Entity Details

Primary name GNB5_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO14775
EntryNameGNB5_HUMAN
FullNameGuanine nucleotide-binding protein subunit beta-5
TaxID9606
Evidenceevidence at protein level
Length395
SequenceStatuscomplete
DateCreated1998-07-15
DateModified2021-06-02

Ontological Relatives

GenesGNB5

GO terms

Show/Hide Table
GOName
GO:0003924 GTPase activity
GO:0005096 GTPase activator activity
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005834 heterotrimeric G-protein complex
GO:0006457 protein folding
GO:0007165 signal transduction
GO:0007186 G protein-coupled receptor signaling pathway
GO:0007212 dopamine receptor signaling pathway
GO:0031682 G-protein gamma-subunit binding
GO:0043547 positive regulation of GTPase activity
GO:0051087 chaperone binding
GO:0098793 presynapse
GO:1901386 negative regulation of voltage-gated calcium channel activity
GO:1902773 GTPase activator complex

Subcellular Location

Show/Hide Table
Subcellular Location
Membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR001632 G-protein, beta subunitDomainDomain
IPR001680 WD40 repeatRepeatRepeat
IPR015943 WD40/YVTN repeat-like-containing domain superfamilyFamilyHomologous superfamily
IPR016346 Guanine nucleotide-binding protein, beta subunitFamilyFamily
IPR019775 WD40 repeat, conserved siteSiteConserved site
IPR020472 G-protein beta WD-40 repeatRepeatRepeat
IPR036322 WD40-repeat-containing domain superfamilyFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617182 OMIMLanguage delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia (LADCI)An autosomal recessive neurodevelopmental disorder characterized by speech impairment and variable expressivity of attention deficit hyperactivity disorder. Some patients manifest developmental and motor delay, hypotonia, and sinus-node dysfunction. The disease is caused by variants affecting the gene represented in this entry.
617173 OMIMIntellectual developmental disorder with cardiac arrhythmia (IDDCA)An autosomal recessive multisystem disorder characterized by delayed psychomotor development, severe intellectual disability with poor or absent speech, and bradycardia and/or cardiac sinus arrhythmias. Additional features include visual abnormalities, seizures, hypotonia, and gastric reflux. The disease is caused by variants affecting the gene represented in this entry.

Interactions

42 interactions

InteractorPartnerSourcesPublicationsLink
GNB5_HUMANMCM2_HUMANBioGRID, HPRD, IntAct16169070 details
GNB5_HUMANMVD1_HUMANBioGRID, HPRD, IntAct16169070 details
GNB5_HUMANEIF3J_HUMANHPRD, IntAct16169070 details
GNB5_HUMANNR6A1_HUMANHPRD, IntAct16169070 details
GNB5_HUMANNOE2_HUMANHPRD, IntAct16169070 details
GNB5_HUMANPSD1_HUMANHPRD, IntAct16169070 details
GNB5_HUMANE2F2_HUMANBioGRID, IntAct21988832 details
GNB5_HUMANPSMD4_HUMANBioGRID, IntAct21988832 details
GNB5_HUMANRFA1_HUMANBioGRID, IntAct21988832 details
GNB5_HUMANANXA7_HUMANBioGRID, MINT21900206 details
GNB5_HUMANBNI3L_HUMANBioGRID, MINT21900206 details
GNB5_HUMANCDN1A_HUMANBioGRID, MINT21900206 details
GNB5_HUMANCSK2B_HUMANBioGRID, MINT21900206 details
GNB5_HUMANT22D1_HUMANBioGRID, MINT21900206 details
GNB5_HUMANGBG7_HUMANBioGRID, HPRD, IntAct25241761 8636150 details
GNB5_HUMANRGS6_HUMANBioGRID, HPRD, IntAct10339615 10521509 28514442 details
GNB5_HUMANRGS7_HUMANBioGRID, HPRD, IntAct10051672 10339615 10521509 19182865 19376773 26186194 28514442 9789084 details
GNB5_HUMANGBG5_HUMANBioGRID, HPRD8636150 details
GNB5_HUMANGBG4_HUMANBioGRID, HPRD16884933 8636150 details
GNB5_HUMANGBG3_HUMANBioGRID, HPRD12606627 8636150 details
GNB5_HUMANGBG13_HUMANBioGRID, HPRD11675383 12606627 details
GNB5_HUMANGBG2_HUMANBioGRID, HPRD10339615 12606627 16301321 19376773 8636150 details
GNB5_HUMANRGS11_HUMANBioGRID, HPRD10339615 12606627 9315921 9789084 details
GNB5_HUMANA4_HUMANBioGRID21832049 details
GNB5_HUMANDRD2_HUMANBioGRID25162404 details
GNB5_HUMANGBG1_HUMANHPRD8636150 details
GNB5_HUMANMLF1_HUMANIntAct25036637 details
GNB5_HUMANMLF2_HUMANIntAct25036637 details
GNB5_HUMANNUDC_HUMANIntAct25036637 details
GNB5_HUMANDNJC7_HUMANIntAct25036637 details
GNB5_HUMANPFD2_HUMANIntAct25036637 details
GNB5_HUMANPSMD2_HUMANIntAct25036637 details
GNB5_HUMANSTIP1_HUMANIntAct25036637 details
GNB5_HUMANPFD5_HUMANBioGRID, IntAct25036637 26186194 details
GNB5_HUMANPTG3L_HUMANIntAct25036637 details
GNB5_HUMANAASD1_HUMANIntAct25036637 details
GNB5_HUMANRGS9_HUMANBioGRID, HPRD, IntAct12119397 21511947 28514442 details
GNB5_HUMANPHLP_HUMANBioGRID, IntAct19376773 26186194 28514442 details
GNB5_HUMANR7BP_HUMANBioGRID16867977 21511947 details
GNB5_HUMANTCPE_HUMANBioGRID19376773 details
GNB5_HUMANMTOR_HUMANBioGRID24462769 details
GNB5_HUMANCUL4A_HUMANBioGRID25982117 details