DisGeNET

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
Displaying entries 4826 - 4850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0006826 Malignant Neoplasms ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0038580 Substance Dependence ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0009402 Colorectal Carcinoma ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0035334 Retinitis Pigmentosa ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0476089 Endometrial Carcinoma ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0007107 Malignant neoplasm of larynx ADH7 131 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide P40394
C0023903 Liver neoplasms COMT 1312 catechol-O-methyltransferase P21964
C1852197 MAJOR AFFECTIVE DISORDER 1 COMT 1312 catechol-O-methyltransferase P21964
C0003469 Anxiety Disorders COMT 1312 catechol-O-methyltransferase P21964
C0006142 Malignant neoplasm of breast COMT 1312 catechol-O-methyltransferase P21964
C1321551 Shprintzen-Goldberg syndrome COMT 1312 catechol-O-methyltransferase P21964
C0030319 Panic Disorder COMT 1312 catechol-O-methyltransferase P21964
C0028768 Obsessive-Compulsive Disorder COMT 1312 catechol-O-methyltransferase P21964
C0013274 Patent ductus arteriosus COMT 1312 catechol-O-methyltransferase P21964
C0700095 Central neuroblastoma COMT 1312 catechol-O-methyltransferase P21964
C0036341 Schizophrenia COMT 1312 catechol-O-methyltransferase P21964
C0036358 Schizophreniform Disorders COMT 1312 catechol-O-methyltransferase P21964
C0494463 Alzheimer Disease, Late Onset COMT 1312 catechol-O-methyltransferase P21964
C0525045 Mood Disorders COMT 1312 catechol-O-methyltransferase P21964
C0005586 Bipolar Disorder COMT 1312 catechol-O-methyltransferase P21964
C0030567 Parkinson Disease COMT 1312 catechol-O-methyltransferase P21964
C0011581 Depressive disorder COMT 1312 catechol-O-methyltransferase P21964
C4721610 Carcinoma, Ovarian Epithelial COMT 1312 catechol-O-methyltransferase P21964
C0022104 Irritable Bowel Syndrome COMT 1312 catechol-O-methyltransferase P21964
C0011265 Presenile dementia COMT 1312 catechol-O-methyltransferase P21964

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024