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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 6476 - 6500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080998 acute necrotizing pancreatitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:9376 Homo sapiens (human) 5562 PRKAA1
  • MGI:6194238
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:4692 endophthalmitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:11714 gestational diabetes HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:36477942
DOID:2841 asthma HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:16424226
DOID:3525 middle cerebral artery infarction HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:14227 azoospermia HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:23064 Homo sapiens (human) 119391 GSTO2
  • PMID:14570706
  • PMID:17194543
DOID:0080502 GM1 gangliosidosis type 1 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:2913 acute pancreatitis HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:14932 Homo sapiens (human) 23409 SIRT4
  • MGI:6194238
DOID:10952 nephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22895845
DOID:12236 primary biliary cholangitis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0111389 mucopolysaccharidosis Ih/s HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0050742 nicotine dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:17223085
  • PMID:17654295
  • PMID:25489907
DOID:0050773 paraganglioma HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • PMID:10657297
  • RGD:7240710
DOID:0050152 aspiration pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14990394
DOID:750 peptic ulcer disease HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:23267857
  • PMID:9867757
DOID:1289 neurodegenerative disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:13413 hepatic encephalopathy HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23624232
  • PMID:25548290
  • PMID:27286263
DOID:9970 obesity HGNC:384 Homo sapiens (human) 1645 AKR1C1
  • PMID:15494612
DOID:162 cancer HGNC:8977 Homo sapiens (human) 5293 PIK3CD
  • MGI:6194238
DOID:83 cataract HGNC:3629 Homo sapiens (human) 2222 FDFT1
  • MGI:6194238

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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: August 19, 2024