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Symbol
Name
ID
Prss12
serine protease 12 neurotrypsin (motopsin)
MGI:1100881
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Strabismus
Nystagmus
Disease(s) Associated with PRSS12
autosomal recessive intellectual developmental disorder 1

Mouse Phenotypes
abnormal eye morphology
Availability Mouse Genotype
Prss12em1(IMPC)Ccpcz/Prss12em1(IMPC)Ccpcz

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