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Symbol
Name
ID
Fbn2
fibrillin 2
MGI:95490
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Keratoconus
Keratoglobus
Astigmatism
Ectopia lentis
Abnormality of retinal pigmentation
Deeply set eye
Abnormal electroretinogram
Strabismus
Duane anomaly
Nystagmus
Horizontal nystagmus
Ophthalmoplegia
Hypermetropia
Myopia
Ptosis
Disease(s) Associated with FBN2
distal arthrogryposis

Mouse Phenotypes
vision/eye phenotype
abnormal eye morphology
Availability Mouse Genotype
Fbn2fp-4J/Fbn2fp-4J *
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
06/04/2019
MGI 6.14
The Jackson Laboratory