KEGG   Homo sapiens (human): 127833
Entry
127833            CDS       T01001                                 
Symbol
SYT2, CMS7, CMS7A, CMS7B, MYSPC, SytII
Name
(RefSeq) synaptotagmin 2
  KO
K19902  synaptotagmin-2
Organism
hsa  Homo sapiens (human)
Disease
H00770  Congenital myasthenic syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    127833 (SYT2)
Membrane trafficking [BR:hsa04131]
 Exocytosis
  Calcium ion-dependent exocytosis
   Synaptotagmins
    127833 (SYT2)
SSDB
Motif
Pfam: C2 TMEM52 PI3K_C2 CEP76-C2 MAP17 DOCK-C2 FAM176 EphA2_TM DUF4153
Other DBs
NCBI-GeneID: 127833
NCBI-ProteinID: NP_001129976
OMIM: 600104
HGNC: 11510
Ensembl: ENSG00000143858
UniProt: Q8N9I0
Structure
Position
1:complement(202590596..202710454)
AA seq 419 aa
MRNIFKRNQEPIVAPATTTATMPIGPVDNSTESGGAGESQEDMFAKLKEKLFNEINKIPL
PPWALIAIAVVAGLLLLTCCFCICKKCCCKKKKNKKEKGKGMKNAMNMKDMKGGQDDDDA
ETGLTEGEGEGEEEKEPENLGKLQFSLDYDFQANQLTVGVLQAAELPALDMGGTSDPYVK
VFLLPDKKKKYETKVHRKTLNPAFNETFTFKVPYQELGGKTLVMAIYDFDRFSKHDIIGE
VKVPMNTVDLGQPIEEWRDLQGGEKEEPEKLGDICTSLRYVPTAGKLTVCILEAKNLKKM
DVGGLSDPYVKIHLMQNGKRLKKKKTTVKKKTLNPYFNESFSFEIPFEQIQKVQVVVTVL
DYDKLGKNEAIGKIFVGSNATGTELRHWSDMLANPRRPIAQWHSLKPEEEVDALLGKNK
NT seq 1260 nt   +upstreamnt  +downstreamnt
atgaggaacattttcaagaggaaccaggagcctattgtggctcctgccaccaccaccgcc
acgatgcccattggacccgtggacaactccactgagagtgggggtgctggggagagccag
gaggacatgtttgccaaactgaaggagaagttattcaatgagataaacaagattccctta
ccaccctgggcactgatcgccattgctgtggttgctgggctcctgcttctcacctgctgc
ttctgcatctgcaagaaatgctgctgcaagaagaagaagaacaagaaggagaagggcaaa
ggcatgaagaatgccatgaacatgaaggacatgaaagggggtcaggatgacgacgacgca
gagacaggcctgactgagggggaaggtgaaggggaggaggagaaagagccagagaacctg
ggcaaactgcagttttccctggactatgattttcaggctaatcagcttactgtgggcgtt
ctgcaggctgctgaactgcctgccctggacatgggaggcacctcagacccttatgtcaag
gtcttcctccttcctgacaagaagaagaaatatgagaccaaagtccatcggaagacactg
aaccctgccttcaatgaaaccttcaccttcaaggtgccataccaggagcttgggggcaaa
actctggtgatggccatctatgactttgaccgcttctccaaacatgacatcattggagag
gtaaaggtgcctatgaacacagtggacctcggccagcccattgaggagtggagagacctg
caaggcggggaaaaggaggagccggagaagctgggcgacatctgcacctccctgcgctat
gtgcccacggccgggaagctcactgtctgcatcctggaggctaagaacctcaagaagatg
gacgtgggcggcctttcagacccgtacgtgaagatccacctgatgcagaatggcaagagg
ctcaagaagaagaagacaaccgtgaagaagaagaccctgaacccatacttcaacgagtcc
ttcagctttgagatccccttcgagcagattcagaaagtccaggtagtggtcaccgtgctg
gactatgacaagctgggcaagaacgaagccataggcaagatcttcgtgggcagcaatgcc
acgggcacagagctgcggcactggtccgacatgctggccaacccccggaggcccatcgcc
cagtggcactcgctcaagcctgaggaggaggtggatgcactcctgggcaagaacaagtag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (16)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (14)   
DNA sequence (30)   
   RefSeq(nuc) (14)   
   GenBank (8)   
   EMBL (8)   
3D Structure (1)   
   PDB (1)   
Protein domain (9)   
   Pfam (9)   
All databases (73)   

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