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Phenotypes Associated with This Genotype
Genotype
MGI:4881721
Allelic
Composition
Wlstm1.1Whsu/Wlstm1.1Whsu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
Wlstm1.1Whsu mutation (1 available); any Wls mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• craniofacial abnormalities are detected at E13.5 and E16.5
• severely impaired development
• severely impaired development
• tooth defects are detected at E16.5
• defects in tissues derived from neural crest cells
• at E16.5

nervous system
• brain abnormalities manifest at E10.5
• absence of mid/hindbrain structures at E10.5
• absence of mid/hindbrain structures at E10.5
• expression analysis indicates defects in the establishment of the isthmic organizer activity
• at E13.5 and E16.5
• at E16.5
• at E13.5 and E16.5
• fail to form properly

endocrine/exocrine glands
• defects are detected at E16.5
• defects are detected at E16.5

digestive/alimentary system
• at E16.5
• defects are detected at E16.5

skeleton
• severely impaired development
• severely impaired development
• tooth defects are detected at E16.5

growth/size/body
• tooth defects are detected at E16.5
• at E16.5


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
04/16/2024
MGI 6.23
The Jackson Laboratory