Symbol Name ID |
Nfix
nuclear factor I/X MGI:97311 |
Darker colors indicate more annotations |
Human Phenotypes | Drooling |
Feeding difficulties |
Autistic behavior |
Disease(s) Associated with NFIX | |||
Marshall-Smith syndrome | |||
Sotos syndrome 2 |
Mouse Phenotypes | impaired active avoidance behavior |
impaired spatial learning |
abnormal long-term spatial reference memory |
abnormal short-term spatial reference memory |
abnormal response to social novelty |
limb grasping |
ataxia |
abnormal social investigation |
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Availability | Mouse Genotype | ||||||||
Nfixtm1Aes/Nfixtm1Aes | |||||||||
Nfixtm1.1Rmg/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 04/30/2024 MGI 6.23 |
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