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Symbol
Name
ID

Psph
phosphoserine phosphatase
MGI:97788

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Microcephaly
Disease(s) Associated with PSPH	Microcephaly
PSPH deficiency

Mouse Phenotypes

abnormal craniofacial morphology

fragmented Meckel's cartilage

short Meckel's cartilage

abnormal sphenoid bone morphology

absent maxilla

abnormal middle ear ossicle morphology

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

Availability

Mouse Genotype

Psph^{tm1.1(KOMP)Vlcg}/Psph^{tm1.1(KOMP)Vlcg}

Psph^{tm1a(EUCOMM)Hmgu}/Psph^{tm1a(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23