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Symbol
Name
ID

Pex7
peroxisomal biogenesis factor 7
MGI:1321392

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Frontal bossing	Micrognathia	Malar flattening	Microcephaly	Flared metaphysis	Rhizomelia	Flexion contracture	Epiphyseal stippling	Kyphoscoliosis	Coronal cleft vertebrae	Calcific stippling of infantile cartilaginous skeleton
Disease(s) Associated with PEX7
rhizomelic chondrodysplasia punctata type 1

Mouse Phenotypes		abnormal osteoclast morphology	abnormal cartilage development	decreased bone mineralization	delayed bone ossification
Availability	Mouse Genotype	abnormal osteoclast morphology	abnormal cartilage development	decreased bone mineralization	delayed bone ossification
	Pex7^tm1Nbra/Pex7^tm1Nbra
	Pex7^tm1Rjaw/Pex7^tm1Rjaw

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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