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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 2601 - 2625 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:0112182 mismatch repair cancer syndrome HGNC:16261 Homo sapiens (human) 114571 SLC22A9 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
DOID:14365 systemic primary carnitine deficiency disease HGNC:10969 Homo sapiens (human) 6584 SLC22A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12408185
  • RGD:7240710
DOID:8778 Crohn's disease HGNC:10969 Homo sapiens (human) 6584 SLC22A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15107849
DOID:655 inherited metabolic disorder HGNC:10969 Homo sapiens (human) 6584 SLC22A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:3974805
DOID:0050700 cardiomyopathy HGNC:10969 Homo sapiens (human) 6584 SLC22A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15487009
DOID:7148 rheumatoid arthritis HGNC:10968 Homo sapiens (human) 6583 SLC22A4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3021 acute kidney failure HGNC:10966 Homo sapiens (human) 6582 SLC22A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19625999
DOID:0060230 basal ganglia calcification HGNC:10947 Homo sapiens (human) 6575 SLC20A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070537 spastic tetraplegia, thin corpus callosum, and progressive microcephaly HGNC:10942 Homo sapiens (human) 6509 SLC1A4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050994 episodic ataxia type 6 HGNC:10941 Homo sapiens (human) 6507 SLC1A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080442 developmental and epileptic encephalopathy 41 HGNC:10940 Homo sapiens (human) 6506 SLC1A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070093 schizophrenia 18 HGNC:10939 Homo sapiens (human) 6505 SLC1A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060650 dicarboxylic aminoaciduria HGNC:10939 Homo sapiens (human) 6505 SLC1A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050659 biotin-responsive basal ganglia disease HGNC:16266 Homo sapiens (human) 80704 SLC19A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:10938 Homo sapiens (human) 10560 SLC19A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10391221
DOID:0090117 thiamine-responsive megaloblastic anemia syndrome HGNC:10938 Homo sapiens (human) 10560 SLC19A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13382 megaloblastic anemia HGNC:10938 Homo sapiens (human) 10560 SLC19A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10391221
DOID:0060770 dextro-looped transposition of the great arteries HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22868813
DOID:12365 malaria HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27198213
DOID:2531 hematologic cancer HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21984221
DOID:9296 cleft lip HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18797703
DOID:612 primary immunodeficiency disease HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7693 abdominal aortic aneurysm HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18635682
DOID:0110672 congenital myasthenic syndrome 21 HGNC:10936 Homo sapiens (human) 6572 SLC18A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:10935 Homo sapiens (human) 6571 SLC18A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16339215
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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: April 7, 2025