Fam20b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fam20b
FAM20B, glycosaminoglycan xylosylkinase
MGI:2443990

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fam20b^{Gt(GST_4283_D8)Lex}/Fam20b^{Gt(GST_4283_D8)Lex} involves: 129S5/SvEvBrd * C57BL/6	abnormal digestive system development	J:186384
	abnormal eye development	J:186384
	abnormal lung development	J:186384
	abnormal skeleton development	J:186384
	decreased embryo size	J:186384
	delayed hepatic development	J:186384
	embryonic lethality, complete penetrance	J:186384
Fam20b^m1Btlr/Fam20b^m1Btlr C57BL/6J-Fam20b^m1Btlr/Btlr	short femur	J:309727
Fam20b^m1Btlr/Fam20b^m1Btlr C57BL/6J-Fam20b^m1Btlr/Btlr	short tibia	J:309727

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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