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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fam76b
family with sequence similarity 76, member B
MGI:1920076
15 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fam76bGt(IST14004H1)Tigm/Fam76bGt(IST14004H1)Tigm
C57BL/6-Fam76bGt(IST14004H1)Tigm 		abnormal macrophage physiology J:358021
abnormal spleen germinal center morphology J:358021
abnormal spleen white pulp morphology J:358021
abnormal splenic cell ratio J:358021
decreased B cell number J:358021
decreased body weight J:358021
enlarged spleen J:358021
increased inflammatory response J:358021
increased interleukin-6 secretion J:358021
increased microglial cell activation J:358021
increased myeloid cell number J:358021
increased response to brain injury J:358021
increased spleen weight J:358021
increased tumor necrosis factor secretion J:358021
microgliosis J:358021
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
12/17/2024
MGI 6.24 		The Jackson Laboratory