About Help FAQ

Symbol
Name
ID

Fscn2
fascin actin-bundling protein 2
MGI:2443337

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Photophobia	Intellectual disability	Hyperreflexia
Disease(s) Associated with FSCN2
retinitis pigmentosa

Mouse Phenotypes

abnormal cochlear hair cell stereociliary bundle morphology

decreased inner hair cell stereocilia number

decreased outer hair cell stereocilia number

short cochlear hair cell stereocilia

cochlear outer hair cell degeneration

abnormal cochlear outer hair cell physiology

abnormal photoreceptor inner segment morphology

photoreceptor inner segment degeneration

abnormal photoreceptor outer segment morphology

abnormal photoreceptor outer segment size

short photoreceptor outer segment

photoreceptor outer segment degeneration

Availability

Mouse Genotype

Fscn2^ahl8/Fscn2^ahl8

Fscn2^em1Fhan/Fscn2^em1Fhan

Fscn2^tm1Sykk/Fscn2^tm1Sykk

Fscn2^tm2Sykk/Fscn2^tm2Sykk

Fscn2^tm1Sykk/Fscn2⁺

Fscn2^tm2Sykk/Fscn2⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/07/2024 MGI 6.23