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Symbol Name ID |
Ntrk1
neurotrophic tyrosine kinase, receptor, type 1 MGI:97383 |
| Darker colors indicate more annotations |
| Human Phenotypes | Functional motor deficit |
Difficulty walking |
| Disease(s) Associated with NTRK1 | ||
| hereditary sensory neuropathy type 4 |
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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