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Symbol Name ID |
Tnfsf11
tumor necrosis factor (ligand) superfamily, member 11 MGI:1100089 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Nystagmus |
Blindness |
| Disease(s) Associated with TNFSF11 | |||
| autosomal recessive osteopetrosis 2 |
| Mouse Phenotypes | optic canal stenosis |
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| Availability | Mouse Genotype | |
| Tnfsf11tm1Ywc/Tnfsf11tm1Ywc | ||
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 04/09/2024 MGI 6.23 |
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