KEGG   Homo sapiens (human): 23176
Entry
23176             CDS       T01001                                 
Symbol
SEPTIN8, SEP2, SEPT8, Septin-8
Name
(RefSeq) septin 8
  KO
K16939  septin 6/8/11
Organism
hsa  Homo sapiens (human)
Pathway
hsa05100  Bacterial invasion of epithelial cells
hsa05131  Shigellosis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05131 Shigellosis
    23176 (SEPTIN8)
   05100 Bacterial invasion of epithelial cells
    23176 (SEPTIN8)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    23176 (SEPTIN8)
   04812 Cytoskeleton proteins [BR:hsa04812]
    23176 (SEPTIN8)
   04147 Exosome [BR:hsa04147]
    23176 (SEPTIN8)
Cilium and associated proteins [BR:hsa03037]
 Motile cilia and associated proteins
  Sperm associated proteins
   23176 (SEPTIN8)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Septins
   Septins
    Group 1
     23176 (SEPTIN8)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   23176 (SEPTIN8)
SSDB
Motif
Pfam: Septin MMR_HSR1 RsgA_GTPase Roc AAA_16 AAA_22 AAA_7 Ras RNA_helicase RHD3_GTPase AIG1 IMD DUF4478 AAA_24 ABC_tran AAA_29 FtsK_SpoIIIE ATG14
Other DBs
NCBI-GeneID: 23176
NCBI-ProteinID: NP_001092281
OMIM: 608418
HGNC: 16511
Ensembl: ENSG00000164402
UniProt: Q92599
Structure
Position
5:complement(132750819..132780083)
AA seq 483 aa
MAATDLERFSNAEPEPRSLSLGGHVGFDSLPDQLVSKSVTQGFSFNILCVGETGIGKSTL
MNTLFNTTFETEEASHHEACVRLRPQTYDLQESNVQLKLTIVDAVGFGDQINKDESYRPI
VDYIDAQFENYLQEELKIRRSLFDYHDTRIHVCLYFITPTGHSLKSLDLVTMKKLDSKVN
IIPIIAKADTISKSELHKFKIKIMGELVSNGVQIYQFPTDDEAVAEINAVMNAHLPFAVV
GSTEEVKVGNKLVRARQYPWGVVQVENENHCDFVKLREMLIRVNMEDLREQTHSRHYELY
RRCKLEEMGFQDSDGDSQPFSLQETYEAKRKEFLSELQRKEEEMRQMFVNKVKETELELK
EKERELHEKFEHLKRVHQEEKRKVEEKRRELEEETNAFNRRKAAVEALQSQALHATSQQP
LRKDKDKKNRSDIGAHQPGMSLSSSKVMMTKASVEPLNCSSWWPAIQCCSCLVRDATWRE
GFL
NT seq 1452 nt   +upstreamnt  +downstreamnt
atggcggccaccgacctggagcgcttctcgaatgcagagccagagccccggagcctctcc
ctgggcggccatgtgggtttcgacagcctccccgaccagctggtcagcaagtcggtcact
cagggcttcagcttcaacatcctctgtgtgggggagaccggcattggcaaatccacactg
atgaacacactcttcaacacgaccttcgagactgaggaagccagtcaccatgaggcatgc
gtgcgcctgcggccccagacctatgacctccaggagagcaacgtgcagctcaagctgacc
attgtggatgccgtgggctttggggatcagatcaataaggatgagagttacaggcccata
gttgactacatcgatgcgcagtttgaaaattatctgcaggaggagctgaagatccgccgc
tcgctcttcgactaccatgacacaaggatccacgtttgcctctacttcatcacgcccaca
gggcactccctgaagtctctagatctagtgaccatgaagaaactagacagcaaggtgaac
attattcccatcatcgccaaggctgacaccatctccaagagcgagctccacaagttcaag
atcaagatcatgggcgagttggtcagcaacggggtccagatctaccagttccccacggat
gatgaggctgttgcagagattaacgcagtcatgaatgcacatctgccctttgccgtggtg
ggcagcaccgaggaggtgaaggtggggaacaagctggtccgagcacggcagtacccctgg
ggagtggtgcaggtggagaatgagaatcactgcgacttcgtgaagctgcgggagatgttg
atccgggtgaacatggaagacctccgcgagcagacccacagccggcactacgagctctac
cggcgctgcaagttggaggagatgggctttcaggacagcgatggtgacagccagcccttc
agcctacaagagacatacgaggccaagaggaaggagttcctaagtgagctgcagaggaag
gaggaagagatgaggcagatgtttgtcaacaaagtgaaggagacagagctggagctgaag
gagaaggaaagggagctccatgagaagtttgagcacctgaagcgggtccaccaggaggag
aagcgcaaggtggaggaaaagcgccgggaactggaggaggagaccaacgccttcaatcgc
cggaaggctgcggtggaggccctgcagtcgcaggccttgcacgccacctcgcagcagccc
ctgaggaaggacaaggacaagaagaacagatcagatataggagcacaccagccgggcatg
agcctctccagctctaaggtgatgatgaccaaggccagtgtggagcccttgaactgcagc
agctggtggcccgccatacagtgctgcagctgcctggtcagggatgcgacgtggagggaa
ggattcctctga

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