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Acad8m1Ytc
Chemically induced Allele Detail
Summary
Symbol: Acad8m1Ytc
Name: acyl-Coenzyme A dehydrogenase family, member 8; mutation 1, Yuan-Tsong Chen
MGI ID: MGI:5693896
Synonyms: Acad8M
Gene: Acad8  Location: Chr9:26885431-26910862 bp, - strand  Genetic Position: Chr9, 12.0 cM
Alliance: Acad8m1Ytc page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C point mutation in exon 2 that results in a frame-shift mutation and premature stop codon that truncates te protein at lysine 50. Western blot analysis confirmed the absence of protein expression in the liver and kidney. (J:222356)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Acad8 Mutation:  29 strains or lines available
References
Original:  J:222356 Sabbagha NG, et al., Alternative splicing in Acad8 resulting a mitochondrial defect and progressive hepatic steatosis in mice. Pediatr Res. 2011 Jul;70(1):31-6
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
11/12/2024
MGI 6.24
The Jackson Laboratory