|
Symbol Name ID |
Nfix
nuclear factor I/X MGI:97311 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Prominent occiput |
Craniosynostosis |
Dolichocephaly |
Short mandibular rami |
Microretrognathia |
Mandibular prognathia |
Retrognathia |
Hyperplasia of the premaxilla |
Prominence of the premaxilla |
Shallow orbits |
Macrocephaly |
Wormian bones |
Long face |
Narrow face |
Triangular face |
Midface retrusion |
Broad forehead |
High forehead |
Prominent forehead |
Everted lower lip vermilion |
Short philtrum |
Eclabion |
Gingival overgrowth |
High palate |
Glossoptosis |
Protruding tongue |
Open mouth |
Narrow mouth |
Irregular dentition |
Microdontia |
Advanced eruption of teeth |
Drooling |
Choanal atresia |
Choanal stenosis |
Anteverted nares |
Depressed nasal bridge |
Short nose |
Recurrent upper respiratory tract infections |
Highly arched eyebrow |
Synophrys |
Thick eyebrow |
Downslanted palpebral fissures |
| Disease(s) Associated with NFIX | |||||||||||||||||||||||||||||||||||||||||||
| Marshall-Smith syndrome | |||||||||||||||||||||||||||||||||||||||||||
| Sotos syndrome 2 |
| Mouse Phenotypes | craniofacial phenotype |
abnormal craniofacial bone morphology |
abnormal cranial suture morphology |
domed cranium |
|
| 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 04/30/2024 MGI 6.23 |
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