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Phenotypes Associated with This Genotype
Genotype
MGI:3698249
Allelic
Composition
Prrx1tm1Tex/Prrx1tm1Tex
Prrx2tm1Hubr/Prrx2+
Genetic
Background
involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prrx1tm1Tex mutation (0 available); any Prrx1 mutation (31 available)
Prrx2tm1Hubr mutation (0 available); any Prrx2 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• at E14.5, Meckel's cartilage is truncated
• newborns exhibit closely spaced incisors
• newborns exhibit shortened dentaries

skeleton
• at E14.5, Meckel's cartilage is truncated
• newborns exhibit closely spaced incisors
• newborns exhibit shortened dentaries
• the base of the metacarpal of the fifth digit is broader and forms an articulation with the trinagular and ulna

growth/size/body
• newborns exhibit closely spaced incisors
• newborns exhibit shortened dentaries

limbs/digits/tail
• the base of the metacarpal of the fifth digit is broader and forms an articulation with the trinagular and ulna


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
12/30/2025
MGI 6.24
The Jackson Laboratory