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 ▲ |
---|---|---|---|---|---|
C0027651 | Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0699791 | Stomach Carcinoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0014116 | Endocardial Cushion Defects | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0019061 | Hemolytic-Uremic Syndrome | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0272286 | Thrombocytopenia due to platelet alloimmunization | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0039585 | Androgen-Insensitivity Syndrome | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C2239176 | Liver carcinoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C1306459 | Primary malignant neoplasm | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0010054 | Coronary Arteriosclerosis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0023895 | Liver diseases | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0011847 | Diabetes | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0948008 | Ischemic stroke | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0018939 | Hematological Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0011849 | Diabetes Mellitus | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0024121 | Lung Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0002395 | Alzheimer's Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0003873 | Rheumatoid Arthritis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0243026 | Sepsis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0034155 | Purpura, Thrombotic Thrombocytopenic | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0038454 | Cerebrovascular accident | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0005779 | Blood Coagulation Disorders | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C3714636 | Pneumonitis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C1956346 | Coronary Artery Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0398650 | Immune thrombocytopenic purpura | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C2717961 | Thrombotic Microangiopathies | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024