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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 6026 - 6050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:1612 breast cancer HGNC:952 Homo sapiens (human) 580 BARD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14550946
  • PMID:16768547
  • PMID:17028982
  • RGD:7240710
DOID:77 gastrointestinal system disease HGNC:12663 Homo sapiens (human) 7412 VCAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11361181
DOID:2043 hepatitis B HGNC:12538 Homo sapiens (human) 54578 UGT1A6 inference by association of genotype from phenotype used in manual assertion
  • PMID:29239247
DOID:11054 urinary bladder cancer HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18272472
  • PMID:18765423
DOID:783 end stage renal disease HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:16385653
  • PMID:20149750
DOID:3969 papillary thyroid carcinoma HGNC:17382 Homo sapiens (human) 57522 SRGAP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:8583 Homo sapiens (human) 5054 SERPINE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19063817
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:1037 Homo sapiens (human) 629 CFB inference by association of genotype from phenotype used in manual assertion
  • PMID:17182750
  • PMID:20513133
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12480694
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2526 prostate adenocarcinoma HGNC:13633 Homo sapiens (human) 9370 ADIPOQ inference by association of genotype from phenotype used in manual assertion
  • PMID:21397927
DOID:7693 abdominal aortic aneurysm HGNC:11186 Homo sapiens (human) 6272 SORT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28698188
DOID:12297 Vogt-Koyanagi-Harada disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17605936
  • PMID:19176112
DOID:1287 cardiovascular system disease HGNC:6623 Homo sapiens (human) 9388 LIPG inference by association of genotype from phenotype used in manual assertion
  • PMID:16023652
DOID:3748 esophagus squamous cell carcinoma HGNC:10471 Homo sapiens (human) 861 RUNX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:30666517
DOID:0050465 Muir-Torre syndrome HGNC:7127 Homo sapiens (human) 4292 MLH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4398 pustulosis of palm and sole HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:12691703
DOID:0080082 nonsyndromic congenital nail disorder 4 HGNC:16175 Homo sapiens (human) 343637 RSPO4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16246971
DOID:8778 Crohn's disease HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15505619
DOID:234 colon adenocarcinoma HGNC:11366 Homo sapiens (human) 6776 STAT5A inference by association of genotype from phenotype used in manual assertion
  • PMID:22121102
DOID:1040 chronic lymphocytic leukemia HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26254371
DOID:0111892 Diamond-Blackfan anemia 11 HGNC:10327 Homo sapiens (human) 6154 RPL26 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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