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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 11251 - 11275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:783 end stage renal disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:22119815
DOID:1612 breast cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • RGD:7240710
DOID:1993 rectum cancer HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:31740231
DOID:10283 prostate cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:22815832
DOID:13001 carotid stenosis HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:28704403
DOID:9256 colorectal cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:0111822 CHILD syndrome HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • RGD:7240710
DOID:12377 spinal muscular atrophy HGNC:4879 Homo sapiens (human) 3074 HEXB
  • PMID:1720305
DOID:0050873 follicular lymphoma HGNC:4021 Homo sapiens (human) 2531 KDSR
  • PMID:8417785
DOID:4852 pleomorphic xanthoastrocytoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25346165
DOID:2986 IgA glomerulonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12220450
DOID:2747 glycogen storage disease HGNC:4699 Homo sapiens (human) 2992 GYG1
  • RGD:7240710
DOID:10024 migraine with aura HGNC:800 Homo sapiens (human) 477 ATP1A2
  • PMID:12953268
DOID:0112223 developmental and epileptic encephalopathy 89 HGNC:4092 Homo sapiens (human) 2571 GAD1
  • RGD:7240710
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19199550
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:17033970
  • PMID:19138334
DOID:10211 cholelithiasis HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:16381022
DOID:2228 thrombocytosis HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:26608331
DOID:1612 breast cancer HGNC:11377 Homo sapiens (human) 6783 SULT1E1
  • PMID:15894657
  • PMID:17372239
DOID:0050546 congenital adrenal insufficiency HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • RGD:7240710
DOID:8499 night blindness HGNC:8082 Homo sapiens (human) 60506 NYX
  • PMID:11062471
  • RGD:7240710
DOID:8692 myeloid leukemia HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:23609856
DOID:0111411 exudative vitreoretinopathy 4 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0080721 calvarial doughnut lesions with bone fragility HGNC:28395 Homo sapiens (human) 166929 SGMS2
  • 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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