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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Aptxtm1b(EUCOMM)Hmgu/Aptxtm1b(EUCOMM)Hmgu
B6N(Cg)-Aptxtm1b(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
Aptxtm1Pmc/Aptxtm1Pmc
129S4/SvJae 		abnormal DNA repair J:170077
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory