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Symbol
Name
ID

Rps19
ribosomal protein S19
MGI:1333780

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Spina bifida occulta	Lethargy	Intellectual disability	Neurodevelopmental delay	Global developmental delay
Disease(s) Associated with RPS19	Microcephaly	Spina bifida occulta	Lethargy	Intellectual disability	Neurodevelopmental delay	Global developmental delay
Diamond-Blackfan anemia
Diamond-Blackfan anemia 1

Mouse Phenotypes		abnormal melanoblast morphology
Availability	Mouse Genotype	abnormal melanoblast morphology
	Rps19^Mhdadsk3/Rps19⁺ Tg(Dct-lacZ)A12Jkn/0

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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