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 Phenotypes | increased muscle spindle number |
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Availability | Mouse Genotype | |
Ntrk1tm2(Ntrk3)Apat/Ntrk1tm2(Ntrk3)Apat |
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 02/23/2021 MGI 6.16 |
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