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)
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