Gene Gene information from NCBI Gene database.
Entrez ID 55530
Gene name SV2 related protein
Gene symbol SVOP
Synonyms (NCBI Gene)
SLC22B4
Chromosome 12
Chromosome location 12q24.11
miRNA miRNA information provided by mirtarbase database.
1805
miRTarBase ID miRNA Experiments Reference
MIRT723942 hsa-miR-193a-3p HITS-CLIP 19536157
MIRT723941 hsa-miR-193b-3p HITS-CLIP 19536157
MIRT723940 hsa-miR-1273g-3p HITS-CLIP 19536157
MIRT723939 hsa-miR-4301 HITS-CLIP 19536157
MIRT723938 hsa-miR-3121-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0008021 Component Synaptic vesicle IEA
GO:0008021 Component Synaptic vesicle ISS
GO:0009925 Component Basal plasma membrane IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611699 25417 ENSG00000166111
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N4V2
Protein name Synaptic vesicle 2-related protein (SV2-related protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 66 347 Sugar (and other) transporter Family
PF07690 MFS_1 376 542 Major Facilitator Superfamily Family
Sequence
Sequence length 548
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
UTERINE FIBROID GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations