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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Has2tm1.2Chg
targeted mutation 1.2, Chin Chiang
MGI:5489765
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Has2tm1.1Chg/Has2tm1.2Chg
Tg(Hoxb6-cre)#Mku/0
involves: 129 * Black Swiss * C57BL/6 * FVB/N * SJL MGI:5489766


Genotype
MGI:5489766
cn1
Allelic
Composition
Has2tm1.1Chg/Has2tm1.2Chg
Tg(Hoxb6-cre)#Mku/0
Genetic
Background
involves: 129 * Black Swiss * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Has2tm1.1Chg mutation (0 available); any Has2 mutation (35 available)
Has2tm1.2Chg mutation (0 available); any Has2 mutation (35 available)
Tg(Hoxb6-cre)#Mku mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• severe cartilage reduction at P0
• reduced chondrocyte differentiation
• joint positioning defects at P0 indicated by prominent changes in phalangeal cartilage nodule organization
• the interphalangeal joints are shifted perpendicularly at P0
• ectopic joints along the digit rays

limbs/digits/tail
• impaired phalangeal mesenchymal condensation
• however, mesenchyme proliferation is normal
• longitudinally oriented cavities that split proximal and medial phalanges
• digit defect in the forelimb is restricted to the posterior digits

embryo
• impaired phalangeal mesenchymal condensation
• however, mesenchyme proliferation is normal





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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
05/14/2024
MGI 6.23
The Jackson Laboratory