Slc5a3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc5a3
solute carrier family 5 (inositol transporters), member 3
MGI:1858226

20 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc5a3^tm1Gtb/Slc5a3⁺ involves: 129X1/SvJ	abnormal amniotic fluid composition	J:83591
Slc5a3^tm1Gtb/Slc5a3⁺ involves: 129X1/SvJ	abnormal homeostasis	J:83591
Slc5a3^tm1Gtb/Slc5a3^tm1Gtb involves: 129X1/SvJ	abnormal amniotic fluid composition	J:83591
	abnormal homeostasis	J:83591
	abnormal nervous system electrophysiology	J:83591
	apnea	J:83591
	cyanosis	J:83591
	hypoventilation	J:83591
	neonatal lethality, complete penetrance	J:83591
	normal nervous system phenotype	J:83591
	respiratory distress	J:83591
	normal respiratory system phenotype	J:83591
Slc5a3^tm1Skc/Slc5a3^tm1Skc involves: 129S7/SvEvBrd	abnormal facial nerve morphology	J:102665
	abnormal nerve conduction	J:102665
	abnormal nervous system morphology	J:102665
	abnormal phrenic nerve morphology	J:102665
	abnormal vagus nerve morphology	J:102665
	absent phrenic nerve	J:102665
	atelectasis	J:102665
	cyanosis	J:102665
	decreased body size	J:102665
	neonatal lethality, incomplete penetrance	J:102665
	respiratory failure	J:102665

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 11/12/2024 MGI 6.24