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 |
---|---|---|---|---|---|
C0024530 | Malaria | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
C0024530 | Malaria | FUT9 | 10690 | fucosyltransferase 9 | Q9Y231 |
C0024530 | Malaria | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0024530 | Malaria | CHI3L1 | 1116 | chitinase 3 like 1 | P36222 |
C0024523 | Malabsorption Syndrome | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0024523 | Malabsorption Syndrome | CD55 | 1604 | CD55 molecule (Cromer blood group) | P08174 |
C0024523 | Malabsorption Syndrome | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
C0024523 | Malabsorption Syndrome | HSD3B7 | 80270 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Q9H2F3 |
C0024523 | Malabsorption Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
C0024523 | Malabsorption Syndrome | PNLIP | 5406 | pancreatic lipase | P16233 |
C0024523 | Malabsorption Syndrome | MMUT | 4594 | methylmalonyl-CoA mutase | P22033 |
C0024523 | Malabsorption Syndrome | TYMP | 1890 | thymidine phosphorylase | P19971 |
C0024523 | Malabsorption Syndrome | SI | 6476 | sucrase-isomaltase | P14410 |
C0024523 | Malabsorption Syndrome | ENPP1 | 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 | P22413 |
C0024523 | Malabsorption Syndrome | OCRL | 4952 | OCRL inositol polyphosphate-5-phosphatase | Q01968 |
C0024523 | Malabsorption Syndrome | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0024523 | Malabsorption Syndrome | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0024523 | Malabsorption Syndrome | MGLL | 11343 | monoglyceride lipase | Q99685 |
C0024523 | Malabsorption Syndrome | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
C0024523 | Malabsorption Syndrome | LCT | 3938 | lactase | P09848 |
C0024523 | Malabsorption Syndrome | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0024523 | Malabsorption Syndrome | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0024523 | Malabsorption Syndrome | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0024523 | Malabsorption Syndrome | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0024523 | Malabsorption Syndrome | AGA | 175 | aspartylglucosaminidase | P20933 |
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Last updated: August 19, 2024