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 3976 - 4000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0004153 Atherosclerosis MGLL 11343 monoglyceride lipase Q99685
C0006870 Cannabis Dependence MGLL 11343 monoglyceride lipase Q99685
C0003469 Anxiety Disorders MGLL 11343 monoglyceride lipase Q99685
C0699790 Colon Carcinoma MGLL 11343 monoglyceride lipase Q99685
C0008373 Cholesteatoma MGLL 11343 monoglyceride lipase Q99685
C0476089 Endometrial Carcinoma MGLL 11343 monoglyceride lipase Q99685
C1332986 Childhood Osteosarcoma MGLL 11343 monoglyceride lipase Q99685
C0524620 Metabolic Syndrome X MGLL 11343 monoglyceride lipase Q99685
C0038586 Substance Use Disorders MGLL 11343 monoglyceride lipase Q99685
C2711227 Steatohepatitis MGLL 11343 monoglyceride lipase Q99685
C0001430 Adenoma MGLL 11343 monoglyceride lipase Q99685
C0085207 Gestational Diabetes MGLL 11343 monoglyceride lipase Q99685
C0600139 Prostate carcinoma MGLL 11343 monoglyceride lipase Q99685
C0007785 Cerebral Infarction MGLL 11343 monoglyceride lipase Q99685
C0700095 Central neuroblastoma MGLL 11343 monoglyceride lipase Q99685
C0242379 Malignant neoplasm of lung MGLL 11343 monoglyceride lipase Q99685
C0585442 Osteosarcoma of bone MGLL 11343 monoglyceride lipase Q99685
C0034152 Henoch-Schoenlein Purpura CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0037773 Spastic Paraplegia, Hereditary CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0524851 Neurodegenerative Disorders CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0037772 Spastic Paraplegia CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C3539507 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0031117 Peripheral Neuropathy CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C1306459 Primary malignant neoplasm CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0085131 Gangliosidosis GM1 CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449

About Release Notes Help Feedback

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