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Phenotypes Associated with This Genotype
Genotype
MGI:2178293
Allelic
Composition
GpnmbR150X/GpnmbR150X
Tyrp1isa/Tyrp1isa
Genetic
Background
involves: C57BL/6J * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
GpnmbR150X mutation (3 available); any Gpnmb mutation (17 available)
Tyrp1isa mutation (3 available); any Tyrp1 mutation (168 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• loss of retinal ganglion cells

pigmentation

nervous system
• loss of retinal ganglion cells

Mouse Models of Human Disease
OMIM ID Ref(s)
Glaucoma-Related Pigment Dispersion Syndrome; GPDS1 600510 J:54013


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/17/2016
MGI 6.05
The Jackson Laboratory