Slc39a2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc39a2
solute carrier family 39 (zinc transporter), member 2
MGI:2684326

7 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc39a2^tm1Gka/Slc39a2^tm1Gka involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	abnormal calcium ion homeostasis	J:121899
	abnormal craniofacial morphology	J:121899
	abnormal limb development	J:121899
	abnormal liver iron level	J:121899
	embryonic growth retardation	J:121899
	ruffled hair	J:121899
	scaly skin	J:121899

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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