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Phenotypes Associated with This Genotype
Genotype
MGI:6315869
Allelic
Composition
Lztr1tm1a(EUCOMM)Wtsi/Lztr1+
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lztr1tm1a(EUCOMM)Wtsi mutation (2 available); any Lztr1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice exhibit reduced longevity, with reduced survival beginning around 20 weeks of age

growth/size/body
• eccentric hypertrophy
• males exhibit facial dysmorphia
• increase in nasal bone width
• males exhibit decreased weight

craniofacial
• shorter skull length in males
• increase in skull width
• decrease in parietal bone length
• males exhibit facial dysmorphia
• increase in nasal bone width

cardiovascular system
• increase in cardiomyocyte area
• eccentric hypertrophy
• increase in stroke volume in females
• decrease in % ejection fraction and fractional shortening in males
• echocardiography indicates decreased left ventricular systolic function and increased diastolic dimensions

cellular
• MEFs exhibit increased growth rate

muscle
• increase in cardiomyocyte area
• decrease in % ejection fraction and fractional shortening in males

skeleton
• shorter skull length in males
• increase in skull width
• decrease in parietal bone length
• increase in nasal bone width

respiratory system
• increase in nasal bone width

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Noonan syndrome 10 DOID:0060588 OMIM:616564
J:268690


Contributing Projects:
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
04/30/2024
MGI 6.23
The Jackson Laboratory