Symbol Name ID

Slc39a13 solute carrier family 39 (metal ion transporter), member 13 MGI:1915677

2 phenotype image(s) for Slc39a13 alleles Showing image(s) 1 to 2

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Caption: Growth retardation, kyphosis, osteopenia, and abnormal cartilage development in Slc39a13tm1Thir/Slc39a13tm1Thir mice (details) Represented Alleles: Slc39a13tm1Thir, solute carrier family 39 (metal ion transporter), member 13; targeted mutation 1, Toshio Hirano Copyright: This image is from Fukada T, PLoS ONE 2008;3(11):e3642, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:143911

Caption: Abnormal teeth and craniofacial development in Slc39a13tm1Thir/Slc39a13tm1Thir mice (details) Represented Alleles: Slc39a13tm1Thir, solute carrier family 39 (metal ion transporter), member 13; targeted mutation 1, Toshio Hirano Copyright: This image is from Fukada T, PLoS ONE 2008;3(11):e3642, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:143911