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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 5976 - 6000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0111650 ectodermal dysplasia 13 HGNC:17550 Homo sapiens (human) 83999 KREMEN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080750 erythema nodosum HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:12198697
DOID:8544 chronic fatigue syndrome HGNC:12338 Homo sapiens (human) 7225 TRPC6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27834303
DOID:12849 autistic disorder HGNC:18541 Homo sapiens (human) 55904 KMT2E inference by association of genotype from phenotype used in manual assertion
  • PMID:25284784
DOID:0112056 X-linked intellectual disability-short stature-overweight syndrome HGNC:19073 Homo sapiens (human) 57187 THOC2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3181 oligodendroglioma HGNC:9884 Homo sapiens (human) 5925 RB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15970925
DOID:0060902 Norman-Roberts syndrome HGNC:9957 Homo sapiens (human) 5649 RELN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13994 cleidocranial dysplasia HGNC:10472 Homo sapiens (human) 860 RUNX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:9182765
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:6407 Homo sapiens (human) 3845 KRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:18772397
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:20147 Homo sapiens (human) 51167 CYB5R4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15504981
DOID:0060917 facioscapulohumeral muscular dystrophy 3 HGNC:30299 Homo sapiens (human) 55791 LRIF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:3273 Homo sapiens (human) 8667 EIF3H inference by association of genotype from phenotype used in manual assertion
  • PMID:11733359
DOID:0111451 progressive myoclonus epilepsy 8 HGNC:14253 Homo sapiens (human) 10715 CERS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:16823505
  • PMID:23828384
DOID:3393 coronary artery disease HGNC:6344 Homo sapiens (human) 9365 KL inference by association of genotype from phenotype used in manual assertion
  • PMID:16579981
  • PMID:16979405
DOID:1612 breast cancer HGNC:11848 Homo sapiens (human) 7097 TLR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22560646
DOID:2349 arteriosclerosis HGNC:9605 Homo sapiens (human) 5743 PTGS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16458279
DOID:2043 hepatitis B HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24407110
  • PMID:29149205
  • PMID:31977279
DOID:2841 asthma HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10733466
DOID:3083 chronic obstructive pulmonary disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19507017
  • PMID:20080081
DOID:684 hepatocellular carcinoma HGNC:1516 Homo sapiens (human) 847 CAT inference by association of genotype from phenotype used in manual assertion
  • PMID:21907168
DOID:2219 Glanzmann's thrombasthenia HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:14687991
DOID:1324 lung cancer HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19901851
DOID:10763 hypertension HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11798899
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:5294 Homo sapiens (human) 3357 HTR2B inference by association of genotype from phenotype used in manual assertion
  • PMID:33081272
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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