About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fyco1tm1.1Arte
targeted mutation 1.1, TaconicArtemis
MGI:7451138
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Fyco1tm1.1Arte/Fyco1tm1.1Arte
Tg(Prm-cre)58Og/0
involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * C57BL/6NTac MGI:7531471
cn2
Fyco1tm1.1Arte/Fyco1tm1.1Arte
Tg(CAG-RFP/EGFP/Map1lc3b)1Hill/0
Tg(Prm-cre)58Og/0
involves: 129S/Sv * C57BL/6J * C57BL/6N * C57BL/6NTac MGI:7531479


Genotype
MGI:7531471
cn1
Allelic
Composition
Fyco1tm1.1Arte/Fyco1tm1.1Arte
Tg(Prm-cre)58Og/0
Genetic
Background
involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fyco1tm1.1Arte mutation (0 available); any Fyco1 mutation (44 available)
Tg(Prm-cre)58Og mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at P60, lens epithelial cells show extensive vacuolization
• at P60, lens fiber cells are large and display irregular shapes
• at P0, P7, and P14, differentiating lens fiber cells show abnormal retention of cellular organelles, including endoplasmic reticulum (ER), mitochondria, and Golgi apparatus (GA), suggesting impaired organelle removal
• mice show initial signs of lens opacities at 4 weeks that develop into mild cataracts at ~8 weeks of age
• mice develop mature bilateral cataracts by 16 weeks of age; extent of lens opacities is variable among mice

cellular
• at P14, lenses show an increased Golgi apparatus mass relative to age-matched wild-type lenses
• at P0, P7, P14 and P21, lenses show an increased ER mass relative to age-matched wild-type lenses
• at P0, lenses show alterations in many autophagy-associated genes, proteins and lipids, including a 1.48-fold increase in the level of SQSTM1/p62 and a modest accumulation of phosphatidylethanolamine (PE) phospholipids, suggesting impaired autophagy

homeostasis/metabolism
• at P0, lenses show alterations in many autophagy-associated genes, proteins and lipids, including a 1.48-fold increase in the level of SQSTM1/p62 and a modest accumulation of phosphatidylethanolamine (PE) phospholipids, suggesting impaired autophagy
• at P0, lenses show a modest accumulation of phosphatidylethanolamine (PE) phospholipids




Genotype
MGI:7531479
cn2
Allelic
Composition
Fyco1tm1.1Arte/Fyco1tm1.1Arte
Tg(CAG-RFP/EGFP/Map1lc3b)1Hill/0
Tg(Prm-cre)58Og/0
Genetic
Background
involves: 129S/Sv * C57BL/6J * C57BL/6N * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fyco1tm1.1Arte mutation (0 available); any Fyco1 mutation (44 available)
Tg(CAG-RFP/EGFP/Map1lc3b)1Hill mutation (1 available)
Tg(Prm-cre)58Og mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• multiphoton laser scanning microscopy showed a 1.3- and 1.6-fold higher GFP intensity in the whole lens and the anterior lens including lens epithelium, respectively, indicating a reduced autophagic flux in mouse lenses

homeostasis/metabolism
• multiphoton laser scanning microscopy showed a 1.3- and 1.6-fold higher GFP intensity in the whole lens and the anterior lens including lens epithelium, respectively, indicating a reduced autophagic flux in mouse lenses





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
09/17/2024
MGI 6.24
The Jackson Laboratory