About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Tctn1
tectonic family member 1
MGI:3603820
16 phenotypes from 2 alleles in 3 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Tctn1em1(IMPC)Mbp/Tctn1+
C57BL/6NCrl-Tctn1em1(IMPC)Mbp/Mmucd 		abnormal eye morphology J:211773
abnormal vitreous body morphology J:211773
hemorrhage J:211773
spina bifida J:211773
Tctn1em1(IMPC)Mbp/Tctn1em1(IMPC)Mbp
C57BL/6NCrl-Tctn1em1(IMPC)Mbp/Mmucd 		hemorrhage J:211773
preweaning lethality, complete penetrance J:211773
spina bifida J:211773
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
B6.129P2-Tctn1Gt(KST296)Byg 		absent floor plate J:103820
holoprosencephaly J:103820
lethality throughout fetal growth and development, complete penetrance J:103820
small embryonic telencephalon J:103820
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
involves: 129P2/OlaHsd 		abnormal embryonic neuroepithelium morphology J:176174
abnormal left-right axis patterning J:176174
abnormal rostral-caudal axis patterning J:176174
absent embryonic cilia J:176174
normal cellular phenotype J:176174
normal embryo phenotype J:176174
preaxial polydactyly J:176174
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 		The Jackson Laboratory