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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 6101 - 6125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:0080379 nephrotic syndrome type 2 HGNC:13394 Homo sapiens (human) 7827 NPHS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11981 morbid obesity HGNC:8032 Homo sapiens (human) 4915 NTRK2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16702999
DOID:1389 polyneuropathy HGNC:11181 Homo sapiens (human) 6649 SOD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:12815947
DOID:4914 esophagus adenocarcinoma HGNC:2594 Homo sapiens (human) 1588 CYP19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21472143
DOID:9352 type 2 diabetes mellitus HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19395279
DOID:0050880 Koolen de Vries syndrome HGNC:24565 Homo sapiens (human) 284058 KANSL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9970 obesity HGNC:7957 Homo sapiens (human) 4887 NPY2R inference by association of genotype from phenotype used in manual assertion
  • PMID:17019604
DOID:0110674 congenital myasthenic syndrome 17 HGNC:6696 Homo sapiens (human) 4038 LRP4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10534 stomach cancer HGNC:6307 Homo sapiens (human) 3791 KDR inference by association of genotype from phenotype used in manual assertion
  • PMID:30380970
DOID:1793 pancreatic cancer HGNC:9948 Homo sapiens (human) 5965 RECQL inference by association of genotype from phenotype used in manual assertion
  • PMID:16540687
  • PMID:19768149
DOID:9164 achalasia HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11837716
  • PMID:30092016
  • PMID:30788115
DOID:0080759 Fanconi renotubular syndrome 3 HGNC:3247 Homo sapiens (human) 1962 EHHADH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081116 benign familial infantile seizures 3 HGNC:10588 Homo sapiens (human) 6326 SCN2A inference by association of genotype from phenotype used in manual assertion
  • PMID:16417554
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2185 Homo sapiens (human) 1300 COL10A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8004099
DOID:0050866 oral squamous cell carcinoma HGNC:76 Homo sapiens (human) 25 ABL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16676365
DOID:0050560 Walker-Warburg syndrome HGNC:19139 Homo sapiens (human) 55624 POMGNT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11709191
  • PMID:15236414
  • PMID:22554691
  • PMID:23689641
DOID:0110060 amelogenesis imperfecta hypomaturation type 2A2 HGNC:7167 Homo sapiens (human) 9313 MMP20 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070252 autosomal dominant Emery-Dreifuss muscular dystrophy 7 HGNC:28472 Homo sapiens (human) 79188 TMEM43 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:6667 Homo sapiens (human) 4018 LPA inference by association of genotype from phenotype used in manual assertion
  • PMID:18775538
DOID:3407 carotid artery disease HGNC:336 Homo sapiens (human) 185 AGTR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16519598
DOID:4448 macular degeneration HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22956172
  • PMID:23538572
DOID:0081101 nonautoimmune hyperthyroidism HGNC:12373 Homo sapiens (human) 7253 TSHR inference by association of genotype from phenotype used in manual assertion
  • PMID:18306976
  • RGD:7240710
DOID:127 leiomyoma HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15760950
DOID:0060563 Char syndrome HGNC:11743 Homo sapiens (human) 7021 TFAP2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:6307 Homo sapiens (human) 3791 KDR inference by association of genotype from phenotype used in manual assertion
  • PMID:24445728
  • PMID:25182707
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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