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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Myl7+
wild type
MGI:2433804
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Myl7tm1(cre)Krc/Myl7+
Prkg1tm2Naw/Prkg1tm2Naw
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) MGI:2668843
cn2
Mapk14tm1Lex/Mapk14tm1Lex
Myl7tm1(cre)Krc/Myl7+
involves: 129S1/Sv * 129S5/SvEvBrd * 129X1/SvJ * C57BL/6 MGI:3580021
cn3
Hcn2tm1Ldw/Hcn2tm2Ldw
Myl7tm1(cre)Krc/Myl7+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3623024


Genotype
MGI:2668843
cn1
Allelic
Composition
Myl7tm1(cre)Krc/Myl7+
Prkg1tm2Naw/Prkg1tm2Naw
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myl7tm1(cre)Krc mutation (0 available); any Myl7 mutation (7 available)
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• cGMP analogues reduce the force of contraction in cardiac muscle from adult controls but not from adult mutants

muscle
• cGMP analogues reduce the force of contraction in cardiac muscle from adult controls but not from adult mutants




Genotype
MGI:3580021
cn2
Allelic
Composition
Mapk14tm1Lex/Mapk14tm1Lex
Myl7tm1(cre)Krc/Myl7+
Genetic
Background
involves: 129S1/Sv * 129S5/SvEvBrd * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1Lex mutation (1 available); any Mapk14 mutation (43 available)
Myl7tm1(cre)Krc mutation (0 available); any Myl7 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• homozygous mice that are heterozygous for Myl7 tm1(cre)Krc, in which cre mediated recombination is induced in cardiomyocytes, display increased mitosis in 4 day old and adult mice cardiomyocytes




Genotype
MGI:3623024
cn3
Allelic
Composition
Hcn2tm1Ldw/Hcn2tm2Ldw
Myl7tm1(cre)Krc/Myl7+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hcn2tm1Ldw mutation (0 available); any Hcn2 mutation (31 available)
Hcn2tm2Ldw mutation (0 available); any Hcn2 mutation (31 available)
Myl7tm1(cre)Krc mutation (0 available); any Myl7 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• variable intervals between heart beats
• sinus dysrhythmia at rest but not during spontaneous activity
• variable intervals between successive heart beats
• regular P wave in a normal PR interval indicating synoatrial node dysfunction
• 30% reduced inward current of sinoatrial cells





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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory