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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0022603 | Seborrheic keratosis | LGALS3 | 3958 | galectin 3 | P17931 |
C0022603 | Seborrheic keratosis | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0022603 | Seborrheic keratosis | NTHL1 | 4913 | nth like DNA glycosylase 1 | P78549 |
C0022603 | Seborrheic keratosis | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0022603 | Seborrheic keratosis | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0022603 | Seborrheic keratosis | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C1282916 | Secondary Raynaud's phenomenon | GAD1 | 2571 | glutamate decarboxylase 1 | Q99259 |
C1282916 | Secondary Raynaud's phenomenon | CNTN3 | 5067 | contactin 3 | Q9P232 |
C0155616 | Secondary hypertension | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C3665349 | Secondary hypothyroidism | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
C3665349 | Secondary hypothyroidism | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C1318533 | Secondary polycythemia | HPRT1 | 3251 | hypoxanthine phosphoribosyltransferase 1 | P00492 |
C1318533 | Secondary polycythemia | ACO1 | 48 | aconitase 1 | P21399 |
C1318533 | Secondary polycythemia | CD177 | 57126 | CD177 molecule | Q8N6Q3 |
C1384406 | Secretory meningioma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0036572 | Seizures | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0036572 | Seizures | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
C0036572 | Seizures | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
C0036572 | Seizures | PIGU | 128869 | phosphatidylinositol glycan anchor biosynthesis class U | Q9H490 |
C0036572 | Seizures | B3GLCT | 145173 | beta 3-glucosyltransferase | Q6Y288 |
C0036572 | Seizures | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
C0036572 | Seizures | EXT1 | 2131 | exostosin glycosyltransferase 1 | Q16394 |
C0036572 | Seizures | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
C0036572 | Seizures | FKTN | 2218 | fukutin | O75072 |
C0036572 | Seizures | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
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Last updated: August 19, 2024