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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 7026 - 7050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:1240 leukemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:18426641
DOID:583 hemolytic anemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:3136561
DOID:2945 severe acute respiratory syndrome HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:15784866
DOID:13406 pulmonary sarcoidosis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:9036208
DOID:2841 asthma HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:16008680
  • PMID:19771478
DOID:1793 pancreatic cancer HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:20103627
DOID:14067 Plasmodium falciparum malaria HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:18003641
DOID:0080600 COVID-19 HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
  • RGD:7240710
DOID:14504 Niemann-Pick disease HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
DOID:653 purine-pyrimidine metabolic disorder HGNC:7892 Homo sapiens (human) 4860 PNP
  • PMID:3029074
DOID:5813 purine nucleoside phosphorylase deficiency HGNC:7892 Homo sapiens (human) 4860 PNP
  • MGI:6194238
  • RGD:7240710
DOID:5453 pulmonary venoocclusive disease HGNC:786 Homo sapiens (human) 468 ATF4
  • MGI:6194238
DOID:10286 prostate carcinoma HGNC:786 Homo sapiens (human) 468 ATF4
  • PMID:25680860
DOID:5154 borna disease HGNC:786 Homo sapiens (human) 468 ATF4
  • MGI:6194238
DOID:10283 prostate cancer HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:26522727
  • PMID:26944919
DOID:2957 pulmonary tuberculosis HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:20856677
DOID:0080488 mucolipidosis HGNC:7758 Homo sapiens (human) 4758 NEU1
  • RGD:7240710
DOID:3343 glycoproteinosis HGNC:7758 Homo sapiens (human) 4758 NEU1
  • MGI:6194238
DOID:0110734 neurodegeneration with brain iron accumulation HGNC:7694 Homo sapiens (human) 4706 NDUFAB1
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:14227 azoospermia HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7681 Homo sapiens (human) 8509 NDST2
  • 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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