Slc39a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc39a1
solute carrier family 39 (zinc transporter), member 1
MGI:1353474

5 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc39a1^tm1.1Gka/Slc39a1^tm1.1Gka involves: 129X1/SvJ * C57BL/6 * FVB/N	abnormal craniofacial development	J:108627
	abnormal embryo development	J:108627
	abnormal limb development	J:108627
	embryonic growth retardation	J:108627
Slc39a1^tm1Gka/Slc39a1^tm1Gka involves: 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:108627

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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