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 |
---|---|---|---|---|---|
C0003466 | Anus, Imperforate | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
C0003466 | Anus, Imperforate | POMT2 | 29954 | protein O-mannosyltransferase 2 | Q9UKY4 |
C0003466 | Anus, Imperforate | PIGO | 84720 | phosphatidylinositol glycan anchor biosynthesis class O | Q8TEQ8 |
C0003466 | Anus, Imperforate | FKRP | 79147 | fukutin related protein | Q9H9S5 |
C0003466 | Anus, Imperforate | LARGE1 | 9215 | LARGE xylosyl- and glucuronyltransferase 1 | O95461 |
C0003466 | Anus, Imperforate | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0242473 | Anus Prolapse | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0003460 | Anuria | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C2936791 | Antley-Bixler Syndrome, Autosomal Dominant | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C2936791 | Antley-Bixler Syndrome, Autosomal Dominant | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C2936791 | Antley-Bixler Syndrome, Autosomal Dominant | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
C1860042 | Antley-Bixler Syndrome with Disordered Steroidogenesis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0272375 | Antithrombin III Deficiency | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
C0272375 | Antithrombin III Deficiency | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
C0272375 | Antithrombin III Deficiency | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0272375 | Antithrombin III Deficiency | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0272375 | Antithrombin III Deficiency | PMM2 | 5373 | phosphomannomutase 2 | O15305 |
C0272375 | Antithrombin III Deficiency | SRD5A3 | 79644 | steroid 5 alpha-reductase 3 | Q9H8P0 |
C0272375 | Antithrombin III Deficiency | PC | 5091 | pyruvate carboxylase | P11498 |
C0272375 | Antithrombin III Deficiency | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0272375 | Antithrombin III Deficiency | LCT | 3938 | lactase | P09848 |
C0272375 | Antithrombin III Deficiency | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
C0003431 | Antisocial Personality Disorder | EXT1 | 2131 | exostosin glycosyltransferase 1 | Q16394 |
C0003431 | Antisocial Personality Disorder | ADH1B | 125 | alcohol dehydrogenase 1B (class I), beta polypeptide | P00325 |
C0003431 | Antisocial Personality Disorder | ACE | 1636 | angiotensin I converting enzyme | P12821 |
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