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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 5001 - 5025 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 RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • MGI:6194238
DOID:1059 intellectual disability RGD:727891 Rattus norvegicus (Norway rat) 317553 Il1rapl1
  • MGI:6194238
DOID:2841 asthma HGNC:16037 Homo sapiens (human) 29095 ORMDL2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:2349 arteriosclerosis RGD:620874 Rattus norvegicus (Norway rat) 89824 Chi3l1
  • MGI:6194238
DOID:13948 bladder neck obstruction HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:7056 Homo sapiens (human) 10724 OGA
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:3571 liver cancer HGNC:24436 Homo sapiens (human) 134526 ACOT12
  • MGI:6194238
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures HGNC:1094 Homo sapiens (human) 670 BPHL
  • MGI:6194238
DOID:2316 brain ischemia MGI:97503 Mus musculus (house mouse) 18538 Pcna
  • MGI:6194238
DOID:850 lung disease MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238
DOID:162 cancer HGNC:9283 Homo sapiens (human) 5501 PPP1CC
  • MGI:6194238
DOID:0110645 long QT syndrome 2 MGI:2146159 Mus musculus (house mouse) 380959 Alg10b
  • MGI:6194238
DOID:820 myocarditis HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00001685 Caenorhabditis elegans 180601 gpd-3
  • MGI:6194238
DOID:893 Wilson disease WB:WBGene00000212 Caenorhabditis elegans 181323 asm-2
  • MGI:6194238
DOID:1324 lung cancer MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
DOID:11714 gestational diabetes MGI:106675 Mus musculus (house mouse) 11450 Adipoq
  • MGI:6194238
DOID:0050827 rheumatic heart disease HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:12858 Huntington's disease RGD:3387 Rattus norvegicus (Norway rat) 65248 Prkaa1
  • MGI:6194238
DOID:2352 hemochromatosis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:6107 Homo sapiens (human) 3651 PDX1
  • 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: August 19, 2024