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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Magoh+
wild type
MGI:2437284
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
MagohGt(AG0150)Wtsi/Magoh+ involves: 129P2/OlaHsd MGI:4462416
ht2
MagohGt(AT0027)Wtsi/Magoh+ involves: 129P2/OlaHsd MGI:4462418
ht3
MagohMos2/Magoh+ involves: BALB/cJ * C57BL/6 MGI:5695271
ht4
MagohMos2/Magoh+ involves: BALB/cJ * C57BL/6J MGI:4462415
ht5
Magohtm1d(KOMP)Dlsi/Magoh+ involves: C57BL/6J * FVB MGI:5695295
cn6
Magohtm1c(KOMP)Dlsi/Magoh+
Emx1tm1(cre)Krj/Emx1+
B6.Cg-Magohtm1c(KOMP)Dlsi Emx1tm1(cre)Krj MGI:5695285
cn7
Emx1tm1(cre)Krj/Emx1+
Magohtm1c(KOMP)Dlsi/Magoh+
involves: 129S2/SvPas * C57BL/6J MGI:7335202


Genotype
MGI:4462416
ht1
Allelic
Composition
MagohGt(AG0150)Wtsi/Magoh+
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MagohGt(AG0150)Wtsi mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• premature death occurs before weaning in some animals
• before weaning with incomplete penetrance

pigmentation

growth/size/body

nervous system




Genotype
MGI:4462418
ht2
Allelic
Composition
MagohGt(AT0027)Wtsi/Magoh+
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MagohGt(AT0027)Wtsi mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• premature death occurs before weaning in some animals
• before weaning with incomplete penetrance

pigmentation

growth/size/body

nervous system




Genotype
MGI:5695271
ht3
Allelic
Composition
MagohMos2/Magoh+
Genetic
Background
involves: BALB/cJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MagohMos2 mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E16.5, cortical thickness is ~50% that of wild-type controls




Genotype
MGI:4462415
ht4
Allelic
Composition
MagohMos2/Magoh+
Genetic
Background
involves: BALB/cJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MagohMos2 mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• at E13.5, heterozygotes show a mild developmental delay relative to wild-type controls

mortality/aging
• premature death occurs before weaning in some animals
• before weaning with incomplete penetrance

pigmentation

growth/size/body
• at E13.5, heterozygotes show a mild developmental delay relative to wild-type controls
• 33% smaller than control littermates

nervous system
• most ectopically produced neurons undergo apoptosis
• brains exhibit extensive apoptosis in the cortex at E14.5
• ectopic and precocious neurogenesis resulting in expanded calretinin-positive cells and ectopically produced Cajal Retzius cells in cortex
• at E18.5 the cortical layers were thinner and disorganized
• adult brain weighed significantly less than those of control littermates (J:159625)
• present prenatally starting between E12.5 and E18.5 (J:159625)
• at E18.5, brain size is disproportionally reduced by 30% relative to body size (J:240595)
• forebrain size is significantly reduced at E18.5
• neocortex size is disproportionally decreased at E13.5
• intermediate neural progenitors in developing cortex was markedly reduced resulting in the smaller number of neurons in E18.5 brains
• brains show ectopic neuron differentiation at E12.5

cellular
• abnormal orientation of the neural stem cell mitotic division plane during cortex development
• most ectopically produced neurons undergo apoptosis
• brains exhibit extensive apoptosis in the cortex at E14.5
• ectopic and precocious neurogenesis resulting in expanded calretinin-positive cells and ectopically produced Cajal Retzius cells in cortex




Genotype
MGI:5695295
ht5
Allelic
Composition
Magohtm1d(KOMP)Dlsi/Magoh+
Genetic
Background
involves: C57BL/6J * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Magohtm1d(KOMP)Dlsi mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• heterozygotes are viable, unlike mice heterozygous for the MagohMos2 allele which show partial postnatal lethality on a C57BL/6J background

nervous system
• heterozygotes display smaller brain size at E16.5
• at E16.5, cortical thickness is significantly reduced relative to wild-type controls, although to a slightly lesser extent than in mice heterozygous for the MagohMos2 allele

pigmentation
• adult heterozygotes exhibit white belly spots
• adult heterozygotes exhibit ventral and dorsal hypopigmentation, similar to adult mice heterozygous for the MagohMos2 allele

integument
• adult heterozygotes exhibit white belly spots




Genotype
MGI:5695285
cn6
Allelic
Composition
Magohtm1c(KOMP)Dlsi/Magoh+
Emx1tm1(cre)Krj/Emx1+
Genetic
Background
B6.Cg-Magohtm1c(KOMP)Dlsi Emx1tm1(cre)Krj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Krj mutation (2 available); any Emx1 mutation (30 available)
Magohtm1c(KOMP)Dlsi mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at P12, mutant mice exhibit significantly smaller brains than heterozygous Emx1tm1(cre)Krj control mice
• at E16.5, cortical thickness is significantly reduced relative to wild-type controls, but thicker than in mice heterozygous for the MagohMos2 allele (likely due to a contribution of ventrally derived neurons which migrate into the dorsal telencephalon, but are not targeted by Emx1-Cre)




Genotype
MGI:7335202
cn7
Allelic
Composition
Emx1tm1(cre)Krj/Emx1+
Magohtm1c(KOMP)Dlsi/Magoh+
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Krj mutation (2 available); any Emx1 mutation (30 available)
Magohtm1c(KOMP)Dlsi mutation (0 available); any Magoh mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• in P12 mice





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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory