|
Symbol Name ID |
Nf1
neurofibromin 1 MGI:97306 |
| Darker colors indicate more annotations |
| Human Phenotypes | Low posterior hairline |
Malar flattening |
Macrocephaly |
Relative macrocephaly |
Abnormality of the face |
Midface retrusion |
Thick vermilion border |
Depressed nasal bridge |
Prominent nasolabial fold |
Abnormal eyelid morphology |
Downslanted palpebral fissures |
Epicanthus |
Lisch nodules |
| Disease(s) Associated with NF1 | |||||||||||||
| neurofibromatosis 1 | |||||||||||||
| neurofibromatosis-Noonan syndrome | |||||||||||||
| spinal neurofibromatosis | |||||||||||||
| Watson syndrome |
| Mouse Phenotypes | abnormal tongue morphology |
increased ear pigmentation |
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| Availability | Mouse Genotype | ||
| Nf1Mhdadsk9/Nf1+ | |||
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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