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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 69301 - 69325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:9884 muscular dystrophy HGNC:1480 Homo sapiens (human) 825 CAPN3
  • PMID:9150160
DOID:1184 nephrotic syndrome HGNC:11180 Homo sapiens (human) 6648 SOD2
  • PMID:9152291
DOID:0060903 thrombosis HGNC:3541 Homo sapiens (human) 2152 F3
  • PMID:9153543
DOID:3907 lung squamous cell carcinoma HGNC:1116 Homo sapiens (human) 682 BSG
  • PMID:9154157
DOID:3007 breast ductal carcinoma HGNC:1116 Homo sapiens (human) 682 BSG
  • PMID:9154157
DOID:1485 cystic fibrosis HGNC:7512 Homo sapiens (human) 4583 MUC2
  • PMID:9155717
DOID:12134 factor VIII deficiency HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:9157572
DOID:3459 breast carcinoma HGNC:7160 Homo sapiens (human) 4323 MMP14
  • PMID:9158005
DOID:13133 HELLP syndrome HGNC:3430 Homo sapiens (human) 2064 ERBB2
  • PMID:9158311
DOID:10591 pre-eclampsia HGNC:3430 Homo sapiens (human) 2064 ERBB2
  • PMID:9158311
DOID:2394 ovarian cancer HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:9166545
DOID:0050328 congenital hypothyroidism HGNC:11040 Homo sapiens (human) 6528 SLC5A5
  • PMID:9171822
DOID:9119 acute myeloid leukemia HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:9171997
DOID:0050908 myelodysplastic syndrome HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:9171997
DOID:4989 pancreatitis HGNC:1228 Homo sapiens (human) 710 SERPING1
  • PMID:9176084
DOID:12241 beta thalassemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:9180253
DOID:1909 melanoma HGNC:6709 Homo sapiens (human) 4049 LTA
  • PMID:9182821
DOID:10223 dermatomyositis HGNC:11920 Homo sapiens (human) 355 FAS
  • PMID:9182923
DOID:3492 mixed connective tissue disease HGNC:11920 Homo sapiens (human) 355 FAS
  • PMID:9182923
DOID:5419 schizophrenia HGNC:3033 Homo sapiens (human) 1822 ATN1
  • PMID:9184318
DOID:3393 coronary artery disease HGNC:9075 Homo sapiens (human) 5345 SERPINF2
  • PMID:9184412
DOID:2377 multiple sclerosis HGNC:6014 Homo sapiens (human) 3565 IL4
  • PMID:9184650
DOID:3209 junctional epidermolysis bullosa HGNC:6142 Homo sapiens (human) 3655 ITGA6
  • PMID:9185503
DOID:11123 Henoch-Schoenlein purpura HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:9186886
DOID:8584 Burkitt lymphoma HGNC:11919 Homo sapiens (human) 958 CD40
  • PMID:9192773

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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: December 9, 2024