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Symbol
Name
ID

Ash1l
ASH1 like histone lysine methyltransferase
MGI:2183158

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Dolichocephaly	Microcephaly	Macrocephaly	Scapular winging	Cervical C2/C3 vertebral fusion	Pectus carinatum	Lumbar hyperlordosis	Lumbar scoliosis
Disease(s) Associated with ASH1L
autosomal dominant intellectual developmental disorder 52

Mouse Phenotypes		increased susceptibility to induced arthritis	abnormal sternum morphology	asymmetric sternocostal joints	increased rib number
Availability	Mouse Genotype	increased susceptibility to induced arthritis	abnormal sternum morphology	asymmetric sternocostal joints	increased rib number
	Ash1l^{Gt(AL0395)Wtsi}/Ash1l^{Gt(AL0395)Wtsi}
	Ash1l^{Tn(pb-Act-RFP)1.AF0-180T25Zhu}/Ash1l^{Tn(pb-Act-RFP)1.AF0-180T25Zhu}

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23