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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Col2a1*R789C)#Waho
transgene insertion, William A Horton
MGI:4941021
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Col2a1*R789C)#Waho/0 involves: C57BL/6 * DBA/2 MGI:4941022


Genotype
MGI:4941022
tg1
Allelic
Composition
Tg(Col2a1*R789C)#Waho/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die soon after birth from respiratory distress

skeleton
• shortened limb bones
• reduction of collagen fibrils in cartilage matrix
• perichondrium is thicker
• cellular organization of the cartilage growth plate is disturbed, with fewer stacks of flattened chondrocytes in the proliferative zone
• mutants exhibit fewer stacks of flattened chondrocytes in the proliferative zone
• mineralization of primary and secondary ossification centers is delayed

growth/size/body
• small thorax
• short trunk
• mutants are severely dwarfed

digestive/alimentary system

limbs/digits/tail
• shortened limb bones

craniofacial

reproductive system
• small litter size, from 2-6 pups

respiratory system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
spondyloepiphyseal dysplasia congenita DOID:14789 OMIM:183900
J:112540





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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory