KEGG   Homo sapiens (human): 6809
Entry
6809              CDS       T01001                                 
Symbol
STX3, DIAR12, MVID2, RDMVID, STX3A
Name
(RefSeq) syntaxin-3 isoform 1
  KO
K08486  syntaxin 1B/2/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa04130  SNARE interactions in vesicular transport
hsa04721  Synaptic vesicle cycle
Disease
H01174  Congenital diarrhea
H02655  Retinal dystrophy and microvillus inclusion disease
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04130 SNARE interactions in vesicular transport
    6809 (STX3)
 09150 Organismal Systems
  09156 Nervous system
   04721 Synaptic vesicle cycle
    6809 (STX3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    6809 (STX3)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    6809 (STX3)
Membrane trafficking [BR:hsa04131]
 SNARE
  Syntaxin (Qa)
   Stx-PM
    6809 (STX3)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of epithelial cells
   6809 (STX3)
  Exosomal proteins of other body fluids (saliva and urine)
   6809 (STX3)
SSDB
Motif
Pfam: Syntaxin SNARE Syntaxin_2 Branch MG280 GyrB_insert DUF3040 YjcZ GlfT2_domain3 ETRAMP Prominin T2SSF SIMPL DUF6584 Relaxase_C
Other DBs
NCBI-GeneID: 6809
NCBI-ProteinID: NP_001427451
OMIM: 600876
HGNC: 11438
UniProt: Q13277
Position
11:59754188..59805878
AA seq 289 aa
MKDRLEQLKAKQLTQDDDTDAVEIAIDNTAFMDEFFSEIEETRLNIDKISEHVEEAKKLY
SIILSAPIPEPKTKDDLEQLTTEIKKRANNVRNKLKSMEKHIEEDEVRSSADLRIRKSQH
SVLSRKFVEVMTKYNEAQVDFRERSKGRIQRQLEITGKKTTDEELEEMLESGNPAIFTSG
IIDSQISKQALSEIEGRHKDIVRLESSIKELHDMFMDIAMLVENQGEMLDNIELNVMHTV
DHVEKARDETKKAVKYQSQARKKLIIIIVLVVVLLGILALIIGLSVGLN
NT seq 870 nt   +upstreamnt  +downstreamnt
atgaaggaccgtctggagcagctgaaggccaagcagctgacacaggatgatgatactgat
gcggttgagattgctatcgacaacacggcttttatggacgagttcttttctgagattgag
gaaactcggcttaacattgacaagatctcagaacatgtagaggaggctaagaaactctac
agtatcattctctctgcaccgattccagagccaaaaaccaaggatgacctagagcagctc
acgactgagattaagaaaagggccaacaacgtccggaacaaactgaagagcatggagaag
catattgaagaagatgaggtcaggtcatcggcagaccttcggattcggaaatcccagcac
tctgtcctttctcggaagtttgtggaggtgatgaccaaatacaatgaagctcaagtggac
ttccgagaacgcagcaaagggcgaatccagcggcagctcgaaattactggcaaaaagaca
accgatgaggagctggaggagatgttggagagtggcaacccggccatcttcacttctggg
atcattgactcacagatttccaagcaagccctcagtgagattgagggacgacacaaggac
attgtgaggctggagagcagcatcaaggagcttcacgacatgtttatggacatcgccatg
ctggtggagaatcagggtgagatgttagataacatagagttgaatgtcatgcacacagtg
gaccacgtggagaaggcacgagatgaaacgaaaaaagctgtgaaataccagagtcaggcc
cggaagaaattgataattatcattgtgctagtagttgtgttgctgggcattttagcattg
attattggactttccgttgggctgaattaa

  All links  
Disease (3)   
   OMIM (3)   
Gene (14)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   RIKEN BRC-DNA (7)   
   OC (1)   
Protein sequence (25)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (22)   
DNA sequence (54)   
   RefSeq(nuc) (22)   
   GenBank (16)   
   EMBL (16)   
Protein domain (15)   
   Pfam (15)   
All databases (111)   

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