Symbol Name ID |
Gnpat
glyceronephosphate O-acyltransferase MGI:1343460 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Optic nerve hypoplasia |
Intellectual disability |
Intellectual disability, severe |
Disease(s) Associated with GNPAT | ||||
rhizomelic chondrodysplasia punctata type 2 |
Mouse Phenotypes | abnormal cerebellar granule cell migration |
abnormal cerebellar foliation |
decreased brain weight |
abnormal cerebral hemisphere morphology |
abnormal Purkinje cell morphology |
small cerebellum |
abnormal paranode morphology |
abnormal paranodal axoglial junction morphology |
optic nerve hypoplasia |
abnormal myelination |
decreased nerve conduction velocity |
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Availability | Mouse Genotype | |||||||||||
Gnpattm1Just/Gnpattm1Just |
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 04/23/2024 MGI 6.23 |
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