Aptx Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Aptx
aprataxin
MGI:1913658

7 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Aptx^{tm1b(EUCOMM)Hmgu}/Aptx^{tm1b(EUCOMM)Hmgu} B6N(Cg)-Aptx^{tm1b(EUCOMM)Hmgu}/J	cataract	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	increased circulating alanine transaminase level	J:211773
	persistence of hyaloid vascular system	J:211773
Aptx^tm1Pmc/Aptx^tm1Pmc 129S4/SvJae	abnormal DNA repair	J:170077
Aptx^tm1Pmc/Aptx^tm1Pmc 129S4/SvJae	abnormal single-strand DNA break repair	J:145730

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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