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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 66576 - 66600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4450 renal cell carcinoma HGNC:1073 Homo sapiens (human) 654 BMP6
  • PMID:20016212
DOID:14323 Marfan syndrome HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:0060180 colitis HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:9970 obesity HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:1612 breast cancer HGNC:1073 Homo sapiens (human) 654 BMP6
  • PMID:17004110
DOID:2355 anemia HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1073 Homo sapiens (human) 654 BMP6
  • PMID:18072288
DOID:2316 brain ischemia HGNC:1073 Homo sapiens (human) 654 BMP6
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:1073 Homo sapiens (human) 654 BMP6
  • PMID:22364398
DOID:0111017 cone-rod dystrophy 10 HGNC:10729 Homo sapiens (human) 64218 SEMA4A
  • RGD:7240710
DOID:0110357 retinitis pigmentosa 35 HGNC:10729 Homo sapiens (human) 64218 SEMA4A
  • RGD:7240710
DOID:0050834 CHARGE syndrome HGNC:10727 Homo sapiens (human) 9723 SEMA3E
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:10727 Homo sapiens (human) 9723 SEMA3E
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:10725 Homo sapiens (human) 10512 SEMA3C
  • PMID:15077297
DOID:0090080 hypogonadotropic hypogonadism 16 with or without anosmia HGNC:10723 Homo sapiens (human) 10371 SEMA3A
  • RGD:7240710
DOID:3407 carotid artery disease HGNC:10722 Homo sapiens (human) 6404 SELPLG
  • PMID:22307784
DOID:4780 anti-basement membrane glomerulonephritis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:8805 intermediate coronary syndrome HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21162967
DOID:0112313 brain small vessel disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20885295
DOID:10652 Alzheimer's disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21484243
DOID:5844 myocardial infarction HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
  • PMID:12165563
  • PMID:17391113
  • PMID:21162967
DOID:0080998 acute necrotizing pancreatitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:17598012
DOID:526 human immunodeficiency virus infectious disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:22156911

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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