Homo sapiens (human): 6622
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Entry
6622 CDS
T01001
Gene name
SNCA, NACP, PARK1, PARK4, PD1
Definition
(RefSeq) synuclein alpha
KO
K04528
alpha-synuclein
Organism
hsa
Homo sapiens (human)
Pathway
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05022
Pathways of neurodegeneration - multiple diseases
Network
nt06410
Calcium signaling
nt06412
Unfolded protein response (UPR) signaling
nt06418
Oxidative phosphorylation
nt06419
Microtubule-based transport
nt06420
Ubiquitin-proteasome system
nt06422
Dopamine metabolism
nt06463
Parkinson disease
Element
N01019
Parkin-mediated ubiquitination
N01020
Mutation-inactivated PRKN to Parkin-mediated ubiquitination
N01030
Mutation-caused aberrant SNCA to 26S proteasome-mediated protein degradation
N01031
Mutation-caused aberrant SNCA to VGCC-Ca2+ -apoptotic pathway
N01033
Mutation-caused aberrant SNCA to ATF6-mediated transcription
N01034
Mutation-caused aberrant SNCA to IRE1a-XBP1 signaling pathway
N01035
Mutation-caused aberrant SNCA to PERK-ATF4 signaling pathway
N01037
Mutation-caused aberrant SNCA to L-DOPA generation
N01041
Mutation-caused aberrant SNCA to transport of dopamine
N01042
Mutation-caused aberrant SNCA to electron transfer in Complex I
N01055
Mutation-caused aberrant SNCA to anterograde axonal transport
Disease
H00057
Parkinson disease
H00066
Lewy body dementia (LBD)
H01600
Parkinsonian syndrome
Drug target
Cinpanemab:
D11467
Prasinezumab:
D11420
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
6622 (SNCA)
05012 Parkinson disease
6622 (SNCA)
05022 Pathways of neurodegeneration - multiple diseases
6622 (SNCA)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
6622 (SNCA)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
6622 (SNCA)
Membrane trafficking [BR:
hsa04131
]
Exocytosis
Calcium ion-dependent exocytosis
Others
6622 (SNCA)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
6622 (SNCA)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Synuclein
Motif
Other DBs
NCBI-GeneID:
6622
NCBI-ProteinID:
NP_000336
OMIM:
163890
HGNC:
11138
Ensembl:
ENSG00000145335
Vega:
OTTHUMG00000130948
Pharos:
P37840
(Tchem)
UniProt:
P37840
LinkDB
All DBs
Structure
PDB:
6OSJ
6OSL
6A6B
6RT0
6OSM
6H6B
6FLT
6RTB
6CU7
6CU8
2N0A
4BXL
2KKW
1XQ8
Thumbnails
Position
4q22.1
AA seq
140 aa
AA seq
DB search
MDVFMKGLSKAKEGVVAAAEKTKQGVAEAAGKTKEGVLYVGSKTKEGVVHGVATVAEKTK
EQVTNVGGAVVTGVTAVAQKTVEGAGSIAAATGFVKKDQLGKNEEGAPQEGILEDMPVDP
DNEAYEMPSEEGYQDYEPEA
NT seq
423 nt
NT seq
+upstream
nt +downstream
nt
atggatgtattcatgaaaggactttcaaaggccaaggagggagttgtggctgctgctgag
aaaaccaaacagggtgtggcagaagcagcaggaaagacaaaagagggtgttctctatgta
ggctccaaaaccaaggagggagtggtgcatggtgtggcaacagtggctgagaagaccaaa
gagcaagtgacaaatgttggaggagcagtggtgacgggtgtgacagcagtagcccagaag
acagtggagggagcagggagcattgcagcagccactggctttgtcaaaaaggaccagttg
ggcaagaatgaagaaggagccccacaggaaggaattctggaagatatgcctgtggatcct
gacaatgaggcttatgaaatgccttctgaggaagggtatcaagactacgaacctgaagcc
taa
DBGET
integrated database retrieval system