About   Help   FAQ
Symbol
Name
ID
Mcoln1
mucolipin 1
MGI:1890498
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Aplasia/Hypoplasia of the abdominal wall musculature
Spastic tetraplegia
Hypotonia
Generalized hypotonia
Muscle weakness
Skeletal muscle atrophy
Disease(s) Associated with MCOLN1
glycoproteinosis
mucolipidosis type IV

Mouse Phenotypes
dilated cardiomyopathy
decreased skeletal muscle mass
Availability Mouse Genotype
Mcoln1tm1Sasl/Mcoln1tm1Sasl

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
The Jackson Laboratory