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Phenotypes Associated with This Genotype
Genotype
MGI:5789378
Allelic
Composition
Alktm2.1Ics/Alk+
Genetic
Background
B6N.129S2(Cg)-Alktm2.1Ics
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Alktm2.1Ics mutation (0 available); any Alk mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• the movement response to hypercapnia is disrupted
• however, mice do not show differences in the Y-maze or the tail suspension tests
• 48% of newborn mutants have a full stomach compared to 61% of wild-type mice, indicating some reduction in milk intake
• during the dark/light test, mice spend less time in the light side, wait longer before going for the first time in the light side and do less light/dark transitions
• mice show increased muscle strength when allowed to grip with all paws
• mice exhibit less rears during the dark phase
• mice exhibit less locomotor activity during the dark phase

homeostasis/metabolism
• slightly higher levels

vision/eye
• 7 of 11 mice exhibit minor abnormalities of the visual system, showing a small zone of higher reflectance under one of the main blood vessels and/or a small white spot under a vein


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
01/28/2026
MGI 6.24
The Jackson Laboratory