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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 14001 - 14025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▼
DOID:12361 Graves' disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10468909
  • PMID:11272094
DOID:12134 factor VIII deficiency HGNC:3546 Homo sapiens (human) 2157 F8 mutant phenotype evidence used in manual assertion
  • PMID:10468616
DOID:583 hemolytic anemia HGNC:10006 Homo sapiens (human) 6005 RHAG inference by association of genotype from phenotype used in manual assertion
  • PMID:10467273
DOID:676 juvenile rheumatoid arthritis HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10457895
DOID:676 juvenile rheumatoid arthritis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10457895
DOID:676 juvenile rheumatoid arthritis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10457895
  • PMID:19908388
DOID:0050700 cardiomyopathy HGNC:7150 Homo sapiens (human) 23417 MLYCD inference by association of genotype from phenotype used in manual assertion
  • PMID:10455107
DOID:2394 ovarian cancer HGNC:6770 Homo sapiens (human) 4089 SMAD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10451707
DOID:1380 endometrial cancer HGNC:1101 Homo sapiens (human) 675 BRCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10451700
DOID:10763 hypertension HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:10450539
DOID:1485 cystic fibrosis HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10449435
DOID:3526 cerebral infarction HGNC:1228 Homo sapiens (human) 710 SERPING1 direct assay evidence used in manual assertion
  • PMID:10446335
DOID:8991 cervix uteri carcinoma in situ HGNC:1100 Homo sapiens (human) 672 BRCA1 direct assay evidence used in manual assertion
  • PMID:10442317
DOID:14761 Greig cephalopolysyndactyly syndrome HGNC:4319 Homo sapiens (human) 2737 GLI3 inference by association of genotype from phenotype used in manual assertion
  • PMID:10441342
  • PMID:15739154
  • PMID:22903559
  • PMID:24736735
  • RGD:7240710
DOID:4621 holoprosencephaly HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:10441331
  • PMID:11919111
  • PMID:8896572
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E MGI:1346523 Mus musculus (house mouse) 24051 Sgcb author statement supported by traceable reference
  • PMID:10441321
  • PMID:10678176
DOID:11446 sciatic neuropathy HGNC:8824 Homo sapiens (human) 5176 SERPINF1 direct assay evidence used in manual assertion
  • PMID:10441236
DOID:0110731 neuronal ceroid lipofuscinosis 3 MGI:107537 Mus musculus (house mouse) 12752 Cln3 author statement supported by traceable reference
  • PMID:10440905
  • PMID:10527801
  • PMID:12374761
  • PMID:15326100
  • PMID:17855597
  • PMID:27101989
  • PMID:32601357
DOID:8924 autoimmune thrombocytopenic purpura HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10435723
DOID:8924 autoimmune thrombocytopenic purpura HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10435723
DOID:684 hepatocellular carcinoma HGNC:2514 Homo sapiens (human) 1499 CTNNB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10435629
  • PMID:19101982
  • PMID:26968103
  • PMID:27276713
  • PMID:28328801
  • RGD:7240710
DOID:0110429 dilated cardiomyopathy 1H HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10432437
  • PMID:15996167
DOID:0110429 dilated cardiomyopathy 1H HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10432437
  • PMID:15498363
  • PMID:15996167
DOID:14793 hypohidrotic ectodermal dysplasia MGI:1343498 Mus musculus (house mouse) 13608 Edar author statement supported by traceable reference
  • PMID:10431242
  • PMID:17148670
  • PMID:9799834
DOID:0111663 ectodermal dysplasia 10A HGNC:2895 Homo sapiens (human) 10913 EDAR inference by association of genotype from phenotype used in manual assertion
  • PMID:10431241
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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 8, 2025