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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 10001 - 10025 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24 inference by association of genotype from phenotype used in manual assertion
  • PMID:11519011
DOID:3146 lipid metabolism disorder HGNC:7958 Homo sapiens (human) 4889 NPY5R inference by association of genotype from phenotype used in manual assertion
  • PMID:17426313
DOID:3146 lipid metabolism disorder HGNC:7530 Homo sapiens (human) 4598 MVK inference by association of genotype from phenotype used in manual assertion
  • PMID:1377680
DOID:3146 lipid metabolism disorder HGNC:2328 Homo sapiens (human) 1374 CPT1A inference by association of genotype from phenotype used in manual assertion
  • PMID:9691089
DOID:3146 lipid metabolism disorder HGNC:9232 Homo sapiens (human) 5465 PPARA inference by association of genotype from phenotype used in manual assertion
  • PMID:10828087
DOID:3151 skin squamous cell carcinoma HGNC:30767 Homo sapiens (human) 90417 KNSTRN inference by association of genotype from phenotype used in manual assertion
  • PMID:25194279
  • PMID:30972880
DOID:3151 skin squamous cell carcinoma HGNC:13723 Homo sapiens (human) 10664 CTCF inference by association of genotype from phenotype used in manual assertion
  • PMID:27974201
DOID:3153 lipomatosis HGNC:1848 Homo sapiens (human) 1056 CEL inference by association of genotype from phenotype used in manual assertion
  • PMID:17259390
DOID:3159 photosensitivity disease HGNC:1103 Homo sapiens (human) 6046 BRD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16516380
DOID:3165 skin benign neoplasm HGNC:5173 Homo sapiens (human) 3265 HRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:22683711
DOID:3168 squamous cell neoplasm HGNC:30796 Homo sapiens (human) 11171 STRAP direct assay evidence used in manual assertion
  • PMID:16778189
DOID:3181 oligodendroglioma HGNC:3229 Homo sapiens (human) 1950 EGF inference by association of genotype from phenotype used in manual assertion
  • PMID:17473192
DOID:3181 oligodendroglioma HGNC:9884 Homo sapiens (human) 5925 RB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15970925
DOID:3181 oligodendroglioma HGNC:7059 Homo sapiens (human) 4255 MGMT inference by association of genotype from phenotype used in manual assertion
  • PMID:15455350
DOID:3204 schwannomatosis HGNC:11103 Homo sapiens (human) 6598 SMARCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22038540
  • PMID:28365909
  • PMID:29409008
DOID:3209 junctional epidermolysis bullosa HGNC:6158 Homo sapiens (human) 3691 ITGB4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6139 Homo sapiens (human) 3675 ITGA3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6490 Homo sapiens (human) 3914 LAMB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:7698759
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa MGI:99909 Mus musculus (house mouse) 16774 Lama3 author statement supported by traceable reference
  • PMID:27729280
DOID:3209 junctional epidermolysis bullosa HGNC:6493 Homo sapiens (human) 3918 LAMC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8012393
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6142 Homo sapiens (human) 3655 ITGA6 inference by association of genotype from phenotype used in manual assertion
  • PMID:9185503
DOID:3209 junctional epidermolysis bullosa MGI:88450 Mus musculus (house mouse) 12821 Col17a1 author statement supported by traceable reference
  • PMID:37796769
DOID:3209 junctional epidermolysis bullosa HGNC:2194 Homo sapiens (human) 1308 COL17A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7550320
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6483 Homo sapiens (human) 3909 LAMA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:8586427
  • RGD:7240710
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:18788 Homo sapiens (human) 22914 KLRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22170554
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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