Disease Info Card

Tyrosinemias

Information about Tyrosinemias: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Tyrosinemias

Most recent studies have shown that Tyrosinemias shares some biological mechanisms with carcinoma, galactosemias, hepatitis, hepatolenticular-degeneration, hereditary-diseases, inborn-errors-of-metabolism, liver-carcinoma, liver-cirrhosis, liver-diseases, liver-failure, liver-neoplasms, malignant-neoplasms, maple-syrup-urine-disease, metabolic-diseases, palmoplantar-keratosis, phenylketonurias, rickets, tyrosine-transaminase-deficiency-disease, tyrosinemia-type-i.

Among the many pathways, these few ones have gauged particular interests from scientists studying Tyrosinemias, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Proliferation, Coagulation, Dna Methylation, Excretion, Fatty Acid Oxidation, Glomerular Filtration, Gluconeogenesis, Glycosylation, Liver Regeneration, Localization, Methylation, Pathogenesis, Regeneration, Reverse Transcription, Secretion, Translation, Transport, Urea Cycle

Quite a number of genes have been found to play important roles in Tyrosinemias, such as AFP, ALAD, ATAT1, F2, FAH, FANCA, GSTZ1, HGD, HPD, LRP2, MCF2L, PAH, QPCT, SLC25A13, TAT, TRIM26, TYR. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Tyrosinemias Related Genes

click to see detail information for each gene

AFP ALAD ATAT1
F2 FAH FANCA
GSTZ1 HGD HPD
LRP2 MCF2L PAH
QPCT SLC25A13 TAT
TRIM26 TYR