Slc23a2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc23a2
solute carrier family 23 (nucleobase transporters), member 2
MGI:1859682

12 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc23a2^tm1Nbm/Slc23a2^tm1Nbm 129S6/SvEvTac-Slc23a2^tm1Nbm	abnormal adrenal gland secretion	J:85988
	abnormal adrenaline level	J:85988
	abnormal adrenergic chromaffin cell morphology	J:85988
	abnormal adrenocortical cell morphology	J:85988
	abnormal dopamine level	J:85988
	abnormal gland physiology	J:76194
	abnormal lung development	J:76194
	abnormal vitamin C level	J:76194
	decreased circulating corticosterone level	J:85988
	intracranial hemorrhage	J:76194
	neonatal lethality, complete penetrance	J:76194
	respiratory failure	J:76194

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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