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 |
---|---|---|---|---|---|
C1306503 | Congenital exomphalos | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C4721532 | Lymphoma, Non-Hodgkin, Familial | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0013415 | Dysthymic Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0346153 | Breast Cancer, Familial | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0033038 | Premature Ejaculation | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0023895 | Liver diseases | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0018818 | Ventricular Septal Defects | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1332979 | Childhood Lymphoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0751571 | Cancer of Urinary Tract | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0266295 | Congenital hypoplasia of kidney | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0042571 | Vertigo | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0917799 | Hypersomnia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0600241 | heroin abuse | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0020179 | Huntington Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0007137 | Squamous cell carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1333990 | Hereditary Nonpolyposis Colorectal Cancer | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0011573 | Endogenous depression | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0027932 | Neurotic Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0001418 | Adenocarcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0020224 | Polyhydramnios | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1336076 | Sporadic Breast Carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0042487 | Venous Thrombosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0021151 | Incipient Schizophrenia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0085159 | Seasonal Affective Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
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