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Symbol
Name
ID
Rpgrip1l
Rpgrip1-like
MGI:1920563
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Encephalocele
Occipital encephalocele
Bowing of the long bones
Genu valgum
Postaxial hand polydactyly
Postaxial foot polydactyly
Postaxial polydactyly
Scoliosis
Disease(s) Associated with RPGRIP1L
Joubert syndrome 7
Meckel syndrome 5

Mouse Phenotypes
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
abnormal rib morphology
abnormal vertebral arch morphology
fusion of vertebral arches
abnormal vertebral body morphology
absent vertebral body
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
04/23/2024
MGI 6.23
The Jackson Laboratory