Species: Hu, Mu
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
Species: Hu, Mu, Rt
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
Species: Hu
Applications: ELISA, ICC/IF, IP, S-ELISA
Host: Mouse Monoclonal
Species: Hu
Applications: WB
Species: Hu
Applications: WB, ELISA, PA, AP
Species: Hu
Applications: WB, ELISA, PA, PAGE, AP
Species: Hu
Applications: WB, ELISA, PA, PAGE, AP
Description
Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26.
Bioinformatics
Entrez |
Human |
Uniprot |
Human Human Human Human |
Product By Gene ID |
3081 |
Alternate Names |
- AKU
- Homogentisicase
- EC 1.13.11.5
- homogentisicase
- Homogentisic acid oxidase
- homogentisate oxidase
- Homogentisate oxygenase
- HGOFLJ94126
- homogentisate 1,2-dioxygenase (homogentisate oxidase)
- homogentisate 1,2-dioxygenase
|
Bioinformatics Tool for HGD
Discover related pathways, diseases and genes to HGD. Need help? Read the
Bioinformatics Tool Guide for instructions on using this tool.