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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:0111676 high molecular weight kininogen deficiency HGNC:6383 Homo sapiens (human) 3827 KNG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7901207
  • RGD:7240710
DOID:3407 carotid artery disease RGD:620410 Rattus norvegicus (Norway rat) 59264 Ltb4r direct assay evidence used in manual assertion
  • PMID:16293697
DOID:1380 endometrial cancer HGNC:392 Homo sapiens (human) 208 AKT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22146979
DOID:1339 Diamond-Blackfan anemia MGI:2444881 Mus musculus (house mouse) 226844 Flvcr1 author statement supported by traceable reference
  • PMID:18258918
DOID:3525 middle cerebral artery infarction RGD:3726 Rattus norvegicus (Norway rat) 25273 Smo mutant phenotype evidence used in manual assertion
  • PMID:23499832
  • PMID:23696546
DOID:0080716 infantile liver failure syndrome HGNC:21876 Homo sapiens (human) 60561 RINT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1749 squamous cell carcinoma HGNC:13726 Homo sapiens (human) 58508 KMT2C inference by association of genotype from phenotype used in manual assertion
  • PMID:25303977
DOID:2920 membranoproliferative glomerulonephritis RGD:69651 Rattus norvegicus (Norway rat) 81810 Tgfbr2 direct assay evidence used in manual assertion
  • PMID:11703592
DOID:9352 type 2 diabetes mellitus HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:24452036
DOID:13269 hereditary coproporphyria MGI:104841 Mus musculus (house mouse) 12892 Cpox author statement supported by traceable reference
  • PMID:23631845
  • PMID:28600349
DOID:6196 reactive arthritis HGNC:43 Homo sapiens (human) 6890 TAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7748224
DOID:0070299 multiple epiphyseal dysplasia 5 MGI:1328350 Mus musculus (house mouse) 17182 Matn3 author statement supported by traceable reference
  • PMID:17517694
DOID:0112072 nuclear type mitochondrial complex I deficiency 20 MGI:1914272 Mus musculus (house mouse) 229211 Acad9 author statement supported by traceable reference
  • PMID:34556413
DOID:1094 attention deficit hyperactivity disorder MGI:1928478 Mus musculus (house mouse) 56710 Brinp1 author statement supported by traceable reference
  • PMID:27042284
DOID:219 colon cancer HGNC:28611 Homo sapiens (human) 253260 RICTOR mutant phenotype evidence used in manual assertion
  • PMID:20226010
DOID:13139 crescentic glomerulonephritis RGD:71069 Rattus norvegicus (Norway rat) 116591 Fcgr2a inference by association of genotype from phenotype used in manual assertion
  • PMID:16482158
DOID:1996 rectum adenocarcinoma HGNC:11368 Homo sapiens (human) 6778 STAT6 inference by association of genotype from phenotype used in manual assertion
  • PMID:22121102
DOID:3389 Papillon-Lefevre disease HGNC:2528 Homo sapiens (human) 1075 CTSC inference by association of genotype from phenotype used in manual assertion
  • PMID:10593994
  • RGD:7240710
DOID:3070 high grade glioma HGNC:8800 Homo sapiens (human) 5155 PDGFB mutant phenotype evidence used in manual assertion
  • PMID:21677873
  • PMID:26945107
DOID:0060788 hypomyelinating leukodystrophy 10 HGNC:30262 Homo sapiens (human) 29920 PYCR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060756 sclerosteosis 1 HGNC:13771 Homo sapiens (human) 50964 SOST inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:9865 Homo sapiens (human) 5915 RARB direct assay evidence used in manual assertion
  • PMID:18349282
  • PMID:23599765
DOID:0060180 colitis RGD:3812 Rattus norvegicus (Norway rat) 25007 Tacr2 mutant phenotype evidence used in manual assertion
  • PMID:12490601
DOID:0060578 Noonan syndrome 1 MGI:99511 Mus musculus (house mouse) 19247 Ptpn11 author statement supported by traceable reference
  • PMID:15273746
  • PMID:17641779
  • PMID:28346493
DOID:0050711 aceruloplasminemia MGI:88476 Mus musculus (house mouse) 12870 Cp author statement supported by traceable reference
  • PMID:10485908
  • PMID:11461924
  • PMID:18804145
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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: December 8, 2025