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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Meox1tm1Bmk
targeted mutation 1, Baljinder S Mankoo
MGI:2674273
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Meox1tm1Bmk/Meox1tm1Bmk involves: 129P2/OlaHsd * C57BL/6 MGI:2674284
cx2
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2tm1Vpa
involves: 129P2/OlaHsd * C57BL/6 MGI:2674285
cx3
Meox1tm1Bmk/Meox1+
Meox2tm1Vpa/Meox2tm1Vpa
involves: 129P2/OlaHsd * C57BL/6 MGI:4365295
cx4
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2+
involves: 129P2/OlaHsd * C57BL/6 MGI:4365367


Genotype
MGI:2674284
hm1
Allelic
Composition
Meox1tm1Bmk/Meox1tm1Bmk
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox1tm1Bmk mutation (0 available); any Meox1 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• relatively mild defects in sclerotome derived rib bones
• relatively mild defects in sclerotome dervived vertebrae
• presence of hemivertebrae
• vertebral and craniovertebral fusions, however no apparent defects in skeletal myogenesis




Genotype
MGI:2674285
cx2
Allelic
Composition
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2tm1Vpa
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox1tm1Bmk mutation (0 available); any Meox1 mutation (17 available)
Meox2tm1Vpa mutation (0 available); any Meox2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are born in Mendelian ratios but die shortly after birth

embryo
• disrupted somite development, patterning, and differentiation
• absence of ventral (ribs and vertebrae) and dorsal (skeletal muscle) somite derivatives
• patterning and specification of the posterior and anterior halves of somites are defective
• newly formed somites are irregular in shape and fail to epithelialize
• newly formed somites are irregularly sized

growth/size/body
• newborn pups present with drastically reduced trunk length

limbs/digits/tail
• tail vertebrae are completely absent
• rudimentary stump lacking skeletal elements

muscle
• myotomes of anterior somites are fused ventrally but separated dorsally, a defect in epithelialization
• epithelial dermomyotome is absent at E10.5
• most skeletal muscles are absent or reduced in size in the mutant, including prevertebral muscles of the neck, the epaxial muscles of the trunk, the hypaxial muscles of the trunk including those of the abdominal wall and intercostal muscles
• the epaxial muscles of the trunk are severely depleted
• the hypaxial muscles of the trunk including those of the abdominal wall and intercostal muscles are severely depleted

skeleton
• mutants lack an axial skeleton
• occipital skull bones are hypoplastic
• sternum develops abnormally
• although centers of ossification are seen at the cervical and thoracic levels, normal ribs are not observed
• vertebral column is absent and largely replaced by two strips of fused cartilage, in a position corresponding to the neural arches
• ossified, deformed vertebrae are formed at the cervical and thoracic level but more posterior lumbar vertebrae are present only as cartilage condensations at the position expected of the neural arches
• tail vertebrae are completely absent
• segmented organization of the ventral sclerotome is lost and instead a uniform unsegmented mesenchyme is observed
• marker analysis indicates perturbed sclerotome differentiation but not specification

adipose tissue
• brown fat overlying the shoulders muscles is absent

craniofacial
• occipital skull bones are hypoplastic

homeostasis/metabolism

nervous system
• dorsal root ganglia are irregular in shape and size and fused together
• spinal nerves are irregular in spacing and direction

integument




Genotype
MGI:4365295
cx3
Allelic
Composition
Meox1tm1Bmk/Meox1+
Meox2tm1Vpa/Meox2tm1Vpa
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox1tm1Bmk mutation (0 available); any Meox1 mutation (17 available)
Meox2tm1Vpa mutation (0 available); any Meox2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• defects affecting the axial skeleton, however ribs and lumbar vertebrae are normal
• vertebral defects apparent only at posterior levels
• tail vertebrae are malformed and fused

limbs/digits/tail
• tail vertebrae are malformed and fused




Genotype
MGI:4365367
cx4
Allelic
Composition
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox1tm1Bmk mutation (0 available); any Meox1 mutation (17 available)
Meox2tm1Vpa mutation (0 available); any Meox2 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• tail vertebrae are fused
• posterior to the pelvic girdle, poorly differentiated cartilaginous elements are seen in place of vertebrae
• vertebral bodies are split at the lumbar level

limbs/digits/tail
• tail vertebrae are fused





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
04/30/2024
MGI 6.23
The Jackson Laboratory