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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 101 - 125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0112275 developmental and epileptic encephalopathy 93 HGNC:851 Homo sapiens (human) 523 ATP6V1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:2082 Homo sapiens (human) 9575 CLOCK inference by association of genotype from phenotype used in manual assertion
  • PMID:20554694
DOID:0050851 glomerulosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7 mutant phenotype evidence used in manual assertion
  • PMID:16213192
DOID:2476 hereditary spastic paraplegia SGD:S000005691 Saccharomyces cerevisiae S288C 854336 SEY1 mutant phenotype evidence used in manual assertion
  • PMID:19665976
DOID:0050651 atrioventricular septal defect MGI:1100864 Mus musculus (house mouse) 13411 Dnah11 author statement supported by traceable reference
  • PMID:20511334
DOID:2018 hyperinsulinism HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:16713443
DOID:1883 hepatitis C HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15942906
  • PMID:31977279
DOID:9452 steatotic liver disease HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11718682
DOID:3969 papillary thyroid carcinoma HGNC:5173 Homo sapiens (human) 3265 HRAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:16035 Homo sapiens (human) 161497 STRC inference by association of genotype from phenotype used in manual assertion
  • PMID:11687802
DOID:9655 oral mucosa leukoplakia HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17290401
DOID:9212 pityriasis rubra pilaris HGNC:16446 Homo sapiens (human) 79092 CARD14 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050696 fetal alcohol spectrum disorder HGNC:8846 Homo sapiens (human) 8864 PER2 direct assay evidence used in manual assertion
  • PMID:31329297
DOID:3082 interstitial lung disease HGNC:10802 Homo sapiens (human) 6440 SFTPC inference by association of genotype from phenotype used in manual assertion
  • PMID:15756222
  • PMID:16423270
  • PMID:19443464
DOID:14791 Leber congenital amaurosis HGNC:7606 Homo sapiens (human) 4647 MYO7A inference by association of genotype from phenotype used in manual assertion
  • PMID:21901789
DOID:639 acute disseminated encephalomyelitis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15201511
  • PMID:19722042
  • PMID:22786832
DOID:5419 schizophrenia MGI:99779 Mus musculus (house mouse) 11441 Chrna7 author statement supported by traceable reference
  • PMID:24983521
DOID:5339 cyclic hematopoiesis HGNC:3309 Homo sapiens (human) 1991 ELANE inference by association of genotype from phenotype used in manual assertion
  • PMID:21425445
  • RGD:7240710
DOID:11650 bronchopulmonary dysplasia HGNC:10798 Homo sapiens (human) 653509 SFTPA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11105614
  • PMID:17264398
DOID:9120 amyloidosis HGNC:4432 Homo sapiens (human) 2805 GOT1 direct assay evidence used in manual assertion
  • PMID:28390893
DOID:0060582 Noonan syndrome 4 HGNC:11187 Homo sapiens (human) 6654 SOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17143282
  • PMID:17143285
  • PMID:17586837
  • RGD:7240710
DOID:11716 prediabetes syndrome HGNC:9677 Homo sapiens (human) 5799 PTPRN2 direct assay evidence used in manual assertion
  • PMID:15004204
DOID:0050473 Alstrom syndrome MGI:1934606 Mus musculus (house mouse) 236266 Alms1 author statement supported by traceable reference
  • MGI:6197902
  • MGI:6197907
  • PMID:16000322
  • PMID:16516152
  • PMID:17206865
  • PMID:28859131
DOID:0090086 hypogonadotropic hypogonadism 6 with or without anosmia HGNC:3686 Homo sapiens (human) 2253 FGF8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:6554 Homo sapiens (human) 3953 LEPR inference by association of genotype from phenotype used in manual assertion
  • PMID:19196818
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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: August 4, 2025