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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
CanxGt(KST286)Byg
gene trap KST286, BayGenomics
MGI:4123998
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
CanxGt(KST286)Byg/CanxGt(KST286)Byg involves: 129P2/OlaHsd * C57BL/6 MGI:4836488


Genotype
MGI:4836488
hm1
Allelic
Composition
CanxGt(KST286)Byg/CanxGt(KST286)Byg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CanxGt(KST286)Byg mutation (0 available); any Canx mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Small size and neurological abnormalities in CanxGt(KST286)Byg/CanxGt(KST286)Byg mice

mortality/aging
N
• mice exhibit normal early postnatal survival

nervous system
N
• mice exhibit normal gross nervous system morphology including normal motor neuron numbers
• the rostral corpus callosum is thinner and, particularly at the medial rise, exhibits areas of patchy and irregular myelination or dysmyelination unlike in wild-type mice
• the internal capsule is less branched and narrower than in wild-type mice
• the cerebellar peduncle exhibits patchy, loose myelination unlike in wild-type mice
• spinal cord neuron myelin is thin, wavy, and decompacted compared to in wild-type neurons
• however, white matter tracts of the spinal cord exhibit no obvious dysmyelination
• spinal cords exhibit perpendicular organization of glial fibers suggesting altered spinal cord development compared to in wild-type mice
• in the spinal cord, rostral corpus callosum, and cerebellar peduncle
• in motor and sensory neurons

behavior/neurological
• mice exhibit lower limb motor defects compared with wild-type mice
• instable gait with hind limb splaying and a rolling walk

growth/size/body
• as early as P7

immune system
N
• mice exhibit normal immune systems





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last database update
10/22/2024
MGI 6.24
The Jackson Laboratory