ENSMUSG00000004591


Mus musculus

Features
Gene ID: ENSMUSG00000004591
  
Biological name :Pkn2
  
Synonyms : Pkn2 / Q8BWW9 / Serine/threonine-protein kinase N2
  
Possible biological names infered from orthology : protein kinase N2 / Q16513
  
Species: Mus musculus
  
Chr. number: 3
Strand: -1
Band: H1
Gene start: 142790902
Gene end: 142882004
  
Corresponding Affymetrix probe sets: 10502484 (MoGene1.0st)   1437295_at (Mouse Genome 430 2.0 Array)   1437296_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000134041
Ensembl peptide - ENSMUSP00000134046
Ensembl peptide - ENSMUSP00000134559
Ensembl peptide - ENSMUSP00000039566
Ensembl peptide - ENSMUSP00000133419
Ensembl peptide - ENSMUSP00000133691
NCBI entrez gene - 109333     See in Manteia.
MGI - MGI:109211
RefSeq - NM_178654
RefSeq Peptide - NP_848769
swissprot - Q8BWW9
swissprot - G3UWT9
swissprot - G3UXH4
swissprot - G3UYD6
swissprot - G3UYE1
swissprot - G3UZM9
Ensembl - ENSMUSG00000004591
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 pkn2ENSDARG00000101983Danio rerio
 zgc:153916ENSDARG00000101293Danio rerio
 PKN2ENSGALG00000006237Gallus gallus
 PKN2ENSG00000065243Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Pkn1 / P70268 / Serine/threonine-protein kinase N1 / Q16512* / protein kinase N1*ENSMUSG0000005767259
Pkn3 / Q8K045 / Serine/threonine-protein kinase N3 / Q6P5Z2* / protein kinase N3*ENSMUSG0000002678547


Protein motifs (from Interpro)
Interpro ID Name
 IPR000008  C2 domain
 IPR000719  Protein kinase domain
 IPR000961  AGC-kinase, C-terminal
 IPR008271  Serine/threonine-protein kinase, active site
 IPR011009  Protein kinase-like domain superfamily
 IPR011072  HR1 rho-binding domain
 IPR017441  Protein kinase, ATP binding site
 IPR017892  Protein kinase, C-terminal
 IPR035892  C2 domain superfamily
 IPR036274  HR1 repeat superfamily
 IPR037313  Serine/threonine-protein kinase N, first HR1 domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006468 protein phosphorylation IEA
 biological_processGO:0006915 apoptotic process IEA
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0007155 cell adhesion IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0010631 epithelial cell migration IEA
 biological_processGO:0016310 phosphorylation IEA
 biological_processGO:0018105 peptidyl-serine phosphorylation IBA
 biological_processGO:0030030 cell projection organization IEA
 biological_processGO:0032467 positive regulation of cytokinesis IEA
 biological_processGO:0035556 intracellular signal transduction IBA
 biological_processGO:0043297 apical junction assembly IEA
 biological_processGO:0045070 positive regulation of viral genome replication IEA
 biological_processGO:0045931 positive regulation of mitotic cell cycle IEA
 biological_processGO:0051301 cell division IEA
 biological_processGO:2000145 regulation of cell motility IEA
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005813 centrosome IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0016604 nuclear body IEA
 cellular_componentGO:0030027 lamellipodium ISS
 cellular_componentGO:0030054 cell junction IEA
 cellular_componentGO:0030496 midbody ISO
 cellular_componentGO:0032154 cleavage furrow ISO
 cellular_componentGO:0032991 protein-containing complex IDA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0043296 apical junction complex IEA
 cellular_componentGO:0045111 intermediate filament cytoskeleton IEA
 cellular_componentGO:0048471 perinuclear region of cytoplasm IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0004672 protein kinase activity IEA
 molecular_functionGO:0004674 protein serine/threonine kinase activity IEA
 molecular_functionGO:0004697 protein kinase C activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016301 kinase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0017049 GTP-Rho binding IEA
 molecular_functionGO:0042826 histone deacetylase binding IEA
 molecular_functionGO:0045296 cadherin binding IEA
 molecular_functionGO:0070063 RNA polymerase binding IEA


Pathways (from Reactome)
Pathway description
RHO GTPases activate PKNs


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0000929 open neural tube "incomplete invagination and fusion of the neuroepithelial layer in early development" [MGI:CLS, J:53370, J:62571]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0001183 overexpanded alveoli "expanded volume of the saclike terminal dilation of the respiratory bronchioles" [J:66345]
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Allelic Composition: Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi,Tg(Tek-cre)12Flv/0
Genetic Background: involves: C3H * C57BL/6 * C57BL/6N

 MP:0001625 cardiac hypertrophy "an increase in size of the cardiac tissue, not due to increased cell number " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi,Tg(Tek-cre)12Flv/0
Genetic Background: involves: C3H * C57BL/6 * C57BL/6N

