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Symbol
Name
ID
Abcd3
ATP-binding cassette, sub-family D member 3
MGI:1349216
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Flat occiput
Micrognathia
Microcephaly
Macrocephaly
Wide anterior fontanel
Epiphyseal stippling
Skeletal dysplasia
Disease(s) Associated with ABCD3
Zellweger syndrome

Mouse Phenotypes
decreased bone mineral content
decreased bone mineral density
Availability Mouse Genotype
Abcd3em1(IMPC)J/Abcd3em1(IMPC)J

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
04/30/2024
MGI 6.23
The Jackson Laboratory