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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Antxr1tm1.2Bstc
targeted mutation 1.2, Brad St Croix
MGI:4353383
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Antxr1tm1.2Bstc/Antxr1tm1.2Bstc B6.Cg-Antxr1tm1.2Bstc MGI:4353403


Genotype
MGI:4353403
hm1
Allelic
Composition
Antxr1tm1.2Bstc/Antxr1tm1.2Bstc
Genetic
Background
B6.Cg-Antxr1tm1.2Bstc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Antxr1tm1.2Bstc mutation (0 available); any Antxr1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• thickened due to increased extracellular matrix compared to in wild-type mice
• overgrowth of upper incisors
• incisors are misaligned
• the peridontal ligament around the incisors and molars is thickened due to increased extracellular matrix compared to in wild-type mice
• tooth overgrowth results from misalignment of incisors and loss of normal abrasion unlike in wild-type mice
• degeneration of the enamel organ associated with dental dysplasia is observed
• degeneration of the enamel organ associated with dental dysplasia is observed
• incisor misalignment worsens with age

skeleton
• thickened due to increased extracellular matrix compared to in wild-type mice
• overgrowth of upper incisors
• incisors are misaligned
• the peridontal ligament around the incisors and molars is thickened due to increased extracellular matrix compared to in wild-type mice
• tooth overgrowth results from misalignment of incisors and loss of normal abrasion unlike in wild-type mice
• degeneration of the enamel organ associated with dental dysplasia is observed
• degeneration of the enamel organ associated with dental dysplasia is observed
• incisor misalignment worsens with age
• the metaphyseal periosteum of the femur is mildly thickened due to increased extracellular matrix
• vertebral periosteal thickening is minimal compared to in wild-type mice

neoplasm
• transplanted B16 tumors grow slower than in wild-type mice
• however, the growth of transplanted LCC tumors is not statistically different from in wild-type mice and B16 tumor cell proliferation, hypoxia, and apoptosis are normal

reproductive system
• mice exhibit loose proteinacious extracellular matrix deposits in the ovaries compared with wild-type mice
• however, follicles develop normally

cardiovascular system
N
• retinal and wound angiogenesis are normal

endocrine/exocrine glands
• mice exhibit loose proteinacious extracellular matrix deposits in the ovaries compared with wild-type mice
• however, follicles develop normally

growth/size/body
• overgrowth of upper incisors
• incisors are misaligned
• the peridontal ligament around the incisors and molars is thickened due to increased extracellular matrix compared to in wild-type mice
• tooth overgrowth results from misalignment of incisors and loss of normal abrasion unlike in wild-type mice
• degeneration of the enamel organ associated with dental dysplasia is observed
• degeneration of the enamel organ associated with dental dysplasia is observed
• incisor misalignment worsens with age

cellular
• mice exhibit increased extracellular matrix in the several organs, including ovaries, uterus, and skin compared with wild-type mice
• subtle increases in the extracellular matrix are observed in the lamina propria of the stomach, small and large intestines, urinary bladder, cervix, and tongue





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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
04/09/2024
MGI 6.23
The Jackson Laboratory