Slc43a2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc43a2
solute carrier family 43, member 2
MGI:2442746

19 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc43a2^{Gt(258C1)Cmhd}/Slc43a2^{Gt(258C1)Cmhd} involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	abnormal amino acid level	J:237439
	abnormal amniotic fluid composition	J:237439
	abnormal circulating amino acid level	J:237439
	abnormal circulating glucose level	J:237439
	abnormal intestinal absorption	J:237439
	abnormal liver physiology	J:237439
	abnormal placental transport	J:237439
	decreased circulating alanine level	J:237439
	decreased circulating histidine level	J:237439
	decreased circulating proline level	J:237439
	decreased circulating serine level	J:237439
	decreased fasting circulating glucose level	J:237439
	decreased fetal weight	J:237439
	fetal growth retardation	J:237439
	increased circulating carnitine level	J:237439
	increased fatty acids level	J:237439
	liver inflammation	J:237439
	postnatal lethality, complete penetrance	J:237439
	slow postnatal weight gain	J:237439

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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