Symbol Name ID |
Slc52a3
solute carrier protein family 52, member 3 MGI:1916948 |
Darker colors indicate more annotations |
Human Phenotypes | Ankle clonus |
Kyphosis |
Scoliosis |
Disease(s) Associated with SLC52A3 | |||
Brown-Vialetto-Van Laere syndrome 1 |
Mouse Phenotypes | short femur |
short tibia |
abnormal pelvic girdle bone morphology |
decreased bone mineral density of femur |
decreased bone mineral density |
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Availability | Mouse Genotype | |||||
Slc52a3tm1.1Said/Slc52a3tm1.1Said Tg(Vil1-cre)997Gum/0 (conditional) |
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 04/16/2024 MGI 6.23 |
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