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Phenotypes Associated with This Genotype
Genotype
MGI:7265077
Allelic
Composition
Myt1lem1Jdd/Myt1l+
Genetic
Background
C57BL/6-Myt1lem1Jdd/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myt1lem1Jdd mutation (1 available); any Myt1l mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• difference in weight from controls is observed at P45 and becomes significant at P94
• difference in weight is more pronounced in females than males

limbs/digits/tail

nervous system
• alterations in chromatin state and gene expression during brain development
• changes in chromatin state are maintained in adult brains
• cortical volume is reduced in proportion with the reduction in brain size
• no change in cell density or ventricular system size
• smaller specific white-matter tracts
• trend towards reduced volume by Nissl staining that was confirmed by magnetic resonance-based diffusion tensor imaging
• decrease in the number of mature mushroom spines and an increase in the number of thin and stubby, immature spines
• decrease in the number of mature mushroom spines and an increase in the number of thin and stubby, immature spines
• decrease in the number of mature mushroom spines and an increase in the number of thin and stubby, immature spines
• layer 2/3 pyramidal neurons in the primary visual cortex display significantly depolarized resting membrane potentials and decreased membrane resistance at P21-P23
• decreased apical progenitor cell density with normal intermediate progenitor (TBR2+) and postmitotic neuron (TBR1+) density and a decrease in the number of proliferating cells at E14 in the cortex
• increase in the number of recently proliferating cells exiting the cell cycle suggesting precocious differentiation of progenitors

behavior/neurological
N
• no tremors are seen
• impaired performance in contextual and cued fear conditioning assays suggesting a decrease in associative memory; however, hyperactivity of the mice may confound this result
• reduced sensitivity to stimulation of the plantar surface of the paw with von Frey filaments
• unable to hold position during the negative geotaxis test
• impaired performance in fore- and hindlimb suspension and grip strength assays
• decreased muscle strength indicated by impaired performance in inverted screen and 90 degree wire assays
• however, performance in balance, coordination, and movement initiation tests is relatively normal
• abnormal hindlimb posture with transient hyperflexions of one or both hindlimbs
• hindlimbs are held at the midline but not clasped
• heightened baseline force measurements in the startle task
• only in females
• increase in the distance traveled in an open field assay and in the social operant task
• males fail to cease nose poking and orient to a social stimulus
• in a social dominance tube test mice tend to be submissive
• display decreased sociability in a social approach assay but still exhibiting social preference
• increased ultrasonic vocalizations by isolated pups suggesting an anxiety like phenotype or increased arousal
• absence of thigmotaxis in the open field assay suggests heightened arousal is more likely than anxiety

cellular
• decreased apical progenitor cell density with normal intermediate progenitor (TBR2+) and postmitotic neuron (TBR1+) density and a decrease in the number of proliferating cells at E14 in the cortex
• increase in the number of recently proliferating cells exiting the cell cycle suggesting precocious differentiation of progenitors

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal dominant intellectual developmental disorder 39 DOID:0070069 OMIM:616521
J:321206


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
04/16/2024
MGI 6.23
The Jackson Laboratory