ENSG00000069966


Homo sapiens

Features
Gene ID: ENSG00000069966
  
Biological name :GNB5
  
Synonyms : GNB5 / G protein subunit beta 5 / O14775
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 15
Strand: -1
Band: q21.2
Gene start: 52115105
Gene end: 52191369
  
Corresponding Affymetrix probe sets: 1554346_at (Human Genome U133 Plus 2.0 Array)   204000_at (Human Genome U133 Plus 2.0 Array)   207124_s_at (Human Genome U133 Plus 2.0 Array)   211871_x_at (Human Genome U133 Plus 2.0 Array)   242404_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000453176
Ensembl peptide - ENSP00000379626
Ensembl peptide - ENSP00000453339
Ensembl peptide - ENSP00000454185
Ensembl peptide - ENSP00000261837
Ensembl peptide - ENSP00000351635
NCBI entrez gene - 10681     See in Manteia.
OMIM - 604447
RefSeq - XM_017021867
RefSeq - NM_006578
RefSeq - NM_016194
RefSeq - XM_011521162
RefSeq - XM_011521163
RefSeq Peptide - NP_057278
RefSeq Peptide - NP_006569
swissprot - A0A024R5V3
swissprot - H0YLU1
swissprot - H0YNW7
swissprot - A0A024R5R9
swissprot - Q96F32
swissprot - O14775
Ensembl - ENSG00000069966
  
Related genetic diseases (OMIM): 617173 - Intellectual developmental disorder with cardiac arrhythmia, 617173
  617182 - Language delay and ADHD/cognitive impairment with or without cardiac arrhythmia, 617182
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 gnb5aENSDARG00000099685Danio rerio
 gnb5bENSDARG00000055377Danio rerio
 GNB5ENSGALG00000039307Gallus gallus
 Gnb5ENSMUSG00000032192Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
GNB4 / Q9HAV0 / G protein subunit beta 4ENSG0000011445045
GNB1 / P62873 / G protein subunit beta 1ENSG0000007836945
GNB2 / P62879 / G protein subunit beta 2ENSG0000017235444
GNB3 / P16520 / G protein subunit beta 3ENSG0000011166444
WDR47 / O94967 / WD repeat domain 47ENSG0000008543329


Protein motifs (from Interpro)
Interpro ID Name
 IPR001632  G-protein, beta subunit
 IPR001680  WD40 repeat
 IPR015943  WD40/YVTN repeat-like-containing domain superfamily
 IPR016346  Guanine nucleotide-binding protein, beta subunit
 IPR017986  WD40-repeat-containing domain
 IPR019775  WD40 repeat, conserved site
 IPR020472  G-protein beta WD-40 repeat
 IPR036322  WD40-repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006457 protein folding TAS
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway IEA
 biological_processGO:0007212 dopamine receptor signaling pathway IDA
 biological_processGO:0043547 positive regulation of GTPase activity IDA
 biological_processGO:1901386 negative regulation of voltage-gated calcium channel activity IDA
 cellular_componentGO:0001750 photoreceptor outer segment IEA
 cellular_componentGO:0001917 photoreceptor inner segment IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0043209 myelin sheath IEA
 cellular_componentGO:1902773 GTPase activator complex TAS
 molecular_functionGO:0003924 GTPase activity NAS
 molecular_functionGO:0004871 obsolete signal transducer activity NAS
 molecular_functionGO:0005096 GTPase activator activity IDA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0031682 G-protein gamma-subunit binding IPI
 molecular_functionGO:0051087 chaperone binding IPI


Pathways (from Reactome)
Pathway description
G-protein activation
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
ADP signalling through P2Y purinoceptor 12
G beta:gamma signalling through PI3Kgamma
Prostacyclin signalling through prostacyclin receptor
Adrenaline,noradrenaline inhibits insulin secretion
Ca2+ pathway
G alpha (q) signalling events
G alpha (12/13) signalling events
G beta:gamma signalling through PLC beta
G alpha (s) signalling events
ADP signalling through P2Y purinoceptor 1
G alpha (i) signalling events
G alpha (z) signalling events
Glucagon-type ligand receptors
Thromboxane signalling through TP receptor
Vasopressin regulates renal water homeostasis via Aquaporins
Thrombin signalling through proteinase activated receptors (PARs)
Presynaptic function of Kainate receptors
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000512 Abnormal electroretinogram "Any abnormality of the electrical responses of various cell types in the retina as measured by electroretinography." [HPO:curators]
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 HP:0000546 Retinal degeneration 
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 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0000750 Impaired language development 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001662 Bradycardia 
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 HP:0007018 Attention deficit hyperactivity disorder "Attention deficit hyperactivity disorder (ADHD) manifests at age 2-3 years or by first grade at the latest. The main symptoms are distractibility, impulsivity, hyperactivity, and often trouble organizing tasks and projects, difficulty going to sleep, and social problems from being aggressive, loud, or impatient." [HPO:curators]
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 HP:0011704 Sick sinus syndrome 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000065675 PRKCQ / Q04759 / protein kinase C theta  / reaction
 ENSG00000108370 RGS9 / O75916 / regulator of G protein signaling 9  / complex / reaction
 ENSG00000136940 PDCL / Q13371 / phosducin like  / complex
 ENSG00000182901 RGS7 / P49802 / regulator of G protein signaling 7  / complex / reaction
 ENSG00000154229 PRKCA / P17252 / protein kinase C alpha  / reaction
 ENSG00000186326 Q6ZS82 / RGS9BP / regulator of G protein signaling 9 binding protein  / complex






 

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