HGD 抗体
(Homogentisate 1,2-Dioxygenase (HGD))
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].
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Latest Publications for our HGD 抗体
: "Adaptation of phenylalanine and tyrosine catabolic pathway to hibernation in bats." in: PLoS ONE, Vol. 8, Issue 4, pp. e62039, (2013) (PubMed).Aliases for HGD 抗体
homogentisate 1,2-dioxygenase (hgo) 抗体homogentisate 1,2-dioxygenase (HGD) 抗体
homogentisate 1,2-dioxygenase (hmgA) 抗体
homogentisate 1,2-dioxygenase (Shewana3_2481) 抗体
homogentisate 1,2-dioxygenase (hgd) 抗体
homogentisate 1,2-dioxygenase (BC1002_0545) 抗体
homogentisate 1,2-dioxygenase (BC1003_0502) 抗体
homogentisate 1,2-dioxygenase (BC1001_0489) 抗体
Homogentisate 1,2-dioxygenase (Sinme_2995) 抗体
Homogentisate 1,2-dioxygenase (Sphch_0441) 抗体
homogentisate 1, 2-dioxygenase (Hgd) 抗体
homogentisate 1,2-dioxygenase L homeolog (hgd.L) 抗体
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