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Symbol Name ID |
Nrf1
nuclear respiratory factor 1 MGI:1332235 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of eye movement |
| Disease(s) Associated with NRF1 | |
| Huntington's disease |
| Mouse Phenotypes | decreased retina ganglion cell number |
decreased retina cone cell number |
decreased retina rod cell number |
short photoreceptor inner segment |
short photoreceptor outer segment |
retina rod cell degeneration |
abnormal retina progenitor cell morphology |
abnormal retina morphology |
abnormal retina layer morphology |
abnormal retina neuronal layer morphology |
absent retina ganglion layer |
thin retina ganglion layer |
thin retina outer nuclear layer |
decreased total retina thickness |
retina hypoplasia |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||||||||||||
| Nrf1tm1c(KOMP)Wtsi/Nrf1tm1c(KOMP)Wtsi Tg(Six3-cre)69Frty/0 (conditional) |
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| Nrf1tm1c(KOMP)Wtsi/Nrf1tm1c(KOMP)Wtsi Tg(Rho-icre)1Ck/0 (conditional) |
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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 04/16/2024 MGI 6.23 |
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