This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Alkaptonuria
Information about Alkaptonuria: 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 Alkaptonuria
Most recent studies have shown that Alkaptonuria shares some biological mechanisms with abnormal-degeneration, abnormal-degeneration, albinism, alcaptonuric-ochronosis, alcaptonuric-ochronosis, alkaptonuria, aortic-valve-stenosis, aortic-valve-stenosis, arthralgia, arthritis, arthritis, arthropathy, arthropathy, back-pain, calcinosis, calcinosis, degenerative-polyarthritis, degenerative-polyarthritis, hereditary-diseases, hereditary-diseases, homocystinuria, inborn-errors-of-metabolism, inborn-errors-of-metabolism, metabolic-diseases, metabolic-diseases, pain, pain, phenylketonurias, pigmentation-disorders, pigmentation-disorders, scleral-diseases, scleral-diseases, spinal-diseases, stenosis, stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Alkaptonuria, and have been seen in publications frequently: Aging, Aging, Amelogenesis, Amelogenesis, Antibody-dependent Cellular Cytotoxicity, Cell Growth, Conjugation, Conjugation, Dna Repair, Excretion, Excretion, Interleukin-2 Production, Locomotion, Ossification, Ossification, Osteoblast Differentiation, Osteoblast Differentiation, Pathogenesis, Pathogenesis, Peroxidase Reaction, Phagocytosis, Phagocytosis, Pigmentation, Pigmentation, Protein Folding, Protein Folding, Protein Oxidation, Protein Oxidation, Regeneration, Renal Tubular Secretion, Renal Tubular Secretion, Reverse Transcription, Reverse Transcription, Secretion, Secretion, Tissue Regeneration, Transport, Transport, Urea Cycle, Urea Cycle
Quite a number of genes have been found to play important roles in Alkaptonuria, such as AMD1, AMY2A, APCS, CAT, CAT, DCXR, DCXR, FAH, FAH, FANCA, FANCA, GSTZ1, GSTZ1, HGD, HGD, HHIP, HPD, HPD, MLYCD, NBN, POMC, PYCARD, PYCARD, QPCT, REG3A, REST, RNF130, RPL29, SH2D1A, ST13, STS, STS, 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.