About   Help   FAQ
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 (153 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 (153 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory