|
Symbol Name ID |
Ift27
intraflagellar transport 27 MGI:1914292 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypogonadism |
External genital hypoplasia |
| Disease(s) Associated with IFT27 | ||
| Bardet-Biedl syndrome 19 |
| 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 flagellum thickness |
disorganized sperm mitochondrial sheath |
abnormal sperm fibrous sheath morphology |
kinked sperm flagellum |
short sperm flagellum |
oligozoospermia |
teratozoospermia |
abnormal sperm head morphology |
globozoospermia |
decreased sperm progressive motility |
asthenozoospermia |
immotile sperm |
abnormal testis physiology |
abnormal spermatogenesis |
abnormal spermiation |
arrest of spermiogenesis |
male infertility |
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| Availability | Mouse Genotype | ||||||||||||||||||||||
| Ift27tm1c(EUCOMM)Hmgu/Ift27tm1c(EUCOMM)Hmgu 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 07/05/2024 MGI 6.24 |
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