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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 |
|---|---|---|---|---|---|
| C0241961 | Angiomyolipoma of kidney | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0162323 | Polyarthritis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0040128 | Thyroid Diseases | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0040149 | Subacute thyroiditis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0278846 | Thymoma malignant invasive | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0393593 | Dystonia Disorders | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0019158 | Hepatitis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C1333969 | Liver Leiomyosarcoma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C2047886 | (Idiopathic) normal pressure hydrocephalus | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0015230 | Exanthema | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0949541 | Hurthle Cell Tumor | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0334618 | Malignant granular cell tumor | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0948008 | Ischemic stroke | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0334276 | Adenocarcinoma in Situ | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0162429 | Malnutrition | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0206732 | Epithelioid hemangioendothelioma | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0033975 | Psychotic Disorders | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C1298681 | Oxalosis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0007134 | Renal Cell Carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0600139 | Prostate carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0027651 | Neoplasms | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0376358 | Malignant neoplasm of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1858328 | Bile acid synthesis defect, congenital, 4 | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1704272 | Benign Prostatic Hyperplasia | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1306459 | Primary malignant neoplasm | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
