|
Symbol Name ID |
Psph
phosphoserine phosphatase MGI:97788 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Cerebral atrophy |
Intellectual disability |
Global developmental delay |
Seizure |
| Disease(s) Associated with PSPH | |||||
| PSPH deficiency |
| Mouse Phenotypes | anastomosis between middle cerebral arteries |
absent segment of posterior cerebral artery |
abnormal vomeronasal organ morphology |
absent vomeronasal organ |
abnormal adenohypophysis morphology |
abnormal neurohypophysis morphology |
absent neurohypophysis |
abnormal pineal gland morphology |
absent pineal gland |
increased trigeminal neuroma incidence |
small superior cervical ganglion |
holoprosencephaly |
abnormal choroid plexus morphology |
abnormal brain commissure morphology |
absent posterior commissure |
abnormal brain internal capsule morphology |
absent brain internal capsule |
abnormal midbrain morphology |
abnormal forebrain morphology |
thin cerebral cortex |
abnormal olfactory bulb morphology |
absent olfactory bulb |
abnormal hindbrain morphology |
basal brain tissue herniation |
absent abducens nerve |
abnormal facial nerve topology |
abnormal hypoglossal nerve topology |
absent hypoglossal nerve |
abnormal olfactory nerve morphology |
absent olfactory nerve |
absent optic chiasm |
absent trochlear nerve |
abnormal dorsal root ganglion topology |
abnormal spinal cord central canal morphology |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||||||||||
| Psphtm1a(EUCOMM)Hmgu/Psphtm1a(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 05/07/2024 MGI 6.23 |
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