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 |
---|---|---|---|---|---|
C0524620 | Metabolic Syndrome X | LIPC | 3990 | lipase C, hepatic type | P11150 |
C0524620 | Metabolic Syndrome X | LGALS3 | 3958 | galectin 3 | P17931 |
C0524620 | Metabolic Syndrome X | LPL | 4023 | lipoprotein lipase | P06858 |
C0524620 | Metabolic Syndrome X | STS | 412 | steroid sulfatase | P08842 |
C0524620 | Metabolic Syndrome X | LTA4H | 4048 | leukotriene A4 hydrolase | P09960 |
C0524620 | Metabolic Syndrome X | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
C0524620 | Metabolic Syndrome X | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C0524620 | Metabolic Syndrome X | CNTN3 | 5067 | contactin 3 | Q9P232 |
C0524620 | Metabolic Syndrome X | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0524620 | Metabolic Syndrome X | PLCG1 | 5335 | phospholipase C gamma 1 | P19174 |
C0524620 | Metabolic Syndrome X | PLA2G2A | 5320 | phospholipase A2 group IIA | P14555 |
C0524620 | Metabolic Syndrome X | PLD2 | 5338 | phospholipase D2 | O14939 |
C0524620 | Metabolic Syndrome X | PNPLA2 | 57104 | patatin like phospholipase domain containing 2 | Q96AD5 |
C0524620 | Metabolic Syndrome X | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
C0524620 | Metabolic Syndrome X | SCD | 6319 | stearoyl-CoA desaturase | O00767 |
C0524620 | Metabolic Syndrome X | SELE | 6401 | selectin E | P16581 |
C0524620 | Metabolic Syndrome X | SELP | 6403 | selectin P | P16109 |
C0524620 | Metabolic Syndrome X | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
C0524620 | Metabolic Syndrome X | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0524620 | Metabolic Syndrome X | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0524620 | Metabolic Syndrome X | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0524620 | Metabolic Syndrome X | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0524620 | Metabolic Syndrome X | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C0524620 | Metabolic Syndrome X | UMOD | 7369 | uromodulin | P07911 |
C0524620 | Metabolic Syndrome X | PTGES2 | 80142 | prostaglandin E synthase 2 | Q9H7Z7 |
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Last updated: August 19, 2024