ENSMUSG00000001151


Mus musculus

Features
Gene ID: ENSMUSG00000001151
  
Biological name :Pcnt
  
Synonyms : Pcnt / pericentrin
  
Possible biological names infered from orthology : O95613
  
Species: Mus musculus
  
Chr. number: 10
Strand: -1
Band: C1
Gene start: 76351263
Gene end: 76442786
  
Corresponding Affymetrix probe sets: 10370127 (MoGene1.0st)   1433873_s_at (Mouse Genome 430 2.0 Array)   1454749_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000151981
Ensembl peptide - ENSMUSP00000001179
Ensembl peptide - ENSMUSP00000151534
NCBI entrez gene - 18541     See in Manteia.
MGI - MGI:102722
RefSeq - XM_017313845
RefSeq - XM_017313840
RefSeq - XM_017313841
RefSeq - XM_017313842
RefSeq - XM_017313843
RefSeq - XM_017313844
RefSeq - NM_001282992
RefSeq - NM_008787
RefSeq - XM_006513348
RefSeq - XM_006513353
RefSeq - XM_006513356
RefSeq - XM_011243382
RefSeq - XM_011243383
RefSeq - XM_011243384
RefSeq - XM_017313838
RefSeq - XM_017313839
RefSeq Peptide - NP_032813
RefSeq Peptide - NP_001269921
swissprot - F8VPV0
swissprot - A0A1W2P8A6
swissprot - A0A1W2P737
Ensembl - ENSMUSG00000001151
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 pcntENSDARG00000033012Danio rerio
 PCNTENSGALG00000007021Gallus gallus
 PCNTENSG00000160299Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Akap9 / A-kinase anchoring protein 9 / Q99996*ENSMUSG0000004040721


Protein motifs (from Interpro)
Interpro ID Name
 IPR019528  Pericentrin/AKAP-450 centrosomal targeting domain
 IPR028745  A-kinase anchor protein 9/Pericentrin


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000226 microtubule cytoskeleton organization IEA
 biological_processGO:0007052 mitotic spindle organization IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0060271 cilium assembly IEA
 biological_processGO:0090316 positive regulation of intracellular protein transport IEA
 cellular_componentGO:0005813 centrosome IEA
 cellular_componentGO:0005814 centriole IEA
 cellular_componentGO:0005815 microtubule organizing center IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0034451 centriolar satellite IEA
 molecular_functionGO:0032947 protein-containing complex scaffold activity IEA


Pathways (from Reactome)
Pathway description
Regulation of PLK1 Activity at G2/M Transition
Loss of Nlp from mitotic centrosomes
Recruitment of mitotic centrosome proteins and complexes
Loss of proteins required for interphase microtubule organization from the centrosome
Recruitment of NuMA to mitotic centrosomes
Anchoring of the basal body to the plasma membrane
AURKA Activation by TPX2


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000111 cleft palate "congenital fissure of the tissues normally uniting to form the palate" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0000259 abnormal vascular development "malformation or aberrant differentiation of the blood vessels" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17509]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0000266 abnormal cardiac morphology "anomalies in the hollow, muscular organ that maintains the circulation of the blood" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0000273 overriding aorta "congenitally mispositioned aorta where the origin straddles the ventral septum and so receives ejected blood from the right ventricle as well as the left." [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cml, J:67826]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000433 microcephaly "an abnormally small head" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0000522 cysts in kidney cortex "abnormal membranous sacs appearing in the renal lobules, tubules and glomeruli" [J:50844]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000562 polydactyly "greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo
Genetic Background: B6.129S1-Tnftm1Ljo

Allelic Composition: Pcntm239Asp/Pcntm239Asp,Tg(mI56i-lacZ)1Mekk/0
Genetic Background: involves: C57BL/6J * FVB/N

Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000564 syndactyly "any degree of webbing or fusion of the digits, may involve only soft tissues or also can include bone" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000774 reduced brain size "smaller appearance of the brain" [J:35802]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000788 abnormal cerebral cortex morphology "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857]
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo
Genetic Background: B6.129S1-Tnftm1Ljo

Allelic Composition: Pcntm239Asp/Pcntm239Asp,Tg(mI56i-lacZ)1Mekk/0
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0000807 abnormal hippocampus morphology "absent or malformed deep lying structure of the cerebrum involved with memory storage and spatial navigation" [The Atlas of Mouse Development:ISBN 0-12-402035-6, MGI:Cls, J:38857]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0000913 abnormal brain development "malformed or incomplete differentiation of the brain" [MGI:cls, J:49840]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0000951 sporadic seizures "occasional seizures occuring at irregular intervals" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo
Genetic Background: B6.129S1-Tnftm1Ljo

Allelic Composition: Pcntm239Asp/Pcnt+,Tg(mI56i-lacZ)1Mekk/0
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0001177 atelectasis "collapse of the lung or any portion of the lung, or decreased or absent air in the lung, resulting in loss of lung volume " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0001178 pulmonary hypoplasia "reduced size of the respiratory organ due to incomplete development of all or part of the organ " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0001293 anophthalmia "congenital absence of all tissues of the eyes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CML, J:71979]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0001297 microphthalmia "reduced average size of the eyes" [J:18048]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0001914 hemorrhage "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0001915 intracranial hemorrhage "bleeding within the skull, including hemorrhage into the brain and within the cranial epidural, subdural, and subarachnoid spaces" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0002081 perinatal lethality "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo
Genetic Background: B6.129S1-Tnftm1Ljo

Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo
Genetic Background: B6.129S1-Tnftm1Ljo

Allelic Composition: Pcntm239Asp/Pcnt+,Tg(mI56i-lacZ)1Mekk/0
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0002092 abnormal eye morphology "abnormal development of the eye tissues resulting in morphological abnormality or abnormal structure of the visual system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0002135 abnormal kidney morphology "abnormal development of the kidney resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Vegfatm2Gne/Vegfatm2Gne,Tg(Pax6-cre,GFP)2Pgr/0
Genetic Background: involves: 129

 MP:0002192 hydrops fetalis "an abnormal accumulation of serous fluid in fetal tissues" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0002741 small olfactory bulb "reduced size of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [J:79871]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0003675 kidney cysts "abnormal membranous sacs in any portion of the pair of organs responsible for urine secretion" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0003935 abnormal craniofacial development "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0004017 duplex kidney "a kidney that is split into two separate collecting systems; there may be a duplex ureter or a single ureter; may present unilaterally or bilaterally" [rbabiuk:Randall Babiuk, Mouse Genome Informatics Curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0004261 abnormal embryonic neuroepithelium morphology "any structural anomaly in the epithelial cell layer that lines the neural tube and develops into the nervous system and into the neural crest cells" [ISBN:0838580343 "Kandel ER, et al. Principles of Neural Science, 3rd edition", MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0004948 abnormal neuronal precursor proliferation "any anomaly in the ability of a neuroblast population to undergo rapid expansion by cell division" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0006009 abnormal neuronal migration "defective or impaired movement of immature neurons from germinal zones to specific positions where they will reside as they mature" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0006042 increased apoptosis "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0006045 mitral valve insufficiency "the mitral valve does not close tightly enough to prevent leakage" [smb:Susan M Bello, Mouse Genome Informatics Curator, RGD:Rat Genome Database submission]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0006047 aortic valve insufficiency "the aortic valve does not close tightly enough to prevent leakage. " [smb:Susan M Bello, Mouse Genome Informatics Curator, RGD:Rat Genome Database submission]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0006113 abnormal heart septum morphology "abnormality in the wall between the atria or ventricles of the heart, usually incomplete closure" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0006138 congestive heart failure "the heart is unable to adequately pump blood throughout the body" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0006254 thin cerebral cortex "decreased depth of the mantle covering the surface of the cerebral hemispheres" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:84683]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0008441 thin cortical plate "reduced thickness of the outer neural tube region in which post-mitotic neuroblasts migrate along radial glia to form the adult cortical layers" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:1812236]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0008458 abnormal cortical ventricular zone morphology "any structural anomaly of a transient region of the developing cerebral cortex that contains migrating neurons, radial glial cells, and a large population of cycling multipotent neural stem cells that generate newborn neurons" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0008772 enlarged heart ventricle "increased average size of the heart ventricles compared to the average for a particular population" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0009743 preaxial polydactyly "duplication of all or part of the first ray on one or more of the autopods" [PMID:19125433]
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Allelic Composition: Gad1tm1.1Tama/Gad1+,Pcntm239Asp/Pcntm239Asp
Genetic Background: involves: C57BL/6 * C57BL/6J * CBA * FVB/N

 MP:0009760 abnormal mitotic spindle "an anomaly in the formation of the ellipsoidal (bipolar) collection of fibers visible during nuclear division and cytokinesis responsible for accurate segregation of chromosomes during mitosis" [ISBN:8185198691 "Rieger R et al Eds Glossary of Genetics Classical and Molecular"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0009937 abnormal neuron differentiation "abnormal growth or development of the cells of the nervous system that receive, conduct, and transmit impulses" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0010403 atrial septal defect "abnormal communications between the two upper chambers of the heart, including such defects in any or all of the ostium primum, ostium secundum, sinus venosus, and coronary sinus regions" [MESH:C14.240.400.560.375]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0010412 atrioventricular septal defect "defects in the thin membranous structure between the right atrium and left ventricle that arise from faulty development of the embryonic endocardial cushions; the spectrum ranges from a primum atrial septal defect and cleft mitral valve, known as a partial atrioventricular septal defect (partial AVSD), to defects of both the primum atrial septum and inlet ventricular septum and the presence of a common atrioventricular valve, referred to as complete atrioventricular septal defect (complete AVSD)" [http://emedicine.medscape.com]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0010865 prenatal growth retardation "slow or limited development during the prenatal period" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0010993 decreased surfactant secretion "decreased production or release from pneumocytes of surfactant, a phospholipid present in the lungs that controls surface tension in the alveoli" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0011099 complete lethality throughout fetal growth and development "death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0011380 enlarged brain ventricle "increased size of one or more of the four communicating cavities within the brain that are continuous with the central canal of the spinal cord" [MGI:smb]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0011495 abnormal head shape "any anomaly in the characteristic surface outline or contour of a head of an organism" [MGI:csmith]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0011682 renal glomerulus cysts "abnormal membranous sacs in any portion of the renal glomerulus" [MGI:csmith]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

 MP:0012285 misaligned sternebrae "abnormal alignment of the sternebrae along the ventral midline" [MGI:anna]
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Allelic Composition: PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
Genetic Background: B6.129P2-PcntGt(RRU388)Byg

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
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