Symbol Name ID |
Maf
MAF bZIP transcription factor MGI:96909 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Microcornea |
Corneal opacity |
Developmental cataract |
Nuclear cataract |
Cerulean cataract |
Cortical pulverulent cataract |
Iris coloboma |
Peters anomaly |
Macular hypoplasia |
Retinal detachment |
Hypertelorism |
High myopia |
Ptosis |
Disease(s) Associated with MAF | |||||||||||||
Ayme-Gripp syndrome | |||||||||||||
cataract | |||||||||||||
cataract 21 multiple types |
Mouse Phenotypes | vision/eye phenotype |
abnormal pupillary reflex |
small pupil |
increased cornea thickness |
abnormal corneal endothelium morphology |
abnormal lens morphology |
abnormal lens development |
abnormal lens induction |
abnormal lens vesicle development |
abnormal lens fiber morphology |
cataract |
nuclear cataract |
small lens |
microphthalmia |
|
Availability | Mouse Genotype | ||||||||||||||
Mafem1(IMPC)Mbp/Mafem1(IMPC)Mbp | |||||||||||||||
MafENU424/MafENU424 | |||||||||||||||
MafOfl/MafOfl | |||||||||||||||
Maftm1Glm/Maftm1Glm | * | ||||||||||||||
Maftm1Gsb/Maftm1Gsb | |||||||||||||||
Maftm1Mym/Maftm1Mym | |||||||||||||||
Mafem1(IMPC)Mbp/Maf+ | |||||||||||||||
MafENU424/Maf+ | |||||||||||||||
MafOfl/Maf+ | ! |
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 03/19/2024 MGI 6.23 |
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