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Loxhd1mpc188H
Chemically induced Allele Detail
Summary
Symbol: Loxhd1mpc188H
Name: lipoxygenase homology domains 1; muta-ped-c3pde 188, Harwell
MGI ID: MGI:5792020
Gene: Loxhd1  Location: Chr18:77369654-77530626 bp, + strand  Genetic Position: Chr18, 52.2 cM
Alliance: Loxhd1mpc188H page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Harwell ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced two point mutations (c.4370T>A and c.5323A>G) that result in the amino acid substitutions of isoleucine with asparagine at position 1457 (p.I1457N) and threonine with alanine at position 1775 (p.T1775A). (J:234901)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Loxhd1 Mutation:  104 strains or lines available
References
Original:  J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
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