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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 9951 - 9975 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:811 lipodystrophy HGNC:325 Homo sapiens (human) 10555 AGPAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11967537
DOID:684 hepatocellular carcinoma HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25700262
DOID:0111577 dehydrated hereditary stomatocytosis 2 HGNC:6293 Homo sapiens (human) 3783 KCNN4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050866 oral squamous cell carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • PMID:28025427
DOID:12205 dengue disease HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:26240159
DOID:576 proteinuria HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10430976
DOID:2942 bronchiolitis HGNC:5981 Homo sapiens (human) 3605 IL17A inference by association of genotype from phenotype used in manual assertion
  • PMID:20437253
DOID:0080855 Parkinsonism HGNC:4177 Homo sapiens (human) 2629 GBA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20838799
DOID:0050545 visceral heterotaxy HGNC:18292 Homo sapiens (human) 55997 CFC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12361 Graves' disease HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:15219383
  • PMID:17348243
  • PMID:19732761
DOID:9155 mucocutaneous leishmaniasis HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:7595196
DOID:0060826 syndromic X-linked intellectual disability Shashi type HGNC:9910 Homo sapiens (human) 27316 RBMX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11335 sarcoidosis HGNC:1142 Homo sapiens (human) 56244 BTNL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22991420
  • RGD:7240710
DOID:2043 hepatitis B HGNC:8760 Homo sapiens (human) 5133 PDCD1 direct assay evidence used in manual assertion
  • PMID:31770816
DOID:0080822 aspirin-induced respiratory disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25975240
DOID:2349 arteriosclerosis HGNC:9596 Homo sapiens (human) 5734 PTGER4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16020747
DOID:0060478 Zika fever HGNC:11363 Homo sapiens (human) 6773 STAT2 mutant phenotype evidence used in manual assertion
  • PMID:29746837
DOID:365 bladder disease HGNC:1952 Homo sapiens (human) 1131 CHRM3 mutant phenotype evidence used in manual assertion
  • PMID:17922784
DOID:8398 osteoarthritis HGNC:9201 Homo sapiens (human) 5443 POMC mutant phenotype evidence used in manual assertion
  • PMID:21378032
DOID:1485 cystic fibrosis HGNC:4311 Homo sapiens (human) 2729 GCLC inference by association of genotype from phenotype used in manual assertion
  • PMID:16690975
DOID:0050884 triosephosphate isomerase deficiency HGNC:12009 Homo sapiens (human) 7167 TPI1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12716 newborn respiratory distress syndrome HGNC:10801 Homo sapiens (human) 6439 SFTPB direct assay evidence used in manual assertion
  • PMID:12490037
DOID:12554 hemolytic-uremic syndrome HGNC:4883 Homo sapiens (human) 3075 CFH inference by association of genotype from phenotype used in manual assertion
  • PMID:14583443
DOID:0050811 congenital adrenal hyperplasia HGNC:2600 Homo sapiens (human) 1589 CYP21A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12930931
DOID:12849 autistic disorder HGNC:4600 Homo sapiens (human) 2918 GRM8 inference by association of genotype from phenotype used in manual assertion
  • PMID:12676915
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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