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 52601 - 52625 of 62743 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0009806 Constipation PRNP 5621 prion protein F7VJQ1
C0009806 Constipation PTEN 5728 phosphatase and tensin homolog P60484
C0009806 Constipation SDHA 6389 succinate dehydrogenase complex flavoprotein subunit A P31040
C0009782 Connective Tissue Diseases B3GALT6 126792 beta-1,3-galactosyltransferase 6 Q96L58
C0009782 Connective Tissue Diseases B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009782 Connective Tissue Diseases GLB1 2720 galactosidase beta 1 P16278
C0009782 Connective Tissue Diseases PLOD3 8985 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 O60568
C0009782 Connective Tissue Diseases HPRT1 3251 hypoxanthine phosphoribosyltransferase 1 P00492
C0009782 Connective Tissue Diseases CYP3A5 1577 cytochrome P450 family 3 subfamily A member 5 P20815
C0009782 Connective Tissue Diseases DCN 1634 decorin P07585
C0009782 Connective Tissue Diseases ACE 1636 angiotensin I converting enzyme P12821
C0009782 Connective Tissue Diseases SLC2A10 81031 solute carrier family 2 member 10 O95528
C0009782 Connective Tissue Diseases CD22 933 CD22 molecule P20273
C0009782 Connective Tissue Diseases COL9A2 1298 collagen type IX alpha 2 chain Q14055
C0009782 Connective Tissue Diseases PCYT1A 5130 phosphate cytidylyltransferase 1, choline, alpha P49585
C0009782 Connective Tissue Diseases PKD1 5310 polycystin 1, transient receptor potential channel interacting P98161
C0009782 Connective Tissue Diseases PKD2 5311 polycystin 2, transient receptor potential cation channel Q13563
C0009782 Connective Tissue Diseases SCP2 6342 sterol carrier protein 2 P22307
C0009766 Allergic Conjunctivitis LGALS3 3958 galectin 3 P17931
C0009763 Conjunctivitis PLD3 23646 phospholipase D family member 3 Q8IV08
C0009763 Conjunctivitis IMPA1 3612 inositol monophosphatase 1 P29218
C0009763 Conjunctivitis LGALS1 3956 galectin 1 P09382
C0009763 Conjunctivitis MBL2 4153 mannose binding lectin 2 P11226
C0009763 Conjunctivitis CD14 929 CD14 molecule P08571
C0009714 Hepatic Fibrosis, Congenital EOGT 285203 EGF domain specific O-linked N-acetylglucosamine transferase Q5NDL2

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