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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nsftm1Himat
targeted mutation 1, Hideo Matsuzaki
MGI:7531287
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nsftm1Himat/Nsftm1Himat C57BL/6N-Nsftm1Himat MGI:7531414
ht2
Nsftm1Himat/Nsf+ C57BL/6N-Nsftm1Himat MGI:7531415


Genotype
MGI:7531414
hm1
Allelic
Composition
Nsftm1Himat/Nsftm1Himat
Genetic
Background
C57BL/6N-Nsftm1Himat
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nsftm1Himat mutation (0 available); any Nsf mutation (152 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• early embryonic lethality




Genotype
MGI:7531415
ht2
Allelic
Composition
Nsftm1Himat/Nsf+
Genetic
Background
C57BL/6N-Nsftm1Himat
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nsftm1Himat mutation (0 available); any Nsf mutation (152 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• in the light/dark box test, mice exhibit a longer latency to enter the light box, indicting increased anxiety
• vertical activity is increased in the open-field test, indicating repetitive behavior
• however, no difference in the total distance traveled is seen in the open-field test
• in a three-chamber social interaction test, mice show less interaction with the stranger mouse during session 2 of the test
• at P6, pups emit fewer calls than wild-type pups

nervous system
• mice show a decrease in postsynaptic density area in postsynaptic membrane of hippocampal -CA1 region
• elevation of fEPSPs upon induction of long term depression (LTD) by low-frequency stimulation of Schaffer collaterals is deceased in hippocampal CA1 neurons
• however, no change in the fEPSPs is seen upon induction of long term potentiation (LTP) by high-frequency stimulation of Schaffer collaterals and no difference is seen in basal synaptic function

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autism spectrum disorder DOID:0060041 J:313900





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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
05/14/2024
MGI 6.23
The Jackson Laboratory