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10 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
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SNCB
synuclein beta
Chromosome 5 Β· 5q35.2
NCBI Gene: 6620Ensembl: ENSG00000074317.11HGNC: HGNC:11140UniProt: G4Y815
82PubMed Papers
20Diseases
0Drugs
1Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
calcium ion bindinginclusion bodyprotein bindingtransition metal ion bindingneurodegenerative diseaseLewy body dementiaintracranial hemorrhageParkinson disease
✦AI Summary

SNCB (synuclein beta) is a small, soluble neural protein belonging to the synuclein family, which arose through whole-genome duplications in early vertebrate evolution 1. Located on chromosome 5, SNCB is highly expressed in brain tissue, particularly in presynaptic terminals and the substantia nigra 23. Mechanistically, SNCB functions as a neuroprotective antagonist to alpha-synuclein (SNCA), inhibiting phospholipase D2 and protecting neurons from apoptosis induced by oxidative stressors through p53-dependent pathways 3. Unlike SNCA, SNCB is poor at assembling into filaments and is notably absent from Lewy body pathology characteristic of Parkinson's disease 4. In disease contexts, SNCB shows complex associations with neurodegenerative conditions. While SNCA mutations cause familial Parkinson's disease, the pathogenic role of SNCB genetic variants remains unclear 5. However, reduced SNCB expression correlates with dementia with Lewy bodies (DLB), with disease-specific genetic variants and haplotypes identified in DLB patients 6. SNCB functions as a non-amyloid component in Alzheimer's disease plaques and contributes to neuroprotection through metal ion binding and synaptic regulation 7. Understanding SNCB's protective mechanisms may inform therapeutic strategies for synucleinopathies.

Sources cited
1
Synucleins are small neural proteins with lipid-binding motifs; alpha- and beta-synuclein found in presynaptic terminals; normal cellular functions not fully determined
PMID: 11806835
2
SNCB arose from whole-genome duplications in vertebrate evolution, with ancestral gene duplications preventing dosage effects in aggregation-prone proteins
PMID: 37626939
3
SNCB highly expressed in brain including substantia nigra; both alpha- and beta-synucleins inhibit phospholipase D2
PMID: 9806846
4
SNCA has established role in Parkinson's disease; pathogenic role of SNCB and SNCG genetic variants in disease is unclear
PMID: 32740728
5
SNCB thought to function as antagonist of alpha-synuclein; dose-dependent decreased apoptosis in RPE cells; triggers inflammatory and oxidative stress responses
PMID: 31128101
6
Beta-synuclein and gamma-synuclein are poor at assembling into filaments and are not present in pathological filamentous lesions; not linked to genetic disease
PMID: 11388653
7
SNCB INDEL variants regulate expression levels; low SNCB expression variants accumulated in dementia with Lewy bodies; disease-specific SNCB haplotypes identified
PMID: 30040713
Disease Associationsβ“˜20
neurodegenerative diseaseOpen Targets
0.47Moderate
Lewy body dementiaOpen Targets
0.45Moderate
intracranial hemorrhageOpen Targets
0.26Weak
Parkinson diseaseOpen Targets
0.12Weak
multiple system atrophyOpen Targets
0.12Weak
Alzheimer diseaseOpen Targets
0.12Weak
melanomaOpen Targets
0.10Suggestive
dementiaOpen Targets
0.09Suggestive
type 2 diabetes mellitusOpen Targets
0.09Suggestive
synucleinopathyOpen Targets
0.08Suggestive
epilepsyOpen Targets
0.08Suggestive
myeloid sarcomaOpen Targets
0.08Suggestive
Krabbe diseaseOpen Targets
0.08Suggestive
Mobius syndromeOpen Targets
0.08Suggestive
meningiomaOpen Targets
0.08Suggestive
supranuclear palsy, progressive, 1Open Targets
0.07Suggestive
HIV-1 infectionOpen Targets
0.07Suggestive
experimental autoimmune encephalomyelitisOpen Targets
0.06Suggestive
obesityOpen Targets
0.06Suggestive
autismOpen Targets
0.06Suggestive
Pathogenic Variants1
NM_003085.5(SNCB):c.208G>A (p.Val70Met)Pathogenic
Lewy body dementia
β˜†β˜†β˜†β˜†2004β†’ Residue 70
View on ClinVar β†—
Related Genes
SNCAProtein interaction100%MTF1Protein interaction75%SNCGShared pathway75%SNCAIPProtein interaction75%MAPTProtein interaction72%UCHL1Protein interaction72%
Tissue Expression6 tissues
Brain
100%
Heart
0%
Liver
0%
Bone Marrow
0%
Ovary
0%
Lung
0%
Gene Interaction Network
Click a node to explore
SNCBSNCAMTF1SNCGSNCAIPMAPTUCHL1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted Β· UniProt Q16143
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
0.69LoF Tolerant
pLIβ“˜
0.49Tolerant
Observed/Expected LoF0.38 [0.22–0.69]
RankingsWhere SNCB stands among ~20K protein-coding genes
  • #5,826of 20,598
    Most Researched82
  • #4,954of 5,498
    Most Pathogenic Variants1
  • #5,187of 17,882
    Most Constrained (LOEUF)0.69
Genes detectedSNCB
Sources retrieved10 papers
Response timeβ€”
πŸ“„ Sources
10β–Ό
1
The synucleins.
PMID: 11806835
Genome Biol Β· 2002
1.00
2
Emergence of the Synucleins.
PMID: 37626939
Biology (Basel) Β· 2023
0.90
3
Genomic organization and expression of the human beta-synuclein gene (SNCB).
PMID: 9806846
Genomics Β· 1998
0.80
4
Genetics of synucleins in neurodegenerative diseases.
PMID: 32740728
Acta Neuropathol Β· 2021
0.70
5
Age-related distribution and potential role of SNCB in topographically different retinal areas of the common marmoset Callithrix jacchus, including the macula.
PMID: 31128101
Exp Eye Res Β· 2019
0.60