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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 4826 - 4850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3073 brain glioblastoma multiforme HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:20219118
DOID:0080737 Ehlers-Danlos syndrome musculocontractural type 2 HGNC:21144 Homo sapiens (human) 29940 DSE
  • RGD:7240710
DOID:3602 toxic encephalopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:12031086
DOID:2871 endometrial carcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:16144912
DOID:4194 glucose metabolism disease HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:0081183 autosomal recessive intellectual developmental disorder 7 HGNC:30242 Homo sapiens (human) 7991 TUSC3
  • RGD:7240710
DOID:1184 nephrotic syndrome HGNC:11178 Homo sapiens (human) 8435 SOAT2
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:14115 toxic shock syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1612 breast cancer HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:16019138
DOID:11476 osteoporosis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:10457 Legionnaires' disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19073229
DOID:0050625 biliary tract benign neoplasm HGNC:7413 Homo sapiens (human) 4507 MTAP
  • PMID:16373701
DOID:1596 depressive disorder HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18348659
DOID:1793 pancreatic cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17019794
  • PMID:17785569
  • PMID:18281514
  • PMID:19843662
DOID:9269 maple syrup urine disease HGNC:2698 Homo sapiens (human) 1629 DBT
  • MGI:6194238
DOID:3407 carotid artery disease HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:16620836
DOID:4450 renal cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19278051
DOID:0070004 myeloid neoplasm HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:27077777
DOID:0060246 MASA syndrome HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • MGI:6194238
  • PMID:7920660
  • PMID:8786080
  • PMID:9643285
  • RGD:7240710
DOID:0050589 inflammatory bowel disease HGNC:8974 Homo sapiens (human) 5289 PIK3C3
  • MGI:6194238
DOID:0080887 vitamin D-dependent rickets type 1B HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • MGI:6194238
  • RGD:7240710
DOID:4079 heart valve disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:16631011

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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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