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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 3601 - 3625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3526 cerebral infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16173529
DOID:9351 diabetes mellitus HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
DOID:9970 obesity HGNC:10606 Homo sapiens (human) 6342 SCP2
  • MGI:6194238
DOID:0080952 AMED syndrome HGNC:253 Homo sapiens (human) 128 ADH5
  • RGD:7240710
DOID:10763 hypertension HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • MGI:6194238
DOID:2755 Mycobacterium avium complex disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:19641295
DOID:1612 breast cancer HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:18719053
DOID:783 end stage renal disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16801331
DOID:9970 obesity HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:3829 pituitary adenoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:12040339
  • PMID:19040046
  • PMID:19046748
  • PMID:19327107
DOID:8472 localized scleroderma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:7916356
DOID:13241 Behcet's disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17206395
DOID:9352 type 2 diabetes mellitus HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
DOID:1875 impotence HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:10763 hypertension HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:2030 anxiety disorder HGNC:4092 Homo sapiens (human) 2571 GAD1
  • PMID:22328461
DOID:2566 corneal dystrophy HGNC:14415 Homo sapiens (human) 6785 ELOVL4
  • PMID:11726641
DOID:0050589 inflammatory bowel disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:29567797
DOID:14499 Fabry disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20941593
DOID:1024 leprosy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20650301
DOID:0014667 disease of metabolism HGNC:6544 Homo sapiens (human) 3948 LDHC
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:5320 Homo sapiens (human) 3373 HYAL1
  • MGI:6194238
DOID:0111261 fumarase deficiency HGNC:3700 Homo sapiens (human) 2271 FH
  • RGD:7240710

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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