About   Help   FAQ
Symbol
Name
ID
Fscn2
fascin actin-bundling protein 2
MGI:2443337
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Attenuation of retinal blood vessels
Chorioretinal atrophy
Bone spicule pigmentation of the retina
Rod-cone dystrophy
Optic atrophy
Nyctalopia
Visual impairment
Disease(s) Associated with FSCN2
retinitis pigmentosa 30

Mouse Phenotypes
abnormal photoreceptor outer segment morphology
short photoreceptor outer segment
abnormal retina morphology
thin retinal inner nuclear layer
thin retinal outer nuclear layer
retinal degeneration
abnormal eye electrophysiology
abnormal cone electrophysiology
abnormal rod electrophysiology
Availability Mouse Genotype
Fscn2tm1Sykk/Fscn2tm1Sykk
Fscn2tm2Sykk/Fscn2tm2Sykk
Fscn2tm1Sykk/Fscn2+
Fscn2tm2Sykk/Fscn2+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/12/2019
MGI 6.13
The Jackson Laboratory