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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Fmnl1tm1.1Sdb/Fmnl1tm1.1Sdb
involves: C3H * C57BL/6 * FVB/N
embryonic lethality, complete penetrance J:250144
Fmnl1tm1.2Sdb/Fmnl1tm1.2Sdb
Lyz2tm1(cre)Ifo/Lyz2tm1(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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last database update
02/23/2021
MGI 6.16
The Jackson Laboratory