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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Prdm13
PR domain containing 13
MGI:2448528
9 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Prdm13em1(IMPC)Tcp/Prdm13em1(IMPC)Tcp
C57BL/6NCrl-Prdm13em1(IMPC)Tcp/Tcp
abnormal spleen morphology J:211773
increased circulating bilirubin level J:211773
increased spleen weight J:211773
Prdm13tm1.1Tfur/Prdm13tm1.1Tfur
Tg(Dkk3-cre)D9Tfur/0
involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N
abnormal optokinetic reflex J:222242
abnormal retina inner plexiform layer morphology J:222242
decreased amacrine cell number J:222242
Prdm13tm1.2Tfur/Prdm13tm1.2Tfur
involves: C57BL/6 * C57BL/6J * C57BL/6N
abnormal optokinetic reflex J:222242
abnormal retina inner plexiform layer morphology J:222242
abnormal visual contrast sensitivity J:222242
decreased amacrine cell number J:222242
thin retina inner nuclear layer J:222242
thin retina inner plexiform layer J:222242

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory