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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 9176 - 9200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:12894 Sjogren's syndrome HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:11359451
DOID:77 gastrointestinal system disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:11361181
DOID:4450 renal cell carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11369057
DOID:9351 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:11372010
DOID:5844 myocardial infarction HGNC:10661 Homo sapiens (human) 6385 SDC4
  • PMID:11372670
DOID:10763 hypertension HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:11378836
  • PMID:15659047
DOID:9970 obesity HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:11381268
  • PMID:17870627
DOID:10283 prostate cancer HGNC:9156 Homo sapiens (human) 5407 PNLIPRP1
  • PMID:11384102
DOID:2352 hemochromatosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11389006
  • PMID:16793930
DOID:409 liver disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11389006
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:3459 breast carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:1686 glaucoma HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • PMID:11391707
DOID:0050771 pheochromocytoma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • PMID:11404820
DOID:224 transient cerebral ischemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:11412877
  • PMID:24053818
DOID:5419 schizophrenia HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:11425011
DOID:10652 Alzheimer's disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • PMID:11430884
DOID:3138 acanthosis nigricans HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:11436180
DOID:4762 vasculogenic impotence RGD:2137 Rattus norvegicus (Norway rat) 25239 Apod
  • PMID:11444882
DOID:11723 Duchenne muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
  • PMID:15833425
  • PMID:7630355
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
DOID:3082 interstitial lung disease HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • PMID:11445799
  • PMID:15756222
  • PMID:16423270
  • PMID:19443464
DOID:3082 interstitial lung disease HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:11445799
  • PMID:9216212
  • RGD:7240710
DOID:0050902 medulloblastoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:11451203
DOID:8805 intermediate coronary syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11451295
  • PMID:15131005

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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