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Symbol
Name
ID
Psat1
phosphoserine aminotransferase 1
MGI:2183441
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Microcephaly
Postnatal microcephaly
Sloping forehead
Cleft palate
High palate
Depressed nasal ridge
Disease(s) Associated with PSAT1
Neu-Laxova syndrome 2
PSAT deficiency

Mouse Phenotypes
abnormal craniofacial morphology
Availability Mouse Genotype
Psat1tm1a(KOMP)Wtsi/Psat1tm1a(KOMP)Wtsi

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
10/08/2019
MGI 6.14
The Jackson Laboratory