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Symbol
Name
ID
Aptx
aprataxin
MGI:1913658
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Hypoalbuminemia
Hypercholesterolemia
Disease(s) Associated with APTX
ataxia with oculomotor apraxia type 1

Mouse Phenotypes
abnormal DNA repair
abnormal single-strand DNA break repair
Availability Mouse Genotype
Aptxtm1Pmc/Aptxtm1Pmc

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
09/18/2018
MGI 6.12
The Jackson Laboratory