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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Disp1tm1Pab
targeted mutation 1, Philip A Beachy
MGI:2672101
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Disp1tm1Pab/Disp1tm1Pab involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:2672102
cn2
Disp1tm1Pab/Disp1tm1Pab
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:3687546


Genotype
MGI:2672102
hm1
Allelic
Composition
Disp1tm1Pab/Disp1tm1Pab
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Disp1tm1Pab mutation (0 available); any Disp1 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• defective heart looping

embryo
• mandibular component of the first branchial arch is severely reduced
• mandibular component is fused in the midline
• mutants exhibit a kink in the truck with dorsal instead of ventral curling of the tail, indicating that embryo turning is impaired
• left/right asymmetry is disrupted as indicated by defective heart looping and disrupted asymmetric expression of Nodal in the left lateral plate mesoderm
• small at E9.5
• midline fusion of the anterior lips of the cephalic neural plate and a poorly defined or absent midline groove
• E8.25 mutants exhibit midline defects of the neural plate in the prospective forebrain
• the ventral neural tube develops as an undifferentiated epithelial tube
• marker analysis indicates somite patterning defects

nervous system
• E8.25 mutants exhibit midline defects of the neural plate in the prospective forebrain
• the ventral neural tube develops as an undifferentiated epithelial tube

growth/size/body
• small at E9.5

vision/eye
• incomplete separation of the bilateral evaginations that form the optic vesicles and by E8.5, the bilateral cup-like evaginations are replaced by a deep single evagination

craniofacial
• mandibular component of the first branchial arch is severely reduced
• mandibular component is fused in the midline




Genotype
MGI:3687546
cn2
Allelic
Composition
Disp1tm1Pab/Disp1tm1Pab
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Disp1tm1Pab mutation (0 available); any Disp1 mutation (61 available)
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (42 available)
Shhtm2Chg mutation (0 available); any Shh mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• survive to at least E18.5

limbs/digits/tail
• digits show segmentation and calcification defects
• develop 6-7 digits per limb (preaxial polydactyly)





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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
09/03/2024
MGI 6.24
The Jackson Laboratory