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 |
---|---|---|---|---|---|
C0272242 | Complement deficiency disease | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0272242 | Complement deficiency disease | FCN3 | 8547 | ficolin 3 | O75636 |
C1257965 | Compensatory Hyperinsulinemia | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
C1257965 | Compensatory Hyperinsulinemia | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C1257965 | Compensatory Hyperinsulinemia | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
C0009460 | Communication impairment | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0009460 | Communication impairment | ARSD | 414 | arylsulfatase D | P51689 |
C0009451 | Communicating Hydrocephalus | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0009451 | Communicating Hydrocephalus | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0043037 | Common wart | FCN3 | 8547 | ficolin 3 | O75636 |
C0043037 | Common wart | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0152424 | Common ventricle | NSDHL | 50814 | NAD(P) dependent steroid dehydrogenase-like | Q15738 |
C0152424 | Common ventricle | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
C0009447 | Common Variable Immunodeficiency | FUT2 | 2524 | fucosyltransferase 2 | Q10981 |
C0009447 | Common Variable Immunodeficiency | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0009447 | Common Variable Immunodeficiency | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0009447 | Common Variable Immunodeficiency | SDC1 | 6382 | syndecan 1 | P18827 |
C0009447 | Common Variable Immunodeficiency | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
C0009447 | Common Variable Immunodeficiency | CD38 | 952 | CD38 molecule | P28907 |
C0009447 | Common Variable Immunodeficiency | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0009447 | Common Variable Immunodeficiency | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C0009447 | Common Variable Immunodeficiency | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C0009447 | Common Variable Immunodeficiency | NCAM1 | 4684 | neural cell adhesion molecule 1 | P13591 |
C0009447 | Common Variable Immunodeficiency | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0009447 | Common Variable Immunodeficiency | CD1D | 912 | CD1d molecule | P15813 |
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