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 |
---|---|---|---|---|---|
C0039101 | synovial sarcoma | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1850889 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020615 | Hypoglycemia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0686353 | Muscular Dystrophies, Limb-Girdle | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0041349 | Nephritis, Tubulointerstitial | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C4551858 | Vesicoureteral Reflux 1 | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020505 | Hyperphagia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0005745 | Blepharoptosis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0085580 | Essential Hypertension | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1857389 | Cystinuria, Type B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1565489 | Renal Insufficiency | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0024796 | Marfan Syndrome | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020538 | Hypertensive disease | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0030319 | Panic Disorder | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0011849 | Diabetes Mellitus | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0001125 | Acidosis, Lactic | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0024523 | Malabsorption Syndrome | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C1257931 | Mammary Neoplasms, Human | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0025517 | Metabolic Diseases | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0028754 | Obesity | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0678222 | Breast Carcinoma | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0006142 | Malignant neoplasm of breast | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0027651 | Neoplasms | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C1306459 | Primary malignant neoplasm | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
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