ENSMUSG00000059481


Mus musculus

Features
Gene ID: ENSMUSG00000059481
  
Biological name :Plg
  
Synonyms : P20918 / Plasminogen Plasmin heavy chain A Activation peptide Angiostatin Plasmin heavy chain A, short form Plasmin light chain B / Plg
  
Possible biological names infered from orthology : lipoprotein(a) / LPA / P00747 / P08519 / plasminogen
  
Species: Mus musculus
  
Chr. number: 17
Strand: 1
Band: A1
Gene start: 12378609
Gene end: 12419384
  
Corresponding Affymetrix probe sets: 10441753 (MoGene1.0st)   1416729_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000014578
NCBI entrez gene - 18815     See in Manteia.
MGI - MGI:97620
RefSeq - NM_008877
RefSeq Peptide - NP_032903
swissprot - P20918
Ensembl - ENSMUSG00000059481
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 plgENSDARG00000023111Danio rerio
 ENSGALG00000028886Gallus gallus
 ENSGALG00000004293Gallus gallus
 LPAENSG00000198670Homo sapiens
 PLGENSG00000122194Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Mst1 / P26928 / macrophage stimulating 1 (hepatocyte growth factor-like) / macrophage stimulating 1*ENSMUSG0000003259136
Hgf / Q08048 / Hepatocyte growth factor Hepatocyte growth factor alpha chain Hepatocyte growth factor beta chain / P14210* / hepatocyte growth factor*ENSMUSG0000002886433
F2 / P19221 / Prothrombin Activation peptide fragment 1 Activation peptide fragment 2 Thrombin light chain Thrombin heavy chain / P00734* / coagulation factor II, thrombin*ENSMUSG0000002724923
Plat / P11214 / Tissue-type plasminogen activator Tissue-type plasminogen activator chain A Tissue-type plasminogen activator chain B / P00750* / plasminogen activator, tissue type*ENSMUSG0000003153822
Hgfac / Q9R098 / hepatocyte growth factor activator / Q04756* / HGF activator*ENSMUSG0000002910220
Habp2 / Mus musculus hyaluronic acid binding protein 2 (Habp2), transcript variant 1, mRNA. / Q14520* / hyaluronan binding protein 2*ENSMUSG0000002507520
F12 / Q80YC5 / Coagulation factor XII Coagulation factor XIIa heavy chain Coagulation factor XIIa light chain / P00748* / coagulation factor XII*ENSMUSG0000002149220
Plau / P06869 / plasminogen activator, urokinase / P00749*ENSMUSG0000002182216


Protein motifs (from Interpro)
Interpro ID Name
 IPR000001  Kringle
 IPR001254  Serine proteases, trypsin domain
 IPR001314  Peptidase S1A, chymotrypsin family
 IPR003609  PAN/Apple domain
 IPR009003  Peptidase S1, PA clan
 IPR013806  Kringle-like fold
 IPR018056  Kringle, conserved site
 IPR018114  Serine proteases, trypsin family, histidine active site
 IPR023317  Peptidase S1A, plasmin
 IPR033116  Serine proteases, trypsin family, serine active site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006508 proteolysis ISO
 biological_processGO:0007596 blood coagulation ISS
 biological_processGO:0007599 hemostasis IEA
 biological_processGO:0010812 negative regulation of cell-substrate adhesion ISO
 biological_processGO:0016525 negative regulation of angiogenesis TAS
 biological_processGO:0022617 extracellular matrix disassembly ISO
 biological_processGO:0042246 tissue regeneration IMP
 biological_processGO:0042730 fibrinolysis IEA
 biological_processGO:0045445 myoblast differentiation IMP
 biological_processGO:0046716 muscle cell cellular homeostasis IMP
 biological_processGO:0048771 tissue remodeling IEA
 biological_processGO:0051603 proteolysis involved in cellular protein catabolic process IEA
 biological_processGO:0051702 interaction with symbiont ISO
 biological_processGO:0051918 negative regulation of fibrinolysis ISO
 biological_processGO:0051919 positive regulation of fibrinolysis ISO
 biological_processGO:0052182 modification by host of symbiont morphology or physiology via secreted substance ISO
 biological_processGO:0052213 interaction with symbiont via secreted substance involved in symbiotic interaction ISO
 biological_processGO:0060707 trophoblast giant cell differentiation IMP
 biological_processGO:0060716 labyrinthine layer blood vessel development IMP
 biological_processGO:0071674 mononuclear cell migration IMP
 cellular_componentGO:0005576 extracellular region TAS
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0009986 cell surface ISO
 cellular_componentGO:0019897 extrinsic component of plasma membrane IDA
 cellular_componentGO:0031232 extrinsic component of external side of plasma membrane ISO
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IEA
 cellular_componentGO:0044218 other organism cell membrane ISO
 molecular_functionGO:0004175 endopeptidase activity IEA
 molecular_functionGO:0004252 serine-type endopeptidase activity TAS
 molecular_functionGO:0005102 signaling receptor binding ISO
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008236 serine-type peptidase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0019899 enzyme binding IEA
 molecular_functionGO:0019900 kinase binding IPI
 molecular_functionGO:0019904 protein domain specific binding ISO
 molecular_functionGO:0034185 apolipoprotein binding ISO
 molecular_functionGO:0051087 chaperone binding ISO
 molecular_functionGO:1904854 proteasome core complex binding ISO
 molecular_functionGO:1990405 protein antigen binding ISO


Pathways (from Reactome)
Pathway description
Platelet degranulation
Degradation of the extracellular matrix
Activation of Matrix Metalloproteinases
Signaling by PDGF
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Dissolution of Fibrin Clot
LDL remodeling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000186 decreased circulating HDL cholesterol level "lower than average level of high density lipoprotein in blood; this molecule transports cholesterol to the liver for excretion in bile" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Apoetm1Bres/Apoetm1Bres,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NIH Black Swiss

 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]
Show

Allelic Composition: Serpine1tm1Mlg/Serpine1tm1Mlg
Genetic Background: B6.129S2-Serpine1tm1Mlg/J

 MP:0000470 abnormal stomach morphology "malformation of the sac-like structure of the digestive canal between the esophagus and the small intestine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000492 abnormal rectum morphology "structural aberration in the terminal portion of the intestinal tube adjacent to the anus" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Plgtm1.1Fjc/Plgtm1.1Fjc
Genetic Background: involves: C57BL/6 * C57BL/6JJcl

 MP:0000493 rectal prolapse "downward movement and external appearance of the rectum through the anus" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Plgtm1Dco/Plgtm1Dco,Tg(Alb-PLG)1Dgi/0
Genetic Background: involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL

Allelic Composition: Plgtm1.1Fjc/Plgtm1.1Fjc
Genetic Background: involves: C57BL/6 * C57BL/6JJcl

 MP:0000495 abnormal colon morphology "malformation of the portion of the large intestine between the cecum and the rectum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000512 intestinal ulcer "lesions in the mucous lining of the intestine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0000598 abnormal liver morphology "malformation or absence of this bile-secreting exocrine gland, which is important for detoxification; for fat, carbohydrate, and protein metabolism; and for glycogen storage " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:23170]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Fgatm1Jld/Fgatm1Jld,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * CF-1

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0000628 abnormal mammary gland development "aberration in the differentiation of the mammary gland during early embryogenesis or during sexual maturity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Hspa4ltm1Imad/Hspa4ltm1Imad
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0000702 enlarged lymph nodes "lymph nodes of increased size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Plgtm1.1Fjc/Plgtm1.1Fjc
Genetic Background: involves: C57BL/6 * C57BL/6JJcl

 MP:0001139 abnormal vagina morphology "malformation of the female reproductive canal located between the uterus and the vulva" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0001175 abnormal lung morphology "malformed organ of respiration" [J:35802]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0001259 abnormal body weight "anomaly in average weight compared to the norm" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Fbn1tm1Hcd/Fbn1+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J

Allelic Composition: Apoetm1Bres/Apoetm1Bres,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NIH Black Swiss

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Plgtm1Dco/Plgtm1Dco,Tg(Alb-PLG)1Dgi/0
Genetic Background: involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL

 MP:0001263 weight loss "progressive reduction of body weight below normal average for age" [J:45400]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
Show

Allelic Composition: Mtm1tm1.2Jman/Y,Tg(ACTA1-cre)79Jme/?
Genetic Background: involves: 129T1/Sv * C57BL/6 * SJL

Allelic Composition: Ngfrtm1Jae/Ngfrtm1Jae,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

 MP:0001273 decreased metastatic potential 
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001310 abnormal conjunctiva morphology "malformation or atrophy of the mucous membrane that lines the inner surface of the eyelids" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0001312 abnormal cornea morphology "malformation or absence of the transparent anterior portion of the fibrous coat of the eye that serves as the chief refractory structure " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001654 hepatic necrosis "pathologic death of cells within, or a portion of, the liver" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Ngfrtm1Jae/Ngfrtm1Jae,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

 MP:0001656 focal hepatic necrosis "a localized area of pathologic death of cells within, or a portion of, the liver" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Fgatm1Jld/Fgatm1Jld,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * CF-1

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Rapgef3tm1.2Chen/Rapgef3tm1.2Chen,Rapgef4tm1.2Chen/Rapgef4tm1.2Chen
Genetic Background: involves: 129 * Black Swiss * C57BL/6 * SJL

 MP:0001792 impaired wound healing "reduced ability or inability to self-repair and close wounds" [J:65302, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0001845 abnormal inflammatory response "aberrant reaction of the microcirculation characterized by movement of fluid and leukocytes from the blood into extravascular tissues" [Pathology:ISBN 0-397-51047-0]
Show

Allelic Composition: Cpb2tm1Efp/Cpb2tm1Efp,Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Dco/Plg+
Genetic Background: involves: 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Cpb2tm1Efp/Cpb2+,Plgtm1Dco/Plg+
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Cpb2tm1Efp/Cpb2tm1Efp,Plgtm1Dco/Plg+
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

 MP:0001851 eye inflammation "local accumulation of fluid, plasma proteins, and leukocytes in the eye" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001852 conjunctivitis "inflammation of the mucous membrane that lines the inner surface of the eyelids" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60896]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001882 abnormal lactation "atypical production of milk from the mammary gland" [J:51296]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001883 mammary adenocarcinoma "higher than normal incidence of malignant tumors of the mammary gland" [J:62919]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0001923 reduced female fertility "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * C57BL/6J

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * 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]
Show

Allelic Composition: Fbn1tm1Hcd/Fbn1+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J

Allelic Composition: Apoetm1Bres/Apoetm1Bres,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NIH Black Swiss

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Ngfrtm1Jae/Ngfrtm1Jae,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

 MP:0002249 abnormal larynx morphology "any structural anomaly of the most superior portion of the respiratory tract" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0002282 abnormal trachea morphology "structral anomaly of the tube descending from the larynx and branching into the right and left main bronchi" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0002551 abnormal blood coagulation "altered ability or inability of the blood to clot" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fgatm1Jld/Fgatm1Jld,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * CF-1

Allelic Composition: Cpb2tm1Efp/Cpb2tm1Efp,Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Dco/Plg+
Genetic Background: involves: 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Cpb2tm1Efp/Cpb2+,Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Cpb2tm1Efp/Cpb2+,Plgtm1Dco/Plg+
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Cpb2tm1Efp/Cpb2tm1Efp,Plgtm1Dco/Plg+
Genetic Background: involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Plgtm1Dco/Plg+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

 MP:0002816 colitis "local accumulation of fluid, plasma proteins, and leukocytes in the colon region of the large intestine" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0003068 enlarged kidney "larger than average size of the kidney" [J:86005, pvb:Pierre Vanden Borre, Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

 MP:0003271 abnormal duodenum morphology "malformation in the first division of the small intestine that extends from the pyloris to the junction with the jejunum " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Fgatm1Jld/Fgatm1Jld,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * CF-1

 MP:0003273 duodenal ulcer "a lesion on the mucosal surface of the duodenum, usually produced by the sloughing of inflammatory necrotic tissue" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0003282 gastric ulcer "a lesion on the mucosal surface of the stomach, usually produced by the sloughing of inflammatory necrotic tissue" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

 MP:0003300 gastrointestinal ulcer "any lesion on the mucosal surface of the gastrointestinal tract, usually produced by the sloughing of inflammatory necrotic tissue" [ncbi:Matthew Mailman, NCBI request, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0003305 proctitis "local accumulation of fluid, plasma proteins, and leukocytes in the mucous membrane of the rectum" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0003333 liver fibrosis "invasion of fibrous connective tissue into the liver, often resulting from inflammation or injury " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Plgtm1.1Fjc/Plgtm1.1Fjc
Genetic Background: involves: C57BL/6 * C57BL/6JJcl

 MP:0003434 resistance to induced choroidal neovascularization "reduction or absence of growth of new, abnormal blood vessels that originate in the choroid through a break in the Bruch membrane into the sub-retinal pigment epithelium or subretinal space and may result in visual loss as a result of chemical or mechanical manipulation (e.g. laser-induced trauma)" [J:82604, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Chrdtm1Emdr/Chrdtm1Emdr,Nogtm1Amc/Nogtm1Amc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J

 MP:0003447 reduced tumor growth/size "less than expected development of tumorous growth when compared to controls" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:65383]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0003633 abnormal nervous system physiology 
Show

Allelic Composition: Dnd1Ter/Dnd1+
Genetic Background: involves: 129S1/Sv * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd

 MP:0003691 abnormal microglial cell function "anomalous activity of the small neuroglial cells, possibly of mesodermal origin, which may become phagocytic, in areas of neural damage or inflammation" [hdene:Howard Dene , Mouse Genome Informatics Curator]
Show

Allelic Composition: G6pctm2.2Jyc/G6pctm2.2Jyc
Genetic Background: involves:129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N

 MP:0003887 increased hepatocyte apoptosis "increase in the number of hepatocytes undergoing programmed cell death" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ngfrtm1Jae/Ngfrtm1Jae,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

 MP:0003893 increased hepatocyte proliferation "anomalous growth and reproduction of hepatocyte cells of the liver" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

Allelic Composition: Ngfrtm1Jae/Ngfrtm1Jae,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

 MP:0004481 abnormal conjunctival epithelium "any structural anomaly in the conjunctival layer of epithelial cells covering inner surface of the eyelid and the front of the eyeball except over the cornea" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0004547 esophageal ulcer "a lesion on the mucosal surface of the esophagus, usually produced by the sloughing of inflammatory necrotic tissue" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0005023 abnormal wound healing "aberrant process of repair of trauma to any tissues of the body, especially that caused by physical means" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Fgatm1Jld/Fgatm1Jld,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * CF-1

 MP:0005035 perianal ulceration "lesion around or near the anus" [cml:Cathy M Lutz , Mouse Genome Informatics Curator, J:71506]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0005048 thrombosis "formation within a tissue or the vascular lumen of a thrombus, an aggregation of coagulated blood containing platelets, fibrin, and entrapped cellular elements " [Pathology:ISBN 0-397-51047-0, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0005150 cachexia "general weight loss and wasting occurring in the course of chronic disease" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0005300 abnormal corneal stroma morphology "structural anomaly of the lamellated connective tissue of the cornea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0005338 atherosclerotic lesions "thickening and loss of elasticity of arterial walls, involving lipid deposition and thickening of intimal layers within arteries" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Apoetm1Bres/Apoetm1Bres,Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NIH Black Swiss

 MP:0005542 corneal vascularization "formation of blood vessels in the cornea, which normally lacks vessels" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0005602 decreased angiogenesis "reduced process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network" [RGD:Rat Genome Database submission]
Show

Allelic Composition: Ttc7fsn/Ttc7fsn
Genetic Background: A/J

Allelic Composition: Plgtm1Jld/Plg+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0006000 abnormal corneal epithelium "malformation in the one or more of the layers of epithelial cells covering the front of the cornea" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 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]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas * C57BL/6J

 MP:0006137 venoocclusion "blockage of blood flow through one or more veins" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cd44tm1Hbg/Cd44tm1Hbg
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0006164 ectropion "abnormal eversion of the upper or lower eyelid that leaves the eye exposed and dry" [smb:Susan M Bello, Mouse Genome Informatics Curator, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0006203 eye hemorrhage "bleeding into the eye" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0006270 abnormal mammary gland growth during lactation "anomaly in the final stage of mammary growth that occurs during the start of lactation" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * C57BL/6J

 MP:0006271 abnormal involution of the mammary gland "anomaly in the process during which mammary glands suspend milk protein production, the mammary alveolar structures collapse and secretory epithelial cells are lost" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * C57BL/6J

