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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Tctn2tm1.1Reit/Tctn2tm1.1Reit
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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last database update
01/04/2022
MGI 6.17
The Jackson Laboratory