Symbol Name ID |
Nfix
nuclear factor I/X MGI:97311 |
Darker colors indicate more annotations |
Human Phenotypes | Omphalocele |
Umbilical hernia |
Short stature |
Tall stature |
Overgrowth |
Decreased body weight |
Failure to thrive |
Disease(s) Associated with NFIX | |||||||
Marshall-Smith syndrome | |||||||
Sotos syndrome 2 |
Mouse Phenotypes | slow postnatal weight gain |
weight loss |
megacephaly |
decreased body size |
|
Availability | Mouse Genotype | ||||
Nfixtm1.1Rmg/Nfixtm1.1Rmg | |||||
Nfixtm1Aes/Nfixtm1Aes | |||||
Nfixtm1Aes/Nfix+ |
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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