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Phenotypes Associated with This Genotype
Genotype
MGI:5770796
Allelic
Composition
Trpm7tm1.1Mkma/Trpm7tm1.1Mkma
Genetic
Background
B6.129-Trpm7tm1.1Mkma
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trpm7tm1.1Mkma mutation (0 available); any Trpm7 mutation (102 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• kinase-inactive homozygotes are viable and develop normally with no significant differences in body weight, food intake, general locomotor activity or serum total Mg2+ and Ca2+ levels relative to wild-type controls
• although basal native channel activity is significantly increased prior to cytoplasmic Mg2+ depletion, maximal current density measured after Mg2+ depletion is not significantly altered in peritoneal macrophages, indicating normal native channel function


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)
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last database update
03/31/2026
MGI 6.24
The Jackson Laboratory