 MP:0008236 decreased susceptibility to neuronal excitotoxicity "less than normal amount of neuronal cell death following exposure to a neurotoxic compound, such as kaniate-induced neuronal cell death mediated via a glutamate excitotoxic process" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: G6pctm2.2Jyc/G6pctm2.2Jyc
Genetic Background: involves:129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N

 MP:0009507 abnormal mammary gland connective tissue morphology "any structural anomaly of the fibrous supportive tissue of the mammary gland" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * C57BL/6J

 MP:0009763 increased sensitivity to induced morbidity/mortality "decrease in the amount of an external agent required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas

 MP:0009764 decreased sensitivity to induced morbidity/mortality "increase in the amount of an external agent required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: B6.129P2-Plgtm1Jld

 MP:0010211 abnormal acute phase protein level "deviation from the normal levels of the series of proteins found in the blood shortly after infection and which participate in the early phases of host defense against infection" [ISBN:0-8153-1691-7 "Immunobiology, The Immune System in Health and Disease"]
Show

Allelic Composition: Chrdtm1Emdr/Chrdtm1Emdr,Nogtm1Amc/Nogtm1Amc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J

 MP:0010249 lactation failure "mammary glands do not secrete milk after parturition" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss * C57BL/6J

 MP:0011507 kidney thrombosis "formation or presence of a thrombus within the blood vessel network of the organ of secretion" [MGI:anna]
Show

Allelic Composition: Plgtm1Jld/Plgtm1Jld
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0012331 increased circulating fibrinogen level "greater levels in the blood of a globulin that is converted into fibrin by the action of thrombin in the presence of ionized calcium to produce coagulation of the blood" [ISBN:0-683-40008-8, MGI:csmith]
Show

Allelic Composition: Plgtm1Dco/Plgtm1Dco
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Plgtm1.1Fjc/Plgtm1.1Fjc
Genetic Background: involves: C57BL/6 * C57BL/6JJcl

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000046070 Igfals / insulin-like growth factor binding protein, acid labile subunit / P35858*  / reaction
 ENSMUSG00000050578 Mmp13 / P33435 / Collagenase 3 / P45452* / matrix metallopeptidase 13*  / reaction
 ENSMUSG00000048583 Igf2 / P09535 / Insulin-like growth factor II Insulin-like growth factor II Preptin / P01344* / insulin like growth factor 2*  / reaction
 ENSMUSG00000031538 Plat / P11214 / Tissue-type plasminogen activator Tissue-type plasminogen activator chain A Tissue-type plasminogen activator chain B / P00750* / plasminogen activator, tissue type*  / reaction / complex
 ENSMUSG00000046223 Plaur / P35456 / plasminogen activator, urokinase receptor / Q03405*  / reaction
 ENSMUSG00000020053 Igf1 / P05017 / Insulin-like growth factor I / P05019* / insulin like growth factor 1*  / reaction
 ENSMUSG00000032006 Pdgfd / Q925I7 / Mus musculus platelet-derived growth factor, D polypeptide (Pdgfd), transcript variant 2, mRNA. / Q9GZP0* / platelet derived growth factor D*  / reaction
 ENSMUSG00000021822 Plau / P06869 / plasminogen activator, urokinase / P00749*  / reaction
 ENSMUSG00000028019 Pdgfc / Q8CI19 / platelet-derived growth factor, C polypeptide / Q9NRA1* / platelet derived growth factor C*  / reaction
 ENSMUSG00000028763 Hspg2 / perlecan (heparan sulfate proteoglycan 2) / P98160* / heparan sulfate proteoglycan 2*  / reaction
 ENSMUSG00000020427 Igfbp3 / P47878 / Insulin-like growth factor-binding protein 3 / P17936*  / reaction
 ENSMUSG00000059481 Plg / P20918 / Plasminogen Plasmin heavy chain A Activation peptide Angiostatin Plasmin heavy chain A, short form Plasmin light chain B / LPA* / P00747* / P08519* / plasminogen* / lipoprotein(a)*  / complex
 ENSMUSG00000022877 Hrg / histidine rich glycoprotein / P04196*  / complex / reaction
 ENSMUSG00000038224 Q61247 / Serpinf2 / serine (or cysteine) peptidase inhibitor, clade F, member 2 / P08697* / serpin family F member 2*  / complex / reaction






 

1 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr