Variegate Porphyria

Overview of Variegate Porphyria

Most recent studies have shown that Variegate Porphyria shares some biological mechanisms with abdominal-pain, acute-intermittent-porphyria, acute-interstitial-pneumonia, bulla, dermatologic-disorders, disorders-of-porphyrin-metabolism, erythropoietic-protoporphyria, hereditary-coproporphyria, hypertensive-disease, liver-diseases, metabolic-diseases, pain, photosensitivity-disorders, porphobilinogen-synthase-deficiency, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic.

Among the many pathways, these few ones have gauged particular interests from scientists studying Variegate Porphyria, and have been seen in publications frequently: Anion Transport, Diuresis, Excretion, Hormone Secretion, Immune Response, Keratinization, Localization, Pathogenesis, Photoprotection, Pigmentation, Reflex, Secretion, Translation, Transport, Vasoconstriction

Quite a number of genes have been found to play important roles in Variegate Porphyria, such as AIP, ALAD, AMBP, AURKAIP1, AVP, BRCA2, CAT, CPOX, EPO, EPX, FANCD2, FECH, HCRT, HFE, HMBS, HRC, PPOX, PSEN1, PTPN6, 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.

Variegate Porphyria Related Genes

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Pathways Related to Variegate Porphyria

This information is being compiled and will come in a future update

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