Symbol Name ID |
Kdm6a
lysine (K)-specific demethylase 6A MGI:1095419 |
* | 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 |
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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) |
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Kdm6atm1.1Kaig/Y Pax7tm2.1(cre/ERT2)Fan/Pax7+ (conditional) |
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 03/12/2024 MGI 6.23 |
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