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Hps5ru2-d
Spontaneous Allele Detail
Summary
Symbol: Hps5ru2-d
Name: HPS5, biogenesis of lysosomal organelles complex 2 subunit 2; ruby-eye 2d
MGI ID: MGI:7489571
Gene: Hps5  Location: Chr7:46409890-46445488 bp, - strand  Genetic Position: Chr7, 30.56 cM
Alliance: Hps5ru2-d page
Mutation
origin
Strain of Origin:  C57BL/10JMsHirRbrc
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Intragenic deletion
    A spontaneous deletion of a single nucleotide results in a frameshift. (J:336412)
Inheritance:    Recessive
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Hps5 Mutation:  90 strains or lines available
References
Original:  J:336412 Hirobe T, How are proliferation and differentiation of melanocytes regulated?. Pigment Cell Melanoma Res. 2011;24(3):462-78
All:  2 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
01/06/2026
MGI 6.24
The Jackson Laboratory