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 ▲ |
---|---|---|---|---|---|
C0376358 | Malignant neoplasm of prostate | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0270853 | Juvenile Myoclonic Epilepsy | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0018802 | Congestive heart failure | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0002395 | Alzheimer's Disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0008370 | Cholestasis | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0011615 | Dermatitis, Atopic | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0036572 | Seizures | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0013595 | Eczema | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0001973 | Alcoholic Intoxication, Chronic | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0010346 | Crohn Disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C1839839 | MAJOR AFFECTIVE DISORDER 2 | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0018784 | Sensorineural Hearing Loss (disorder) | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C3536893 | Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0019158 | Hepatitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0006840 | Candidiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0018889 | Helminthiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0024117 | Chronic Obstructive Airway Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0700345 | Candidiasis, Vulvovaginal | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1394891 | Intrinsic Factor Deficiency | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0022568 | Keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0026946 | Mycoses | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0041296 | Tuberculosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C1262117 | Fungal keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0037299 | Skin Ulcer | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0345904 | Malignant neoplasm of liver | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
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