Tctn2 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/10/2024 MGI 6.24