mortality/aging
• no homozygous mice are obtained
|
Allele Symbol Allele Name Allele ID |
Prkar1atm1.1Geno targeted mutation 1.1, Genoway MGI:6682077 |
||||||||||||
Summary |
2 genotypes
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no homozygous mice are obtained
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no litters are obtained when heterozygous females are bred with either wild-type mice or heterozygous males
|
• mice exhibit slightly shorter and blunt snouts
|
• plasma parathyroid hormone levels are increased
• however, mice exhibit normal thyroid stimulating hormone levels and normal plasma calcium and phosphorus concentrations
|
• basal urinary cAMP levels are increased
• however, urine/calcium/creatinine clearance ratio and urinary phosphorus normalized by urinary creatinine are normal in males
|
• shorter cranial and skull bone lengths
|
• shortening of the diaphysis of endochondral bone at P4
|
• shortening of the metaphysis of endochondral bone at P4
|
• skeletal bone mineral density is decreased at P4
|
• bone volume and bone surface are decreased
|
• tibia is smaller and appears to have reduced formation of primary spongiosa and trabecular bone, suggesting a defect in bone mineralization
|
• mice exhibit peripheral acrodysostosis affecting the endochondral skeleton as indicated by short stature, short tail, and short forelimbs and hindlimbs
• however, joint formation is normal
|
• growth plate shows more diffuse and columnar PCNA+ cells which are also present in the zone in proximity of the cartilage/bone junction
• the number of PCNA+ cells per prehypertrophic/hypertrophic chondrocyte column is increased
|
• increase in the height of the columnar proliferative prehypertrophic chondrocyte layer
|
• decrease in the height of the hypertrophic chondrocyte layer
|
• delay in mineralization of the cartilage and epiphyseal secondary ossification centers is seen in forelimb and hindlimb bones indicating a delay in endochondral bone development
|
• facial dysostosis as indicated by shorter cranial and skull bone lengths and foramen magnum diameters
|
• shorter cranial and skull bone lengths
|
• mice exhibit slightly shorter and blunt snouts
|
• mice exhibit shorter digits affecting both forelimbs and hindlimbs
|
• mice exhibit shorter forelimbs and hindlimbs
|
• basal urinary cAMP levels are increased
• however, urine/calcium/creatinine clearance ratio and urinary phosphorus normalized by urinary creatinine are normal in males
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
acrodysostosis | DOID:14669 |
OMIM:101800 OMIM:614613 |
J:303060 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 12/17/2024 MGI 6.24 |
![]() |
|