Symbol Name ID |
Slc39a13
solute carrier family 39 (metal ion transporter), member 13 MGI:1915677 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Bifid uvula |
High palate |
Hypodontia |
Delayed eruption of teeth |
Dental malocclusion |
Depressed nasal bridge |
Downslanted palpebral fissures |
Disease(s) Associated with SLC39A13 | ||||||||
Ehlers-Danlos syndrome spondylodysplastic type 3 |
Mouse Phenotypes | abnormal jaw morphology |
abnormal alveolar process morphology |
abnormal tooth morphology |
abnormal incisor morphology |
abnormal molar root morphology |
brittle teeth |
malocclusion |
small mandible |
small maxilla |
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Availability | Mouse Genotype | |||||||||
Slc39a13tm1Thir/Slc39a13tm1Thir |
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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last database update 09/03/2024 MGI 6.24 |
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