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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 13176 - 13200 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:585 nephrolithiasis HGNC:11019 Homo sapiens (human) 6569 SLC34A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22396660
DOID:0090142 cystathioninuria MGI:1339968 Mus musculus (house mouse) 107869 Cth author statement supported by traceable reference
  • PMID:20566639
DOID:0110477 autosomal recessive nonsyndromic deafness 2 HGNC:7606 Homo sapiens (human) 4647 MYO7A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060746 basal laminar drusen HGNC:4883 Homo sapiens (human) 3075 CFH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:848 arthritis HGNC:19100 Homo sapiens (human) 149233 IL23R inference by association of genotype from phenotype used in manual assertion
  • PMID:19035472
DOID:8778 Crohn's disease HGNC:8104 Homo sapiens (human) 100506658 OCLN direct assay evidence used in manual assertion
  • PMID:21748286
DOID:0110423 dilated cardiomyopathy 1C MGI:1344412 Mus musculus (house mouse) 24131 Ldb3 author statement supported by traceable reference
  • PMID:19028670
DOID:1168 familial hyperlipidemia RGD:2998 Rattus norvegicus (Norway rat) 300438 Ldlr mutant phenotype evidence used in manual assertion
  • PMID:29459263
DOID:1059 intellectual disability HGNC:18683 Homo sapiens (human) 9775 EIF4A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:23376982
DOID:224 transient cerebral ischemia RGD:2581 Rattus norvegicus (Norway rat) 24890 Esr1 direct assay evidence used in manual assertion
  • PMID:24548484
  • PMID:25098259
DOID:7148 rheumatoid arthritis HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:12563673
DOID:0060877 bullous congenital ichthyosiform erythroderma MGI:96699 Mus musculus (house mouse) 16681 Krt2 author statement supported by traceable reference
  • PMID:12533510
DOID:10603 glucose intolerance HGNC:11621 Homo sapiens (human) 6927 HNF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:15277395
DOID:0070068 autosomal dominant intellectual developmental disorder 38 MGI:1096317 Mus musculus (house mouse) 13628 Eef1a2 author statement supported by traceable reference
  • PMID:32160274
DOID:0111377 fetal akinesia deformation sequence syndrome 1 HGNC:7525 Homo sapiens (human) 4593 MUSK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1935 Bardet-Biedl syndrome HGNC:967 Homo sapiens (human) 583 BBS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11285252
DOID:0111078 tibial muscular dystrophy HGNC:12403 Homo sapiens (human) 7273 TTN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080584 autosomal dominant Wolfram syndrome HGNC:12762 Homo sapiens (human) 7466 WFS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease MGI:1342774 Mus musculus (house mouse) 19017 Ppargc1a author statement supported by traceable reference
  • PMID:32439544
DOID:0080484 peroxisome biogenesis disorder 10A HGNC:8858 Homo sapiens (human) 8504 PEX3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:14709372
  • PMID:15059615
DOID:0050955 spinocerebellar ataxia type 2 HGNC:10555 Homo sapiens (human) 6311 ATXN2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110282 autosomal recessive limb-girdle muscular dystrophy type 2H FB:FBgn0265356 Drosophila melanogaster (fruit fly) 37190 tn combinatorial experimental and author inference evidence used in manual assertion
  • PMID:33296226
DOID:684 hepatocellular carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • PMID:23907815
  • PMID:25123086
  • PMID:25339005
  • PMID:26575952
  • PMID:28416747
DOID:0070270 hereditary nonpolyposis colorectal cancer type 8 HGNC:11529 Homo sapiens (human) 4072 EPCAM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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: December 8, 2025