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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 ▼ |
|---|---|---|---|---|---|
| C0006012 | Borderline Personality Disorder | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0038379 | Strabismus | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0019693 | HIV Infections | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0085636 | Photophobia | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0028077 | Nyctalopia | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0015397 | Disorder of eye | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0009398 | Color vision defect | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C3489532 | Cone-Rod Dystrophy 2 | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0004936 | Mental disorders | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0004238 | Atrial Fibrillation | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0028738 | Nystagmus | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C1864849 | RETINAL CONE DYSTROPHY 4 | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C0003850 | Arteriosclerosis | CACNA2D4 | 93589 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Q7Z3S7 |
| C1140680 | Malignant neoplasm of ovary | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C1306459 | Primary malignant neoplasm | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0019158 | Hepatitis | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0006826 | Malignant Neoplasms | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0025286 | Meningioma | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0007847 | Malignant tumor of cervix | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0001973 | Alcoholic Intoxication, Chronic | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0019159 | Hepatitis A | TIPARP | 25976 | TCDD inducible poly(ADP-ribose) polymerase | Q7Z3E1 |
| C0919267 | ovarian neoplasm | PRSS41 | 360226 | serine protease 41 | Q7RTY9 |
| C1846896 | Deafness, Autosomal Recessive 22 | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0268237 | Cytochrome-c Oxidase Deficiency | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1846647 | DEAFNESS, AUTOSOMAL RECESSIVE (disorder) | OTOA | 146183 | otoancorin | Q7RTW8 |
