About   Help   FAQ
Symbol
Name
ID
Rps6ka3
ribosomal protein S6 kinase polypeptide 3
MGI:104557
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Hypotonia
Disease(s) Associated with RPS6KA3
Coffin-Lowry syndrome
non-syndromic X-linked intellectual disability 19

Mouse Phenotypes
muscle phenotype
decreased skeletal muscle glycogen level
Availability Mouse Genotype
Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry *
Rps6ka3tm1.1Kry/Rps6ka3+ *
Rps6ka3tm1Ljg/Y

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
04/30/2024
MGI 6.23
The Jackson Laboratory