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Symbol
Name
ID
Prdm5
PR domain containing 5
MGI:1918029
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Dentinogenesis imperfecta
Macrocephaly
Congenital hip dislocation
Scoliosis
Spondylolisthesis
Joint laxity
Recurrent fractures
Disease(s) Associated with PRDM5
brittle cornea syndrome

Mouse Phenotypes
abnormal bone structure
abnormal bone collagen fibril morphology
decreased bone mineral content
decreased bone mineral density
decreased compact bone volume
decreased trabecular bone volume
decreased bone volume
abnormal osteoblast morphology
delayed bone ossification
Availability Mouse Genotype
Prdm5Gt(AV0702)Wtsi/Prdm5Gt(AV0702)Wtsi

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory