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Symbol
Name
ID
Nphp3
nephronophthisis 3 (adolescent)
MGI:1921275
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Oligohydramnios
Polyhydramnios
Disease(s) Associated with NPHP3
Meckel syndrome 7
renal-hepatic-pancreatic dysplasia

Mouse Phenotypes
abnormal embryo turning
abnormal left-right axis patterning
Availability Mouse Genotype
Nphp3tm1Cbe/Nphp3tm1Cbe

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