Symbol Name ID |
Maf
MAF bZIP transcription factor MGI:96909 |
Darker colors indicate more annotations |
Human Phenotypes | Cerebral atrophy |
Chiari type I malformation |
Intellectual disability |
Seizure |
Disease(s) Associated with MAF | ||||
Ayme-Gripp syndrome |
Mouse Phenotypes | abnormal axon morphology |
abnormal Meissner's corpuscle morphology |
abnormal pacinian corpuscle morphology |
decreased pacinian corpuscle number |
small pacinian corpuscles |
axon degeneration |
abnormal nervous system electrophysiology |
decreased nerve conduction velocity |
decreased prepulse inhibition |
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Availability | Mouse Genotype | |||||||||
Mafem1(IMPC)Mbp/Maf+ | ||||||||||
Maftm1.1Cbm/Maftm2.1Cbm Isl1tm1(cre)Tmj/Isl1+ (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 05/28/2024 MGI 6.13 |
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