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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 6676 - 6700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:206 hereditary multiple exostoses HGNC:3515 Homo sapiens (human) 2134 EXTL1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:10811 nasal cavity cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19950227
DOID:13450 coccidioidomycosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19083122
DOID:11054 urinary bladder cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15596044
DOID:3407 carotid artery disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:19717975
DOID:11713 diabetic angiopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22246459
DOID:1936 atherosclerosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:12451000
DOID:9744 type 1 diabetes mellitus HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:22210567
DOID:1324 lung cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:11906 Homo sapiens (human) 8794 TNFRSF10C
  • MGI:6194238
DOID:4780 anti-basement membrane glomerulonephritis HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:0111077 pyruvate kinase deficiency of red cells HGNC:9020 Homo sapiens (human) 5313 PKLR
  • MGI:6194238
  • PMID:16704447
  • PMID:19755962
  • RGD:7240710
DOID:0060350 adenine phosphoribosyltransferase deficiency HGNC:626 Homo sapiens (human) 353 APRT
  • MGI:6194238
  • RGD:7240710
DOID:824 periodontitis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15491310
DOID:10534 stomach cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:27323394
  • PMID:28387921
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:15685 Homo sapiens (human) 11041 B4GAT1
  • MGI:6194238
DOID:1214 tympanosclerosis HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
DOID:0050557 congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
DOID:1924 hypogonadism HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:21987487
DOID:14717 centronuclear myopathy HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16875506
DOID:1289 neurodegenerative disease HGNC:17074 Homo sapiens (human) 23098 SARM1
  • 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