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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 5351 - 5375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2048 autoimmune hepatitis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:20208391
DOID:0110818 hereditary spastic paraplegia 73 HGNC:18540 Homo sapiens (human) 126129 CPT1C
  • RGD:7240710
DOID:0111392 mucopolysaccharidosis type IVB HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:0050571 congenital disorder of glycosylation type II HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:14897 Homo sapiens (human) 80271 ITPKC
  • PMID:33470690
DOID:0111068 congenital bile acid synthesis defect 4 HGNC:451 Homo sapiens (human) 23600 AMACR
  • RGD:7240710
DOID:8534 gastroesophageal reflux disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:21426732
DOID:3008 invasive ductal carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:8102204
DOID:10283 prostate cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:18645193
DOID:684 hepatocellular carcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:16750516
DOID:3211 lysosomal storage disease HGNC:9251 Homo sapiens (human) 5476 CTSA
  • PMID:8514852
DOID:8719 in situ carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18617777
DOID:9970 obesity HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21372607
DOID:9352 type 2 diabetes mellitus HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:27281273
DOID:0050562 West syndrome HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:9993 hypoglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:15963101
DOID:3070 high grade glioma HGNC:8977 Homo sapiens (human) 5293 PIK3CD
  • MGI:6194238
DOID:10763 hypertension HGNC:2648 Homo sapiens (human) 11283 CYP4F8
  • MGI:6194238
DOID:0060256 Dowling-Degos disease HGNC:14988 Homo sapiens (human) 23509 POFUT1
  • RGD:7240710
DOID:14080 glucocorticoid-remediable aldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • RGD:7240710
DOID:4971 myelofibrosis HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24997152
  • PMID:25860380
  • RGD:7240710
DOID:14183 alcoholic neuropathy HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • 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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