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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Itga5tm1Hyn
targeted mutation 1, Richard Hynes
MGI:1857207
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Itga5tm1Hyn/Itga5tm1Hyn involves: 129S2/SvPas * C57BL/6J MGI:2180820
cn2
Itga5tm1Hyn/Itga5tm2Hyn
Tg(H2-K1-tsA58)6Kio/0
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca * SJL MGI:4818936
cn3
Gt(ROSA)26Sortm1Sho/0
Itga5tm2Hyn/Itga5tm1Hyn
Itgavtm2Hyn/Itgav+
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * SJL MGI:4818939
cn4
Gt(ROSA)26Sortm1Sho/0
Itga5tm2Hyn/Itga5tm1Hyn
Itgavtm1Hyn/Itgavtm2Hyn
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * SJL MGI:4818940
cn5
Itga5tm1Hyn/Itga5tm2Hyn
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * SJL MGI:4818935
cx6
Itga5tm1Hyn/Itga5+
Nischedsn/Nischedsn
C3H.Cg-Nischedsn Itga5tm1Hyn MGI:6101182
cx7
Itga5tm1Hyn/Itga5+
Nischedsn/Nisch+
C3H.Cg-Nischedsn Itga5tm1Hyn MGI:6101183
cx8
Itga3tm1Jak/Itga3+
Itga5tm1Hyn/Itga5+
Itga8tm1Lfr/Itga8+
involves: 129S2/SvPas * 129S4/SvJae * 129X1/SvJ * C57BL/6J MGI:3583667


Genotype
MGI:2180820
hm1
Allelic
Composition
Itga5tm1Hyn/Itga5tm1Hyn
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die between E10.0 and E11.0

embryo
• at E9.5, mutant embryos are only partially turned into the fetal position
• at E8.5, homozygotes display an abnormal curvature
• at E9.5, the posterior trunk of mutant embryos is deformed and only 1/3 of E9.0 wild-type length
• although delayed, the anterior region (including heads, branchial arches and heart) appears relatively unaffected
• at E8.5, homozygotes display a slightly truncated anterior-posterior axis
• at E9.5, mutant embryos are developmentally retarded and equivalent in size to E9.0 wild-type embryos
• by E10.5, mutant embryos are equivalent in size to E9.5 wild-type embryos
• at E9.5, homozygotes display a deficit in paraxial mesoderm in the region flanking the neural tube
• mesenchymeal cells, normally found on the dorsal side of somites are absent
• at E9.5, homozygotes exhibit kinked neural tubes in the posterior trunk region
• at E9.5, mutant embryos lack somites in the truncated posterior regions; however, normal somite numbers (7-10 pairs) are noted anteriorly
• at E8.0-E8.5, most mutant embryos exhibit normal numbers of somites relative to wild-type embryos (4-13 pairs)
• at E9.5, mutant yolk sacs display abnormal blood vessels, with large numbers of blood cells leaking into the exocoelomic space
• at E9.5, the extraembryonic mesodermal layer is reduced and separated from the extraembryonic endoderm

growth/size/body
• at E9.5, mutant embryos are developmentally retarded and equivalent in size to E9.0 wild-type embryos
• by E10.5, mutant embryos are equivalent in size to E9.5 wild-type embryos

nervous system
• at E9.5, homozygotes exhibit kinked neural tubes in the posterior trunk region

cardiovascular system
• all homozygotes form hearts and a vascular system; however, primitive blood vessels are distended and leaky
• at E9.5, homozygotes show vascular defects both in the embryo and in extraembryonic vasculature, with fewer blood cells present in the heart and blood vessels
• at E9.5, the mutant dorsal aortae are not fully closed, with leakage of primitive blood cells into the mesoderm-deficient space
• at E9.5, mutant yolk sacs display abnormal blood vessels, with large numbers of blood cells leaking into the exocoelomic space

cellular
N
• mutant embryonic fibroblasts are able to assemble fibronectin matrix, form focal contacts, and migrate on fibronectin




