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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 |
|---|---|---|---|---|---|
| C0241910 | Autoimmune Chronic Hepatitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0241910 | Autoimmune Chronic Hepatitis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0241910 | Autoimmune Chronic Hepatitis | INPP5D | 3635 | inositol polyphosphate-5-phosphatase D | Q92835 |
| C0241910 | Autoimmune Chronic Hepatitis | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
| C0241910 | Autoimmune Chronic Hepatitis | UMOD | 7369 | uromodulin | P07911 |
| C0241910 | Autoimmune Chronic Hepatitis | CD1D | 912 | CD1d molecule | P15813 |
| C0241910 | Autoimmune Chronic Hepatitis | CD74 | 972 | CD74 molecule | P04233 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0241910 | Autoimmune Chronic Hepatitis | PDIA3 | 2923 | protein disulfide isomerase family A member 3 | P30101 |
| C0004352 | Autistic Disorder | EXT1 | 2131 | exostosin glycosyltransferase 1 | Q16394 |
| C0004352 | Autistic Disorder | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0004352 | Autistic Disorder | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0004352 | Autistic Disorder | ST8SIA2 | 8128 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 | Q92186 |
| C0004352 | Autistic Disorder | GALNT14 | 79623 | polypeptide N-acetylgalactosaminyltransferase 14 | Q96FL9 |
| C0004352 | Autistic Disorder | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C0004352 | Autistic Disorder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0004352 | Autistic Disorder | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0004352 | Autistic Disorder | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0004352 | Autistic Disorder | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C0004352 | Autistic Disorder | SRD5A3 | 79644 | steroid 5 alpha-reductase 3 | Q9H8P0 |
| C0004352 | Autistic Disorder | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
