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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 5326 - 5350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1184 nephrotic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • MGI:6194238
  • PMID:15292677
DOID:423 myopathy HGNC:16781 Homo sapiens (human) 80896 NPL
  • MGI:6194238
DOID:10763 hypertension HGNC:17423 Homo sapiens (human) 55501 CHST12
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:18693542
DOID:0111619 combined D-2- and L-2-hydroxyglutaric aciduria HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
  • RGD:7240710
DOID:0060496 respiratory allergy HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16487239
DOID:5082 liver cirrhosis HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:30950843
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:17997 Homo sapiens (human) 79147 FKRP
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16195162
DOID:3071 gliosarcoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0050152 aspiration pneumonia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:162 cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:0111156 spermatogenic failure 9 HGNC:19414 Homo sapiens (human) 283417 DPY19L2
  • RGD:7240710
DOID:0112022 non-syndromic X-linked intellectual disability 21 HGNC:5996 Homo sapiens (human) 11141 IL1RAPL1
  • RGD:7240710
DOID:5138 leiomyomatosis HGNC:3700 Homo sapiens (human) 2271 FH
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:8977 Homo sapiens (human) 5293 PIK3CD
  • MGI:6194238
DOID:583 hemolytic anemia HGNC:8896 Homo sapiens (human) 5230 PGK1
  • PMID:16740138
DOID:2043 hepatitis B HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12915457
  • PMID:27644568
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:4928 intrahepatic cholangiocarcinoma HGNC:5382 Homo sapiens (human) 3417 IDH1
  • PMID:26245674
DOID:9744 type 1 diabetes mellitus HGNC:4006 Homo sapiens (human) 2517 FUCA1
  • PMID:7304074
DOID:783 end stage renal disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:16421163
DOID:3908 lung non-small cell carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:20592629
DOID:6000 congestive heart failure HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
DOID:9282 ocular hypertension HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024