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Phenotypes Associated with This Genotype
Genotype
MGI:4440539
Allelic
Composition
Rettm1.2Pern/Rettm1.2Pern
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rettm1.2Pern mutation (0 available); any Ret mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

renal/urinary system
• kidney development fails

nervous system
• synapse development is abnormal; postsynaptic acetylcholine receptor (AChR) clustering is reduced and shows a lack of streaks of more intense specializations at neuromuscular synapses in the tongue compared to wild-type
• nerve terminal sprouting from intact terminals is often observed in contrast to control mice


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
01/06/2026
MGI 6.24
The Jackson Laboratory