Slc23a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc23a1
solute carrier family 23 (nucleobase transporters), member 1
MGI:1341903

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc23a1^tm1Mlev/Slc23a1⁺ involves: 129S6/SvEvTac * C57BL/6J	abnormal blood homeostasis	J:159697
	abnormal urine homeostasis	J:159697
	abnormal vitamin absorption	J:159697
	abnormal vitamin homeostasis	J:159697
	lethargy	J:159697
	postnatal lethality	J:159697
Slc23a1^tm1Mlev/Slc23a1^tm1Mlev involves: 129S6/SvEvTac * C57BL/6J	abnormal renal filtration rate	J:159697
	abnormal urine homeostasis	J:159697
	abnormal vitamin absorption	J:159697
	abnormal vitamin C level	J:159697
	absent gastric milk in neonates	J:159697
	aminoaciduria	J:159697
	lethargy	J:159697
	maternal effect	J:159697
	perinatal lethality, incomplete penetrance	J:159697
	postnatal lethality, complete penetrance	J:159697

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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