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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 July 29, 2024
Displaying entries 1376 - 1400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:7148 rheumatoid arthritis HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:20676650
  • PMID:22505706
DOID:9970 obesity HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:16328014
  • PMID:16491645
DOID:10611 protein-losing enteropathy HGNC:2665 Homo sapiens (human) 1604 CD55
  • RGD:7240710
DOID:77 gastrointestinal system disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:11361181
DOID:0050861 colorectal adenocarcinoma HGNC:2648 Homo sapiens (human) 11283 CYP4F8
  • PMID:27354594
DOID:2841 asthma HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:18382474
  • PMID:18774397
  • PMID:19910030
  • PMID:20860503
DOID:0111507 Lenz-Majewski hyperostotic dwarfism HGNC:9587 Homo sapiens (human) 9791 PTDSS1
  • RGD:7240710
DOID:13922 eosinophilic esophagitis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26416193
DOID:11476 osteoporosis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:17002564
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17923109
DOID:0111677 familial benign fleck retina HGNC:9038 Homo sapiens (human) 5322 PLA2G5
  • RGD:7240710
DOID:9828 neonatal abstinence syndrome HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:23632726
  • PMID:26233486
  • PMID:27983768
DOID:2154 nephroblastoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:9070652
DOID:0050453 lissencephaly HGNC:19743 Homo sapiens (human) 29954 POMT2
  • PMID:17559086
DOID:853 polymyalgia rheumatica HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:12375325
DOID:0110669 congenital myasthenic syndrome 14 HGNC:23159 Homo sapiens (human) 85365 ALG2
  • RGD:7240710
DOID:0111110 maturity-onset diabetes of the young type 13 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:2280 hidradenitis suppurativa HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:23106544
DOID:417 autoimmune disease HGNC:5382 Homo sapiens (human) 3417 IDH1
  • PMID:31121195
DOID:0060075 estrogen-receptor positive breast cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • PMID:28881720
DOID:0090139 cortisone reductase deficiency HGNC:4795 Homo sapiens (human) 9563 H6PD
  • PMID:12858176
DOID:7148 rheumatoid arthritis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:19221398
DOID:10283 prostate cancer HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:20663522
DOID:12140 Chagas disease HGNC:11177 Homo sapiens (human) 6646 SOAT1
  • PMID:31236660
DOID:1612 breast cancer HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:18497059

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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 19, 2024