About   Help   FAQ
Symbol
Name
ID
Fbxl4
F-box and leucine-rich repeat protein 4
MGI:2140367
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Plagiocephaly
Microcephaly
Short foot
Scoliosis
Disease(s) Associated with FBXL4
mitochondrial DNA depletion syndrome 13

Mouse Phenotypes
kyphosis
Availability Mouse Genotype
Fbxl4tm1.2Lrsn/Fbxl4tm1.2Lrsn

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory