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Symbol
Name
ID
Psph
phosphoserine phosphatase
MGI:97788
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Intrauterine growth retardation
Postnatal growth retardation
Disease(s) Associated with PSPH
PSPH deficiency

Mouse Phenotypes
abnormal oral cavity morphology
absent tongue
tongue hypoplasia
abnormal nasal cavity morphology
abnormal nasal septum morphology
abnormal vomeronasal organ morphology
absent vomeronasal organ
abnormal outer ear morphology
abnormal external auditory canal morphology
absent external auditory canal
embryonic growth retardation
abnormal embryo size
embryo cyst
thoracoschisis
epithelioid cyst
fetal growth retardation
heterochrony
Availability Mouse Genotype
Psphtm1.1(KOMP)Vlcg/Psphtm1.1(KOMP)Vlcg
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
04/16/2024
MGI 6.23
The Jackson Laboratory