SNCG synuclein gamma
Gene ID: 6623, updated on 3-Nov-2024Gene type: protein coding
Also known as: SR; BCSG1
- See all available tests in GTR for this gene
- Go to complete Gene record for SNCG
- Go to Variation Viewer for SNCG variants
Summary
This gene encodes a member of the synuclein family of proteins which are believed to be involved in the pathogenesis of neurodegenerative diseases. Mutations in this gene have also been associated with breast tumor development. [provided by RefSeq, Jan 2010]
Genomic context
- Location:
- 10q23.2
- Sequence:
- Chromosome: 10; NC_000010.11 (86955759..86963258)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for SNCG variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ALSoD/SNCG genetic mutations
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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