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Symbol
Name
ID
Psph
phosphoserine phosphatase
MGI:97788
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Hypertonia
Cerebral atrophy
Intellectual disability
Global developmental delay
Seizures
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
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
trigeminal neuroma
absent trochlear nerve
abnormal dorsal root ganglion topology
abnormal spinal cord central canal morphology
Availability Mouse Genotype
Psphtm1a(EUCOMM)Hmgu/Psphtm1a(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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last database update
11/12/2019
MGI 6.14
The Jackson Laboratory