Slc52a3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc52a3
solute carrier protein family 52, member 3
MGI:1916948

29 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc52a3^tm1.1Said/Slc52a3^tm1.1Said Tg(Vil1-cre)997Gum/0 involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N * SJL	abnormal ocular surface morphology	J:278571
	abnormal pelvic girdle bone morphology	J:278571
	abnormal vitamin level	J:278571
	decreased body weight	J:278571
	decreased bone mineral density	J:278571
	decreased bone mineral density of femur	J:278571
	hunched posture	J:278571
	lethargy	J:278571
	postnatal growth retardation	J:278571
	postnatal lethality, incomplete penetrance	J:278571
	short femur	J:278571
	short tibia	J:278571
Slc52a3^{tm2a(KOMP)Wtsi}/Slc52a3⁺ B6JTyr;B6N-Slc52a3^{tm2a(KOMP)Wtsi}/Wtsi	abnormal vibrissa morphology	J:175295
	increased body weight	J:175295
Slc52a3^{tm2a(KOMP)Wtsi}/Slc52a3^{tm2a(KOMP)Wtsi} involves: C57BL/6N	abnormal lipid homeostasis	J:236029
	abnormal placental transport	J:236029
	abnormal vitamin homeostasis	J:236029
	abnormal vitamin level	J:236029
	decreased birth weight	J:236029
	decreased body weight	J:236029
	decreased fatty acid beta-oxidation	J:236029
	decreased fetal weight	J:236029
	decreased food intake	J:236029
	decreased placenta weight	J:236029
	glutaricadicuria	J:236029
	normal homeostasis/metabolism phenotype	J:236029
	hyperlipidemia	J:236029
	hypoglycemia	J:236029
	increased circulating carnitine level	J:236029
	neonatal lethality, incomplete penetrance	J:236029
	postnatal lethality, incomplete penetrance	J:236029
	premature death	J:236029

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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