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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mab21l2tm1Nao
targeted mutation 1, Naoki Takahashi
MGI:3511363
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mab21l2tm1Nao/Mab21l2tm1Nao involves: 129 * C57BL/6 MGI:3512037


Genotype
MGI:3512037
hm1
Allelic
Composition
Mab21l2tm1Nao/Mab21l2tm1Nao
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mab21l2tm1Nao mutation (1 available); any Mab21l2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

pigmentation
• the retinal pigment epithelium was not formed in E10.5 or E11.5 mutants

cardiovascular system
• abnormal heart position due to reduced ventral body wall thickness

vision/eye
• absent lens vesicle at E10.5
• the lens was absent at E11.5
• at E9.5, the optic vesicle in the area in contact with the surface ectoderm was narrower than in heterozygotes and at E10.5, the optic vesicle did not contact the surface ectoderm and lacked a lens vesicle
• at E11.5, mutants exhibited malformation of the rudiment retina
• the retinal pigment epithelium was not formed in E10.5 or E11.5 mutants
• reduced retinal progenitor cell proliferation in the dorsal side of the optic vesicle at E9.5

growth/size/body
• extruded abdominal organs with an umbilical hernia containing part of the liver
• reduced ventral body wall thickness, with reduced cell numbers at E10.5 and reduced cell proliferation at E11.5, leading to abnormal heart position and extrusion of abdominal organs





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last database update
05/14/2024
MGI 6.23
The Jackson Laboratory