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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 71176 - 71200 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12842 Guillain-Barre syndrome HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:0050523 adult T-cell leukemia/lymphoma HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:16790753
DOID:9538 multiple myeloma HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:22705596
DOID:2518 orchitis HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:12449 aplastic anemia HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:21234821
DOID:2917 cryoglobulinemia HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:23840845
DOID:11123 Henoch-Schoenlein purpura HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:27030970
DOID:1040 chronic lymphocytic leukemia HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:23154584
DOID:2799 bronchiolitis obliterans HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:10124 corneal disease HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:24283754
DOID:2957 pulmonary tuberculosis HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:17713660
DOID:9119 acute myeloid leukemia HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:16115907
DOID:3525 middle cerebral artery infarction HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
DOID:2841 asthma HGNC:1705 Homo sapiens (human) 942 CD86
  • MGI:6194238
  • PMID:17513529
  • PMID:9449507
DOID:6432 pulmonary hypertension HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:19693657
DOID:8924 autoimmune thrombocytopenic purpura HGNC:1705 Homo sapiens (human) 942 CD86
  • PMID:19379594
  • PMID:20581660
DOID:0110810 hereditary spastic paraplegia 5A HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:0111070 congenital bile acid synthesis defect 3 HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:5844 myocardial infarction RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
  • PMID:21329947
DOID:10591 pre-eclampsia RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
  • PMID:20720407
DOID:783 end stage renal disease RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • PMID:16543713
DOID:11400 pyelonephritis RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:9074 systemic lupus erythematosus RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238

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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: December 9, 2024