Symbol Name ID |
Plekhm1
pleckstrin homology domain containing, family M (with RUN domain) member 1 MGI:2443207 |
Darker colors indicate more annotations |
Human Phenotypes | Optic nerve compression |
Abnormality of visual evoked potentials |
Hydrocephalus |
Tremor |
Cranial nerve paralysis |
Abnormality of movement |
Disease(s) Associated with PLEKHM1 | ||||||
osteopetrosis |
Mouse Phenotypes | abnormal optic disk morphology |
decreased prepulse inhibition |
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Availability | Mouse Genotype | ||
Plekhm1tm1b(EUCOMM)Hmgu/Plekhm1tm1b(EUCOMM)Hmgu |
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 08/02/2024 MGI 6.24 |
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