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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
03/13/2019
MGI 6.13
The Jackson Laboratory