Fmnl1 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/17/2024 MGI 6.24