About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf
transgene insertion, Veronique Lefebvre
MGI:5426519
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Sox9tm1Gsr/Sox9tm1Gsr
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
involves: 129P2/OlaHsd * C57BL/6 MGI:5426540
cn2
Adgrg6tm1Arte/Adgrg6tm1Arte
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
involves: 129S5/SvEvBrd MGI:7266839
cn3
Prmt5tm2c(EUCOMM)Wtsi/Prmt5tm2c(EUCOMM)Wtsi
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
involves: C57BL/6N MGI:7277816


Genotype
MGI:5426540
cn1
Allelic
Composition
Sox9tm1Gsr/Sox9tm1Gsr
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox9tm1Gsr mutation (2 available); any Sox9 mutation (32 available)
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• with doxycycline treatment from E15.5 on, columnar zones are shortened in growth plates of mutants
• with doxycycline treatment from E15.5 onward, severe dwarfism results
• endochondral bones stop elongating by E17.5 with doxycycline treatment from E15.5 onward
• chondrocytes lose ability to enlarge by E17.5 when doxycycline treatment takes place from E15.5 onward
• columnar cells stop proliferating at a rate 3 times greater than control cells with doxycycline treatment starting at E15.5; number of apoptotic cells in the columnar zone of growth plates is about 28 fold higher and about 5 times higher in the prehypertrophic zone of controls with 2 days of doxycycline treatment




Genotype
MGI:7266839
cn2
Allelic
Composition
Adgrg6tm1Arte/Adgrg6tm1Arte
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
Genetic
Background
involves: 129S5/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Adgrg6tm1Arte mutation (0 available); any Adgrg6 mutation (63 available)
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• altered extracellular matrix component expression and endplate-oriented disk herniations at 8 months of age
• embryonic induction of recombinase induction resulted in scoliosis in 25% and 16.7% of mice with Cobb angles of 11 to 43 degrees at P20 and P180, respectively




Genotype
MGI:7277816
cn3
Allelic
Composition
Prmt5tm2c(EUCOMM)Wtsi/Prmt5tm2c(EUCOMM)Wtsi
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf/0
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prmt5tm2c(EUCOMM)Wtsi mutation (1 available); any Prmt5 mutation (44 available)
Tg(Col2a1/Acan-rtTA,tetO-cre)#Vlf mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
N
• no signs of scoliosis are seen following induction of recombinase expression at either 2 or 4 weeks of age
• at 4 months of age, 3 months post induction of recombinase expression, there is a minor increase in acellular clefts at the midline of the endplate
• however, no gross signs of degenerative histopathology are seen





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
05/07/2024
MGI 6.23
The Jackson Laboratory