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 ▼ |
---|---|---|---|---|---|
C0086543 | Cataract | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0009691 | Congenital cataract | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C1306459 | Primary malignant neoplasm | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0376358 | Malignant neoplasm of prostate | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0023467 | Leukemia, Myelocytic, Acute | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0525045 | Mood Disorders | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0006142 | Malignant neoplasm of breast | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0004364 | Autoimmune Diseases | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0345904 | Malignant neoplasm of liver | CRYL1 | 51084 | crystallin lambda 1 | Q9Y2S2 |
C0014457 | Eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0400966 | Non-alcoholic Fatty Liver Disease | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0155877 | Allergic asthma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0004096 | Asthma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C1800706 | Idiopathic Pulmonary Fibrosis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0006826 | Malignant Neoplasms | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0206062 | Lung Diseases, Interstitial | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0004623 | Bacterial Infections | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0036421 | Systemic Scleroderma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0002390 | Extrinsic allergic alveolitis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0242459 | Simple Pulmonary Eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0034069 | Pulmonary Fibrosis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C3714636 | Pneumonitis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0206061 | Pneumonia, Interstitial | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0032285 | Pneumonia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0085584 | Encephalopathies | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
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