This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Facts about GDH/6PGL endoplasmic bifunctional protein.
Human | |
---|---|
Gene Name: | H6PD |
Uniprot: | O95479 |
Entrez: | 9563 |
Belongs to: |
---|
No superfamily |
6-phosphogluconolactonase; DKFZp686A01246; EC 1.1.1.49; EC 2.7.4.3; EC 3.1.1.31; G6PD, H form; G6PDH; GDH/6PGL endoplasmic bifunctional protein; GDHglucose 1- dehydrogenase; glucose dehydrogenase; glucose dehyrogenase; glucose-6-phosphate dehydrogenase, salivary; hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase); MGC87643
Mass (kDA):
88.893 kDA
Human | |
---|---|
Location: | 1p36.22 |
Sequence: | 1; NC_000001.11 (9234767..9271337) |
Present in most tissues examined, strongest in liver.
Endoplasmic reticulum lumen.
PMID: 10349511 by Mason P.J., et al. Human hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) encoded at 1p36: coding sequence and expression.
PMID: 12858176 by Draper N., et al. Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.