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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 5751 - 5775 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:0060797 hypomyelinating leukodystrophy 8 HGNC:30348 Homo sapiens (human) 55703 POLR3B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050866 oral squamous cell carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • PMID:28025427
DOID:0060774 congenital diarrhea HGNC:12781 Homo sapiens (human) 7482 WNT2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:11140 Homo sapiens (human) 6620 SNCB inference by association of genotype from phenotype used in manual assertion
  • PMID:17556099
DOID:0111626 D-glyceric aciduria HGNC:24247 Homo sapiens (human) 132158 GLYCTK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:20103627
DOID:10283 prostate cancer HGNC:6358 Homo sapiens (human) 5655 KLK10 inference by association of genotype from phenotype used in manual assertion
  • PMID:11920956
DOID:0111401 congenital dyserythropoietic anemia type II HGNC:10702 Homo sapiens (human) 10483 SEC23B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111542 familial expansile osteolysis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070046 Coffin-Siris syndrome 4 HGNC:11100 Homo sapiens (human) 6597 SMARCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3310 atopic dermatitis HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:22533231
DOID:9256 colorectal cancer HGNC:4553 Homo sapiens (human) 2876 GPX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19428376
DOID:10595 Charcot-Marie-Tooth disease HGNC:7225 Homo sapiens (human) 4359 MPZ inference by association of genotype from phenotype used in manual assertion
  • PMID:11080237
  • RGD:7240710
DOID:10763 hypertension RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15775781
  • PMID:16467505
DOID:12306 vitiligo HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16409268
DOID:0110759 type 1 diabetes mellitus 22 HGNC:1606 Homo sapiens (human) 1234 CCR5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:3273 Homo sapiens (human) 8667 EIF3H inference by association of genotype from phenotype used in manual assertion
  • PMID:11733359
DOID:0110070 arrhythmogenic right ventricular dysplasia 1 HGNC:11769 Homo sapiens (human) 7043 TGFB3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11383 cryptorchidism HGNC:17318 Homo sapiens (human) 122042 RXFP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12217959
DOID:3587 pancreatic ductal carcinoma HGNC:7059 Homo sapiens (human) 4255 MGMT inference by association of genotype from phenotype used in manual assertion
  • PMID:16844323
DOID:11716 prediabetes syndrome HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18096169
DOID:0110982 Joubert syndrome 13 HGNC:26113 Homo sapiens (human) 79600 TCTN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome HGNC:2209 Homo sapiens (human) 1289 COL5A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10777716
  • PMID:11278977
  • PMID:12145749
  • PMID:8752669
DOID:1993 rectum cancer HGNC:2602 Homo sapiens (human) 1591 CYP24A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31740231
DOID:0090128 Carvajal syndrome HGNC:3052 Homo sapiens (human) 1832 DSP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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International Collaboration

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