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Symbol
Name
ID
Rpgrip1l
Rpgrip1-like
MGI:1920563
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Encephalocele
Occipital encephalocele
Cleft upper lip
Cleft palate
Disease(s) Associated with RPGRIP1L
Joubert syndrome 7
Meckel syndrome 5

Mouse Phenotypes
persistent right 6th pharyngeal arch artery
abnormal cranium morphology
abnormal basioccipital bone morphology
abnormal basisphenoid bone morphology
abnormal viscerocranium morphology
abnormal hyoid bone morphology
abnormal incisor morphology
abnormal mandible morphology
mandible hypoplasia
abnormal maxilla morphology
cleft upper lip
abnormal palate morphology
cleft palate
decreased tongue size
abnormal nasal cavity morphology
abnormal nasal septum morphology
Availability Mouse Genotype
Rpgrip1ltm1a(EUCOMM)Wtsi/Rpgrip1ltm1a(EUCOMM)Wtsi
Rpgrip1ltm1Urt/Rpgrip1ltm1Urt

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
11/05/2019
MGI 6.14
The Jackson Laboratory