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 |
---|---|---|---|---|---|
C0020538 | Hypertensive disease | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
C0020538 | Hypertensive disease | SDHC | 6391 | succinate dehydrogenase complex subunit C | Q99643 |
C0020538 | Hypertensive disease | SELL | 6402 | selectin L | P14151 |
C0020538 | Hypertensive disease | SELP | 6403 | selectin P | P16109 |
C0020538 | Hypertensive disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0020538 | Hypertensive disease | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
C0020538 | Hypertensive disease | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0020538 | Hypertensive disease | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
C0020538 | Hypertensive disease | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
C0020538 | Hypertensive disease | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0020538 | Hypertensive disease | UMOD | 7369 | uromodulin | P07911 |
C0020538 | Hypertensive disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0020538 | Hypertensive disease | TBXAS1 | 6916 | thromboxane A synthase 1 | P24557 |
C0020538 | Hypertensive disease | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C0020538 | Hypertensive disease | PTGES2 | 80142 | prostaglandin E synthase 2 | Q9H7Z7 |
C0020538 | Hypertensive disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0020538 | Hypertensive disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0020538 | Hypertensive disease | CAT | 847 | catalase | P04040 |
C0020538 | Hypertensive disease | DEGS1 | 8560 | delta 4-desaturase, sphingolipid 1 | O15121 |
C0020538 | Hypertensive disease | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0020538 | Hypertensive disease | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C0020538 | Hypertensive disease | FCN3 | 8547 | ficolin 3 | O75636 |
C0020538 | Hypertensive disease | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0020538 | Hypertensive disease | VNN1 | 8876 | vanin 1 | O95497 |
C0020538 | Hypertensive disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
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