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Symbol
Name
ID

Stk36
serine/threonine kinase 36
MGI:1920831

Phenotype annotations related to nervous system

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Morphological central nervous system abnormality	Hydrocephalus	Ventriculomegaly	Delayed speech and language development
Disease(s) Associated with STK36
primary ciliary dyskinesia

Mouse Phenotypes		hydrocephaly	non-obstructive hydrocephaly	increased prepulse inhibition
Availability	Mouse Genotype	hydrocephaly	non-obstructive hydrocephaly	increased prepulse inhibition
	Stk36^tm1Fjs/Stk36^tm1Fjs		!
	Stk36^tm1Lex/Stk36^tm1Lex
	Stk36^em1(IMPC)J/Stk36⁺

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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