ENSMUSG00000042632


Mus musculus

Features
Gene ID: ENSMUSG00000042632
  
Biological name :Pla2g6
  
Synonyms : P97819 / phospholipase A2, group VI / Pla2g6
  
Possible biological names infered from orthology : O60733
  
Species: Mus musculus
  
Chr. number: 15
Strand: -1
Band: E1
Gene start: 79286228
Gene end: 79328390
  
Corresponding Affymetrix probe sets: 10430489 (MoGene1.0st)   1422147_a_at (Mouse Genome 430 2.0 Array)   1431277_at (Mouse Genome 430 2.0 Array)   1431278_s_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000134672
Ensembl peptide - ENSMUSP00000044234
Ensembl peptide - ENSMUSP00000131081
Ensembl peptide - ENSMUSP00000132071
Ensembl peptide - ENSMUSP00000133554
Ensembl peptide - ENSMUSP00000133578
Ensembl peptide - ENSMUSP00000133998
Ensembl peptide - ENSMUSP00000134456
NCBI entrez gene - 53357     See in Manteia.
MGI - MGI:1859152
RefSeq - XM_017316698
RefSeq - XM_006521152
RefSeq - XM_006521153
RefSeq - XM_006521154
RefSeq - XM_006521155
RefSeq - XM_006521156
RefSeq - XM_006521157
RefSeq - XM_006521158
RefSeq - XM_006521159
RefSeq - XM_006521160
RefSeq - NM_001199023
RefSeq - NM_001199024
RefSeq - NM_001199025
RefSeq - NM_016915
RefSeq Peptide - NP_058611
RefSeq Peptide - NP_001185952
RefSeq Peptide - NP_001185953
RefSeq Peptide - NP_001185954
swissprot - G3UX52
swissprot - Q3UN31
swissprot - G3UX73
swissprot - P97819
swissprot - G3UY97
Ensembl - ENSMUSG00000042632
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 pla2g6ENSDARG00000060921Danio rerio
 PLA2G6ENSGALG00000012281Gallus gallus
 O60733ENSG00000184381Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Pnpla8 / Q8K1N1 / Calcium-independent phospholipase A2-gamma / Q9NP80* / patatin like phospholipase domain containing 8*ENSMUSG0000003625716


Protein motifs (from Interpro)
Interpro ID Name
 IPR002110  Ankyrin repeat
 IPR002641  Patatin-like phospholipase domain
 IPR016035  Acyl transferase/acyl hydrolase/lysophospholipase
 IPR020683  Ankyrin repeat-containing domain
 IPR036770  Ankyrin repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001934 positive regulation of protein phosphorylation IEA
 biological_processGO:0006629 lipid metabolic process IEA
 biological_processGO:0006935 chemotaxis IEA
 biological_processGO:0007204 positive regulation of cytosolic calcium ion concentration IEA
 biological_processGO:0007613 memory IEA
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0014832 urinary bladder smooth muscle contraction IEA
 biological_processGO:0016042 lipid catabolic process IEA
 biological_processGO:0019731 antibacterial humoral response ISO
 biological_processGO:0032049 cardiolipin biosynthetic process ISO
 biological_processGO:0034976 response to endoplasmic reticulum stress IEA
 biological_processGO:0035774 positive regulation of insulin secretion involved in cellular response to glucose stimulus IEA
 biological_processGO:0045921 positive regulation of exocytosis IEA
 biological_processGO:0051967 negative regulation of synaptic transmission, glutamatergic IEA
 biological_processGO:0060135 maternal process involved in female pregnancy IEA
 biological_processGO:0090037 positive regulation of protein kinase C signaling IEA
 biological_processGO:0090200 positive regulation of release of cytochrome c from mitochondria IEA
 biological_processGO:0090238 positive regulation of arachidonic acid secretion IEA
 biological_processGO:0097755 positive regulation of blood vessel diameter IEA
 biological_processGO:1901339 regulation of store-operated calcium channel activity IEA
 biological_processGO:2000304 positive regulation of ceramide biosynthetic process IEA
 cellular_componentGO:0005615 extracellular space ISO
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005739 mitochondrion IEA
 cellular_componentGO:0005815 microtubule organizing center ISO
 cellular_componentGO:0005829 cytosol ISO
 cellular_componentGO:0016020 membrane IEA
 molecular_functionGO:0004623 phospholipase A2 activity IEA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0005516 calmodulin binding IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0017171 serine hydrolase activity IDA
 molecular_functionGO:0019901 protein kinase binding IEA
 molecular_functionGO:0043008 ATP-dependent protein binding IEA
 molecular_functionGO:0047499 calcium-independent phospholipase A2 activity IEA
 molecular_functionGO:0102567 phospholipase A2 activity (consuming 1,2-dipalmitoylphosphatidylcholine) IEA
 molecular_functionGO:0102568 phospholipase A2 activity consuming 1,2-dioleoylphosphatidylethanolamine) IEA


