About   Help   FAQ
Symbol
Name
ID
Fbxw7
F-box and WD-40 domain protein 7
MGI:1354695
Phenotype annotations related to reproductive system
Darker colors indicate more annotations
Human Phenotypes
Cryptorchidism
Disease(s) Associated with FBXW7
developmental delay, hypotonia, and impaired language

Mouse Phenotypes
oligozoospermia
decreased male germ cell number
increased male germ cell apoptosis
abnormal male germ cell physiology
abnormal seminiferous tubule epithelium morphology
abnormal Sertoli cell barrier morphology
abnormal Sertoli cell morphology
decreased Sertoli cell number
ectopic Sertoli cells
seminiferous tubule degeneration
abnormal testis development
decreased testis weight
small testis
testicular atrophy
testis degeneration
arrest of spermatogenesis
abnormal epididymis morphology
decreased epididymis weight
small epididymis
decreased litter size
male infertility
reduced male fertility
Availability Mouse Genotype
Fbxw7tm1Iaai/Fbxw7tm1Iaai
Tg(Amh-cre)8815Reb/0  (conditional)

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
05/21/2024
MGI 6.23
The Jackson Laboratory