About Help FAQ

Symbol
Name
ID

Ocln
occludin
MGI:106183

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Spasticity	Hypotonia	Axial hypotonia
Disease(s) Associated with OCLN
pseudo-TORCH syndrome 1

Mouse Phenotypes		abnormal stomach muscularis externa morphology	abnormal muscle morphology
Availability	Mouse Genotype	abnormal stomach muscularis externa morphology	abnormal muscle morphology
	Ocln^{Gt(ROSA)39Tshi}/Ocln^{Gt(ROSA)39Tshi}
	Ocln^tm1Tshi/Ocln^tm1Tshi

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 04/23/2024 MGI 6.23