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Hps1tvrm32
Chemically induced Allele Detail
Summary
Symbol: Hps1tvrm32
Name: HPS1, biogenesis of lysosomal organelles complex 3 subunit 1; translational vision research model 32
MGI ID: MGI:4867885
Gene: Hps1  Location: Chr19:42743544-42768417 bp, - strand  Genetic Position: Chr19, 36.56 cM
Alliance: Hps1tvrm32 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Undefined
 
Mutation detailsThis ENU induced mutation was determined to be an allele of Hps1 by failed complementation test with another allele in this gene. (J:166679)
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 Hps1 Mutation:  35 strains or lines available
References
Original:  J:166679 Won J, et al., Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384
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
05/28/2024
MGI 6.13
The Jackson Laboratory