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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
sickle cell anemia
Summary
- Synonym
-
- Hb SC disease
- Hb-S/Hb-C disease
- Hb-SS disease without crisis
- Hemoglobin S disease without crisis
- Sickle-cell/Hb-C disease without crisis
- drepanocytosis
- haemoglobin SC disease
- hemoglobin SC disease
- sickle cell anaemia
- Definition
- A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.
- Super Class
- autosomal recessive disease blood protein disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 54579 | UGT1A5 | UDP glucuronosyltransferase family 1 member A5 | |
| 54600 | UGT1A9 | UDP glucuronosyltransferase family 1 member A9 | |
| 54657 | UGT1A4 | UDP glucuronosyltransferase family 1 member A4 | |
| 54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 | |
| 54659 | UGT1A3 | UDP glucuronosyltransferase family 1 member A3 | |
| 56886 | UGGT1 | UDP-glucose glycoprotein glucosyltransferase 1 | |
| 79888 | LPCAT1 | lysophosphatidylcholine acyltransferase 1 | |
| 79966 | SCD5 | stearoyl-CoA desaturase 5 | |
| 114805 | GALNT13 | polypeptide N-acetylgalactosaminyltransferase 13 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P14555 | Phospholipase A2, membrane associated | |
| P16109 | P-selectin | |
| P16442 | Histo-blood group ABO system transferase | |
| P16581 | E-selectin | |
| P16662 | UDP-glucuronosyltransferase 2B7 | |
| P17405 | Sphingomyelin phosphodiesterase | |
| P17931 | Galectin-3 | |
| P19224 | UDP-glucuronosyltransferase 1-6 | |
| P19320 | Vascular cell adhesion protein 1 | |
| P19526 | Galactoside alpha-(1,2)-fucosyltransferase 1 |
