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Symbol Name ID |
Slc39a13
solute carrier family 39 (metal ion transporter), member 13 MGI:1915677 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Camptodactyly of finger |
Short phalanx of finger |
Tapered finger |
Flat capital femoral epiphysis |
Broad femoral neck |
Short femoral neck |
Flared metaphysis |
Dislocated radial head |
Short metacarpal |
Joint contracture of the hand |
Joint hypermobility |
Flattened epiphysis |
Kyphoscoliosis |
Irregular vertebral endplates |
Platyspondyly |
Osteopenia |
| Disease(s) Associated with SLC39A13 | |||||||||||||||||
| Ehlers-Danlos syndrome spondylodysplastic type 3 |
| Mouse Phenotypes | abnormal osteoblast physiology |
abnormal jaw morphology |
abnormal alveolar process morphology |
abnormal tooth morphology |
abnormal incisor morphology |
abnormal molar root morphology |
brittle teeth |
malocclusion |
small mandible |
small maxilla |
abnormal long bone morphology |
abnormal long bone epiphyseal plate proliferative zone |
abnormal long bone hypertrophic chondrocyte zone |
abnormal long bone epiphysis morphology |
thickened long bone epiphysis |
abnormal long bone metaphysis morphology |
decreased length of long bones |
kyphosis |
abnormal bone structure |
decreased bone mineral density of femur |
decreased bone mineral density |
decreased compact bone thickness |
decreased bone trabecula number |
abnormal epiphyseal plate morphology |
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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 04/30/2024 MGI 6.23 |
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