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Phenotypes Associated with This Genotype
Genotype
MGI:4367885
Allelic
Composition
Aplnrtm1.1Tq/Aplnrtm1.1Tq
Genetic
Background
C57BL/6-Aplnrtm1.1Tq
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aplnrtm1.1Tq mutation (0 available); any Aplnr mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected mice are produced from heterozygous parents even when the deficit of maternal care is corrected with fostering

cardiovascular system
• some embryos exhibit cardiac development defects unlike wild-type mice
• mice exhibit decreased fractional shortening compared with wild-type mice
• cardiomyocyte sarcomeric function is decreased with impaired velocity of contraction and relaxation compared to in wild-type mice
• however, intracellular calcium is unchanged

homeostasis/metabolism
• mice exhibit decreased exercise endurance compared with wild-type mice

behavior/neurological
• poor maternal care is more pronounced than in heterozygous mice
• mice exhibit decreased exercise endurance compared with wild-type mice

embryo
• some embryos exhibit evidence of overall developmental failure

muscle
• mice exhibit decreased fractional shortening compared with wild-type mice


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
03/25/2025
MGI 6.24
The Jackson Laboratory