KEGG   Homo sapiens (human): 6811
Entry
6811              CDS       T01001                                 
Symbol
STX5, CDG2AA, SED5, STX5A
Name
(RefSeq) syntaxin 5
  KO
K08490  syntaxin 5
Organism
hsa  Homo sapiens (human)
Pathway
hsa04130  SNARE interactions in vesicular transport
Disease
H00119  Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04130 SNARE interactions in vesicular transport
    6811 (STX5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    6811 (STX5)
Membrane trafficking [BR:hsa04131]
 SNARE
  Syntaxin (Qa)
   Stx-cisGolgi
    6811 (STX5)
SSDB
Motif
Pfam: SNARE Syntaxin-5_N Syntaxin Apolipoprotein DUF16 SKA1 Vac_Fusion DUF5063 DUF3130 MCPsignal DUF1664
Other DBs
NCBI-GeneID: 6811
NCBI-ProteinID: NP_003155
OMIM: 603189
HGNC: 11440
Ensembl: ENSG00000162236
UniProt: Q13190
Structure
Position
11:complement(62806860..62832051)
AA seq 355 aa
MIPRKRYGSKNTDQGVYLGLSKTQVLSPATAGSSSSDIAPLPPPVTLVPPPPDTMSCRDR
TQEFLSACKSLQTRQNGIQTNKPALRAVRQRSEFTLMAKRIGKDLSNTFAKLEKLTILAK
RKSLFDDKAVEIEELTYIIKQDINSLNKQIAQLQDFVRAKGSQSGRHLQTHSNTIVVSLQ
SKLASMSNDFKSVLEVRTENLKQQRSRREQFSRAPVSALPLAPNHLGGGAVVLGAESHAS
KDVAIDMMDSRTSQQLQLIDEQDSYIQSRADTMQNIESTIVELGSIFQQLAHMVKEQEET
IQRIDENVLGAQLDVEAAHSEILKYFQSVTSNRWLMVKIFLILIVFFIIFVVFLA
NT seq 1068 nt   +upstreamnt  +downstreamnt
atgatcccgcggaaacgctacgggtctaagaacacggatcagggtgtctacctgggtctc
tcaaagacacaggtcctgtcccctgcaactgctggcagtagcagcagcgacatcgcccct
ctgccccccccagtgaccctcgtccctccccctcccgacaccatgtcctgccgggatcgg
acccaggagtttctgtctgcctgcaagtcgctgcagacccgtcagaatggaatccagaca
aataagccagctttgcgtgctgtccgacaacgcagtgaattcaccctcatggccaagcgc
attgggaaagaccttagcaacacatttgccaagctggagaagctgacaatcttggcaaag
cgcaagtccctctttgatgataaagcagtggaaattgaagagctaacatatatcatcaaa
caggacatcaatagcctcaacaaacaaattgctcagctccaggatttcgtgagagccaag
ggcagccagagtggccggcacctgcagacccactccaacaccattgtggtctccttgcag
tcgaaactggcttctatgtccaatgacttcaaatcggttttagaagtgaggacagagaac
ctgaagcagcagaggagccggagagagcagttctcccgggcacctgtgtcagccctgccc
cttgcccctaaccacctgggcggtggtgctgtggttctgggggcagagtcccatgcctcc
aaggatgtcgccatcgacatgatggactctcggaccagccagcagctgcagctcattgac
gagcaggattcctacatccagagtcgggcagacaccatgcagaacattgagtcgacaatt
gttgagttgggctccatctttcagcagttggcacacatggttaaggaacaggaggaaacc
attcagaggatcgacgagaacgtgctaggagcccagctggacgttgaggccgcccattca
gagatcctcaagtacttccagtctgtcacctccaaccggtggctcatggtcaaaatcttc
ctcatcctcattgtcttcttcatcatctttgtggtcttccttgcttga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (9)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (29)   
   RefSeq(nuc) (7)   
   GenBank (11)   
   EMBL (11)   
3D Structure (1)   
   PDB (1)   
Protein domain (11)   
   Pfam (11)   
All databases (69)   

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