Tctn2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tctn2
tectonic family member 2
MGI:1915228

12 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Tctn2^tm1.1Reit/Tctn2^tm1.1Reit involves: 129P2/OlaHsd * C57BL/6	abnormal embryonic neuroepithelium morphology	J:176174
	abnormal limb mesenchyme morphology	J:176174
	abnormal rostral-caudal axis patterning	J:176174
	absent embryonic cilia	J:176174
	absent floor plate	J:173396
	cleft palate	J:173396
	exencephaly	J:173396
	microphthalmia	J:173396
	open neural tube	J:173396
	preaxial polydactyly	J:173396
	right-sided stomach	J:173396
	ventricular septal defect	J:173396

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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