Please wait while page loads....
Details of ALDOB gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| ALDOB | ALDB | P05062 | ALDOB_HUMAN | 229
| ENSG00000136872
| Fructose-bisphosphate aldolase B | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Hereditary fructose intolerance (HFI) [MIM:229600]: Autosomal recessive disease that results in an inability to metabolize fructose and related sugars. Complete exclusion of fructose results in dramatic recovery however, if not treated properly, HFI subjects suffer episodes of hypoglycemia, general ill condition, and risk of death the remainder of life. Note=The disease is caused by mutations affecting the gene represented in this entry. |
229600 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Aldob | Ald | aldo-1 | |
