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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Tctn3em1(IMPC)J/Tctn3+
C57BL/6NJ-Tctn3em1(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
Tctn3em1(IMPC)J/Tctn3em1(IMPC)J
C57BL/6NJ-Tctn3em1(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
Tctn3tm1.2Blnw/Tctn3tm1.2Blnw
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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory