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Symbol
Name
ID

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

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Nystagmus	Visual impairment
Disease(s) Associated with NTRK2
developmental and epileptic encephalopathy 58

Mouse Phenotypes		abnormal pupillary reflex	decreased amacrine cell number	decreased retina ganglion cell number	abnormal retina ganglion cell morphology	abnormal retina rod cell outer segment morphology	abnormal optic nerve morphology	abnormal retina development	abnormal eyelid morphology	abnormal rod electrophysiology	abnormal vision
Availability	Mouse Genotype	abnormal pupillary reflex	decreased amacrine cell number	decreased retina ganglion cell number	abnormal retina ganglion cell morphology	abnormal retina rod cell outer segment morphology	abnormal optic nerve morphology	abnormal retina development	abnormal eyelid morphology	abnormal rod electrophysiology	abnormal vision
	Ntrk2^tm1Lfr/Ntrk2^tm1Lfr
	Ntrk2^tm1Rohr/Ntrk2^tm1Rohr
	Ntrk2^tm1Lfr/Ntrk2⁺
	Ntrk2^tm2Lfr/Ntrk2^tm2Lfr Tg(Six3-cre)69Frty/? Tg(Thy1-YFP)HJrs/? (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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