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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Vcpip1em1Zlou
endonuclease-mediated mutation 1, Zhenkun Lou
MGI:6515598
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Vcpip1em1Zlou/Vcpip1em1Zlou C57BL/6NHsd-Vcpip1em1Zlou MGI:6515750


Genotype
MGI:6515750
hm1
Allelic
Composition
Vcpip1em1Zlou/Vcpip1em1Zlou
Genetic
Background
C57BL/6NHsd-Vcpip1em1Zlou
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vcpip1em1Zlou mutation (0 available); any Vcpip1 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• significant senescence of inguinal adipose tissue (IAT)

cellular
• large increase in number of abnormal chromosomes in mouse embryo fibroblasts (MEFs)
• significant increase in number of micronuclei in normochromic erythrocytes (NCEs)
• increased accumulation of camptothecin (CPT)-induced topoisomerase 1 cleavage complex (Top1cc) foci in liver at age 4 months and in MEFs
• hypersensitive to DNA-protein crosslink (DPC)-inducing agents formaldehyde (FA), camptothecin (CPT) and cisplatin in mouse embryo fibroblasts (MEFs)
• failure to repair DNA-protein crosslinks (DPCs) in mouse embryo fibroblasts (MEFs)
• increased accumulation of camptothecin (CPT)-induced topoisomerase 1 cleavage complex (Top1cc) foci in liver at age 4 months and in MEFs
• large increase in number of abnormal chromosomes in mouse embryo fibroblasts (MEFs)
• failure to repair DNA-protein crosslinks (DPCs) in mouse embryo fibroblasts (MEFs)
• significant increase in number of micronuclei in normochromic erythrocytes (NCEs)
• increased accumulation of camptothecin (CPT)-induced topoisomerase 1 cleavage complex (Top1cc) foci in liver at age 4 months and in MEFs

growth/size/body

homeostasis/metabolism
• failure to repair DNA-protein crosslinks (DPCs) in mouse embryo fibroblasts (MEFs)
• increased accumulation of camptothecin (CPT)-induced topoisomerase 1 cleavage complex (Top1cc) foci in liver at age 4 months and in MEFs

mortality/aging
• reduced median lifespan

skeleton
• at age 10 months
• at age 10 months

vision/eye
• increased incidence of cataracts at age 10 months

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
progeria DOID:3911 OMIM:176670
J:297179





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory