- abnormal stomach morphology / MGI
- abnormal rectum morphology / MGI
- rectal prolapse / MGI
- abnormal colon morphology / MGI
- intestinal ulcer / MGI
- abnormal liver morphology / MGI
- abnormal mammary gland development / MGI
- enlarged lymph nodes / MGI
- abnormal vagina morphology / MGI
- abnormal lung morphology / MGI
- abnormal body weight / MGI
- decreased body weight / MGI
- weight loss / MGI
- abnormal conjunctiva morphology / MGI
- abnormal cornea morphology / MGI
- hepatic necrosis / MGI
- postnatal growth retardation / MGI
- impaired wound healing / MGI
- abnormal inflammatory response / MGI
- eye inflammation / MGI
- conjunctivitis / MGI
- abnormal lactation / MGI
- reduced female fertility / MGI
- premature death / MGI
- abnormal larynx morphology / MGI
- abnormal trachea morphology / MGI
- abnormal blood coagulation / MGI
- colitis / MGI
- enlarged kidney / MGI
- duodenal ulcer / MGI
- gastric ulcer / MGI
- gastrointestinal ulcer / MGI
- proctitis / MGI
- liver fibrosis / MGI
- decreased susceptibility to induced choroidal neovascularization / MGI
- decreased tumor growth/size / MGI
- abnormal nervous system physiology / MGI
- abnormal microglial cell physiology / MGI
- increased hepatocyte proliferation / MGI
- abnormal conjunctival epithelium morphology / MGI
- esophageal ulcer / MGI
- perianal ulcer / MGI
- abnormal thrombosis / MGI
- cachexia / MGI
- abnormal corneal stroma morphology / MGI
- cardiovascular system phenotype / MGI
- corneal vascularization / MGI
- decreased angiogenesis / MGI
- abnormal corneal epithelium morphology / MGI
- pulmonary fibrosis / MGI
- venoocclusion / MGI
- ectropion / MGI
- eye hemorrhage / MGI
- abnormal mammary gland growth during lactation / MGI
- abnormal involution of the mammary gland / MGI
- decreased susceptibility to neuronal excitotoxicity / MGI
- abnormal mammary gland connective tissue morphology / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- decreased sensitivity to induced morbidity/mortality / MGI
- abnormal acute phase protein level / MGI
- lactation failure / MGI
- abnormal kidney thrombosis / MGI
- increased circulating fibrinogen level / MGI
- absent corneal epithelium / MGI
C57BL/6NCrl-Plgem1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:12790 |
Citation information | RRID:IMSR_EM:12790 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6NCrl-Plgem1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Plgem1(IMPC)Ccpcz |
Gene/Transgene symbol | Plg |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- PLG-related hereditary angioedema with normal C1Inh / Orphanet_537072
- Hypoplasminogenemia / Orphanet_722
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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