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Symbol
Name
ID
Rps6ka3
ribosomal protein S6 kinase polypeptide 3
MGI:104557
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Ventriculomegaly
Delayed speech and language development
Intellectual disability
Intellectual disability, mild
Global developmental delay
Motor delay
Seizure
Disease(s) Associated with RPS6KA3
Coffin-Lowry syndrome
non-syndromic X-linked intellectual disability 19

Mouse Phenotypes
nervous system phenotype
abnormal dendritic spine morphology
abnormal synapse morphology
abnormal postsynaptic density morphology
abnormal CNS synaptic transmission
short excitatory postsynaptic current decay time
abnormal excitatory postsynaptic potential
reduced AMPA-mediated synaptic currents
Availability Mouse Genotype
Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry *
Rps6ka3tm1.1Kry/Rps6ka3+ *

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)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory