Disease Info Card

Amino Acid Metabolism, Inborn Errors

Information about Amino Acid Metabolism, Inborn Errors: 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 Amino Acid Metabolism, Inborn Errors

Most recent studies have shown that Amino Acid Metabolism, Inborn Errors shares some biological mechanisms with acidosis, aminoaciduria, cystinosis, cystinuria, fanconi-syndrome, hartnup-disease, homocystinuria, hyperglycinemia, inborn-errors-of-metabolism, kidney-diseases, maple-syrup-urine-disease, metabolic-diseases, nonketotic-hyperglycinemia, phenylketonurias, phosphate-diabetes, proteinuria-of-undiagnosed-cause, renal-aminoacidurias, rickets.

Among the many pathways, these few ones have gauged particular interests from scientists studying Amino Acid Metabolism, Inborn Errors, and have been seen in publications frequently: Amino Acid Transport, Cardiac Conduction, Carnitine Transport, Chromosome Localization, Conjugation, Excretion, Fatty Acid Oxidation, Glomerular Filtration, Intestinal Absorption, Localization, Muscle Atrophy, Myelination, Neutral Amino Acid Transport, Pathogenesis, Pigmentation, Reflex, Secretion, Transepithelial Transport, Transport, Urea Cycle

Quite a number of genes have been found to play important roles in Amino Acid Metabolism, Inborn Errors, such as ACADS, ALB, CAT, CBS, CSF2, DAO, GCDH, GLS2, HNF1A, HNF1B, LAMC2, MYOC, OAT, OCRL, PAH, PTH, SPP1. 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.

Amino Acid Metabolism, Inborn Errors Related Genes

click to see detail information for each gene

ACADS ALB CAT
CBS CSF2 DAO
GCDH GLS2 HNF1A
HNF1B LAMC2 MYOC
OAT OCRL PAH
PTH SPP1