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Plg Gene Detail
Summary
  • Symbol
    Plg
  • Name
    plasminogen
  • Synonyms
    Pg
  • Feature Type
    protein coding gene
  • IDs
    MGI:97620
    NCBI Gene: 18815
  • Gene Overview
    MyGene.info: PLG
Location & Maps
more
  • Sequence Map
    Chr17:12378609-12419384 bp, + strand
  • From NCBI annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      40776 bp   ±  kb flank

  • Genome Browsers
Homology
more
  • Human Ortholog
    PLG, plasminogen
  • Vertebrate Orthologs
    10
  • Human Ortholog
    PLG, plasminogen
    Orthology source: HGNC, HomoloGene
  • Links
    NCBI Gene ID: 5340
    neXtProt AC: NX_P00747

  • Chr Location
    6q26; chr6:160702193-160754054 (+)  GRCh38.p2

  • HomoloGene
    Vertebrate Homology Class 55452
    1 human;1 mouse;1 rat;1 chimpanzee;1 rhesus macaque;1 cattle;1 dog;1 chicken;1 western clawed frog;1 zebrafish
  • HCOP
    human homology predictions: PLG
  • Protein SuperFamily
  • Gene Tree
    Plg
Human Diseases
more
  • Diseases
    1 with Plg mouse models; 1 with human PLG associations

Human Disease Mouse Models
       Plasminogen Deficiency, Type I   OMIM: 217090 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    63 phenotypes from 3 alleles in 13 genetic backgrounds
    26 phenotypes from multigenic genotypes
    3 images
    115 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryogenesis
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
tumorigenesis
vision/eye

Click cells to view annotations.
  • All Mutations and Alleles
    5
  • Targeted
    3
  • Transgenic
    2
  • Incidental Mutations
Homozygous null mutants exhibit retarded growth, variable rectal prolapse, impaired fertility and lactation in females, early mortality, and widespread fibrin deposition and thrombotic lesions in liver, lung, stomach and other tissues.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
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Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
Interactions
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Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 18815 NCBI Gene Model | MGI Sequence Detail 40776 C57BL/6J ±  kb
transcript NM_008877 RefSeq | MGI Sequence Detail 2755 C57BL/6  
polypeptide P20918 UniProt | EBI | MGI Sequence Detail 812 Not Applicable  
For the selected sequence
Polymorphisms
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  • SNPs within 2kb
    296 from dbSNP Build 142
  • RFLP
Protein
Information
less
Molecular
Reagents
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  • All nucleic 172
    Genomic 10
    cDNA 157
    Primer pair 3
    Other 2

    Microarray probesets 5
Other
Accession IDs
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MGD-MRK-13360, MGI:2146904
References
more
  • Summaries
    All 173
    Developmental Gene Expression 6
    Diseases 1
    Gene Ontology 9
    Phenotypes 115
  • Earliest
    J:47228 Miyata T, et al., Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site. Proc Natl Acad Sci U S A. 1982 Oct;79(20):6132-6
  • Latest
    J:225798 Yuasa M, et al., Fibrinolysis is essential for fracture repair and prevention of heterotopic ossification. J Clin Invest. 2015 Aug 3;125(8):3117-31

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/26/2016
MGI 6.03
The Jackson Laboratory