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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 11301 - 11325 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:0112160 autosomal dominant nonsyndromic deafness 79 HGNC:21088 Homo sapiens (human) 79966 SCD5
  • RGD:7240710
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:589 congenital hemolytic anemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:8499925
  • PMID:9856489
DOID:0080554 congenital disorder of glycosylation Ib HGNC:7216 Homo sapiens (human) 4351 MPI
  • RGD:7240710
DOID:9538 multiple myeloma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:18285692
DOID:612 primary immunodeficiency disease HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • RGD:7240710
DOID:6132 bronchitis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:14593914
DOID:3908 lung non-small cell carcinoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • PMID:25576295
DOID:4248 coronary stenosis HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:34262949
DOID:0080923 bilateral parasagittal parieto-occipital polymicrogyria HGNC:16873 Homo sapiens (human) 9896 FIG4
  • RGD:7240710
DOID:0112313 brain small vessel disease HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • PMID:23083441
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:18823627
DOID:11054 urinary bladder cancer HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:16985032
DOID:0050848 obstructive sleep apnea HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:18204169
DOID:0070215 familial hyperinsulinemic hypoglycemia 4 HGNC:4799 Homo sapiens (human) 3033 HADH
  • RGD:7240710
DOID:0080071 mucolipidosis III alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • RGD:7240710
DOID:8778 Crohn's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21702710
DOID:1059 intellectual disability HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • PMID:11889465
DOID:2738 pseudoxanthoma elasticum HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:17693525
DOID:0060898 Parkinson's disease 20 HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • RGD:7240710
DOID:4247 coronary restenosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15790942
DOID:9975 cocaine dependence HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:19255376
DOID:2841 asthma HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:15266299
  • PMID:18547625

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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