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 |
---|---|---|---|---|---|
C1510586 | Autism Spectrum Disorders | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
C1510586 | Autism Spectrum Disorders | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
C1510586 | Autism Spectrum Disorders | CAT | 847 | catalase | P04040 |
C1510586 | Autism Spectrum Disorders | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C1510586 | Autism Spectrum Disorders | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
C1510586 | Autism Spectrum Disorders | PTGES | 9536 | prostaglandin E synthase | O14684 |
C1510586 | Autism Spectrum Disorders | PTGES3 | 10728 | prostaglandin E synthase 3 | Q15185 |
C1510586 | Autism Spectrum Disorders | MACROD2 | 140733 | mono-ADP ribosylhydrolase 2 | A1Z1Q3 |
C1510586 | Autism Spectrum Disorders | UPP2 | 151531 | uridine phosphorylase 2 | O95045 |
C1510586 | Autism Spectrum Disorders | GLO1 | 2739 | glyoxalase I | Q04760 |
C1510586 | Autism Spectrum Disorders | AMY1A | 276 | amylase alpha 1A | P04745 |
C1510586 | Autism Spectrum Disorders | AMY1C | 278 | amylase alpha 1C | P04745 |
C1510586 | Autism Spectrum Disorders | AMY1B | 277 | amylase alpha 1B | P04745 |
C1510586 | Autism Spectrum Disorders | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C1510586 | Autism Spectrum Disorders | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
C1510586 | Autism Spectrum Disorders | BST1 | 683 | bone marrow stromal cell antigen 1 | Q10588 |
C1510586 | Autism Spectrum Disorders | SDC4 | 6385 | syndecan 4 | P31431 |
C1510586 | Autism Spectrum Disorders | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
C1510586 | Autism Spectrum Disorders | CDH13 | 1012 | cadherin 13 | P55290 |
C1510586 | Autism Spectrum Disorders | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C1510586 | Autism Spectrum Disorders | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C1510586 | Autism Spectrum Disorders | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C1510586 | Autism Spectrum Disorders | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
C1510586 | Autism Spectrum Disorders | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C1510586 | Autism Spectrum Disorders | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
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