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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 6126 - 6150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12858 Huntington's disease HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
  • PMID:6237280
DOID:11394 adult respiratory distress syndrome HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:19858233
DOID:14501 Sjogren-Larsson syndrome HGNC:411 Homo sapiens (human) 222 ALDH3B2
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:15638228
DOID:3083 chronic obstructive pulmonary disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19493329
  • PMID:20096799
  • PMID:20156752
DOID:3770 pulmonary fibrosis HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:2355 anemia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:18156303
  • PMID:23141116
DOID:10581 metachromatic leukodystrophy HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:12894 Sjogren's syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:399 tuberculosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20537163
DOID:552 pneumonia HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:15928955
DOID:2747 glycogen storage disease HGNC:9725 Homo sapiens (human) 5836 PYGL
  • PMID:9536091
DOID:3393 coronary artery disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15059615
DOID:11446 sciatic neuropathy HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:22783049
DOID:1612 breast cancer HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19810822
  • PMID:22560646
  • PMID:23510418
DOID:0111582 hereditary arterial and articular multiple calcification syndrome HGNC:8021 Homo sapiens (human) 4907 NT5E
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:23348713
  • PMID:9631454
DOID:9352 type 2 diabetes mellitus HGNC:9235 Homo sapiens (human) 5467 PPARD
  • MGI:6194238
  • PMID:16804087
DOID:1826 epilepsy HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
DOID:0111395 mucopolysaccharidosis type IIIA HGNC:10818 Homo sapiens (human) 6448 SGSH
  • MGI:6194238
  • RGD:7240710
DOID:6543 acne HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17033191
DOID:1612 breast cancer HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:10739169

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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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Last updated: August 19, 2024