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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 October 9, 2024
Displaying entries 71201 - 71225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:3021 acute kidney failure MGI:87874 Mus musculus (house mouse) 11421 Ace
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
DOID:14256 adult-onset Still's disease HGNC:4893 Homo sapiens (human) 3082 HGF
  • PMID:24387171
DOID:5199 ureteral obstruction HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus FB:FBgn0042711 Drosophila melanogaster (fruit fly) 117364 Hex-t1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:3432 Homo sapiens (human) 2066 ERBB4
  • MGI:6194238
DOID:2841 asthma WB:WBGene00003930 Caenorhabditis elegans 175504 pat-3
  • MGI:6194238
DOID:784 chronic kidney disease MGI:1098733 Mus musculus (house mouse) 52466 Slc46a1
  • MGI:6194238
DOID:0050697 chorioamnionitis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:1389 polyneuropathy HGNC:602 Homo sapiens (human) 337 APOA4
  • PMID:19589605
DOID:0090130 cortical dysplasia-focal epilepsy syndrome HGNC:13830 Homo sapiens (human) 26047 CNTNAP2
  • MGI:6194238
  • RGD:7240710
DOID:11383 cryptorchidism RGD:619831 Rattus norvegicus (Norway rat) 246097 Fas
  • PMID:29606031
DOID:12466 secondary hyperparathyroidism MGI:1351351 Mus musculus (house mouse) 12374 Casr
  • MGI:6194238
DOID:10608 celiac disease MGI:1858745 Mus musculus (house mouse) 54167 Icos
  • MGI:6194238
DOID:2527 nephrosis HGNC:12692 Homo sapiens (human) 7431 VIM
  • MGI:6194238
DOID:0060060 non-Hodgkin lymphoma WB:WBGene00017089 Caenorhabditis elegans 171999 poml-2
  • MGI:6194238
DOID:8991 cervix uteri carcinoma in situ MGI:97798 Mus musculus (house mouse) 19225 Ptgs2
  • MGI:6194238
DOID:0110853 rhizomelic chondrodysplasia punctata type 3 HGNC:327 Homo sapiens (human) 8540 AGPS
  • MGI:6194238
  • RGD:7240710
DOID:14753 isovaleric acidemia RGD:2936 Rattus norvegicus (Norway rat) 24513 Ivd
  • MGI:6194238
DOID:9266 cystinuria SGD:S000003519 Saccharomyces cerevisiae S288C 853204 IMA1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease FB:FBgn0004057 Drosophila melanogaster (fruit fly) 32974 G6pd
  • MGI:6194238
DOID:13141 uveitis MGI:98759 Mus musculus (house mouse) 21872 Tjp1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:9204 Homo sapiens (human) 5444 PON1
  • PMID:17949258
DOID:824 periodontitis HGNC:7159 Homo sapiens (human) 4322 MMP13
  • MGI:6194238
DOID:0070273 hereditary nonpolyposis colorectal cancer type 6 RGD:69651 Rattus norvegicus (Norway rat) 81810 Tgfbr2
  • MGI:6194238

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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 9, 2024