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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 6001 - 6025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:4947 cholangiocarcinoma HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:24131658
  • PMID:28347255
DOID:684 hepatocellular carcinoma HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:26389641
DOID:0090068 giant axonal neuropathy 1 HGNC:4137 Homo sapiens (human) 8139 GAN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081423 familial focal epilepsy with variable foci 3 HGNC:14124 Homo sapiens (human) 8131 NPRL3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080448 developmental and epileptic encephalopathy 48 HGNC:567 Homo sapiens (human) 8120 AP3B2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080960 amelogenesis imperfecta type 2A6 HGNC:4519 Homo sapiens (human) 8111 GPR68 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11719 oculopharyngeal muscular dystrophy HGNC:8565 Homo sapiens (human) 8106 PABPN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14681 Silver-Russell syndrome HGNC:5009 Homo sapiens (human) 8091 HMGA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:127 leiomyoma HGNC:5009 Homo sapiens (human) 8091 HMGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8954805
DOID:3315 lipoma HGNC:5009 Homo sapiens (human) 8091 HMGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:7606786
DOID:2394 ovarian cancer HGNC:5009 Homo sapiens (human) 8091 HMGA2 mutant phenotype evidence used in manual assertion
  • PMID:18452175
DOID:0081343 congenital myopathy 9A HGNC:4023 Homo sapiens (human) 8087 FXR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081344 congenital myopathy 9B HGNC:4023 Homo sapiens (human) 8087 FXR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9164 achalasia HGNC:13666 Homo sapiens (human) 8086 AAAS inference by association of genotype from phenotype used in manual assertion
  • PMID:16098009
DOID:0050602 triple-A syndrome HGNC:13666 Homo sapiens (human) 8086 AAAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:25112956
  • PMID:29627316
  • PMID:33665490
DOID:3969 papillary thyroid carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:32024448
DOID:3907 lung squamous cell carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:24323028
  • PMID:28177435
  • PMID:30885352
DOID:10941 intracranial aneurysm HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:30121816
DOID:3748 esophagus squamous cell carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:25151357
DOID:0060473 Kabuki syndrome HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:24633898
  • PMID:26300940
  • RGD:7240710
DOID:5409 lung small cell carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:27873319
  • PMID:28007623
  • PMID:29627316
  • PMID:29748005
DOID:3717 gastric adenocarcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D mutant phenotype evidence used in manual assertion
  • PMID:30177394
DOID:14004 thoracic aortic aneurysm HGNC:29673 Homo sapiens (human) 8076 MFAP5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050948 autosomal dominant hypophosphatemic rickets HGNC:3680 Homo sapiens (human) 8074 FGF23 inference by association of genotype from phenotype used in manual assertion
  • PMID:11062477
  • PMID:19655082
  • 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: April 7, 2025