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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 October 9, 2024
Displaying entries 65401 - 65425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0090135 complex cortical dysplasia with other brain malformations 5 HGNC:12412 Homo sapiens (human) 7280 TUBB2A
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • PMID:31825269
DOID:3526 cerebral infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17016617
DOID:5041 esophageal cancer HGNC:13861 Homo sapiens (human) 11178 LZTS1
  • PMID:10097140
DOID:0070040 autosomal dominant intellectual developmental disorder 10 HGNC:1406 Homo sapiens (human) 10369 CACNG2
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:24758241
DOID:10908 hydrocephalus HGNC:7208 Homo sapiens (human) 8777 MPDZ
  • RGD:7240710
DOID:0080827 human cytomegalovirus infection HGNC:6340 Homo sapiens (human) 3813 KIR3DS1
  • PMID:25253288
DOID:1993 rectum cancer HGNC:1919 Homo sapiens (human) 1108 CHD4
  • PMID:25407497
DOID:9974 drug dependence HGNC:8156 Homo sapiens (human) 4988 OPRM1
  • PMID:33402148
DOID:3627 aortic aneurysm HGNC:3603 Homo sapiens (human) 2200 FBN1
  • PMID:7762551
DOID:12849 autistic disorder HGNC:14295 Homo sapiens (human) 22941 SHANK2
  • RGD:7240710
DOID:9952 acute lymphoblastic leukemia HGNC:7989 Homo sapiens (human) 4893 NRAS
  • PMID:25204082
DOID:3393 coronary artery disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12975417
DOID:0060222 Scheie syndrome HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:9970 obesity HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:16025115
  • RGD:7240710
DOID:9970 obesity HGNC:3176 Homo sapiens (human) 1906 EDN1
  • PMID:17444275
DOID:1405 primary angle-closure glaucoma HGNC:1181 Homo sapiens (human) 745 MYRF
  • PMID:36129575
DOID:2843 long QT syndrome HGNC:6242 Homo sapiens (human) 9992 KCNE2
  • PMID:15840476
DOID:0110566 autosomal dominant nonsyndromic deafness 40 HGNC:2418 Homo sapiens (human) 1428 CRYM
  • RGD:7240710
DOID:302 substance abuse HGNC:3025 Homo sapiens (human) 1815 DRD4
  • PMID:33544778
  • PMID:34828440
DOID:684 hepatocellular carcinoma HGNC:18437 Homo sapiens (human) 84868 HAVCR2
  • PMID:27034168
DOID:0050470 Donohue syndrome HGNC:6091 Homo sapiens (human) 3643 INSR
  • RGD:7240710
DOID:4948 gallbladder carcinoma HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:7795450
DOID:1405 primary angle-closure glaucoma HGNC:171 Homo sapiens (human) 90 ACVR1
  • PMID:32641001

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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: December 9, 2024