Results for "homogentisate metabolic process": 4 genes

Name

HGD Gene

homogentisate 1,2-dioxygenase

This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]

AOMS1 Gene

Abdominal obesity-metabolic syndrome QTL1

AOMS2 Gene

abdominal obesity-metabolic syndrome QTL2

ASMER1 Gene

adipocyte associated metabolic related lncRNA 1