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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
placental insufficiency
Summary
- Definition
- A placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy.
- Super Class
- placenta disease
External Links
- Disease Ontology
- DOID:3891
- Mondo Disease Ontology
- MeSH
- UMLS
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1727 | CYB5R3 | cytochrome b5 reductase 3 | |
| 1737 | DLAT | dihydrolipoamide S-acetyltransferase | |
| 1836 | SLC26A2 | solute carrier family 26 member 2 | |
| 2182 | ACSL4 | acyl-CoA synthetase long chain family member 4 | |
| 2218 | FKTN | fukutin | |
| 2220 | FCN2 | ficolin 2 | |
| 2530 | FUT8 | fucosyltransferase 8 | |
| 2538 | G6PC1 | glucose-6-phosphatase catalytic subunit 1 | |
| 2581 | GALC | galactosylceramidase | |
| 2584 | GALK1 | galactokinase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q12860 | Contactin-1 | |
| Q12918 | Killer cell lectin-like receptor subfamily B member 1 | |
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q13563 | Polycystin-2 | |
| Q15392 | Delta(24)-sterol reductase | |
| Q15485 | Ficolin-2 | |
| Q16831 | Uridine phosphorylase 1 | |
| Q16836 | Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial | |
| Q5H8A4 | GPI ethanolamine phosphate transferase 2 | |
| Q6NSJ0 | Myogenesis-regulating glycosidase |
