Symbol Name ID |
Pfn4
profilin family, member 4 MGI:1920121 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | cellular phenotype |
abnormal sperm flagellum morphology |
abnormal sperm connecting piece morphology |
abnormal sperm midpiece morphology |
abnormal sperm mitochondrial sheath morphology |
coiled sperm flagellum |
necrospermia |
abnormal sperm head morphology |
abnormal acrosome morphology |
abnormal acrosome assembly |
abnormal proacrosomal vesicle fusion |
globozoospermia |
abnormal sperm nucleus morphology |
small sperm head |
abnormal spermatid morphology |
abnormal manchette morphology |
abnormal manchette assembly |
absent manchette |
abnormal Golgi apparatus morphology |
impaired autophagy |
decreased sperm progressive motility |
asthenozoospermia |
abnormal Golgi vesicle transport |
|
Availability | Mouse Genotype | |||||||||||||||||||||||
Pfn4em1Hsc/Pfn4em1Hsc | * | |||||||||||||||||||||||
Pfn4em2Hsc/Pfn4em2Hsc | * |
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 09/17/2024 MGI 6.24 |
|
|