Inf2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Inf2
inverted formin, FH2 and WH2 domain containing
MGI:1917685

8 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Inf2^{tm1.1(KOMP)Vlcg}/Inf2^{tm1.1(KOMP)Vlcg} C57BL/6N-Inf2^{tm1.1(KOMP)Vlcg}/Ucd	decreased hematocrit	J:211773
Inf2^{tm1.1(KOMP)Vlcg}/Inf2^{tm1.1(KOMP)Vlcg} involves: C57BL/6NTac	abnormal blood vessel physiology	J:255715
	abnormal placenta vasculature	J:255715
	decreased fetal weight	J:255715
	decreased placental labyrinth size	J:255715
	fetal growth retardation	J:255715
	increased systemic arterial blood pressure	J:255715
	long gestation period	J:255715

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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