Symbol Name ID |
Ift140
intraflagellar transport 140 MGI:2146906 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hypogonadism |
Abnormal testis morphology |
Disease(s) Associated with IFT140 | ||
retinitis pigmentosa |
Mouse Phenotypes | reproductive system phenotype |
abnormal sperm flagellum morphology |
abnormal outer dense fiber morphology |
abnormal sperm axoneme morphology |
abnormal sperm end piece morphology |
abnormal sperm mitochondrial morphology |
abnormal sperm fibrous sheath morphology |
kinked sperm flagellum |
short sperm flagellum |
oligozoospermia |
teratozoospermia |
abnormal sperm head morphology |
abnormal sperm nucleus morphology |
abnormal spermatid morphology |
abnormal manchette morphology |
decreased sperm progressive motility |
asthenozoospermia |
immotile sperm |
abnormal spermiogenesis |
abnormal spermiation |
male infertility |
impaired fertilization |
|
Availability | Mouse Genotype | ||||||||||||||||||||||
Ift140tm1c(KOMP)Wtsi/Ift140tm1c(KOMP)Wtsi Tg(Stra8-icre)1Reb/0 (conditional) |
* |
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 08/02/2024 MGI 6.24 |
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