Tctn3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tctn3
tectonic family member 3
MGI:1914840

17 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tctn3^em1(IMPC)J/Tctn3⁺ C57BL/6NJ-Tctn3^em1(IMPC)J/Mmjax	abnormal cholesterol homeostasis	J:211773
	abnormal lens morphology	J:211773
	decreased circulating calcium level	J:211773
	decreased circulating total protein level	J:211773
Tctn3^em1(IMPC)J/Tctn3^em1(IMPC)J C57BL/6NJ-Tctn3^em1(IMPC)J/Mmjax	abnormal body wall morphology	J:211773
	abnormal embryo size	J:211773
	anophthalmia	J:211773
	polydactyly	J:211773
	preweaning lethality, complete penetrance	J:211773
Tctn3^tm1.2Blnw/Tctn3^tm1.2Blnw involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SW	abnormal cilium morphology	J:249241
	abnormal direction of heart looping	J:249241
	absent floor plate	J:249241
	decreased embryonic neuroepithelium primary cilium number	J:249241
	edema	J:249241
	holoprosencephaly	J:249241
	lethality throughout fetal growth and development, incomplete penetrance	J:249241
	neonatal lethality, complete penetrance	J:249241
	polydactyly	J:249241

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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