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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 January 28, 2025
Displaying entries 6026 - 6050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0050773 paraganglioma RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b inference by association of genotype from phenotype used in manual assertion
  • PMID:12036912
DOID:1935 Bardet-Biedl syndrome HGNC:967 Homo sapiens (human) 583 BBS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11285252
DOID:0081231 autosomal recessive intellectual developmental disorder 70 HGNC:24152 Homo sapiens (human) 51319 RSRC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:4187 Homo sapiens (human) 2638 GC inference by association of genotype from phenotype used in manual assertion
  • PMID:12137326
DOID:0080199 colorectal carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53 inference by association of genotype from phenotype used in manual assertion
  • PMID:29560751
DOID:0080081 nonsyndromic congenital nail disorder 3 HGNC:9060 Homo sapiens (human) 5333 PLCD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12306 vitiligo HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16420246
  • PMID:9653015
DOID:13241 Behcet's disease HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18408113
DOID:2841 asthma HGNC:1331 Homo sapiens (human) 727 C5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15278436
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110019 age related macular degeneration 7 HGNC:1318 Homo sapiens (human) 718 C3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19899988
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6554 Homo sapiens (human) 3953 LEPR inference by association of genotype from phenotype used in manual assertion
  • PMID:22215535
  • PMID:27257426
DOID:8947 diabetic retinopathy HGNC:381 Homo sapiens (human) 231 AKR1B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16701918
  • PMID:19587357
DOID:0111646 congenital lactase deficiency HGNC:6530 Homo sapiens (human) 3938 LCT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1205 allergic disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10689122
  • PMID:15853900
  • PMID:16112029
DOID:0050745 diffuse large B-cell lymphoma HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:27282998
DOID:6364 migraine HGNC:1437 Homo sapiens (human) 796 CALCA inference by association of genotype from phenotype used in manual assertion
  • PMID:20959432
DOID:1798 pancreatic endocrine carcinoma HGNC:2681 Homo sapiens (human) 1616 DAXX inference by association of genotype from phenotype used in manual assertion
  • PMID:29212165
DOID:0112334 pontocerebellar hypoplasia type 1C HGNC:17035 Homo sapiens (human) 11340 EXOSC8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110450 dilated cardiomyopathy 1II HGNC:2389 Homo sapiens (human) 1410 CRYAB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5683 hereditary breast ovarian cancer syndrome HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:83 cataract HGNC:11179 Homo sapiens (human) 6647 SOD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21921984
DOID:10534 stomach cancer HGNC:12637 Homo sapiens (human) 7403 KDM6A inference by association of genotype from phenotype used in manual assertion
  • PMID:32867456
DOID:350 mastocytosis HGNC:5973 Homo sapiens (human) 3596 IL13 inference by association of genotype from phenotype used in manual assertion
  • PMID:19178408
DOID:1588 thrombocytopenia HGNC:3749 Homo sapiens (human) 2313 FLI1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15232614
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International Collaboration

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: April 7, 2025