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Dync2h1m152Asp
Chemically induced Allele Detail
Summary
Symbol: Dync2h1m152Asp
Name: dynein cytoplasmic 2 heavy chain 1; mutation 152, Andrew S Peterson
MGI ID: MGI:3799301
Synonyms: Dnchc2Q397Stop
Gene: Dync2h1  Location: Chr9:6928550-7177619 bp, - strand  Genetic Position: Chr9, Syntenic
Alliance: Dync2h1m152Asp page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsThe molecular lesion is a C to A transversion in exon 8 that creates a stop codon at amino acid position 397 (Dnchc2Q397Stop). (J:103514)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Dync2h1 Mutation:  215 strains or lines available
References
Original:  J:136795 Zarbalis K, et al., A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development. PLoS Biol. 2004 Aug;2(8):E219
All:  2 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
04/16/2024
MGI 6.23
The Jackson Laboratory