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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Map3k1tm1Yxia
targeted mutation 1, Ying Xia
MGI:2676654
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Map3k1tm1Yxia/Map3k1tm1Yxia involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:5699113
hm2
Map3k1tm1Yxia/Map3k1tm1Yxia involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:6384030
hm3
Map3k1tm1Yxia/Map3k1tm1Yxia involves: 129/Sv * C57BL/6 MGI:2676659
ht4
Map3k1tm1Yxia/Map3k1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:5699114
ht5
Map3k1goya/Map3k1tm1Yxia involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:5699115
cx6
Map3k1tm1Yxia/Map3k1+
Mapk8tm1Wag/Mapk8tm1Wag
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1 MGI:6384031
cx7
Map3k1tm1Yxia/Map3k1+
Mapk8tm1Wag/Mapk8+
Mapk9tm1Mka/Mapk9+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1 MGI:6384032


Genotype
MGI:5699113
hm1
Allelic
Composition
Map3k1tm1Yxia/Map3k1tm1Yxia
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• at 2 weeks
• however, mice exhibit normal outer hair cell proliferation
• at 4 weeks with increasing severity from apex to base
• further degeneration at 9 weeks
• very severe in small patches
• inner hair cells, outer hair cells and pillar cells are replaced with rosette-like formation composed of Claudius and Hensen cells at 9 weeks

nervous system
• at 2 weeks
• however, mice exhibit normal outer hair cell proliferation
• at 4 weeks with increasing severity from apex to base
• further degeneration at 9 weeks




Genotype
MGI:6384030
hm2
Allelic
Composition
Map3k1tm1Yxia/Map3k1tm1Yxia
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• the number of apoptotic cells is increased in the retina at P14-P21
• iris overgrowth
• however, Meibomian glands are normal
• stromal neovascularization and thickening of the cornea
• corneas show macrophage invasion in the stroma
• surgical suture of the eyelid partially restores normal corneal appearance and reduces macrophage invasion
• stromal thickening
• surgical suture of the eyelid partially restores normal corneal appearance and reduces corneal thickening
• cloudiness of the cornea
• eyes open at birth
• retinas start to show misallocated cell bodies at the posterior side at P7 and develop sporadic rosette structures posterior to the photoreceptor layers at P15
• retina shows invasion of macrophages at 1 year of age
• localized neo-vascularization in RPE and outer nuclear layer
• an increase in late-born Muller glial cells is seen in retinas
• Muller glial processes protrude beyond the boundary of the outer limiting membrane and displace the rod photoreceptors in hyperplastic lesions
• mice show broken down retinal pigment epithelium (RPE) resulting in focal RPE leak
• the number of mitotic progenitors is slightly increased at P6 and significantly higher at P7 and P8 at the outer edge of the retina and some mitotic progenitors are located in unusual positions in the inner segment of the retinas
• S-phase+ cells are more abundant at P6-P10 in the retina, especially in peripheral regions
• however, mitosis ceases at P12 in the retina as in controls
• regional dislocalization in the outer nuclear layer and rosette-like arrangements in this layer
• mice with opened eyelids sutured closed right after birth and suture removed at P14 when eyelids open normally show rosette structure in the outer nuclear layer at P15
• thinner outer nuclear layer at 1 year of age
• signs of retinal degeneration are seen at 1 year of age
• some Muller glia nuclei undergo mitosis and migrate out of the inner nuclear layer, indicating proliferative gliosis

cardiovascular system
• localized neo-vascularization in RPE and outer nuclear layer

cellular
• the number of apoptotic cells is increased in the retina at P14-P21

nervous system
• an increase in late-born Muller glial cells is seen in retinas
• Muller glial processes protrude beyond the boundary of the outer limiting membrane and displace the rod photoreceptors in hyperplastic lesions

pigmentation
• mice show broken down retinal pigment epithelium (RPE) resulting in focal RPE leak




Genotype
MGI:2676659
hm3
Allelic
Composition
Map3k1tm1Yxia/Map3k1tm1Yxia
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at E15.5, the eyelid tip epithelium is thinner than normal; however, number of cell layers is normal
• at E15.5, the mutant eyelid epithelium displays tight cell-cell contacts with signifcantly fewer and smaller intercellular spaces, unlike in wild-type controls
• no abnormal eyelid morphology is noted at E14.5
• by E16, the mutant eyelid fails to move forward, leaving the ocular surface exposed
• impaired eyelid closure is noted at E16
• at E15.5, no clumps of round cells are detected along the mutant eyelid margin, unlike in wild-type controls
• all homozygotes exhibit eyelids open at birth

integument
• keratinocytes ineffective in wound closure




Genotype
MGI:5699114
ht4
Allelic
Composition
Map3k1tm1Yxia/Map3k1+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• however, mice do not exhibit outer hair cell degeneration

nervous system
• however, mice do not exhibit outer hair cell degeneration




Genotype
MGI:5699115
ht5
Allelic
Composition
Map3k1goya/Map3k1tm1Yxia
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1goya mutation (0 available); any Map3k1 mutation (62 available)
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• at 9 weeks of age with an apical-to-basal gradient




Genotype
MGI:6384031
cx6
Allelic
Composition
Map3k1tm1Yxia/Map3k1+
Mapk8tm1Wag/Mapk8tm1Wag
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
Mapk8tm1Wag mutation (1 available); any Mapk8 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• eyes are open at birth
• however, mice exhibit normal retinal morphology




Genotype
MGI:6384032
cx7
Allelic
Composition
Map3k1tm1Yxia/Map3k1+
Mapk8tm1Wag/Mapk8+
Mapk9tm1Mka/Mapk9+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k1tm1Yxia mutation (0 available); any Map3k1 mutation (62 available)
Mapk8tm1Wag mutation (1 available); any Mapk8 mutation (71 available)
Mapk9tm1Mka mutation (1 available); any Mapk9 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• eyes are open at birth
• however, mice exhibit normal retinal morphology





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory