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Symbol
Name
ID
Rpgrip1l
Rpgrip1-like
MGI:1920563
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Generalized hypotonia
Disease(s) Associated with RPGRIP1L
Joubert syndrome 7

Mouse Phenotypes
abnormal eye muscle morphology
Availability Mouse Genotype
Rpgrip1ltm1a(EUCOMM)Wtsi/Rpgrip1ltm1a(EUCOMM)Wtsi

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