Entity Details

Primary name ARHG1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ92888
EntryNameARHG1_HUMAN
FullNameRho guanine nucleotide exchange factor 1
TaxID9606
Evidenceevidence at protein level
Length912
SequenceStatuscomplete
DateCreated2003-08-29
DateModified2021-06-02

Ontological Relatives

GenesARHGEF1

GO terms

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GOName
GO:0001664 G protein-coupled receptor binding
GO:0003723 RNA binding
GO:0005085 guanyl-nucleotide exchange factor activity
GO:0005096 GTPase activator activity
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007266 Rho protein signal transduction
GO:0043065 positive regulation of apoptotic process
GO:0043547 positive regulation of GTPase activity
GO:0051056 regulation of small GTPase mediated signal transduction

Subcellular Location

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Subcellular Location
Cytoplasm
Membrane

Domains

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DomainNameCategoryType
IPR000219 Dbl homology (DH) domainDomainDomain
IPR001849 Pleckstrin homology domainDomainDomain
IPR011993 PH-like domain superfamilyFamilyHomologous superfamily
IPR015212 Regulator of G protein signalling-like domainDomainDomain
IPR035899 Dbl homology (DH) domain superfamilyFamilyHomologous superfamily
IPR036305 RGS domain superfamilyFamilyHomologous superfamily
IPR037887 p115RhoGEF, RGS domainDomainDomain
IPR041020 ARHGEF1-like, PH domainDomainDomain

Diseases

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Disease IDSourceNameDescription
618459 OMIMImmunodeficiency 62 (IMD62)An autosomal recessive, primary immunologic disorder characterized by recurrent severe respiratory tract infections and bronchiectasis, due to antibody deficiency. Affected individuals have an abnormal B cell immunophenotype, with low levels of circulating memory B cells. The disease is caused by variants affecting the gene represented in this entry.