Homo sapiens (human): 127833
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C2
PI3K_C2
DOCK-C2
CEP76-C2
MAP17
TMEM52
FAM176
EphA2_TM
Motif
Other DBs
NCBI-GeneID:
127833
NCBI-ProteinID:
NP_001129976
OMIM:
600104
HGNC:
11510
Ensembl:
ENSG00000143858
UniProt:
Q8N9I0
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(202590596..202710454)
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AA seq
419 aa
AA seq
DB search
MRNIFKRNQEPIVAPATTTATMPIGPVDNSTESGGAGESQEDMFAKLKEKLFNEINKIPL
PPWALIAIAVVAGLLLLTCCFCICKKCCCKKKKNKKEKGKGMKNAMNMKDMKGGQDDDDA
ETGLTEGEGEGEEEKEPENLGKLQFSLDYDFQANQLTVGVLQAAELPALDMGGTSDPYVK
VFLLPDKKKKYETKVHRKTLNPAFNETFTFKVPYQELGGKTLVMAIYDFDRFSKHDIIGE
VKVPMNTVDLGQPIEEWRDLQGGEKEEPEKLGDICTSLRYVPTAGKLTVCILEAKNLKKM
DVGGLSDPYVKIHLMQNGKRLKKKKTTVKKKTLNPYFNESFSFEIPFEQIQKVQVVVTVL
DYDKLGKNEAIGKIFVGSNATGTELRHWSDMLANPRRPIAQWHSLKPEEEVDALLGKNK
NT seq
1260 nt
NT seq
+upstream
nt +downstream
nt
atgaggaacattttcaagaggaaccaggagcctattgtggctcctgccaccaccaccgcc
acgatgcccattggacccgtggacaactccactgagagtgggggtgctggggagagccag
gaggacatgtttgccaaactgaaggagaagttattcaatgagataaacaagattccctta
ccaccctgggcactgatcgccattgctgtggttgctgggctcctgcttctcacctgctgc
ttctgcatctgcaagaaatgctgctgcaagaagaagaagaacaagaaggagaagggcaaa
ggcatgaagaatgccatgaacatgaaggacatgaaagggggtcaggatgacgacgacgca
gagacaggcctgactgagggggaaggtgaaggggaggaggagaaagagccagagaacctg
ggcaaactgcagttttccctggactatgattttcaggctaatcagcttactgtgggcgtt
ctgcaggctgctgaactgcctgccctggacatgggaggcacctcagacccttatgtcaag
gtcttcctccttcctgacaagaagaagaaatatgagaccaaagtccatcggaagacactg
aaccctgccttcaatgaaaccttcaccttcaaggtgccataccaggagcttgggggcaaa
actctggtgatggccatctatgactttgaccgcttctccaaacatgacatcattggagag
gtaaaggtgcctatgaacacagtggacctcggccagcccattgaggagtggagagacctg
caaggcggggaaaaggaggagccggagaagctgggcgacatctgcacctccctgcgctat
gtgcccacggccgggaagctcactgtctgcatcctggaggctaagaacctcaagaagatg
gacgtgggcggcctttcagacccgtacgtgaagatccacctgatgcagaatggcaagagg
ctcaagaagaagaagacaaccgtgaagaagaagaccctgaacccatacttcaacgagtcc
ttcagctttgagatccccttcgagcagattcagaaagtccaggtagtggtcaccgtgctg
gactatgacaagctgggcaagaacgaagccataggcaagatcttcgtgggcagcaatgcc
acgggcacagagctgcggcactggtccgacatgctggccaacccccggaggcccatcgcc
cagtggcactcgctcaagcctgaggaggaggtggatgcactcctgggcaagaacaagtag
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