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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 8026 - 8050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:635 acquired immunodeficiency syndrome HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26885809
DOID:0060180 colitis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:0060903 thrombosis HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • MGI:6194238
DOID:3450 cutaneous Paget's disease HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • PMID:22522847
DOID:2349 arteriosclerosis HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:15961705
DOID:8778 Crohn's disease HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:22398043
DOID:6000 congestive heart failure HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:22785609
DOID:783 end stage renal disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
  • PMID:11162628
DOID:1612 breast cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:9703922
DOID:3498 pancreatic ductal adenocarcinoma HGNC:12705 Homo sapiens (human) 8876 VNN1
  • PMID:32663515
DOID:4450 renal cell carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:12833185
  • PMID:17284111
DOID:8398 osteoarthritis HGNC:18185 Homo sapiens (human) 54206 ERRFI1
  • MGI:6194238
DOID:10763 hypertension HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • PMID:17264398
DOID:3803 Crigler-Najjar syndrome HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • MGI:6194238
  • PMID:16019265
  • PMID:16337205
  • PMID:22094718
  • PMID:24285217
  • PMID:9497253
  • RGD:7240710
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:9491 Homo sapiens (human) 5652 PRSS8
  • MGI:6194238
DOID:162 cancer HGNC:1801 Homo sapiens (human) 8760 CDS2
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • PMID:21220706
DOID:841 extrinsic allergic alveolitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19218674
DOID:10763 hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:0081331 glycogen storage disease Ic HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:2799 bronchiolitis obliterans HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:4481 allergic rhinitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17069098
  • PMID:19763595
  • PMID:22402138
  • PMID:22555057
  • PMID:22577387
  • PMID:23639307
DOID:5517 stomach carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:29179459

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

Acknowledgements

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