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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 13676 - 13700 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:0050776 non-syndromic X-linked intellectual disability SGD:S000004872 Saccharomyces cerevisiae S288C 855301 TRM732 sequence similarity evidence used in manual assertion
  • PMID:25404562
DOID:0060041 autism spectrum disorder MGI:98248 Mus musculus (house mouse) 110876 Scn2a author statement supported by traceable reference
  • PMID:34156984
DOID:9744 type 1 diabetes mellitus HGNC:20580 Homo sapiens (human) 120227 CYP2R1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17607662
DOID:14557 primary pulmonary hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS inference by association of genotype from phenotype used in manual assertion
  • PMID:32236489
DOID:0080199 colorectal carcinoma HGNC:9801 Homo sapiens (human) 5879 RAC1 mutant phenotype evidence used in manual assertion
  • PMID:23559092
DOID:0060882 renal hypomagnesemia 4 HGNC:3229 Homo sapiens (human) 1950 EGF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:10632 Homo sapiens (human) 6352 CCL5 inference by association of genotype from phenotype used in manual assertion
  • PMID:19335954
DOID:1790 malignant mesothelioma HGNC:172 Homo sapiens (human) 91 ACVR1B mutant phenotype evidence used in manual assertion
  • PMID:30061637
DOID:0110790 hereditary spastic paraplegia 39 HGNC:16268 Homo sapiens (human) 10908 PNPLA6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1883 hepatitis C HGNC:1606 Homo sapiens (human) 1234 CCR5 inference by association of genotype from phenotype used in manual assertion
  • PMID:27304910
  • RGD:7240710
DOID:1923 disorder of sexual development HGNC:464 Homo sapiens (human) 268 AMH inference by association of genotype from phenotype used in manual assertion
  • PMID:1483695
DOID:8761 acute megakaryocytic leukemia HGNC:6193 Homo sapiens (human) 3718 JAK3 mutant phenotype evidence used in manual assertion
  • PMID:16843266
DOID:0050156 idiopathic pulmonary fibrosis HGNC:9605 Homo sapiens (human) 5743 PTGS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21319594
DOID:12716 newborn respiratory distress syndrome MGI:104719 Mus musculus (house mouse) 15531 Ndst1 author statement supported by traceable reference
  • PMID:10664446
  • PMID:10852901
DOID:0080528 bronchiectasis 3 HGNC:10602 Homo sapiens (human) 6340 SCNN1G inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer HGNC:9646 Homo sapiens (human) 5783 PTPN13 inference by association of genotype from phenotype used in manual assertion
  • PMID:24338422
DOID:332 amyotrophic lateral sclerosis HGNC:11179 Homo sapiens (human) 6647 SOD1 direct assay evidence used in manual assertion
  • PMID:26826269
DOID:0111358 Floating-Harbor syndrome HGNC:16974 Homo sapiens (human) 10847 SRCAP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19252927
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1 author statement supported by traceable reference
  • PMID:28545977
DOID:1245 vulva cancer HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12543794
DOID:5844 myocardial infarction HGNC:336 Homo sapiens (human) 185 AGTR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16061119
DOID:9976 heroin dependence HGNC:4083 Homo sapiens (human) 2562 GABRB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19500151
  • PMID:25025424
DOID:0070094 oculocutaneous albinism type IA HGNC:12442 Homo sapiens (human) 7299 TYR direct assay evidence used in manual assertion
  • PMID:19436266
DOID:9743 diabetic neuropathy HGNC:12680 Homo sapiens (human) 7422 VEGFA direct assay evidence used in manual assertion
  • PMID:26201024
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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