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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 451 - 475 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:2671 transitional cell carcinoma HGNC:5472 Homo sapiens (human) 3486 IGFBP3 direct assay evidence used in manual assertion
  • PMID:17541304
DOID:11758 iron deficiency anemia HGNC:11740 Homo sapiens (human) 7018 TF inference by association of genotype from phenotype used in manual assertion
  • PMID:11703331
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:0070552 epidermolytic palmoplantar keratoderma 1 HGNC:6447 Homo sapiens (human) 3857 KRT9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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: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: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: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:6196 reactive arthritis HGNC:43 Homo sapiens (human) 6890 TAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7748224
DOID:219 colon cancer HGNC:28611 Homo sapiens (human) 253260 RICTOR mutant phenotype evidence used in manual assertion
  • PMID:20226010
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:0060438 Cole-Carpenter syndrome HGNC:10706 Homo sapiens (human) 9871 SEC24D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110035 Alzheimer's disease 2 HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12120 pulmonary alveolar proteinosis HGNC:2436 Homo sapiens (human) 1439 CSF2RB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:10593 Homo sapiens (human) 6331 SCN5A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:2731 Homo sapiens (human) 4921 DDR2 direct assay evidence used in manual assertion
  • PMID:28476831
DOID:14018 alcoholic liver cirrhosis HGNC:404 Homo sapiens (human) 217 ALDH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11051375
  • PMID:23550892
  • PMID:29779728
DOID:0050641 Rh deficiency syndrome HGNC:10006 Homo sapiens (human) 6005 RHAG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060455 Thiel-Behnke corneal dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10632 Wolfram syndrome HGNC:12762 Homo sapiens (human) 7466 WFS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9771706
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Supported by JST NBDC Grant Number JPMJND2204

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