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Disease Info Card
Hepatoerythropoietic Porphyria
Information about Hepatoerythropoietic Porphyria: 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 Hepatoerythropoietic Porphyria
Most recent studies have shown that Hepatoerythropoietic Porphyria shares some biological mechanisms with acute-intermittent-porphyria, anemia, de-novo-mutation, dermatologic-disorders, disorders-of-porphyrin-metabolism, erythropoietic-protoporphyria, familial-porphyria-cutanea-tarda, hereditary-diseases, hypertrichosis, liver-cirrhosis, liver-diseases, liver-failure, pain, photosensitivity-disorders, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic, variegate-porphyria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hepatoerythropoietic Porphyria, and have been seen in publications frequently: Aging, Complement Activation, Cornification, Dna Repair, Drug Resistance, Excretion, Hypersensitivity, Lactation, Localization, Mast Cell Degranulation, Methylation, Pathogenesis, Photoprotection, Pigmentation, Response To Stress, Rna Splicing, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Hepatoerythropoietic Porphyria, such as ABCG2, AIP, ALAD, AMBP, AURKAIP1, CPOX, EPHB6, EPX, FECH, HCRT, HMBS, HPSE, HRC, PPA1, PPOX, PPY, QPCT, TNFSF14, UROD. 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.