KEGG   Homo sapiens (human): 9900
Entry
9900              CDS       T01001                                 
Symbol
SV2A, DEE113, SLC22B1, SV2
Name
(RefSeq) synaptic vesicle glycoprotein 2A
  KO
K06258  MFS transporter, VNT family, synaptic vesicle glycoprotein 2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04512  ECM-receptor interaction
Disease
H00606  Early infantile epileptic encephalopathy
Drug target
Brivaracetam: D08879<JP/US>
Levetiracetam: D00709<JP/US>
Padsevonil: D11842
Piracetam: D01914<JP>
Plosaracetam: D13077
Seletracetam: D05817
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04512 ECM-receptor interaction
    9900 (SV2A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    9900 (SV2A)
Transporters [BR:hsa02000]
 Major facilitator superfamily (MFS)
  Protein transporters
   Vesicular neurotransmitter transporter (VNT) [TC:2.A.1.22]
    9900 (SV2A)
SSDB
Motif
Pfam: LD_SV2 Sugar_tr MFS_1 MFS_2 Pentapeptide_4 MFS_3 Pentapeptide Pentapeptide_3
Other DBs
NCBI-GeneID: 9900
NCBI-ProteinID: NP_001315603
OMIM: 185860
HGNC: 20566
Ensembl: ENSG00000159164
UniProt: Q7L0J3
Structure
Position
1:complement(149903318..149917844)
AA seq 742 aa
MEEGFRDRAAFIRGAKDIAKEVKKHAAKKVVKGLDRVQDEYSRRSYSRFEEEDDDDDFPA
PSDGYYRGEGTQDEEEGGASSDATEGHDEDDEIYEGEYQGIPRAESGGKGERMADGAPLA
GVRGGLSDGEGPPGGRGEAQRRKEREELAQQYEAILRECGHGRFQWTLYFVLGLALMADG
VEVFVVGFVLPSAEKDMCLSDSNKGMLGLIVYLGMMVGAFLWGGLADRLGRRQCLLISLS
VNSVFAFFSSFVQGYGTFLFCRLLSGVGIGGSIPIVFSYFSEFLAQEKRGEHLSWLCMFW
MIGGVYAAAMAWAIIPHYGWSFQMGSAYQFHSWRVFVLVCAFPSVFAIGALTTQPESPRF
FLENGKHDEAWMVLKQVHDTNMRAKGHPERVFSVTHIKTIHQEDELIEIQSDTGTWYQRW
GVRALSLGGQVWGNFLSCFGPEYRRITLMMMGVWFTMSFSYYGLTVWFPDMIRHLQAVDY
ASRTKVFPGERVEHVTFNFTLENQIHRGGQYFNDKFIGLRLKSVSFEDSLFEECYFEDVT
SSNTFFRNCTFINTVFYNTDLFEYKFVNSRLINSTFLHNKEGCPLDVTGTGEGAYMVYFV
SFLGTLAVLPGNIVSALLMDKIGRLRMLAGSSVMSCVSCFFLSFGNSESAMIALLCLFGG
VSIASWNALDVLTVELYPSDKRTTAFGFLNALCKLAAVLGISIFTSFVGITKAAPILFAS
AALALGSSLALKLPETRGQVLQ
NT seq 2229 nt   +upstreamnt  +downstreamnt
atggaagagggcttccgagaccgggcagctttcatccgtggggccaaagacattgctaag
gaagtcaaaaagcatgcggccaagaaggtggtgaagggcctggacagagtccaggacgaa
tattcccgaagatcgtactcccgctttgaggaggaggatgatgatgatgacttccctgct
cccagtgatggttattaccgaggagaagggacccaggatgaggaggaaggtggtgcatcc
agtgatgctactgagggccatgacgaggatgatgagatctatgaaggggaatatcagggc
attccccgggcagagtctgggggcaaaggcgagcggatggcagatggggcgcccctggct
ggagtaagggggggcttgagtgatggggagggtccccctgggggccggggggaggcacaa
cgacggaaagaacgagaagaactggcccaacagtatgaagccatcctacgggagtgtggc
cacggccgcttccagtggacactgtattttgtgcttggtctggcgctgatggctgacggt
gtggaggtctttgtggtgggcttcgtgctgcccagcgctgagaaagacatgtgcctgtcc
gactccaacaaaggcatgctaggcctcatcgtctacctgggcatgatggtgggagccttc
ctctggggaggtctggctgaccggctgggtcggaggcagtgtctgctcatctcgctctca
gtcaacagcgtcttcgccttcttctcatcttttgtccagggttacggcactttcctcttc
tgccgcctactttctggggttgggattggagggtccatccccattgtcttctcctatttc
tccgagtttctggcccaggagaaacgaggggagcatttgagctggctctgcatgttttgg
atgattggtggcgtgtacgcagctgctatggcctgggccatcatcccccactatgggtgg
agttttcagatgggttctgcctaccagttccacagctggagggtcttcgtcctcgtctgc
gcctttccttctgtgtttgccattggggctctgaccacgcagcctgagagcccccgtttc
ttcctagagaatggaaagcatgatgaggcctggatggtgctgaagcaggtccatgatacc
aacatgcgagccaaaggacatcctgagcgagtgttctcagtaacccacattaagacgatt
catcaggaggatgaattgattgagatccagtcggacacagggacctggtaccagcgctgg
ggggtccgggccttgagcctaggggggcaggtttgggggaattttctctcctgttttggt
cccgaatatcggcgcatcactctgatgatgatgggtgtgtggttcaccatgtcattcagc
tactatggcctgaccgtctggtttcctgacatgatccgccatctccaggcagtggactac
gcatcccgcaccaaagtgttccccggggagcgcgtagagcatgtaacttttaacttcacg
ttggagaatcagatccaccgaggcgggcagtacttcaatgacaagttcattgggctgcgg
ctcaagtcagtgtcctttgaggattccctgtttgaagagtgttattttgaggatgtcaca
tccagcaacacgtttttccgcaactgcacattcatcaacactgtgttctataacactgac
ctgttcgagtacaagtttgtgaacagccgtctgataaacagtacattcctgcacaacaag
gagggctgcccgctagacgtgacagggacgggcgaaggtgcctacatggtatactttgtg
agcttcctggggacactggcagtgcttcctgggaatatcgtgtctgccctgctcatggac
aagatcggcaggctcagaatgcttgctggctccagcgtgatgtcctgtgtctcctgcttc
ttcctgtcttttgggaacagtgagtcggccatgatcgctctgctctgcctttttggcggg
gtcagcattgcatcctggaatgcgctggacgtgttgactgttgaactctacccctcagac
aagaggaccacagcttttggcttcctgaatgccctgtgtaagctggcagctgtgctgggg
atcagcatcttcacatccttcgtgggaatcaccaaggctgcacccatcctctttgcctca
gctgcccttgcccttggcagctctctggccctgaagctgcctgagacccgggggcaggtg
ctgcagtga

  All links  
Disease (2)   
   OMIM (2)   
Gene (13)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (26)   
   RefSeq(nuc) (4)   
   GenBank (11)   
   EMBL (11)   
3D Structure (14)   
   PDB (14)   
Protein domain (8)   
   Pfam (8)   
All databases (69)   

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