Metazoan complexes |
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Emili & Marcotte labs |
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Details of SLC2A2 gene in Homo sapiens
IDs | |||||||||
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Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| SLC2A2 | GLUT2 | P11168 | GTR2_HUMAN | 6514 | ENSG00000163581 | Solute carrier family 2, facilitated glucose transporter member 2 | SPROT |
Disease | |||||||||
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Disease | OMIM id | ||||||||
Fanconi-Bickel syndrome (FBS) [MIM:227810]: Rare, well- defined clinical entity, inherited in an autosomal recessive mode and characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose. Note=The disease is caused by mutations affecting the gene represented in this entry. | 227810 |
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Slc2a2 | FBgn0261914 | fgt-1... | Sp-Rlp2 |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
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