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Symbol
Name
ID

Kdm6a
lysine (K)-specific demethylase 6A
MGI:1095419

Phenotype annotations related to muscle

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Congenital diaphragmatic hernia	Hypotonia	Generalized hypotonia
Disease(s) Associated with KDM6A
Kabuki syndrome

Mouse Phenotypes		muscle phenotype	myocardial trabeculae hypoplasia	abnormal muscle precursor cell morphology	impaired skeletal muscle regeneration
Availability	Mouse Genotype	muscle phenotype	myocardial trabeculae hypoplasia	abnormal muscle precursor cell morphology	impaired skeletal muscle regeneration
	Kdm6a^{Gt(RRA094)Byg}/Kdm6a^{Gt(RRA094)Byg}
	Kdm6a^{tm1b(EUCOMM)Wtsi}/Kdm6a^{tm1b(EUCOMM)Wtsi}
	Kdm6a^tm2.1Kaig/Kdm6a^tm2.1Kaig	*
	Kdm6a^tm2.1Kaig/Y	*
	Kdm6a^tm1.1Kaig/Kdm6a^tm1.1Kaig Pax7^{tm2.1(cre/ERT2)Fan}/Pax7⁺ (conditional)
	Kdm6a^tm1.1Kaig/Y Pax7^{tm2.1(cre/ERT2)Fan}/Pax7⁺ (conditional)

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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