Pathways (from Reactome)
Pathway description
Acyl chain remodelling of PC
Acyl chain remodelling of PE
Role of phospholipids in phagocytosis
COPI-independent Golgi-to-ER retrograde traffic


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000160 kyphosis "forward curvature of the spine, characterized by extensive flexion. " [J:62023, J:66943, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000745 tremors "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0000755 hindlimb paralysis "loss of power of voluntary movement in the muscles of the hindlimb through injury or disease of it or its nerve supply" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0000955 abnormal spinal cord morphology "malformation or disorganization of the cylindrical tissue of the vertebral canal that extends from the medulla oblongata to the conus medullaris" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0001263 weight loss "progressive reduction of body weight below normal average for age" [J:45400]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Tnfsf13btm1Msc/Tnfsf13btm1Msc,Traf2tm1Rbr/Traf2tm1Rbr
Genetic Background: involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Tnfsf13btm1Msc/Tnfsf13btm1Msc,Traf2tm1Rbr/Traf2tm1Rbr
Genetic Background: involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0001405 impaired coordination "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001406 abnormal gait "unusual or distinctive way of walking" [J:65038]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001415 increased exploration in new environment "greater amount of time spent investigating new location" [J:28825]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0001516 abnormal motor coordination/ balance "altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0001524 impaired limb coordination "reduced ability to organize limb movements to execute complex maneuvers, such as walking" [J:64962, MGI:CLS, J:17123]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001922 reduced male fertility "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001925 male infertility "inability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Scn1atm1Kea/Scn1a+
Genetic Background: (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1

 MP:0002001 blindness "loss of the sense of sight" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Scn1atm1Kea/Scn1a+
Genetic Background: (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1

 MP:0002066 abnormal motor capabilities/coordination/movement "altered ability to coordinate voluntary movement or repetitive, compulsive movements" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cacna1atm1Nobs/Cacna1atm2Nobs
Genetic Background: involves: 129 * C57BL/6J

 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: Cd19tm1(cre)Cgn/Cd19+,Tnfsf13btm1Msc/Tnfsf13btm1Msc,Traf2tm1Rbr/Traf2tm1Rbr
Genetic Background: involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0002152 abnormal brain morphology "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0002229 CNS neurodegeneration "a retrogressive impairment of function or destruction of neural tissue" [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: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0002269 muscular atrophy "a wasting of muscle tissue resulting in a derangement of the muscle fibers; occurs with age, immobilization, weightlessness, malnutrition or denervation" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
Show

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0002651 abnormal sciatic nerve "malformation, absence or misprojection of the nerve which originates in the lumbar and sacral spinal cord (L4 to S3) and supplies motor and sensory innervation to the lower extremity" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002675 asthenozoospermia "loss or reduction of the mobility of the spermatozoa, frequently associated with infertility" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0003225 axonal dystrophy "axon degeneration resulting from inadequate or faulty metabolism" [RGD:Rat Genome Database submission]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0003312 abnormal locomotor coordination "reduced ability of an animal to maintain skillful and effective interaction of movements while engaging in locomotor activity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tcirg1tm1Utku/Tcirg1tm1Utku
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0003632 abnormal nervous system morphology 
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0003871 abnormal myelin sheath morphology "malformation of the insulating envelope that surrounds nerve fibers or axons" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003982 increased cholesterol level "greater than normal concentration in the body of these most abundant steroids in animal tissues, and precursors to steroid hormones and bile salts; also components of plasma membranes" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Scn1atm1Kea/Scn1a+
Genetic Background: (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1

 MP:0005092 decreased double-positive T cell count "less than the expected number of the subset of T cells found in the thymus that express both CD4 and CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0005112 abnormal anterior horn morphology "anomalous structure of the ventral gray column of the spinal cord" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005277 abnormal brainstem morphology "anomalous structure of the midbrain, pons, or medulla" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82670]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0005404 abnormal axon morphology "anomaly in the structure of the single process of a nerve cell that normally conducts impulses away from the cell body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0005405 axon degeneration "retrogressive pathologic change in the single process of a nerve cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0006035 abnormal mitochondrial morphology "anomalous structure of the mitochondria" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008026 abnormal brain white matter morphology "any structural anomaly of the regions of the brain that are largely or entirely composed of myelinated nerve cell axons and contain few or no neural cell bodies or dendrites" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0008503 abnormal spinal cord gray matter morphology "any structural anomaly of the regions of the spinal cord that are largely or entirely composed of nerve cell bodies and their dendrites and some supportive tissue" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008571 abnormal synaptic bouton morphology "any structural anomaly of the knoblike enlargements along the course of axons, or more commonly at the distal terminations of axons which are specialized for the release of neurotransmitters" [MESH:A08.663.542.145.750]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008916 abnormal astrocyte physiology "any functional anomaly of one of the large neuroglia cells of nervous tissue" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0009417 skeletal muscle atrophy "a wasting of skeletal muscle tissue resulting in a derangement of the muscle fibers; occurs with age, immobilization, weightlessness, malnutrition or denervation" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

 MP:0010047 axonal spheroids "focal 10-50 micron diameter swellings of axons, which are sometimes, but not always, terminal endbulbs, and are filled with disorganized neurofilaments, tubules, organelles or multi-lamellar inclusions" [PMID:15644421]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010053 decreased grip strength "reduced ability to grasp and hold objects, often measured as time spent hanging from an object or wire" [ISBN:0471316393 "Crawley, JN, What s Wrong with my Mouse: Behavioral Phenotyping of Transgenic and Knockout Mice"]
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Allelic Composition: Pla2g6m1Sein/Pla2g6m1Sein
Genetic Background: C57BL/6JJcl-Pla2g6m1Sein

Allelic Composition: Pla2g6m1J/Pla2g6m1J
Genetic Background: C3H/HeJ-Pla2g6m1J

 MP:0010331 abnormal apolipoprotein level "anomaly in the amount of the a protein that is frequently a component of a lipoprotein complex" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Scn1atm1Kea/Scn1a+
Genetic Background: (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1

 MP:0011635 abnormal mitochondrial crista morphology "Any of the inward folds of the mitochondrial inner membrane; crista number, extent, and shape differ in mitochondria from different tissues and organisms; crista appear to be devices for increasing the surface area of the mitochondrial inner membrane, where the enzymes of electron transport and oxidative phosphorylation are found; the shape can vary with the respiratory state of the mitochondria" [GO:0030061]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0020378 abnormal cell cytoskeleton morphology "any anomaly in the structure of the various filamentous elements that form the internal framework of cells, and typically remain after treatment of the cells with mild detergent to remove membrane constituents and soluble components of the cytoplasm" [GO:0005856, MGI:mberry]
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Allelic Composition: Pla2g6tm1Tsu/Pla2g6tm1Tsu
Genetic Background: involves: 129S2/SvPas * C57BL/6

  


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






 

0 s.

 
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