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 12826 - 12850 of 62743 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0699790 Colon Carcinoma REG1B 5968 regenerating family member 1 beta P48304
C0699790 Colon Carcinoma GOLPH3 64083 golgi phosphoprotein 3 Q9H4A6
C0699790 Colon Carcinoma SHMT1 6470 serine hydroxymethyltransferase 1 P34896
C0699790 Colon Carcinoma SHMT2 6472 serine hydroxymethyltransferase 2 P34897
C0699790 Colon Carcinoma SOAT1 6646 sterol O-acyltransferase 1 P35610
C0699790 Colon Carcinoma LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0699790 Colon Carcinoma SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C0699790 Colon Carcinoma TKT 7086 transketolase P29401
C0699790 Colon Carcinoma DGKZ 8525 diacylglycerol kinase zeta Q13574
C0699790 Colon Carcinoma TKTL1 8277 transketolase like 1 P51854
C0699790 Colon Carcinoma TKTL2 84076 transketolase like 2 Q9H0I9
C0699790 Colon Carcinoma PLA2G7 7941 phospholipase A2 group VII Q13093
C0699790 Colon Carcinoma CA4 762 carbonic anhydrase 4 P22748
C0699790 Colon Carcinoma PCYT1B 9468 phosphate cytidylyltransferase 1, choline, beta Q9Y5K3
C0699790 Colon Carcinoma MTMR3 8897 myotubularin related protein 3 Q13615
C0699790 Colon Carcinoma DGKE 8526 diacylglycerol kinase epsilon P52429
C0699744 Infection of ear CD44 960 CD44 molecule (Indian blood group) P16070
C0699743 Congenital muscular dystrophy (disorder) POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0699743 Congenital muscular dystrophy (disorder) B3GALNT2 148789 beta-1,3-N-acetylgalactosaminyltransferase 2 Q8NCR0
C0699743 Congenital muscular dystrophy (disorder) FKTN 2218 fukutin O75072
C0699743 Congenital muscular dystrophy (disorder) POMT2 29954 protein O-mannosyltransferase 2 Q9UKY4
C0699743 Congenital muscular dystrophy (disorder) POMGNT1 55624 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) Q8WZA1
C0699743 Congenital muscular dystrophy (disorder) FKRP 79147 fukutin related protein Q9H9S5
C0699743 Congenital muscular dystrophy (disorder) POMK 84197 protein O-mannose kinase Q9H5K3
C0699743 Congenital muscular dystrophy (disorder) LARGE1 9215 LARGE xylosyl- and glucuronyltransferase 1 O95461

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