Genotype
MGI:4818936
cn2
Allelic
Composition
Itga5tm1Hyn/Itga5tm2Hyn
Tg(H2-K1-tsA58)6Kio/0
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Itga5tm2Hyn mutation (2 available); any Itga5 mutation (47 available)
Tg(H2-K1-tsA58)6Kio mutation (2 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• endothelial cells showed reduced adhesion to fibronectin




Genotype
MGI:4818939
cn3
Allelic
Composition
Gt(ROSA)26Sortm1Sho/0
Itga5tm2Hyn/Itga5tm1Hyn
Itgavtm2Hyn/Itgav+
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1Sho mutation (4 available); any Gt(ROSA)26Sor mutation (993 available)
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Itga5tm2Hyn mutation (2 available); any Itga5 mutation (47 available)
Itgavtm2Hyn mutation (2 available); any Itgav mutation (54 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at P21 fewer mice are alive than wild type

cardiovascular system
• in several of the mice
• ventricular septation defects

cellular
• in several of the mice




Genotype
MGI:4818940
cn4
Allelic
Composition
Gt(ROSA)26Sortm1Sho/0
Itga5tm2Hyn/Itga5tm1Hyn
Itgavtm1Hyn/Itgavtm2Hyn
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1Sho mutation (4 available); any Gt(ROSA)26Sor mutation (993 available)
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Itga5tm2Hyn mutation (2 available); any Itga5 mutation (47 available)
Itgavtm1Hyn mutation (1 available); any Itgav mutation (54 available)
Itgavtm2Hyn mutation (2 available); any Itgav mutation (54 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die at E14.5 of severe dorsal edema and sometimes hemorrhage

cardiovascular system
• aorta vascular ring
• absent ascending aorta
• in one of two surviving mice
• ventricular septation defects

cellular
• in one of two surviving mice




Genotype
MGI:4818935
cn5
Allelic
Composition
Itga5tm1Hyn/Itga5tm2Hyn
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Itga5tm2Hyn mutation (2 available); any Itga5 mutation (47 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:6101182
cx6
Allelic
Composition
Itga5tm1Hyn/Itga5+
Nischedsn/Nischedsn
Genetic
Background
C3H.Cg-Nischedsn Itga5tm1Hyn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Nischedsn mutation (0 available); any Nisch mutation (73 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• more so than in Nischedsn homozygotes at 4 and 20 weeks
• at 4 weeks
• more so than in Nischedsn homozygotes at 4 and 20 weeks
• cavity is filled with cellular exudate and thickened mucoperiosteum due to inflammation

immune system
• more so than in Nischedsn homozygotes at 4 and 20 weeks
• cavity is filled with cellular exudate and thickened mucoperiosteum due to inflammation




Genotype
MGI:6101183
cx7
Allelic
Composition
Itga5tm1Hyn/Itga5+
Nischedsn/Nisch+
Genetic
Background
C3H.Cg-Nischedsn Itga5tm1Hyn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Nischedsn mutation (0 available); any Nisch mutation (73 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• mild with onset at 12 weeks unlike single heterozygotes
• from 12 weeks with muscosal thickening unlike single heterozygotes

immune system
• from 12 weeks with muscosal thickening unlike single heterozygotes




Genotype
MGI:3583667
cx8
Allelic
Composition
Itga3tm1Jak/Itga3+
Itga5tm1Hyn/Itga5+
Itga8tm1Lfr/Itga8+
Genetic
Background
involves: 129S2/SvPas * 129S4/SvJae * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga3tm1Jak mutation (0 available); any Itga3 mutation (53 available)
Itga5tm1Hyn mutation (1 available); any Itga5 mutation (47 available)
Itga8tm1Lfr mutation (2 available); any Itga8 mutation (75 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• nearly complete elimination of long term potentiation after 60 minutes

behavior/neurological
• deficient in spatial memory in a Morris water maze test
• normal fear conditioning however





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory