Fam72a Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fam72a
family with sequence similarity 72, member A
MGI:1919669

7 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fam72a^{tm1.1(KOMP)Vlcg}/Fam72a^{tm1.1(KOMP)Vlcg} C57BL/6N-Fam72a^{tm1.1(KOMP)Vlcg}/Ucd	abnormal kidney morphology	J:211773
	increased blood urea nitrogen level	J:211773
	polycystic kidney	J:211773
Fam72a^{tm1.1(KOMP)Vlcg}/Fam72a^{tm1.1(KOMP)Vlcg} C57BL/6NTac-Fam72a^{tm1.1(KOMP)Vlcg}	abnormal class switch recombination	J:326431
	abnormal somatic hypermutation frequency	J:326431
	increased B cell apoptosis	J:326431
	increased germinal center B cell number	J:326431

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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