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Alx4lst
Chemically induced Allele Detail
Summary
Symbol: Alx4lst
Name: aristaless-like homeobox 4; Strong's luxoid
MGI ID: MGI:1856068
Synonyms: lstD, Springville luxoid
Gene: Alx4  Location: Chr2:93472779-93511686 bp, + strand  Genetic Position: Chr2, 51.62 cM
Alliance: Alx4lst page
Mutation
origin
Strain of Origin:  NHO/Brpb
Mutation
description
Allele Type:    Chemically induced (other)
Mutation:    Single point mutation
 
Mutation detailsThe G to A transition point mutation in codon 206 is predicted to alter amino acid arginine to glutamine in the corresponding amino acid located in the homeodomain. (J:49152)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 28 assay results
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 Alx4 Mutation:  21 strains or lines available
Notes
This mutation arose after treatment of mice with methylcholanthrene.
References
Original:  J:34255 Strong LC, et al., A new Luxoid mutant in mice. J Hered. 1956;47(6):277-84
All:  17 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
11/19/2024
MGI 6.24
The Jackson Laboratory