- decreased grip strength / IMPC
- decreased total retina thickness / IMPC
- decreased NK cell number / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal spleen morphology / IMPC
- abnormal uterus morphology / IMPC
- abnormal eye morphology / IMPC
- increased prepulse inhibition / IMPC
- small seminal vesicle / IMPC
- immune system phenotype / IMPC
- increased circulating creatinine level / IMPC
- increased fasting circulating glucose level / IMPC
- abnormal seminal vesicle morphology / IMPC
- microphthalmia / IMPC
- increased effector memory CD8-positive, alpha-beta T cell number / IMPC
- enlarged spleen / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
STOCK Parp1tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:10037 |
Citation information | RRID:IMSR_EM:10037 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 | STOCK Parp1tm1a(EUCOMM)Hmgu/IcsOrl |
Alternative name | HEPD0555_6_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Parp1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Parp1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0555_6_C04. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased cell proliferation / MGI
- skin hyperplasia / MGI
- decreased body weight / MGI
- increased mortality induced by gamma-irradiation / MGI
- abnormal inflammatory response / MGI
- decreased inflammatory response / MGI
- decreased litter size / MGI
- abnormal macrophage physiology / MGI
- enhanced wound healing / MGI
- no phenotypic analysis / MGI
- abnormal leukocyte migration / MGI
- decreased neuron apoptosis / MGI
- abnormal response/metabolism to endogenous compounds / MGI
- abnormal microglial cell physiology / MGI
- elevated level of mitotic sister chromatid exchange / MGI
- increased mortality induced by ionizing radiation / MGI
- induced chromosome breakage / MGI
- decreased susceptibility to kidney reperfusion injury / MGI
- abnormal cell cycle checkpoint function / MGI
- decreased susceptibility to noise-induced hearing loss / MGI
- decreased susceptibility to injury / MGI
- immune system phenotype / MGI
- increased renal glomerular filtration rate / MGI
- decreased circulating creatinine level / MGI
- increased apoptosis / MGI
- abnormal DNA repair / MGI
- decreased circulating tumor necrosis factor level / MGI
- decreased circulating interleukin-1 beta level / MGI
- decreased susceptibility to endotoxin shock / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- prenatal lethality, incomplete penetrance / MGI
- decreased renal tubule apoptosis / MGI
- decreased susceptibility to dopaminergic neuron neurotoxicity / MGI
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