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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lrp4tm1Her
targeted mutation 1, Joachim Herz
MGI:3621893
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lrp4tm1Her/Lrp4tm1Her involves: 129S/SvEvBrd * 129S6/SvEvTac * C57BL/6J MGI:5561076
hm2
Lrp4tm1Her/Lrp4tm1Her involves: 129S6/SvEvTac MGI:4455051
hm3
Lrp4tm1Her/Lrp4tm1Her involves: 129S6/SvEvTac * C57BL/6 MGI:3622272
cx4
Apptm1Dbo/App+
Lrp4tm1Her/Lrp4tm1Her
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:5561077
cx5
Apptm1Dbo/Apptm1Dbo
Lrp4tm1Her/Lrp4+
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:5561078
cx6
Apptm1Dbo/Apptm1Dbo
Lrp4tm1Her/Lrp4tm1Her
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:5561079
cx7
Aplp2tm1Dbo/Aplp2tm1Dbo
Lrp4tm1Her/Lrp4tm1Her
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:5561080


Genotype
MGI:5561076
hm1
Allelic
Composition
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S/SvEvBrd * 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• acetylcholine receptor density is reduced compared to in wild-type mice
• neuromuscular junction are smaller with reduced innervation compared to in wild-type mice
• however, neuromuscular synapses are present at E16.5




Genotype
MGI:4455051
hm2
Allelic
Composition
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• distinct grooved incisor labial surfaces
• over one third show supernumerary maxillary incisor tooth germs at birth
• grooves on incisors result from a localized reduction of enamel on the labial surface

growth/size/body
• distinct grooved incisor labial surfaces
• over one third show supernumerary maxillary incisor tooth germs at birth
• grooves on incisors result from a localized reduction of enamel on the labial surface

skeleton
• distinct grooved incisor labial surfaces
• over one third show supernumerary maxillary incisor tooth germs at birth
• grooves on incisors result from a localized reduction of enamel on the labial surface




Genotype
MGI:3622272
hm3
Allelic
Composition
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• number of homozygotes identified at P5 is much lower than expected, but up to approximately E13, numbers of each genotype is as expected

embryo
• the Fgf8-expressing AER is thickened and broadened in mutants

growth/size/body
• mutants have mild craniofacial defects usually in the form of incisor defects
• homozygotes show significantly reduced body weights and postnatal growth compared with wild-type and heterozygotes

limbs/digits/tail
• the Fgf8-expressing AER is thickened and broadened in mutants
• examination 14 day-old mutants revealed fused digital bones and tendons, club-shaped deformities of digital tips and metaphyseal defects
• homozygous mice have fully penetrant polysyndactyly of both the fore- and hindlimbs;
• extensive bone fusion can be seen in the forelimb
• extensive bone fusion can be seen in the hindlimb

craniofacial
• mutants have mild craniofacial defects usually in the form of incisor defects

skeleton
• mutants have mild craniofacial defects usually in the form of incisor defects
• at E12.5, chondrocye compaction is apparent in the fore- and hindlimbs of mutants; the digital cartilage is broadly fused in mutants as seen at P0




Genotype
MGI:5561077
cx4
Allelic
Composition
Apptm1Dbo/App+
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm1Dbo mutation (4 available); any App mutation (89 available)
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 20 of 49 mice die within 5 months




Genotype
MGI:5561078
cx5
Allelic
Composition
Apptm1Dbo/Apptm1Dbo
Lrp4tm1Her/Lrp4+
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm1Dbo mutation (4 available); any App mutation (89 available)
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 6 of 45 mice die within 5 months




Genotype
MGI:5561079
cx6
Allelic
Composition
Apptm1Dbo/Apptm1Dbo
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm1Dbo mutation (4 available); any App mutation (89 available)
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• despite Mendelian ratios at E18.5, fewer than expected mice are present at weaning

nervous system
• increased nerve terminal sprouting
• reduced size and density of acetylcholine clusters compared with either single homozygote

cellular
• increased nerve terminal sprouting




Genotype
MGI:5561080
cx7
Allelic
Composition
Aplp2tm1Dbo/Aplp2tm1Dbo
Lrp4tm1Her/Lrp4tm1Her
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aplp2tm1Dbo mutation (1 available); any Aplp2 mutation (30 available)
Lrp4tm1Her mutation (1 available); any Lrp4 mutation (97 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory