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Symbol
Name
ID

Ntrk2
neurotrophic tyrosine kinase, receptor, type 2
MGI:97384

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Secondary microcephaly
Disease(s) Associated with NTRK2	Secondary microcephaly
developmental and epileptic encephalopathy 58

Mouse Phenotypes		decreased width of hypertrophic chondrocyte zone	decreased long bone epiphyseal plate size	abnormal rib morphology	kyphosis
Availability	Mouse Genotype	decreased width of hypertrophic chondrocyte zone	decreased long bone epiphyseal plate size	abnormal rib morphology	kyphosis
	Ntrk2^{tm1b(EUCOMM)Wtsi}/Ntrk2⁺
	Ntrk2^tm2Lfp/Ntrk2^tm2Lfp Tg(Col2a1-cre)1Bhr/0 (conditional)

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)
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