|
Symbol Name ID |
Nfix
nuclear factor I/X MGI:97311 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Astigmatism |
Optic atrophy |
Optic nerve hypoplasia |
Blue sclerae |
Hypertelorism |
Proptosis |
Strabismus |
Nystagmus |
Hypermetropia |
Myopia |
High myopia |
Glaucoma |
| Disease(s) Associated with NFIX | |||||||||||||
| Marshall-Smith syndrome | |||||||||||||
| Sotos syndrome 2 |
| Mouse Phenotypes | abnormal timing of postnatal eyelid opening |
delayed eyelid opening |
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| Availability | Mouse Genotype | ||
| Nfixtm1.1Rmg/Nfixtm1.1Rmg | |||
| Nfixtm1Aes/Nfixtm1Aes | |||
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 04/23/2024 MGI 6.23 |
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