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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Vsx2+
wild type
MGI:2430130
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Vsx2tm1.1(DTA)Kash/Vsx2+ involves: 129S4/SvJae * C57BL/6 MGI:3836039
cn2
Shox2tm1.1(cre)Oki/Shox2+
Tg(CAG-Bgeo/GFP)21Lbe/0
Vsx2tm1(DTA)Kash/Vsx2+
involves: 129S/SvEv * 129X1/SvJ * C57BL/6J MGI:5576700
cx3
Vsx2or-J/Vsx2+
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
involves: 129/Sv * C57BL/6 * FVB/N * SJL MGI:3052553


Genotype
MGI:3836039
ht1
Allelic
Composition
Vsx2tm1.1(DTA)Kash/Vsx2+
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vsx2tm1.1(DTA)Kash mutation (0 available); any Vsx2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within 24 hours of birth likely due to respiratory defects

nervous system
• at E11.5, Vsx2+ spinal cords contain 57% fewer neurons than in wild-type mice, and by P0 no Chx+ interneurons are detected in the spinal cord
• at E13.5, Vsx2+ interneurons are reduced 4-fold compared to in wild-type mice with only newly generated Vsx2+ interneurons remaining in medial locations
• at P0, ventral vGlut2+ (Slc17a6+) neurons are decreased 30% compared to in wild-type mice
• V2a class excitatory interneurons are ablated
• the variability in burst amplitude and cycle period are greater in spinal cords and exhibit increased variability over additional cycles compared to in wild-type mice indicating that locomotor rhythms are destabilized
• however, commissurally projecting inhibitory glycinergic interneuron signaling, chemically-induced intrinsic rhythmogenic activity of spinal cord interneurons, and ipsilateral flexor-extensor alternations are normal
• signaling of left-right coordination is disrupted in the spinal cord compared to in wild-type mice
• neurally evoked locomotor rhythm initiation by the brainstem or sensory afferents is inhibited unlike in wild-type mice




Genotype
MGI:5576700
cn2
Allelic
Composition
Shox2tm1.1(cre)Oki/Shox2+
Tg(CAG-Bgeo/GFP)21Lbe/0
Vsx2tm1(DTA)Kash/Vsx2+
Genetic
Background
involves: 129S/SvEv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shox2tm1.1(cre)Oki mutation (0 available); any Shox2 mutation (20 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Vsx2tm1(DTA)Kash mutation (1 available); any Vsx2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• number of Shox2-expressing V2a interneurons is reduced by 98%; total number of Shox2-expressing interneurons is reduced by >80%
• variability in locomotor parameters (cycle period, burst duration, amplitude) that are observed in isolated neonatal spinal cords exposed to low NMDA concentrations is increased in mutants compared to controls; higher NMDA concentrations reduce this variability
• other parameters such as burst frequency and flexor-extensor alternation are not significantly different




Genotype
MGI:3052553
cx3
Allelic
Composition
Vsx2or-J/Vsx2+
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
Genetic
Background
involves: 129/Sv * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Chx10-EGFP/cre,-ALPP)2Clc mutation (1 available)
Vsx2or-J mutation (1 available); any Vsx2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• more Muller cells are observed in the retina

nervous system
• more Muller cells are observed in the retina

cellular
• more Muller cells are observed in the retina





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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
03/18/2025
MGI 6.24
The Jackson Laboratory