ENSG00000101333


Homo sapiens

Features
Gene ID: ENSG00000101333
  
Biological name :PLCB4
  
Synonyms : phospholipase C beta 4 / PLCB4 / Q15147
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 20
Strand: 1
Band: p12.3
Gene start: 9068763
Gene end: 9481242
  
Corresponding Affymetrix probe sets: 203895_at (Human Genome U133 Plus 2.0 Array)   203896_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000385805
Ensembl peptide - ENSP00000367762
Ensembl peptide - ENSP00000390616
Ensembl peptide - ENSP00000412982
Ensembl peptide - ENSP00000395753
Ensembl peptide - ENSP00000391614
Ensembl peptide - ENSP00000278655
Ensembl peptide - ENSP00000367734
Ensembl peptide - ENSP00000367754
NCBI entrez gene - 5332     See in Manteia.
OMIM - 600810
RefSeq - XM_017027886
RefSeq - XM_006723569
RefSeq - XM_011529254
RefSeq - XM_017027880
RefSeq - XM_017027881
RefSeq - XM_017027882
RefSeq - XM_017027883
RefSeq - XM_017027884
RefSeq - XM_017027885
RefSeq - NM_000933
RefSeq - NM_001172646
RefSeq - NM_182797
RefSeq - XM_005260724
RefSeq - XM_005260728
RefSeq - XM_006723568
RefSeq Peptide - NP_877949
RefSeq Peptide - NP_000924
RefSeq Peptide - NP_001166117
swissprot - B1AJW4
swissprot - B1AJW1
swissprot - Q15147
swissprot - B1AJW3
swissprot - B1AJW2
Ensembl - ENSG00000101333
  
Related genetic diseases (OMIM): 614669 - Auriculocondylar syndrome 2, 614669
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
 PLCB4ENSDARG00000100786Danio rerio
 PLCB4ENSGALG00000008907Gallus gallus
 Plcb4ENSMUSG00000039943Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PLCB1 / Q9NQ66 / phospholipase C beta 1ENSG0000018262139
PLCB3 / Q01970 / phospholipase C beta 3ENSG0000014978238
PLCB2 / Q00722 / phospholipase C beta 2ENSG0000013784134
PLCH1 / Q4KWH8 / phospholipase C eta 1ENSG0000011480524
PLCH2 / O75038 / phospholipase C eta 2ENSG0000014952724
PLCL1 / Q15111 / phospholipase C like 1 (inactive)ENSG0000011589621
PLCL2 / Q9UPR0 / phospholipase C like 2ENSG0000015482221
PLCD4 / Q9BRC7 / phospholipase C delta 4ENSG0000011555621
PLCD1 / P51178 / phospholipase C delta 1ENSG0000018709120
PLCD3 / Q8N3E9 / phospholipase C delta 3ENSG0000016171420
PLCZ1 / Q86YW0 / phospholipase C zeta 1ENSG0000013915117


Protein motifs (from Interpro)
Interpro ID Name
 IPR000008  C2 domain
 IPR000909  Phosphatidylinositol-specific phospholipase C, X domain
 IPR001192  Phosphoinositide phospholipase C family
 IPR001711  Phospholipase C, phosphatidylinositol-specific, Y domain
 IPR009535  Phospholipase C-beta, conserved site
 IPR011992  EF-hand domain pair
 IPR011993  PH-like domain superfamily
 IPR015359  Phosphoinositide-specific phospholipase C, EF-hand-like domain
 IPR016280  Phosphatidylinositol-4, 5-bisphosphate phosphodiesterase beta
 IPR017946  PLC-like phosphodiesterase, TIM beta/alpha-barrel domain superfamily
 IPR035892  C2 domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006629 lipid metabolic process IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway TAS
 biological_processGO:0016042 lipid catabolic process IEA
 biological_processGO:0035556 intracellular signal transduction IEA
 biological_processGO:0043647 inositol phosphate metabolic process TAS
 cellular_componentGO:0005622 intracellular IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005790 smooth endoplasmic reticulum IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0014069 postsynaptic density IEA
 cellular_componentGO:0030425 dendrite IEA
 molecular_functionGO:0004435 phosphatidylinositol phospholipase C activity TAS
 molecular_functionGO:0004629 phospholipase C activity TAS
 molecular_functionGO:0004871 obsolete signal transducer activity IEA
 molecular_functionGO:0005509 calcium ion binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008081 phosphoric diester hydrolase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA


Pathways (from Reactome)
Pathway description
PLC beta mediated events
Synthesis of IP3 and IP4 in the cytosol
G alpha (q) signalling events


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant 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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 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:0000160 Microstomia "The presence of an abnormally small `mouth` (FMA:49184)." [HPO:curators]
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 HP:0000162 Glossoptosis 
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 HP:0000175 Cleft palate "Cleft palate is a developmental defect of the `palate` (FMA:54549) resulting from a failure of fusion of the palatine processes." [HPO:curators]
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 HP:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
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 HP:0000311 Round face "An unusually round appearance of the face." [HPO:curators]
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 HP:0000358 Posteriorly rotated ears "A type of `abnormal location of the ears` (HP:0000357) in which the position of the ears is characterized by posterior rotation (the superior part of the ears is rotated towards the back of the head, and the inferior part of the ears towards the front)." [HPO:probinson]
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 HP:0000369 Low-set ears "Low-set ears are defined to be set below an arbitrary line drawn between the lateral canthus of the eye and the occipital protruberance." [HPO:curators]
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 HP:0000678 Dental overcrowding 
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 HP:0000689 Dental malocclusion "Dental malocclusion refers to an abnormality of the occlusion, or alignment, of the teeth and the way the upper and lower teeth fit together, resulting in overcrowding of teeth or in abnormal bite patterns." [HPO:curators]
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 HP:0002104 Apnea "Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event." [HPO:curators]
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 HP:0004453 Overfolding of the superior helices 
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 HP:0007627 Mandibular condyle aplasia 
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 HP:0007628 Mandibular condyle hypoplasia 
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 HP:0008537 Cleft at the superior portion of the pinna 
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 HP:0008559 Hypoplastic superior helix 
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 HP:0009088 Speech articulation difficulties 
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 HP:0025267 Snoring "Deep, noisy breathing during sleep accompanied by hoarse or harsh sounds caused by the vibration of respiratory structures (especially the soft palate) resulting in sound due to obstructed air movement during breathing while sleeping." []
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000088256 GNA11 / P29992 / G protein subunit alpha 11  / complex / reaction
 ENSG00000060558 GNA15 / P30679 / G protein subunit alpha 15  / reaction / complex
 ENSG00000137841 PLCB2 / Q00722 / phospholipase C beta 2  / reaction
 ENSG00000149782 PLCB3 / Q01970 / phospholipase C beta 3  / reaction
 ENSG00000182621 PLCB1 / Q9NQ66 / phospholipase C beta 1  / reaction
 ENSG00000101333 PLCB4 / Q15147 / phospholipase C beta 4  / reaction
 ENSG00000156052 GNAQ / P50148 / G protein subunit alpha q  / reaction / complex
 ENSG00000156049 GNA14 / O95837 / G protein subunit alpha 14  / reaction / complex






 

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