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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 ▲ |
|---|---|---|---|---|---|
| C0003850 | Arteriosclerosis | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0025202 | melanoma | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0014859 | Esophageal Neoplasms | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0021400 | Influenza | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0027583 | Nematode infections | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0006826 | Malignant Neoplasms | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0036220 | Kaposi Sarcoma | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0600139 | Prostate carcinoma | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0019163 | Hepatitis B | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0022658 | Kidney Diseases | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0014070 | Encephalomyelitis | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0010068 | Coronary heart disease | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C1853195 | Prostate Cancer, Hereditary, 7 | SIGLEC1 | 6614 | sialic acid binding Ig like lectin 1 | Q9BZZ2 |
| C0008925 | Cleft Palate | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C0027651 | Neoplasms | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C0206624 | Hepatoblastoma | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C0025958 | Microcephaly | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C1956346 | Coronary Artery Disease | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C2239176 | Liver carcinoma | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C0037773 | Spastic Paraplegia, Hereditary | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
| C0004153 | Atherosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011849 | Diabetes Mellitus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041296 | Tuberculosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0004238 | Atrial Fibrillation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011847 | Diabetes | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
