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Symbol Name ID |
Nfkb1
nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 MGI:97312 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spastic paraparesis |
Myelopathy |
Abnormal pyramidal sign |
| Disease(s) Associated with NFKB1 | |||
| HTLV-1-associated myelopathy/tropical spastic paraparesis |
| Mouse Phenotypes | abnormal cochlear inner hair cell morphology |
decreased cochlear nerve compound action potential |
cochlear ganglion degeneration |
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| Availability | Mouse Genotype | |||
| Nfkb1tm1Bal/Nfkb1tm1Bal | ||||
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 04/07/2026 MGI 6.24 |
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