 MP:0001688 abnormal somite development "anomalous formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0001700 abnormal embryo turning "atypical axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (Mus:E8.5-E9.5) such that the curvature of the entire trunk region is reversed and the neural ectoderm moves to the convex region and the midgut region becomes located in the concave region" [The Atlas of Mouse Development:ISBN 0-12-402035-6, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0001719 absent vitelline blood vessels "missing vasculature of the yolk sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:62571, J:12623]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0001723 disorganized vascular plexus 
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0001787 pericardial edema "accumulation of watery fluid in the pericardial sac of the heart" [J:52597]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 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: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0002084 abnormal developmental patterning "abnormal systematic arrangement of the developing body along an axis" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

Allelic Composition: Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi,Tg(Tek-cre)12Flv/0
Genetic Background: involves: C3H * C57BL/6 * C57BL/6N

 MP:0002950 abnormal neural crest cell migration "defect in the dispersion of the transient and migratory group of cells that emerge from the dorsal region of the neural tube and migrate to many peripheral locations to form various tissues of the adult" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0003229 abnormal vitelline vasculature "malformation in the vessels of the yolk sac" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93257]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0003874 absent branchial arches "missing the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0003885 abnormal rostro-caudal body axis extension "anomaly in or failure of the long (rostral-caudal) axis of the body to elongate normally once patterning has been established" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0004046 abnormal mitosis "anomaly in the process of cell division including both division of the nucleus (karyokinesis) and the cytoplasm (cytokinesis) " [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0004759 decreased mitotic index "decreased number of cells in G2/M phase" [Bertram_Weiss:Bayer_Schering_Pharma_AG]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0004837 abnormal neural fold formation "any anomaly in the process by which the edges of the neural plate thicken and move up to form a U-shaped structure called the neural groove" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0006050 pulmonary fibrosis "formation of fibrous tissue within the lung often resulting from inflammation or injury " [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi,Tg(Tek-cre)12Flv/0
Genetic Background: involves: C3H * C57BL/6 * C57BL/6N

 MP:0006301 abnormal mesenchyme morphology "abnormality in the loosely packed, unspecialized cells that derive mostly from the mesoderm and contribute to connective tissue, bone, cartilage and circulatory and lymphatic systems." [J:120305, mnk:Michelle Knowlton_MGI Curator]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0008784 craniorachischisis "congenital fissure of the skull and vertebral column" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0009328 delayed heart looping "late onset of the initiation and/or completion of cardiac looping" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0010831 partial lethality "the appearance of lower than Mendelian ratios of offspring of a given genotype due to death of some, but not all of the organisms" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi,Tg(Tek-cre)12Flv/0
Genetic Background: involves: C3H * C57BL/6 * C57BL/6N

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0011702 abnormal fibroblast proliferation "anomaly in the ability of the a fibroblast cell population to undergo expansion by cell division" [MGI:csmith]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0011704 decreased fibroblast proliferation "reduction in the expansion rate of a fibroblast cell population by cell division" [MGI:csmith]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0012176 abnormal head development "anomaly in the process in which the anatomical structures of the head are generated and organized" [GO:0060323]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0013504 increased embryonic tissue cell apoptosis "increase in the timing or the number of cells in embryonic tissue undergoing programmed cell death" [MGI:csmith]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0013925 abnormal vascular plexus formation 
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0014134 abnormal embryo morphology "any structural anomaly of an embryo " [MGI:csmith]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

 MP:0014138 abnormal germ layer morphology "any structural anomaly of the layer of cells produced during the process of gastrulation during the early development of the animal embryo, which is distinct from other such layers of cells, as an early step of cell differentiation" [ISBN:0-683-40008-8]
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Allelic Composition: Pkn1tm1Ajmc/Pkn1tm1Ajmc,Pkn2tm1a(KOMP)Wtsi/Pkn2+,Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac

 MP:0014141 abnormal mesoderm morphology "any structural anomaly of the middle germ layer of the embryo, between the endoderm and ectoderm" [UBERON:0000926]
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Allelic Composition: Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+,Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
Genetic Background: involves: C57BL/6N * C57BL/6NTac

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000054364 Rhob / P62746 / ras homolog family member B / P62745*  / reaction / complex
 ENSMUSG00000007815 Rhoa / Q9QUI0 / ras homolog family member A / P61586*  / reaction / complex
 ENSMUSG00000002233 Rhoc / Q62159 / Rho-related GTP-binding protein RhoC / P08134* / ras homolog family member C*  / reaction / complex
 ENSMUSG00000024122 Pdpk1 / Q9Z2A0 / 3-phosphoinositide-dependent protein kinase 1 / O15530*  / complex / reaction






 

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