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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 3/07/2006 |
Symbol | GGM |
Location | 22q12.3 |
Name | glucose-galactose malabsorption |
Other name(s) | monosaccharide malabsorption |
Corresponding gene | SLC5A1 |
Other symbol(s) | SGLT1 |
Main clinical features |
|
Genetic determination | autosomal recessive |
Function/system disorder | metabolism/membrane transport |
Type | disease |
Gene product |
Name | cotransporter 1, Na+/glucose, small intestine |
Remark(s) |