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Hps5ru2-mr
Spontaneous Allele Detail
Summary
Symbol: Hps5ru2-mr
Name: HPS5, biogenesis of lysosomal organelles complex 2 subunit 2; maroon
MGI ID: MGI:1856146
Synonyms: mr
Gene: Hps5  Location: Chr7:46409890-46445488 bp, - strand  Genetic Position: Chr7, 30.56 cM
Alliance: Hps5ru2-mr page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsA spontaneous mutation that arose in a "lactation" stock. Maroon was shown to be allelic to ru2 by complementation testing.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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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 Hps5 Mutation:  90 strains or lines available
References
Original:  J:15003 Bateman N, Maroon - allele of silver?. Mouse News Lett. 1957;16:7
All:  7 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
12/10/2024
MGI 6.24
The Jackson Laboratory