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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mapk14tm1.1Dvb
targeted mutation 1.1, Dmitry V Bulavin
MGI:3706998
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mapk14tm1.1Dvb/Mapk14tm1.1Dvb B6(FVB)-Mapk14tm1.1Dvb MGI:5500172
ht2
Mapk14tm1.1Dvb/Mapk14+ B6(FVB)-Mapk14tm1.1Dvb MGI:5500173
cx3
Mapk14tm1.1Dvb/Mapk14+
Ppm1dtm1Lad/Ppm1dtm1Lad
Tg(IghMyc)22Bri/0
involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL MGI:3710181
cx4
Mapk14tm1.1Dvb/Mapk14+
Ppm1dtm1Lad/Ppm1dtm1Lad
involves: 129S7/SvEvBrd * C57BL/6 MGI:5500175


Genotype
MGI:5500172
hm1
Allelic
Composition
Mapk14tm1.1Dvb/Mapk14tm1.1Dvb
Genetic
Background
B6(FVB)-Mapk14tm1.1Dvb
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1.1Dvb mutation (1 available); any Mapk14 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die by E11.5 as a result of placental and heart defects




Genotype
MGI:5500173
ht2
Allelic
Composition
Mapk14tm1.1Dvb/Mapk14+
Genetic
Background
B6(FVB)-Mapk14tm1.1Dvb
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1.1Dvb mutation (1 available); any Mapk14 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• injection with the beta cell toxin streptozocin (STZ) results in lowered blood glucose levels in 4-6 month old mice (11 weeks post treatment) as compared to wild-type
• injection with the beta cell toxin streptozocin (STZ) results in lowered blood glucose levels in 9-14 month old mice (7 weeks post treatment) as compared to wild-type
• islet cell proliferation is increased in 10-12 month old mutant mice at 3 and at 30 days post-STZ treatment as compared to wild-type

endocrine/exocrine glands
• injection with the beta cell toxin streptozocin (STZ) results in lowered blood glucose levels in 4-6 month old mice (11 weeks post treatment) as compared to wild-type
• injection with the beta cell toxin streptozocin (STZ) results in lowered blood glucose levels in 9-14 month old mice (7 weeks post treatment) as compared to wild-type
• islet cell proliferation is increased in 10-12 month old mutant mice at 3 and at 30 days post-STZ treatment as compared to wild-type

homeostasis/metabolism
• pancreatic islet proliferation is decreased in aged (22-24 month old) mice, but is similar to wild-type in young mice




Genotype
MGI:3710181
cx3
Allelic
Composition
Mapk14tm1.1Dvb/Mapk14+
Ppm1dtm1Lad/Ppm1dtm1Lad
Tg(IghMyc)22Bri/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1.1Dvb mutation (1 available); any Mapk14 mutation (41 available)
Ppm1dtm1Lad mutation (1 available); any Ppm1d mutation (28 available)
Tg(IghMyc)22Bri mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• the median lifespan of 130 days

neoplasm
• similar to mice carrying double Ppm1dtm1Lad allele without Mapk14tm1Dvb allele, based on increased median survival time, mice carrying single Mapk14tm1Dvb allele were considerably more resistant to tumor formation induced by myc than mice with homozygous wild-type Ppm1d+ allele




Genotype
MGI:5500175
cx4
Allelic
Composition
Mapk14tm1.1Dvb/Mapk14+
Ppm1dtm1Lad/Ppm1dtm1Lad
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1.1Dvb mutation (1 available); any Mapk14 mutation (41 available)
Ppm1dtm1Lad mutation (1 available); any Ppm1d mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
N
• double mutant Ppm1dtm1Lad Mapk14tm1.1Dvb mice exhibit pancreatic islet proliferation similar to wild-type, correcting the phenotype observed in Ppm1dtm1Lad mutant mice
• double mutant Ppm1dtm1Lad Mapk14tm1.1Dvb mice do not exhibit impaired glucose tolerance, correcting the phenotype observed in Ppm1dtm1Lad/ mutant mice





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory