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Phenotypes Associated with This Genotype
Genotype
MGI:3694209
Allelic
Composition
Ddr2tm1Kln/Ddr2tm1Kln
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ddr2tm1Kln mutation (0 available); any Ddr2 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Skull comparison of Ddr1tm1Wfv/Ddr1tm1Wfv, Ddr2tm1Kln/Ddr2tm1Kln and Ddr2tm1Kln/Ddr2+ mice

growth/size/body
• altered nasal bone
• obvious at 10 days of age
• although normal at birth, homozygotes fail to thrive

cellular
• slow proliferation of skin fibroblasts
• reduced proliferation of epidermal keratinocytes during wound healing
• fewer proliferating cells in growth plates of bones

skeleton
• spherical skull shape
• skulls are jolted as shown by a reduced length
• skull length reduced up to 20% by 4 months of age (J:74580)
• irregular growth of flat bones (J:74580)
• neurocranium shows a more round shape
• altered nasal bone
• shortened by 12-15% in length by 4 months of age
• growth plate height reduced 16% in metatarsals at 2 weeks of age
• chondrocyte apoptosis is normal
• marked reduction in the number of proliferating cells in the metatarsal growth plate, particularly at 2 weeks of age but also at 3 weeks

craniofacial
• spherical skull shape
• skulls are jolted as shown by a reduced length
• skull length reduced up to 20% by 4 months of age (J:74580)
• irregular growth of flat bones (J:74580)
• neurocranium shows a more round shape
• altered nasal bone

homeostasis/metabolism
• reduced proliferative response in epidermal keratinocytes during skin wound healing

respiratory system
• altered nasal bone


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
04/16/2024
MGI 6.23
The Jackson Laboratory