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 |
---|---|---|---|---|---|
C0004096 | Asthma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C1527304 | Allergic Reaction | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0021051 | Immunologic Deficiency Syndromes | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0024141 | Lupus Erythematosus, Systemic | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0021053 | Immune System Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C4551595 | Biliary Cirrhosis, Primary, 1 | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0003873 | Rheumatoid Arthritis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0002395 | Alzheimer's Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C3837958 | Diabetes Mellitus, Ketosis-Prone | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0033860 | Psoriasis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0018621 | Hay fever | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C3495559 | Juvenile arthritis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0152268 | Nodular Sclerosis Classical Hodgkin Lymphoma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0205734 | Diabetes, Autoimmune | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0011847 | Diabetes | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0004943 | Behcet Syndrome | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C2607914 | Allergic rhinitis (disorder) | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0011615 | Dermatitis, Atopic | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0271650 | Impaired glucose tolerance | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0013595 | Eczema | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0007570 | Celiac Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0264408 | Childhood asthma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0524851 | Neurodegenerative Disorders | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C1561643 | Chronic Kidney Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0009447 | Common Variable Immunodeficiency | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
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