ENSMUSG00000019817


Mus musculus

Features
Gene ID: ENSMUSG00000019817
  
Biological name :Plagl1
  
Synonyms : Plagl1
  
Possible biological names infered from orthology : PLAG1 like zinc finger 1 / Q9UM63
  
Species: Mus musculus
  
Chr. number: 10
Strand: 1
Band: A2
Gene start: 13060504
Gene end: 13131694
  
Corresponding Affymetrix probe sets: 10361771 (MoGene1.0st)   1426208_x_at (Mouse Genome 430 2.0 Array)   1438588_at (Mouse Genome 430 2.0 Array)   1450533_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000115595
Ensembl peptide - ENSMUSP00000141514
Ensembl peptide - ENSMUSP00000120581
Ensembl peptide - ENSMUSP00000117321
Ensembl peptide - ENSMUSP00000112847
Ensembl peptide - ENSMUSP00000112889
Ensembl peptide - ENSMUSP00000113710
NCBI entrez gene - 22634     See in Manteia.
MGI - MGI:1100874
RefSeq - NM_009538
RefSeq Peptide - NP_033564
swissprot - Q3UQW2
swissprot - B0QZX5
swissprot - Q9JLQ4
swissprot - B0QZX4
swissprot - A0A0A6YWE3
Ensembl - ENSMUSG00000019817
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 PLAGL1ENSGALG00000013754Gallus gallus
 PLAGL1ENSG00000118495Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Plag1 / Q9QYE0 / Zinc finger protein PLAG1 / Q6DJT9* / PLAG1 zinc finger*ENSMUSG0000000328227
Plagl2 / PLAG1 like zinc finger 2 / Q9UPG8*ENSMUSG0000005141323


Protein motifs (from Interpro)
Interpro ID Name
 IPR013087  Zinc finger C2H2-type
 IPR027770  Zinc finger protein PLAGL1
 IPR036236  Zinc finger C2H2 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IEA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0006915 apoptotic process IBA
 biological_processGO:0010468 regulation of gene expression IGI
 biological_processGO:0035914 skeletal muscle cell differentiation IMP
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II ISO
 cellular_componentGO:0005634 nucleus IBA
 cellular_componentGO:0005794 Golgi apparatus ISO
 cellular_componentGO:0016604 nuclear body ISO
 cellular_componentGO:0043231 intracellular membrane-bounded organelle ISO
 molecular_functionGO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding ISO
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IBA
 molecular_functionGO:0001228 transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding ISO
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding ISO
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 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]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0001211 wrinkled skin "irregular folds and/or indentations on the skin" [J:19212]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0001954 respiratory distress "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0002080 prenatal lethality "death anytime between fertilization and E18.5" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cacna1atm1.2Sher/Cacna1atm1.2Sher
Genetic Background: involves: 129S4/SvJae

 MP:0002082 postnatal lethality "premature death anytime after postnatal day 1 to weaning age (3 weeks)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Plagl1tm1Jour/Plagl1+
Genetic Background: B6.129P2-Plagl1tm1Jour

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

 MP:0002759 abnormal caudal vertebrae morphology "malformed bony segments of the tail, usually 27-30 present" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82849]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0002834 decreased heart weight "less than average weight of the heart compared to the average for a particular strain" [RGD:Rat Genome Database submission]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0003051 curly tail "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0003122 maternal imprinting "specific loci are inactivated during oogenesis and are not expressed in offspring" [llw2:Linda Washburn, Mouse Genome Informatics Curator, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

Allelic Composition: Plagl1tm1Jour/Plagl1+
Genetic Background: CBA.129P2-Plagl1tm1Jour

 MP:0003123 paternal imprinting "specific loci are inactivated during spermatogenesis and are not expressed in offspring " [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator, llw2:Linda Washburn, Mouse Genome Informatics Curator]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

 MP:0003720 abnormal neural tube closure "abnormal invagination and fusion of the neuroepithelial layer in early development" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:99099]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0005109 abnormal talus morphology "malformation of the bone that articlulates with the tibia and fibula" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0005306 abnormal phalanx morphology "aberrant structure of any of the long bones of the digits" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0008271 abnormal bone ossification "any anomaly in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance" [GO:0001503]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0008770 decreased survivor rate "a smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0009431 decreased fetal weight "reduced weight of a fetus compared to controls (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

 MP:0009674 decreased birth weight "reduction in average weight at birth compared to controls" [RGD:cur "Rat Genome Database submission"]
Show

Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm,Tg(TRAMP)8247Ng/?
Genetic Background: involves: 129S2/SvPas * BALB/c * C57BL/6

Allelic Composition: Plagl1tm1Jour/Plagl1+
Genetic Background: B6.129P2-Plagl1tm1Jour

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 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]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0010420 muscular ventricular septal defect "abnormal communications between the two lower chambers of the heart, involving the muscular septum and often occurring as multiple communications, and includes central muscular or midmuscular, apical, or marginal communications when the defect is along the RV-septal junction; any single defect observed from the LV aspect may have several openings on the RV aspect" [http://emedicine.medscape.com]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1+
Genetic Background: involves: 129S5/SvEvBrd

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Plagl1tm1Jour/Plagl1+
Genetic Background: B6.129P2-Plagl1tm1Jour

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

 MP:0011088 partial neonatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith]
Show

Allelic Composition: Plagl1tm1Jour/Plagl1+
Genetic Background: B6.129P2-Plagl1tm1Jour

 MP:0011101 partial prenatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Plagl1Gt(OST181461)Lex/Plagl1Gt(OST181461)Lex
Genetic Background: involves: 129S5/SvEvBrd

  


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






 

0 s.

 
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