|
Symbol Name ID |
Ptdss1
phosphatidylserine synthase 1 MGI:1276575 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Facial palsy |
Anterior pituitary hypoplasia |
Hydrocephalus |
Ventriculomegaly |
Cerebral cortical atrophy |
Dysplastic corpus callosum |
Agenesis of corpus callosum |
Absent septum pellucidum |
Spina bifida occulta |
Intellectual disability |
Moderate intellectual disability |
Global developmental delay |
Specific learning disability |
| Disease(s) Associated with PTDSS1 | ||||||||||||||
| Lenz-Majewski hyperostotic dwarfism |
| Mouse Phenotypes | nervous system phenotype |
increased prepulse inhibition |
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| Availability | Mouse Genotype | ||
| Ptdss1tm1b(EUCOMM)Hmgu/Ptdss1tm1b(EUCOMM)Hmgu | |||
| Ptdss1tm1Jev/Ptdss1tm1Jev | * | ||
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 07/08/2026 MGI 6.24 |
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