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 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024