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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 51 - 75 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050156 idiopathic pulmonary fibrosis HGNC:13575 Homo sapiens (human) 23476 BRD4 direct assay evidence used in manual assertion
  • PMID:23759512
DOID:0050156 idiopathic pulmonary fibrosis HGNC:7516 Homo sapiens (human) 727897 MUC5B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050156 idiopathic pulmonary fibrosis MGI:104798 Mus musculus (house mouse) 21926 Tnf author statement supported by traceable reference
  • PMID:7542280
DOID:0050156 idiopathic pulmonary fibrosis HGNC:14129 Homo sapiens (human) 10919 EHMT2 direct assay evidence used in manual assertion
  • PMID:24652950
DOID:0050161 lower respiratory tract disease FB:FBgn0035976 Drosophila melanogaster (fruit fly) 39063 PGRP-LC CG4432 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:33826881
DOID:0050161 lower respiratory tract disease FB:FBgn0030695 Drosophila melanogaster (fruit fly) 32534 PGRP-LE CG8995 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:33826881
DOID:0050168 autoimmune polyendocrine syndrome type 2 HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21388354
DOID:0050168 autoimmune polyendocrine syndrome type 2 HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21388354
DOID:0050168 autoimmune polyendocrine syndrome type 2 HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21388354
DOID:0050185 erythema multiforme HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9627123
DOID:0050200 Korean hemorrhagic fever RGD:2895 Rattus norvegicus (Norway rat) 25704 Il2ra mutant phenotype evidence used in manual assertion
  • PMID:17878294
DOID:0050211 swine influenza HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • PMID:29867955
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1950 Homo sapiens (human) 1128 CHRM1 mutant phenotype evidence used in manual assertion
  • PMID:17764462
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1389 Homo sapiens (human) 774 CACNA1B direct assay evidence used in manual assertion
  • PMID:16289869
DOID:0050214 Lambert-Eaton myasthenic syndrome MGI:109482 Mus musculus (house mouse) 12286 Cacna1a author statement supported by traceable reference
  • PMID:18653245
DOID:0050328 congenital hypothyroidism HGNC:13273 Homo sapiens (human) 50506 DUOX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12110737
DOID:0050328 congenital hypothyroidism RGD:621458 Rattus norvegicus (Norway rat) 83613 Nefl direct assay evidence used in manual assertion
  • PMID:18845185
DOID:0050328 congenital hypothyroidism RGD:3911 Rattus norvegicus (Norway rat) 25360 Tshr mutant phenotype evidence used in manual assertion
  • PMID:29507327
DOID:0050328 congenital hypothyroidism RGD:3160 Rattus norvegicus (Norway rat) 24588 Nefm direct assay evidence used in manual assertion
  • PMID:18845185
DOID:0050328 congenital hypothyroidism HGNC:11040 Homo sapiens (human) 6528 SLC5A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:9171822
DOID:0050328 congenital hypothyroidism HGNC:12015 Homo sapiens (human) 7173 TPO inference by association of genotype from phenotype used in manual assertion
  • PMID:7550241
DOID:0050328 congenital hypothyroidism MGI:98813 Mus musculus (house mouse) 22018 Tpo author statement supported by traceable reference
  • PMID:16762971
DOID:0050328 congenital hypothyroidism MGI:98849 Mus musculus (house mouse) 22095 Tshr author statement supported by traceable reference
  • MGI:5571363
  • PMID:10575115
  • PMID:12432094
  • PMID:17932107
DOID:0050328 congenital hypothyroidism MGI:98733 Mus musculus (house mouse) 21819 Tg author statement supported by traceable reference
  • PMID:3803305
DOID:0050328 congenital hypothyroidism MGI:99829 Mus musculus (house mouse) 12393 Runx2 author statement supported by traceable reference
  • PMID:20375239
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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

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Last updated: August 4, 2025