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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 |
|---|---|---|---|---|---|
| C1565489 | Renal Insufficiency | MSLN | 10232 | mesothelin | Q13421 |
| C1565489 | Renal Insufficiency | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C1565489 | Renal Insufficiency | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1565489 | Renal Insufficiency | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C1565489 | Renal Insufficiency | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C1565489 | Renal Insufficiency | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C1565489 | Renal Insufficiency | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C1565489 | Renal Insufficiency | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C1565489 | Renal Insufficiency | HAGH | 3029 | hydroxyacylglutathione hydrolase | Q16775 |
| C1565489 | Renal Insufficiency | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
| C1565489 | Renal Insufficiency | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
| C1565489 | Renal Insufficiency | ME1 | 4199 | malic enzyme 1 | P48163 |
| C1565489 | Renal Insufficiency | OCRL | 4952 | OCRL inositol polyphosphate-5-phosphatase | Q01968 |
| C1565489 | Renal Insufficiency | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C1565489 | Renal Insufficiency | PKD1 | 5310 | polycystin 1, transient receptor potential channel interacting | P98161 |
| C1565489 | Renal Insufficiency | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
| C1565489 | Renal Insufficiency | MASP1 | 5648 | mannan binding lectin serine peptidase 1 | P48740 |
| C1565489 | Renal Insufficiency | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
| C1565489 | Renal Insufficiency | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C1563719 | Kallmann Syndrome 1 | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C1563705 | Nephrogenic Diabetes Insipidus, Type I | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1563705 | Nephrogenic Diabetes Insipidus, Type I | L1CAM | 3897 | L1 cell adhesion molecule | P32004 |
| C1563705 | Nephrogenic Diabetes Insipidus, Type I | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
| C1562894 | Thiel-Behnke corneal dystrophy | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
| C1562113 | Fleck corneal dystrophy | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
