| Entry |
|
| Symbol |
LCT
|
| Name |
|
| Pathway |
| map04973 | Carbohydrate digestion and absorption |
|
| Reaction |
| R01678 | lactose galactohydrolase |
|
| Disease |
| H00116 | Congenital lactase deficiency |
|
| Brite |
KEGG Orthology (KO) [BR:ko00001]
09100 Metabolism
09101 Carbohydrate metabolism
00052 Galactose metabolism
K01229 LCT; lactase-phlorizin hydrolase
09150 Organismal Systems
09154 Digestive system
04973 Carbohydrate digestion and absorption
K01229 LCT; lactase-phlorizin hydrolase
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03110 Chaperones and folding catalysts
K01229 LCT; lactase-phlorizin hydrolase
Enzymes [BR:ko01000]
3. Hydrolases
3.2 Glycosylases
3.2.1 Glycosidases, i.e. enzymes that hydrolyse O- and S-glycosyl compounds
3.2.1.62 glycosylceramidase
K01229 LCT; lactase-phlorizin hydrolase
3.2.1.108 lactase
K01229 LCT; lactase-phlorizin hydrolase
Chaperones and folding catalysts [BR:ko03110]
Intramolecular chaperones
Others
K01229 LCT; lactase-phlorizin hydrolase
|
| Other DBs |
|
| Genes |
» show all
|
| Reference |
|
| Authors |
Ingram CJ, Mulcare CA, Itan Y, Thomas MG, Swallow DM |
| Title |
Lactose digestion and the evolutionary genetics of lactase persistence. |
| Journal |
|
| Reference |
|
| Authors |
Boll W, Wagner P, Mantei N |
| Title |
Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase. |
| Journal |
Am J Hum Genet 48:889-902 (1991) |
| Sequence |
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| LinkDB |
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