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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pdk4tm1Rhar
targeted mutation 1, Robert A Harris
MGI:3521806
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pdk4tm1Rhar/Pdk4tm1Rhar B6.129-Pdk4tm1Rhar MGI:3697306
cn2
Pdk1tm1c(EUCOMM)Hmgu/Pdk1tm1c(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk3em1Eze/Pdk3em1Eze
Pdk4tm1Rhar/Pdk4tm1Rhar
Tg(Prrx1-cre)1Cjt/0
involves: 129 * C57BL/6J * C57BL/6N * SJL/J MGI:6712414
cx3
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk3em1Eze/Pdk3em1Eze
Pdk4tm1Rhar/Pdk4tm1Rhar
involves: 129 * C57BL/6J * C57BL/6N MGI:6712416
cx4
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk4tm1Rhar/Pdk4tm1Rhar
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N MGI:6712269
cx5
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk4tm1Rhar/Pdk4tm1Rhar
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N MGI:6712417


Genotype
MGI:3697306
hm1
Allelic
Composition
Pdk4tm1Rhar/Pdk4tm1Rhar
Genetic
Background
B6.129-Pdk4tm1Rhar
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdk4tm1Rhar mutation (1 available); any Pdk4 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• lower serum concentration of pyruvate in mice fasted for 48 h compared to wild-type mice
• higher serum concentration of branched chain amino acids in mice fasted for 48 h compared to wild-type mice
• lower serum concentration of alanine in mice fasted for 48 h compared to wild-type mice
• lower serum concentration of lactate in mice fasted for 48 h compared to wild-type mice
• higher serum concentration of non-esterified fatty acids in mice fasted for 48 h compared to wild-type mice
• after 48 h of starvation, livers contain 42% less free glucose compared to similarly starved wild-type mice
• glucose oxidation rate is 36% greater in diaphragms; however, lactase release and net glycolysis rates are reduced by 37% and 35%, respectively
• 30% and 58% lower in 24 h and 48 h fasted mice, respectively, compared to similarly fasted wild-type mice
• however, in the fed state blood glucose levels are similar to wild-type
• small but significant increase in insulin levels after 48 h of starvation compared to wild-type mice
• slight but significant increase in glucose tolerance
• however, no difference is seen in insulin sensitivity
• larger decrease in liver glycogen levels induced by 24 h of starvation and a smaller rebound in levels between 24 and 48 h of starvation compared to wild-type mice
• however, the starvation-induced reduction in skeletal muscle glycogen is similar to wild-type
• higher serum concentration of triacylglycerol in mice fasted for 48 h compared to wild-type mice
• ketone body levels are elevated in the liver after 48 h of starvation
• higher serum concentration of acetoacetate and beta-hydroxybutyrate in mice fasted for 48 h compared to wild-type mice

liver/biliary system
• larger decrease in liver glycogen levels induced by 24 h of starvation and a smaller rebound in levels between 24 and 48 h of starvation compared to wild-type mice
• however, the starvation-induced reduction in skeletal muscle glycogen is similar to wild-type




Genotype
MGI:6712414
cn2
Allelic
Composition
Pdk1tm1c(EUCOMM)Hmgu/Pdk1tm1c(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk3em1Eze/Pdk3em1Eze
Pdk4tm1Rhar/Pdk4tm1Rhar
Tg(Prrx1-cre)1Cjt/0
Genetic
Background
involves: 129 * C57BL/6J * C57BL/6N * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdk1tm1c(EUCOMM)Hmgu mutation (0 available); any Pdk1 mutation (28 available)
Pdk2tm1Rhar mutation (1 available); any Pdk2 mutation (23 available)
Pdk3em1Eze mutation (0 available); any Pdk3 mutation (8 available)
Pdk4tm1Rhar mutation (1 available); any Pdk4 mutation (30 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice are viable

reproductive system
N
• mice are fertile

skeleton
N
• mice exhibit normal embryonic bone development




Genotype
MGI:6712416
cx3
Allelic
Composition
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk3em1Eze/Pdk3em1Eze
Pdk4tm1Rhar/Pdk4tm1Rhar
Genetic
Background
involves: 129 * C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdk1tm1a(EUCOMM)Hmgu mutation (0 available); any Pdk1 mutation (28 available)
Pdk2tm1Rhar mutation (1 available); any Pdk2 mutation (23 available)
Pdk3em1Eze mutation (0 available); any Pdk3 mutation (8 available)
Pdk4tm1Rhar mutation (1 available); any Pdk4 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die between P0 and P4

homeostasis/metabolism
• at P1, but not E18.5
• increased serum 3-beta-hydroxybutyrate levels at P1, but not E18.5
• decreased pyruvate and lactate serum levels

skeleton
N
• mice exhibit normal embryonic bone development




Genotype
MGI:6712269
cx4
Allelic
Composition
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk2tm1Rhar/Pdk2tm1Rhar
Pdk4tm1Rhar/Pdk4tm1Rhar
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdk1tm1a(EUCOMM)Hmgu mutation (0 available); any Pdk1 mutation (28 available)
Pdk2tm1Rhar mutation (1 available); any Pdk2 mutation (23 available)
Pdk4tm1Rhar mutation (1 available); any Pdk4 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are viable

reproductive system
• mice are fertile

skeleton
• mice exhibit normal embryonic bone development




Genotype
MGI:6712417
cx5
Allelic
Composition
Pdk1tm1a(EUCOMM)Hmgu/Pdk1tm1a(EUCOMM)Hmgu
Pdk4tm1Rhar/Pdk4tm1Rhar
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdk1tm1a(EUCOMM)Hmgu mutation (0 available); any Pdk1 mutation (28 available)
Pdk4tm1Rhar mutation (1 available); any Pdk4 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are viable

reproductive system
• mice are fertile

skeleton
• mice exhibit normal embryonic bone development





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory