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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
Flexion contracture
Micrognathia
Malar flattening
Microcephaly
Frontal bossing
Short fourth metatarsal
Flared metaphysis
Rhizomelia
Epiphyseal stippling
Coronal cleft vertebrae
Kyphoscoliosis
Calcific stippling of infantile cartilaginous skeleton
Multiple epiphyseal dysplasia
Disease(s) Associated with PEX7
Refsum disease
rhizomelic chondrodysplasia punctata type 1

Mouse Phenotypes
abnormal osteoclast morphology
abnormal cartilage development
decreased bone mineralization
delayed bone ossification
Availability Mouse Genotype
Pex7tm1Nbra/Pex7tm1Nbra
Pex7tm1Rjaw/Pex7tm1Rjaw

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
08/13/2019
MGI 6.14
The Jackson Laboratory