Symbol Name ID |
Piga
phosphatidylinositol glycan anchor biosynthesis, class A MGI:99461 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Secondary microcephaly |
Stroke |
Dysphagia |
Spasticity |
Lower limb spasticity |
Upper limb spasticity |
Gliosis |
Delayed myelination |
Abnormal pons morphology |
Lateral ventricle dilatation |
Cerebral cortical atrophy |
Abnormal cerebral white matter morphology |
Hypoplasia of the corpus callosum |
Absent septum pellucidum |
Olfactory lobe agenesis |
Cerebellar hypoplasia |
Neuronal loss in central nervous system |
Hypsarrhythmia |
Absent speech |
Lethargy |
Hyperreflexia |
Brisk reflexes |
Epileptic encephalopathy |
Headache |
Global developmental delay |
Generalized myoclonic seizure |
Disease(s) Associated with PIGA | |||||||||||||||||||||||||||
multiple congenital anomalies-hypotonia-seizures syndrome 2 | |||||||||||||||||||||||||||
paroxysmal nocturnal hemoglobinuria |
Mouse Phenotypes | abnormal brain development |
exencephaly |
|
Availability | Mouse Genotype | ||
Pigatm1.1Tak/Piga+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|