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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 9551 - 9575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3312 bipolar disorder HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • RGD:7240710
DOID:8552 chronic myeloid leukemia HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17900686
DOID:8552 chronic myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25436036
DOID:824 periodontitis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:783 end stage renal disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:14654 prostatitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • MGI:6194238
DOID:583 hemolytic anemia HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:10733484
DOID:9471 meningitis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:7521338
DOID:0050700 cardiomyopathy HGNC:4432 Homo sapiens (human) 2805 GOT1
  • MGI:6194238
DOID:0111265 Boucher-Neuhauser syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:9021 Homo sapiens (human) 5315 PKM
  • MGI:6194238
DOID:14749 methylmalonic acidemia HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation HGNC:924 Homo sapiens (human) 2683 B4GALT1
  • PMID:11901181
DOID:576 proteinuria HGNC:10658 Homo sapiens (human) 6382 SDC1
  • MGI:6194238
DOID:13250 diarrhea HGNC:6530 Homo sapiens (human) 3938 LCT
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:19474411
DOID:13241 Behcet's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21044750
DOID:0014667 disease of metabolism HGNC:2898 Homo sapiens (human) 1738 DLD
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • MGI:6194238
  • PMID:10091405
  • PMID:15753292
  • PMID:16609363
  • PMID:21993917
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:250 Homo sapiens (human) 125 ADH1B
  • RGD:7240710
DOID:1596 depressive disorder HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:7998 hyperthyroidism HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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