Scnn1a Phenotype Annotations

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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)
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