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 ▲ |
---|---|---|---|---|---|
C0003873 | Rheumatoid Arthritis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0005586 | Bipolar Disorder | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0036341 | Schizophrenia | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C4048328 | cervical cancer | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0524851 | Neurodegenerative Disorders | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0019623 | Malignant histiocytosis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0302592 | Cervix carcinoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0007570 | Celiac Disease | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0152230 | Cholinergic urticaria | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0011603 | Dermatitis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0014457 | Eosinophilia | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0282687 | Hemorrhagic Fever, Ebola | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0010346 | Crohn Disease | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0042769 | Virus Diseases | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0036341 | Schizophrenia | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0009404 | Colorectal Neoplasms | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C1319315 | Adenocarcinoma of large intestine | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0005586 | Bipolar Disorder | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0037928 | Spinal Cord Diseases | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0005956 | Bone Marrow Diseases | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0004936 | Mental disorders | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
C0007102 | Malignant tumor of colon | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
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