Tctn1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tctn1
tectonic family member 1
MGI:3603820

21 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tctn1^em1(IMPC)Mbp/Tctn1⁺ C57BL/6NCrl-Tctn1^em1(IMPC)Mbp/Mmucd	abnormal eye morphology	J:211773
	abnormal vitreous body morphology	J:211773
	anophthalmia	J:211773
	hemorrhage	J:211773
	microcephaly	J:211773
	microphthalmia	J:211773
	polydactyly	J:211773
	spina bifida	J:211773
	syndactyly	J:211773
Tctn1^em1(IMPC)Mbp/Tctn1^em1(IMPC)Mbp C57BL/6NCrl-Tctn1^em1(IMPC)Mbp/Mmucd	anophthalmia	J:211773
	hemorrhage	J:211773
	microcephaly	J:211773
	microphthalmia	J:211773
	polydactyly	J:211773
	preweaning lethality, complete penetrance	J:211773
	spina bifida	J:211773
	syndactyly	J:211773
Tctn1^{Gt(KST296)Byg}/Tctn1^{Gt(KST296)Byg} B6.129P2-Tctn1^{Gt(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
Tctn1^{Gt(KST296)Byg}/Tctn1^{Gt(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 04/16/2024 MGI 6.23