|
Symbol Name ID |
Cfh
complement component factor h MGI:88385 |
| Darker colors indicate more annotations |
| Human Phenotypes | Keratoconjunctivitis sicca |
Cataract |
Macular degeneration |
Retinopathy |
Drusen |
Uveitis |
Blindness |
Progressive visual loss |
Glaucoma |
| Disease(s) Associated with CFH | |||||||||
| age related macular degeneration 4 | |||||||||
| basal laminar drusen | |||||||||
| sarcoidosis | |||||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | abnormal retina vasculature morphology |
increased susceptilbility to retina ischemic injury |
abnormal retina rod bipolar cell morphology |
abnormal retina photoreceptor morphology |
disorganized photoreceptor outer segment |
abnormal retina pigment epithelium morphology |
white pupil |
abnormal retina morphology |
abnormal retina layer morphology |
retina detachment |
abnormal Bruch membrane morphology |
decreased a-wave amplitude |
decreased b-wave amplitude |
decreased visual acuity |
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| Availability | Mouse Genotype | ||||||||||||||
| Cfhtm1.1Song/Cfhtm1.1Song | |||||||||||||||
| Cfhtm1Mbo/Cfhtm1Mbo | |||||||||||||||
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 08/21/2024 MGI 6.24 |
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