Symbol Name ID |
Th
tyrosine hydroxylase MGI:98735 |
Darker colors indicate more annotations |
Human Phenotypes | Diplopia |
Color vision defect |
Disease(s) Associated with TH | ||
Parkinson's disease |
Mouse Phenotypes | abnormal eye physiology |
abnormal eye electrophysiology |
abnormal vision |
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Availability | Mouse Genotype | |||
Thtm4.1Rpa/Thtm4.1Rpa Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (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 03/19/2024 MGI 6.23 |
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