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Disc1m1H
Chemically induced Allele Detail
Summary
Symbol: Disc1m1H
Name: disrupted in schizophrenia 1; mutation 1, Harwell
MGI ID: MGI:5752777
Synonyms: DISC1D453G, Disc1enu1H
Gene: Disc1  Location: Chr8:125780934-125988597 bp, + strand  Genetic Position: Chr8, 73.26 cM
Alliance: Disc1m1H page
Mutation
origin
Strain of Origin:  BALB/cAnN
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced an A to G point mutation that results in the amino acid substitution of glycine for aspartic acid at position 453 (D453G). (J:229661)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Disc1 Mutation:  69 strains or lines available
References
Original:  J:229661 Dachtler J, et al., Missense mutation in DISC1 C-terminal coiled-coil has GSK3beta signaling and sex-dependent behavioral effects in mice. Sci Rep. 2016;6:18748
All:  1 reference(s)

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