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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 66026 - 66050 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1324 lung cancer HGNC:7325 Homo sapiens (human) 4436 MSH2
  • PMID:25252909
DOID:0050545 visceral heterotaxy HGNC:4214 Homo sapiens (human) 2657 GDF1
  • RGD:7240710
DOID:10941 intracranial aneurysm HGNC:2464 Homo sapiens (human) 1462 VCAN
  • PMID:16917090
DOID:9952 acute lymphoblastic leukemia HGNC:12441 Homo sapiens (human) 7298 TYMS
  • PMID:25007187
DOID:0081216 autosomal recessive intellectual developmental disorder 54 HGNC:30765 Homo sapiens (human) 23043 TNIK
  • RGD:7240710
DOID:0060558 lethal congenital contracture syndrome HGNC:13841 Homo sapiens (human) 57211 ADGRG6
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:11364 Homo sapiens (human) 6774 STAT3
  • PMID:22269120
DOID:12306 vitiligo HGNC:5438 Homo sapiens (human) 3458 IFNG
  • PMID:23777204
DOID:0111780 TARP syndrome HGNC:9896 Homo sapiens (human) 8241 RBM10
  • RGD:7240710
DOID:13810 familial hypercholesterolemia HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:9699897
DOID:0080527 bronchiectasis 2 HGNC:10599 Homo sapiens (human) 6337 SCNN1A
  • RGD:7240710
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:4914 esophagus adenocarcinoma HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:21472143
DOID:0111530 linear nevus sebaceous syndrome HGNC:5173 Homo sapiens (human) 3265 HRAS
  • PMID:22683711
  • RGD:7240710
DOID:0110661 congenital myasthenic syndrome 20 HGNC:14025 Homo sapiens (human) 60482 SLC5A7
  • RGD:7240710
DOID:2236 congenital afibrinogenemia HGNC:3662 Homo sapiens (human) 2244 FGB
  • PMID:12393540
  • RGD:7240710
DOID:2355 anemia HGNC:492 Homo sapiens (human) 286 ANK1
  • PMID:11372755
DOID:9296 cleft lip HGNC:4221 Homo sapiens (human) 392255 GDF6
  • PMID:18716610
DOID:1024 leprosy HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:18177245
  • RGD:7240710
DOID:1612 breast cancer HGNC:10050 Homo sapiens (human) 6041 RNASEL
  • PMID:15330212
DOID:10325 silicosis HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:12096683
DOID:0060805 Prieto syndrome HGNC:14543 Homo sapiens (human) 65267 WNK3
  • RGD:7240710
DOID:1324 lung cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20303010
DOID:3393 coronary artery disease HGNC:1142 Homo sapiens (human) 56244 BTNL2
  • PMID:19882345
DOID:0050902 medulloblastoma HGNC:583 Homo sapiens (human) 324 APC
  • PMID:17238184

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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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