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SVOP - SV2 related protein Gene

Also Known as SLC22B4

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 55530

About SVOP

Cytogenetic location: 12q24.11 Genomic coordinates (GRCh38): 12:108,907,741-109,021,068 (from NCBI)

This gene has 5 transcripts (splice variants), 206 orthologues and 22 paralogues. Biased expression in brain (RPKM 14.1) and adrenal (RPKM 0.9).

Summary

Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in synaptic vesicle. [provided by Alliance of Genome Resources, Apr 2022]

SVOP Products (1)

mRNA	Protein	Name
NM_018711.5	NP_061181.1	synaptic vesicle 2-related protein

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	32296183	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SVOP Protein Structure

Sugar_tr

MFS_1

0
100
200
300
400
483 a.a.

Protein Preferred Names	Protein Names
synaptic vesicle 2-related protein	SV2 related protein homolog

SVOP Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	SVOP	Q8N4V2	FXYD6	Homo sapiens	Q9H0Q3	Validated Y2H	32296183
Intra	SVOP	Q8N4V2	FXYD6	Homo sapiens	Q9H0Q3	Complementation	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Developmental And Epileptic Encephalopathy 4	DEE4 Epileptic Encephalopathy, Early Infantile, 4 Eiee4 Early Infantile Epileptic Encephalopathy 4 Stxbp1-Related Early-Onset Encephalopathy Early Myoclonic Encephalopathy Developmental And Epileptic Encephalopathy, 4 Stxbp1 Disorders Stxbp1 Encephalopathy Developmental And Epileptic Encephalopathy, Type 4 Early-Infantile Epileptic Encephalopathy 4 Stxbp1 Encephalopathy With Epilepsy Stxbp1 Epileptic Encephalopathy Stxbp1-Related Developmental And Epileptic Encephalopathy Stxbp1-Related Epileptic Encephalopathy Eme Neonatal Epilepsy With Suppression-Burst Pattern Encephalopathy, Epileptic, Early Infantile, Type 4

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14061	SVOP Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SVOP	MGD	MGI:1915916
Canis familiaris	SVOP	VGNC	VGNC:47008
Felis catus	SVOP	VGNC	VGNC:65865
Rattus norvegicus	SVOP	RGD	RGD:620277
Macaca mulatta	SVOP	VGNC	VGNC:78208
Bos taurus	SVOP	VGNC	VGNC:35498
Others	SVOP	NCBI