Entity Details

Primary name SHRM4_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9ULL8
EntryNameSHRM4_HUMAN
FullNameProtein Shroom4
TaxID9606
Evidenceevidence at protein level
Length1493
SequenceStatuscomplete
DateCreated2007-05-15
DateModified2021-06-02

Ontological Relatives

GenesSHROOM4

GO terms

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GOName
GO:0001725 stress fiber
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005884 actin filament
GO:0005912 adherens junction
GO:0005925 focal adhesion
GO:0007015 actin filament organization
GO:0007420 brain development
GO:0009898 cytoplasmic side of plasma membrane
GO:0009925 basal plasma membrane
GO:0016324 apical plasma membrane
GO:0030036 actin cytoskeleton organization
GO:0030864 cortical actin cytoskeleton
GO:0043231 intracellular membrane-bounded organelle
GO:0043296 apical junction complex
GO:0045159 myosin II binding
GO:0050890 cognition
GO:0051015 actin filament binding

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR001478 PDZ domainDomainDomain
IPR014799 Apx/Shrm Domain 2DomainDomain
IPR027685 Shroom familyFamilyFamily
IPR027687 Shroom4FamilyFamily
IPR036034 PDZ superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
300434 OMIMMental retardation, X-linked, syndromic, Stocco dos Santos type (SDSX)A syndrome characterized by severe mental retardation with hyperactivity, aggressive behavior, delayed or no speech, and seizures. Additional features include congenital bilateral hip luxation, short stature, and kyphosis. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

InteractorPartnerSourcesPublicationsLink