Scnn1a Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Scnn1a
sodium channel, nonvoltage-gated 1 alpha
MGI:101782

8 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Scnn1a^tm1.1Hum/Scnn1a^tm1.1Hum involves: 129	no abnormal phenotype detected	J:75110
Scnn1a^tm1.1Hum/Scnn1a^tm1.1Hum Tg(Hoxb7-cre)13Amc/0 involves: 129/Sv * C57BL/6	abnormal renal transport	J:161474
Scnn1a^tm1.2Hum/Scnn1a^tm1.2Hum involves: 129	preweaning lethality, complete penetrance	J:75110
Scnn1a^tm1Hum/Scnn1a^tm1Hum involves: 129	no abnormal phenotype detected	J:75110
Scnn1a^tm1Rss/Scnn1a^tm1Rss involves: 129P2/OlaHsd * C57BL/6J	abnormal eating behavior	J:31762
	cyanosis	J:31762
	decreased locomotor activity	J:31762
	neonatal lethality, complete penetrance	J:31762
	respiratory distress	J:31762

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 12/17/2024 MGI 6.24