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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 7226 - 7250 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11650 bronchopulmonary dysplasia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22882323
DOID:6039 uveal melanoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • RGD:7240710
DOID:3748 esophagus squamous cell carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:15205355
  • PMID:25162968
DOID:0080199 colorectal carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:10637515
DOID:1324 lung cancer HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:18495292
DOID:7148 rheumatoid arthritis HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:20676650
  • PMID:22505706
DOID:0060575 3MC syndrome 1 HGNC:6901 Homo sapiens (human) 5648 MASP1
  • RGD:7240710
DOID:219 colon cancer HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23027623
  • PMID:23859041
DOID:3717 gastric adenocarcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:32243890
DOID:14330 Parkinson's disease HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23624232
  • PMID:25548290
  • PMID:27286263
DOID:1993 rectum cancer HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23859041
DOID:9261 nasopharynx carcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:32449282
DOID:11476 osteoporosis HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:4780 anti-basement membrane glomerulonephritis HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:3633 beta-mannosidosis HGNC:6831 Homo sapiens (human) 4126 MANBA
  • MGI:6194238
  • RGD:7240710
DOID:3413 alpha-mannosidosis HGNC:6826 Homo sapiens (human) 4125 MAN2B1
  • MGI:6194238
  • RGD:7240710
DOID:5419 schizophrenia HGNC:6825 Homo sapiens (human) 4122 MAN2A2
  • MGI:6194238
DOID:1338 congenital dyserythropoietic anemia HGNC:6824 Homo sapiens (human) 4124 MAN2A1
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:6824 Homo sapiens (human) 4124 MAN2A1
  • MGI:6194238
DOID:0081097 Rafiq syndrome HGNC:6823 Homo sapiens (human) 11253 MAN1B1
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:6783 Homo sapiens (human) 4099 MAG
  • PMID:2419505
DOID:3525 middle cerebral artery infarction HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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


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