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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
Central hypotonia
Muscular 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
Kdm6aGt(RRA094)Byg/Kdm6aGt(RRA094)Byg
Kdm6atm1b(EUCOMM)Wtsi/Kdm6atm1b(EUCOMM)Wtsi
Kdm6atm2.1Kaig/Kdm6atm2.1Kaig *
Kdm6atm2.1Kaig/Y *
Kdm6atm1.1Kaig/Kdm6atm1.1Kaig
Pax7tm2.1(cre/ERT2)Fan/Pax7+  (conditional)
Kdm6atm1.1Kaig/Y
Pax7tm2.1(cre/ERT2)Fan/Pax7+  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/04/2018
MGI 6.13
The Jackson Laboratory