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Details of GPD1 gene in Homo sapiens
IDs | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
|
| GPD1 | --- | P21695 | GPDA_HUMAN | 2819 | ENSG00000167588 | Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic | SPROT | |
Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | OMIM id | ||||||||
| Hypertriglyceridemia, transient infantile (HTGTI) [MIM:614480]: An autosomal recessive disorder characterized by onset of moderate to severe transient hypertriglyceridemia in infancy that normalizes with age. The hypertriglyceridemia is associated with hepatomegaly, moderately elevated transaminases, persistent fatty liver, and the development of hepatic fibrosis. Note=The disease is caused by mutations affecting the gene represented in this entry. | 614480 | ||||||||
Orthologs in other species | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
| Gpd1 | Gpdh | gpdh-2 | Sp-Gpd1 | ||||||
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
|---|---|---|---|---|---|---|---|---|---|
| GPD1 | GNPNAT1 | 0.524528142 | GPD1 | GNPNAT1 | cpx124 | no | no | no | Novel |
| ACO2 | GPD1 | 0.791423488 | ACO2 | GPD1 | cpx124 | no | yes | no | Known |