Symbol Name ID |
Ntrk2
neurotrophic tyrosine kinase, receptor, type 2 MGI:97384 |
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 |
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Availability | Mouse Genotype | ||||||||||
Ntrk2tm1Lfr/Ntrk2tm1Lfr | |||||||||||
Ntrk2tm1Rohr/Ntrk2tm1Rohr | |||||||||||
Ntrk2tm1Lfr/Ntrk2+ | |||||||||||
Ntrk2tm2Lfr/Ntrk2tm2Lfr Tg(Six3-cre)69Frty/? Tg(Thy1-YFP)HJrs/? (conditional) |
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 08/02/2024 MGI 6.24 |
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