KEGG   Homo sapiens (human): 6857
Entry
6857              CDS       T01001                                 
Symbol
SYT1, BAGOS, P65, SVP65, SYT
Name
(RefSeq) synaptotagmin 1
  KO
K15290  synaptotagmin-1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04721  Synaptic vesicle cycle
Disease
H02397  Neurodevelopmental disorder with movement abnormalities or hypotonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09156 Nervous system
   04721 Synaptic vesicle cycle
    6857 (SYT1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    6857 (SYT1)
Membrane trafficking [BR:hsa04131]
 Exocytosis
  Calcium ion-dependent exocytosis
   Synaptotagmins
    6857 (SYT1)
SSDB
Motif
Pfam: C2 Comm DUF5381 TssR_C DUF1258 GmrSD_N
Other DBs
NCBI-GeneID: 6857
NCBI-ProteinID: NP_001129277
OMIM: 185605
HGNC: 11509
Ensembl: ENSG00000067715
UniProt: P21579
Structure
Position
12:78863982..79452008
AA seq 422 aa
MVSESHHEALAAPPVTTVATVLPSNATEPASPGEGKEDAFSKLKEKFMNELHKIPLPPWA
LIAIAIVAVLLVLTCCFCICKKCLFKKKNKKKGKEKGGKNAINMKDVKDLGKTMKDQALK
DDDAETGLTDGEEKEEPKEEEKLGKLQYSLDYDFQNNQLLVGIIQAAELPALDMGGTSDP
YVKVFLLPDKKKKFETKVHRKTLNPVFNEQFTFKVPYSELGGKTLVMAVYDFDRFSKHDI
IGEFKVPMNTVDFGHVTEEWRDLQSAEKEEQEKLGDICFSLRYVPTAGKLTVVILEAKNL
KKMDVGGLSDPYVKIHLMQNGKRLKKKKTTIKKNTLNPYYNESFSFEVPFEQIQKVQVVV
TVLDYDKIGKNDAIGKVFVGYNSTGAELRHWSDMLANPRRPIAQWHTLQVEEEVDAMLAV
KK
NT seq 1269 nt   +upstreamnt  +downstreamnt
atggtgagcgagagtcaccatgaggccctggcagccccgcctgtcaccactgtcgcgact
gttctgccaagcaacgccacagagccagccagtcctggagaaggaaaggaagatgcattt
tctaagctgaaggagaagtttatgaatgagttgcataaaattccattgccaccgtgggcc
ttaattgcaatagccatagtcgcagtccttttagtcctgacctgctgcttttgtatctgt
aagaaatgtttgttcaaaaagaaaaacaagaagaagggaaaggaaaaaggagggaagaat
gccattaacatgaaagatgtaaaagacttagggaagacgatgaaagatcaggccctcaag
gatgatgatgctgaaactggattgacagatggagaagaaaaagaagaacccaaagaagag
gagaaactgggaaaacttcagtattcactggattatgatttccaaaataaccagctgctg
gtagggatcattcaggctgccgaactgcccgccttggacatggggggcacatctgatcct
tacgtgaaagtgtttctgctacctgataagaagaagaaatttgagacaaaagtccaccga
aaaacccttaatcctgtcttcaatgagcaatttactttcaaggtaccatactcggaattg
ggtggcaaaaccctagtgatggctgtatatgattttgatcgtttctctaagcatgacatc
attggagaatttaaagtccctatgaacacagtggattttggccatgtaactgaggaatgg
cgtgacctgcaaagtgctgagaaggaagagcaagagaaattgggtgatatctgcttctcc
cttcgctacgtacctactgctggtaagctgactgttgtcattctggaggcaaagaacctg
aagaagatggatgtgggtggcttatccgatccttatgtgaagattcatctgatgcagaat
ggtaagaggctgaagaagaaaaagacaacaattaaaaagaacacacttaacccctactac
aatgagtcattcagctttgaagtaccttttgaacaaatccagaaagtgcaggtggtggta
actgttttggactatgacaagattggcaagaacgatgccatcggcaaagtctttgtgggc
tacaacagcaccggcgcggagctgcgacactggtcagacatgctggccaaccccaggcga
cctattgcccagtggcacaccctgcaggtagaggaggaagttgatgccatgctggccgtc
aagaagtaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (27)   
   RefGene (18)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (22)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (20)   
DNA sequence (48)   
   RefSeq(nuc) (20)   
   GenBank (14)   
   EMBL (14)   
3D Structure (24)   
   PDB (24)   
Protein domain (6)   
   Pfam (6)   
All databases (129)   

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