Fmnl1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fmnl1
formin-like 1
MGI:1888994

11 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Fmnl1^tm1.1Sdb/Fmnl1^tm1.1Sdb involves: C3H * C57BL/6 * FVB/N	embryonic lethality, complete penetrance	J:250144
Fmnl1^tm1.2Sdb/Fmnl1^tm1.2Sdb Lyz2^tm1(cre)Ifo/Lyz2^tm1(cre)Ifo involves: C3H * C57BL/6 * FVB/N	abnormal Kupffer cell morphology	J:250144
	abnormal macrophage morphology	J:250144
	abnormal macrophage physiology	J:250144
	normal cardiovascular system phenotype	J:250144
	decreased macrophage cell number	J:250144
	normal growth/size/body region phenotype	J:250144
	normal hematopoietic system phenotype	J:250144
	impaired macrophage chemotaxis	J:250144
	normal mortality/aging	J:250144
	normal reproductive system phenotype	J:250144

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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