Basic Information

SYN3

Full name: synapsin III

Gene type: protein coding

HGNC ID: HGNC:11496

Gene location: 22q12.3

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/8224

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:11496

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_003490.4

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/O14994

AlphaFold: https://alphafold.ebi.ac.uk/entry/O14994

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/602705

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=8224

Pathway resources

Variant resources

Gene	Disease type	Variant type	NCBI dbSNP	Alleles	Variant location
SYN3	AMD	Intron Variant	rs9621532	A>C	chr22:32688525 (GRCh38.p13)
SYN3	Drusen Area in Central Circle	Intron Variant	rs5749482	G>A / G>C / G>T	chr22:32663679 (GRCh38.p13)
SYN3	AMD	Intron Variant	rs5754227	T>C	chr22:32709831 (GRCh38.p13)
SYN3	AMD	Intron Variant	rs756481	A>G	chr22:32709241 (GRCh38.p13)
SYN3	AMD	Intron Variant	rs5749498	G>A / G>T	chr22:32710961 (GRCh38.p13)
SYN3	AMD	Intron Variant	rs12170368	C>T	chr22:32715261 (GRCh38.p13)