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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	Encephalocele	Occipital encephalocele	Cleft upper lip	Cleft palate
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

Rpgrip1l^{tm1a(EUCOMM)Wtsi}/Rpgrip1l^{tm1a(EUCOMM)Wtsi}

Rpgrip1l^tm1Urt/Rpgrip1l^tm1Urt

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23