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Symbol
Name
ID

Plekhm1
pleckstrin homology domain containing, family M (with RUN domain) member 1
MGI:2443207

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic nerve compression	Abnormality of visual evoked potentials	Nystagmus	Opsoclonus	Visual impairment
Disease(s) Associated with PLEKHM1
osteopetrosis

Mouse Phenotypes		abnormal optic disk morphology
Availability	Mouse Genotype	abnormal optic disk morphology
	Plekhm1^{tm1b(EUCOMM)Hmgu}/Plekhm1^{tm1b(EUCOMM)Hmgu}

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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