Erf Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Erf
Ets2 repressor factor
MGI:109637

37 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Erf^{tm1.1(KOMP)Mbp}/Erf⁺ C57BL/6N-Erf^{tm1.1(KOMP)Mbp}/MbpMmucd	abnormal embryo size	J:211773
	embryonic growth retardation	J:211773
Erf^{tm1.1(KOMP)Mbp}/Erf⁺ C57BL/6N-Erf^{tm1.1(KOMP)Mbp}/Ucd	abnormal heart morphology	J:211773
	abnormal snout morphology	J:211773
	abnormal tooth morphology	J:211773
	abnormal uterus morphology	J:211773
	enlarged heart	J:211773
	hydrometra	J:211773
	urinary bladder obstruction	J:211773
Erf^{tm1.1(KOMP)Mbp}/Erf^{tm1.1(KOMP)Mbp} C57BL/6N-Erf^{tm1.1(KOMP)Mbp}/MbpMmucd	embryonic lethality prior to tooth bud stage	J:211773
Erf^{tm1.1(KOMP)Mbp}/Erf^{tm1.1(KOMP)Mbp} C57BL/6N-Erf^{tm1.1(KOMP)Mbp}/Ucd	preweaning lethality, complete penetrance	J:211773
Erf^tm1Gmav/Erf^tm1Gmav involves: 129S4/SvJae * C57BL/6 * CBA	abnormal allantois morphology	J:123628
	abnormal chorion morphology	J:123628
	abnormal ectoplacental cone morphology	J:123628
	abnormal placenta morphology	J:123628
	abnormal spongiotrophoblast layer morphology	J:123628
	abnormal trophoblast giant cell morphology	J:123628
	abnormal vitelline vasculature morphology	J:123628
	absent placental labyrinth	J:123628
	absent umbilical cord	J:123628
	anemia	J:123628
	decreased embryo size	J:123628
	decreased embryo weight	J:123628
	decreased spongiotrophoblast size	J:123628
	edema	J:123628
	embryonic lethality during organogenesis, incomplete penetrance	J:123628
	failure of chorioallantoic fusion	J:123628
	forebrain hypoplasia	J:123628
	hindbrain hypoplasia	J:123628
	increased apoptosis	J:123628
	midbrain hypoplasia	J:123628
	open neural tube	J:123628
	pale yolk sac	J:123628
Erf^tm1Gmav/Erf^tm2Gmav involves: 129/Sv * C57BL/6 * CBA	delayed bone ossification	J:198059
	domed cranium	J:198059
	premature cranial suture closure	J:198059
Erf^tm2Gmav/Erf^tm2.1Gmav involves: 129/Sv * C57BL/6 * CBA	delayed bone ossification	J:198059
	domed cranium	J:198059
	premature cranial suture closure	J:198059
Erf^tm2Gmav/Erf^tm2Gmav involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	no abnormal phenotype detected	J:198059

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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