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Symbol
Name
ID
Fbn2
fibrillin 2
MGI:95490
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Mandibular prognathia
Trismus
Malar flattening
Microcephaly
Mild microcephaly
Macrocephaly
Frontal bossing
Brachycephaly
Cranial asymmetry
Dolichocephaly
Scaphocephaly
Decreased facial expression
Mask-like facies
Facial asymmetry
Flat face
Round face
Narrow face
Triangular face
Chin with H-shaped crease
Dimple chin
Tall chin
Low anterior hairline
Prominent forehead
Deep philtrum
Long philtrum
Cleft palate
Submucous cleft hard palate
Bifid uvula
High palate
Pursed lips
Whistling appearance
Narrow mouth
Dental crowding
Furrowed tongue
Anteverted nares
Underdeveloped nasal alae
Bulbous nose
Short nose
Depressed nasal bridge
Wide nasal bridge
Prominent nasolabial fold
Highly arched eyebrow
Blepharophimosis
Downslanted palpebral fissures
Epicanthus
Telecanthus
Low posterior hairline
Disease(s) Associated with FBN2
distal arthrogryposis

Mouse Phenotypes
micrognathia
Availability Mouse Genotype
Fbn2timon/Fbn2timon

Contributing Projects:
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
08/13/2019
MGI 6.14
The Jackson Laboratory