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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 |
|---|---|---|---|
| 9896 | FIG4 | FIG4 phosphoinositide 5-phosphatase | |
| 10327 | AKR1A1 | aldo-keto reductase family 1 member A1 | |
| 10466 | COG5 | component of oligomeric golgi complex 5 | |
| 10559 | SLC35A1 | solute carrier family 35 member A1 | |
| 10585 | POMT1 | protein O-mannosyltransferase 1 | |
| 10891 | PPARGC1A | PPARG coactivator 1 alpha | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 | |
| 11141 | IL1RAPL1 | interleukin 1 receptor accessory protein like 1 | |
| 22933 | SIRT2 | sirtuin 2 | |
| 23483 | TGDS | TDP-glucose 4,6-dehydratase |
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 |
