About   Help   FAQ
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
Loading...
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)
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