About Help FAQ

Symbol
Name
ID

Ntrk1
neurotrophic tyrosine kinase, receptor, type 1
MGI:97383

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Functional motor deficit	Difficulty walking
Disease(s) Associated with NTRK1	Functional motor deficit	Difficulty walking
hereditary sensory neuropathy type 4

Mouse Phenotypes		increased muscle spindle number
Availability	Mouse Genotype	increased muscle spindle number
	Ntrk1^{tm2(Ntrk3)Apat}/Ntrk1^{tm2(Ntrk3)Apat}

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support.	last database update 02/23/2021 MGI 6.16