|
Symbol Name ID |
Spata7
spermatogenesis associated 7 MGI:2144877 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Nystagmus |
Nyctalopia |
Constriction of peripheral visual field |
Visual loss |
| Disease(s) Associated with SPATA7 | ||||
| Leber congenital amaurosis 3 |
| Mouse Phenotypes | vision/eye phenotype |
abnormal photoreceptor connecting cilium morphology |
abnormal retina cone cell morphology |
retina cone cell degeneration |
abnormal retina rod cell morphology |
retina rod cell degeneration |
retina photoreceptor degeneration |
abnormal retina morphology |
thin retina outer nuclear layer |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
|
| Availability | Mouse Genotype | |||||||||||
| Spata7tm1.1(KOMP)Vlcg/Spata7tm1.1(KOMP)Vlcg | ||||||||||||
| Spata7tm1Mrd/Spata7tm1Mrd | ||||||||||||
| Spata7tm2.1Mrd/Spata7tm2.1Mrd | ||||||||||||
| Spata7tm1Mrd/Spata7tm2Mrd Tg(Crx-cre)1Tfur/0 (conditional) |
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| Spata7tm1Mrd/Spata7tm2Mrd Tg(BEST1-cre)1Jdun/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 04/30/2024 MGI 6.23 |
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