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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1257931 | Mammary Neoplasms, Human | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C1257931 | Mammary Neoplasms, Human | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1257931 | Mammary Neoplasms, Human | CAT | 847 | catalase | P04040 |
| C1257931 | Mammary Neoplasms, Human | CD74 | 972 | CD74 molecule | P04233 |
| C1257931 | Mammary Neoplasms, Human | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C1257931 | Mammary Neoplasms, Human | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C1257931 | Mammary Neoplasms, Human | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
| C1257931 | Mammary Neoplasms, Human | GPNMB | 10457 | glycoprotein nmb | Q14956 |
| C1257931 | Mammary Neoplasms, Human | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C1257931 | Mammary Neoplasms, Human | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
| C1257931 | Mammary Neoplasms, Human | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C1257931 | Mammary Neoplasms, Human | FASN | 2194 | fatty acid synthase | P49327 |
| C1257931 | Mammary Neoplasms, Human | GPX2 | 2877 | glutathione peroxidase 2 | P18283 |
| C1257931 | Mammary Neoplasms, Human | HADHB | 3032 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | P55084 |
| C1257931 | Mammary Neoplasms, Human | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C1257931 | Mammary Neoplasms, Human | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C1257931 | Mammary Neoplasms, Human | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C1257958 | Glucose Metabolism Disorders | HK1 | 3098 | hexokinase 1 | P19367 |
| C1257958 | Glucose Metabolism Disorders | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C1257958 | Glucose Metabolism Disorders | G6PC | 2538 | glucose-6-phosphatase catalytic subunit | P35575 |
| C1257958 | Glucose Metabolism Disorders | GCK | 2645 | glucokinase | P35557 |
| C1257958 | Glucose Metabolism Disorders | DHCR24 | 1718 | 24-dehydrocholesterol reductase | Q15392 |
| C1257958 | Glucose Metabolism Disorders | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
| C1257960 | Mannosidase Deficiency Diseases | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C1257965 | Compensatory Hyperinsulinemia | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
