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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 9601 - 9625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:17968 Homo sapiens (human) 51146 A4GNT
  • PMID:16441422
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2
  • RGD:7240710
DOID:10763 hypertension HGNC:17855 Homo sapiens (human) 26035 GLCE
  • PMID:27699767
DOID:6713 cerebrovascular disease HGNC:17855 Homo sapiens (human) 26035 GLCE
  • PMID:27699767
DOID:5679 retinal disease HGNC:17852 Homo sapiens (human) 56994 CHPT1
  • MGI:6194238
DOID:4440 seminoma HGNC:17825 Homo sapiens (human) 11145 PLAAT3
  • PMID:11526504
DOID:162 cancer HGNC:1769 Homo sapiens (human) 10423 CDIPT
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:1769 Homo sapiens (human) 10423 CDIPT
  • MGI:6194238
DOID:0060728 NGLY1-deficiency HGNC:17646 Homo sapiens (human) 55768 NGLY1
  • MGI:6194238
  • RGD:7240710
DOID:2871 endometrial carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18519763
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:1612 breast cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17764565
  • PMID:8673923
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:4362 cervical cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17548682
DOID:2394 ovarian cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:10493953
DOID:303 substance-related disorder HGNC:1753 Homo sapiens (human) 1012 CDH13
  • MGI:6194238
DOID:4247 coronary restenosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18387661
DOID:11054 urinary bladder cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18094410
DOID:2841 asthma HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:15192232
  • PMID:16179638
  • PMID:20226308
DOID:12053 cryptococcosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:0050127 sinusitis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:19379605

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Supported by JST NBDC Grant Number JPMJND2204

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


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