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Symbol
Name
ID

Aptx
aprataxin
MGI:1913658

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Hypercholesterolemia	Hypoalbuminemia	Elevated circulating creatine kinase concentration
Disease(s) Associated with APTX
ataxia with oculomotor apraxia type 1

Mouse Phenotypes		abnormal DNA repair	abnormal single-strand DNA break repair	increased circulating alanine transaminase level
Availability	Mouse Genotype	abnormal DNA repair	abnormal single-strand DNA break repair	increased circulating alanine transaminase level
	Aptx^{tm1b(EUCOMM)Hmgu}/Aptx^{tm1b(EUCOMM)Hmgu}
	Aptx^tm1Pmc/Aptx^tm1Pmc

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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