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Phenotypes Associated with This Genotype
Genotype
MGI:6477405
Allelic
Composition
Trp63tm2.1Aam/Trp63tm3Aam
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trp63tm2.1Aam mutation (0 available); any Trp63 mutation (59 available)
Trp63tm3Aam mutation (0 available); any Trp63 mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• 95% of neonates exhibit cleft palate

digestive/alimentary system
• 95% of neonates exhibit cleft palate

growth/size/body
• 95% of neonates exhibit cleft palate

integument
• dermis is thicker in large areas of the skin
• epidermis is abnormal with the stratum basale and stratum spinosum affected; thickening of Trp63-, K14-, and K10-expressing layers in patches of the epidermis covering the skin surface

limbs/digits/tail
• 100% of neonates exhibit limb defects, ranging from lack of hindlimbs to single ectrodactyly
• single ectrodactyly in some neonates


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
03/18/2025
MGI 6.24
The Jackson Laboratory