|
Symbol Name ID |
Fbn1
fibrillin 1 MGI:95489 |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
Broad skull |
Dolichocephaly |
Micrognathia |
Retrognathia |
Hypoplasia of the maxilla |
Malar flattening |
Shallow orbits |
Long face |
Round face |
Narrow face |
Full cheeks |
Midface retrusion |
Depressed glabella |
Thick lower lip vermilion |
Deep philtrum |
Long philtrum |
Smooth philtrum |
Thin upper lip vermilion |
High palate |
High, narrow palate |
Narrow palate |
Narrow mouth |
Abnormal dental morphology |
Tooth malposition |
Dental crowding |
Anteverted nares |
Bulbous nose |
Depressed nasal bridge |
Short nose |
Abnormal eyebrow morphology |
Long eyelashes |
Downslanted palpebral fissures |
| Disease(s) Associated with FBN1 | |||||||||||||||||||||||||||||||||
| acromicric dysplasia | |||||||||||||||||||||||||||||||||
| autosomal dominant isolated ectopia lentis 1 | |||||||||||||||||||||||||||||||||
| geleophysic dysplasia 2 | |||||||||||||||||||||||||||||||||
| Marfan syndrome | |||||||||||||||||||||||||||||||||
| mitral valve prolapse | |||||||||||||||||||||||||||||||||
| stiff skin syndrome | |||||||||||||||||||||||||||||||||
| Weill-Marchesani syndrome |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools