Entity Details

Primary name SVBP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N300
EntryNameSVBP_HUMAN
FullNameSmall vasohibin-binding protein
TaxID9606
Evidenceevidence at protein level
Length66
SequenceStatuscomplete
DateCreated2006-05-02
DateModified2021-06-02

Ontological Relatives

GenesSVBP

GO terms

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GOName
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0006508 proteolysis
GO:0008017 microtubule binding
GO:0009306 protein secretion
GO:0010596 negative regulation of endothelial cell migration
GO:0031397 negative regulation of protein ubiquitination
GO:0045177 apical part of cell
GO:0061564 axon development
GO:1905048 regulation of metallopeptidase activity

Subcellular Location

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Subcellular Location
Cytoplasm
Secreted

Domains

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DomainNameCategoryType
IPR031378 Small vasohibin-binding proteinFamilyFamily

Diseases

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Disease IDSourceNameDescription
618569 OMIMNeurodevelopmental disorder with ataxia, hypotonia, and microcephaly (NEDAHM)An autosomal recessive neurodevelopmental disorder characterized by intellectual disability, microcephaly, ataxia, and muscular hypotonia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
SVBP_HUMANVASH1_HUMANBioGRID, DIP20736312 31235910 31270470 details