Entry |
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Symbol |
LCT
|
Name |
|
Pathway |
map04973 | Carbohydrate digestion and absorption |
|
Disease |
H00116 | Congenital lactase deficiency |
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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
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Other DBs |
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Genes |
» show all
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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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