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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 |
|---|---|---|---|---|---|
| C1565887 | Newborn physiological jaundice | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C1565662 | Acute Kidney Insufficiency | HEXB | 3074 | hexosaminidase subunit beta | P07686 |
| C1565662 | Acute Kidney Insufficiency | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
| C1565662 | Acute Kidney Insufficiency | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C1565662 | Acute Kidney Insufficiency | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C1565662 | Acute Kidney Insufficiency | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
| C1565662 | Acute Kidney Insufficiency | GPNMB | 10457 | glycoprotein nmb | Q14956 |
| C1565662 | Acute Kidney Insufficiency | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C1565662 | Acute Kidney Insufficiency | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1565662 | Acute Kidney Insufficiency | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
| C1565489 | Renal Insufficiency | GCNT2 | 2651 | glucosaminyl (N-acetyl) transferase 2 (I blood group) | Q8N0V5 |
| C1565489 | Renal Insufficiency | A4GALT | 53947 | alpha 1,4-galactosyltransferase (P blood group) | Q9NPC4 |
| C1565489 | Renal Insufficiency | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1565489 | Renal Insufficiency | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1565489 | Renal Insufficiency | GLA | 2717 | galactosidase alpha | P06280 |
| C1565489 | Renal Insufficiency | ARSA | 410 | arylsulfatase A | P15289 |
| C1565489 | Renal Insufficiency | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C1565489 | Renal Insufficiency | COG1 | 9382 | component of oligomeric golgi complex 1 | Q8WTW3 |
| C1565489 | Renal Insufficiency | OGA | 10724 | O-GlcNAcase | O60502 |
| C1565489 | Renal Insufficiency | HPSE | 10855 | heparanase | Q9Y251 |
| C1565489 | Renal Insufficiency | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C1565489 | Renal Insufficiency | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
| C1565489 | Renal Insufficiency | AKR1B1 | 231 | aldo-keto reductase family 1 member B | P15121 |
| C1565489 | Renal Insufficiency | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C1565489 | Renal Insufficiency | HPRT1 | 3251 | hypoxanthine phosphoribosyltransferase 1 | P00492 |
