRAEALGHKTPEPAPRRTEITIVKPQESAHRRME
SPASKIPEMPTAPAVDAAPKRVEIQVPKPAEGPASPLPPQTLENSEHALVSQLQSRLEPK
PQPPVVEALPKSQEAPEAAPGCVGDMAETPRDAGLKQAPAPRNEKAPADFGYVGIDSILE
QMRRKAMKQGFEFNIMVVGQSGLGKSTLINTLFKSKISRKSVQPTSEERIPKTIEIKSIT
HDIEEKGVRMKLTVIDTPGFGDHINNENCWQPIMKFINDQYEKYLQEEVNINRKKRIPDT
RVHCCLYFIPATGHSLRPLDIEFMKRLSKVVNIVPVIAKADTLTLEERVYFKQRITADLL
SNGIDVYPQKEFDEDPEDRLVNEKFREMIPFAVVGSDHEYQVNGKRILGRKTKWGTIEVE
NTTHCEFAYLRDLLIRTHMQNIKDITSSIHFEAYRVKRLHEGSNAMANGVEEKGPEAQEM
NT seq
1803 nt
NT seq
+upstream
nt +downstream
nt
atgccagggggcccccaaagcaggcttgagctcctctccttccgccttctccccctcccc
ccaggagtcacgcggacctccagcaaccgtctccggaagctcggcgaccccaccggccca
gccctgaagagatcttttgaggtcgaggaggccgagacgcccaactccactccgcaccgg
agggtccagacccccgtgctccgggccactgtggccagctccacccagaagttccaggac
ctgggggtgaagaactccgagcccgcagcccgccatgtagactccctcagccagcgatcc
cccaaggctgccctgcggagggtcgagctctcagggcctaaggccgagcccgtgtcccgg
cgcacagagatctccatcgacatctcgtccaagcaggtggagagcgccggcgctgccggg
ccgtcccgcttcgggctcaaacgagcggaggcgctgggccacaagacaccggagcctgcc
cctcggaggacggagatcaccatagtcaagccccaggagtcagcccacaggaggatggag
agccctgcctccaagatccccgagatgcccacagctcccgctgtggatgcggcccccaag
agggtcgagatccaggtgcccaaaccggccgaggggccagcctccccgctcccaccccag
accctggagaattcggaacacgccttggtgtctcagctgcagagccggctggagcccaag
ccccagccccctgtggtcgaggccctcccgaagagccaagaggcccccgaggcggctcct
ggctgtgttggcgacatggctgagacccccagagacgccgggctgaagcaggcgcccgcg
ccccgcaacgagaaggcccccgcggacttcggctatgtgggcatcgactccatcctggag
cagatgcgcaggaaggccatgaagcagggcttcgagttcaacatcatggtggtcgggcag
agcggcttggggaagtccaccttgatcaatacccttttcaagtccaaaatcagccggaag
tcggtgcagcccacctcggaggaacgcatccccaagaccattgagatcaagtccatcacg
cacgatattgaggagaagggcgtccgcatgaagctcacggtcatcgacacgccgggcttt
ggggaccacatcaacaatgagaactgctggcagccgatcatgaagttcatcaacgaccag
tacgagaagtacctgcaggaggaggtcaacatcaaccggaagaagcgcatcccggacacg
cgcgtgcactgctgcctctacttcatccccgccaccggccactccctcaggcccctggac
atcgagttcatgaagcgcctcagcaaagtcgtcaacatcgtccctgtcatcgccaaggct
gacacgctgaccctggaggagagggtctacttcaaacagcggatcaccgcggacctgctg
tccaacggcatcgacgtgtacccccagaaggagtttgacgaggacccggaggaccggctg
gtgaatgagaagttccgagagatgatcccgttcgccgtggtgggcagtgaccacgagtac
caagtgaacgggaagaggatccttggcaggaaaaccaaatggggcaccatcgaagtcgag
aacaccacccactgtgagtttgcgtaccttcgggacctcctcatcaggacgcacatgcag
aacatcaaggacatcaccagcagcatccacttcgaagcctaccgtgtgaagcgtctgcac
gagggcagcaacgccatggccaacggcgtcgaggaaaaggggccggaggcccaggagatg
tag
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