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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 10026 - 10050 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:5031 Homo sapiens (human) 3178 HNRNPA1 direct assay evidence used in manual assertion
  • PMID:11984596
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25729550
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22170554
DOID:3210 Pelizaeus-Merzbacher disease HGNC:9086 Homo sapiens (human) 5354 PLP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10425042
  • RGD:7240710
DOID:3210 Pelizaeus-Merzbacher disease MGI:97623 Mus musculus (house mouse) 18823 Plp1 author statement supported by traceable reference
  • PMID:11872612
  • PMID:17133418
  • PMID:17394578
  • PMID:18835559
  • PMID:20091761
DOID:3211 lysosomal storage disease WB:WBGene00021546 Caenorhabditis elegans 3565323 laat-1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:22822152
DOID:3211 lysosomal storage disease HGNC:9251 Homo sapiens (human) 5476 CTSA inference by association of genotype from phenotype used in manual assertion
  • PMID:8514852
DOID:3211 lysosomal storage disease MGI:1924105 Mus musculus (house mouse) 235504 Slc17a5 author statement supported by traceable reference
  • MGI:3609573
DOID:3211 lysosomal storage disease WB:WBGene00021546 Caenorhabditis elegans 3565323 laat-1 mutant phenotype evidence used in manual assertion
  • PMID:22822152
DOID:3211 lysosomal storage disease FB:FBgn0030141 Drosophila melanogaster (fruit fly) 31902 Gga combinatorial experimental and author inference evidence used in manual assertion
  • PMID:21923734
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA inference by association of genotype from phenotype used in manual assertion
  • PMID:1703489
DOID:3213 demyelinating disease RGD:2906 Rattus norvegicus (Norway rat) 29385 Cxcr2 mutant phenotype evidence used in manual assertion
  • PMID:19616545
DOID:3213 demyelinating disease HGNC:7553 Homo sapiens (human) 4609 MYC inference by association of genotype from phenotype used in manual assertion
  • PMID:22076651
DOID:3213 demyelinating disease HGNC:6367 Homo sapiens (human) 5653 KLK6 inference by association of genotype from phenotype used in manual assertion
  • PMID:12023317
DOID:322 myelitis HGNC:4940 Homo sapiens (human) 3115 HLA-DPB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22884298
DOID:3227 tracheal stenosis HGNC:11766 Homo sapiens (human) 7040 TGFB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20172396
DOID:3234 central nervous system lymphoma HGNC:1699 Homo sapiens (human) 974 CD79B inference by association of genotype from phenotype used in manual assertion
  • PMID:28619981
DOID:3234 central nervous system lymphoma HGNC:1133 Homo sapiens (human) 695 BTK mutant phenotype evidence used in manual assertion
  • PMID:28552327
DOID:3234 central nervous system lymphoma HGNC:7562 Homo sapiens (human) 4615 MYD88 inference by association of genotype from phenotype used in manual assertion
  • PMID:28619981
DOID:3234 central nervous system lymphoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:22628023
DOID:326 ischemia RGD:2082 Rattus norvegicus (Norway rat) 25233 Akt2 mutant phenotype evidence used in manual assertion
  • PMID:19084003
DOID:326 ischemia RGD:621861 Rattus norvegicus (Norway rat) 89805 Angpt2 direct assay evidence used in manual assertion
  • PMID:19672036
DOID:326 ischemia WB:WBGene00003168 Caenorhabditis elegans 181728 mec-4 mutant phenotype evidence used in manual assertion
  • PMID:15543143
DOID:326 ischemia HGNC:10618 Homo sapiens (human) 6347 CCL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15308783
DOID:326 ischemia RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a direct assay evidence used in manual assertion
  • PMID:14970118
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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