Symbol Name ID |
Nf1
neurofibromin 1 MGI:97306 |
Darker colors indicate more annotations |
Human Phenotypes | Low posterior hairline |
Neoplasm of the breast |
Abnormal hair quantity |
Freckling |
Axillary freckling |
Inguinal freckling |
Generalized hyperpigmentation |
Cafe-au-lait spot |
Multiple cafe-au-lait spots |
Hypopigmented skin patches |
Melanocytic nevus |
Macule |
Hypopigmented macule |
Subcutaneous nodule |
Neoplasm of the skin |
Neurofibroma |
Spinal neurofibroma |
Symmetric spinal nerve root neurofibromas |
Plexiform neurofibroma |
Disease(s) Associated with NF1 | |||||||||||||||||||
neurofibromatosis 1 | |||||||||||||||||||
neurofibromatosis-Noonan syndrome | |||||||||||||||||||
spinal neurofibromatosis | |||||||||||||||||||
Watson syndrome |
Mouse Phenotypes | increased ear pigmentation |
dermatitis |
disheveled coat |
abnormal hair cycle anagen phase |
pallor |
increased foot pad pigmentation |
increased tail pigmentation |
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Availability | Mouse Genotype | |||||||
Nf1tm1Tyj/Nf1tm1Tyj | ||||||||
Nf1Mhdadsk9/Nf1+ | ||||||||
Nf1tm1a(KOMP)Wtsi/Nf1+ | ||||||||
Nf1tm1c(KOMP)Wtsi/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 (conditional) |
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Nf1tm1Par/Nf1tm1Par Tg(Mx1-cre)1Cgn/0 (conditional) |
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Nf1tm1.1Kest/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 (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 04/16/2024 MGI 6.23 |
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