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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 5626 - 5650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1733 cryptosporidiosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19827946
DOID:0060322 mastoiditis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:24690988
DOID:5016 hepatocellular clear cell carcinoma HGNC:5382 Homo sapiens (human) 3417 IDH1
  • PMID:25355558
  • PMID:28403884
DOID:1826 epilepsy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:13580 cholestasis HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:29749584
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10195920
  • PMID:14587643
  • PMID:17436151
DOID:9352 type 2 diabetes mellitus HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:18613291
  • PMID:7516306
  • PMID:9789717
DOID:3320 Tay-Sachs disease HGNC:4878 Homo sapiens (human) 3073 HEXA
  • MGI:6194238
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10831941
DOID:11394 adult respiratory distress syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:21317313
DOID:3146 lipid metabolism disorder HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • PMID:9691089
DOID:0070342 adult-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • PMID:10369257
  • PMID:11153906
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
DOID:150 disease of mental health HGNC:4416 Homo sapiens (human) 8443 GNPAT
  • MGI:6194238
DOID:0111391 mucopolysaccharidosis IVA HGNC:4122 Homo sapiens (human) 2588 GALNS
  • RGD:7240710
DOID:0060710 autosomal recessive congenital ichthyosis 2 HGNC:430 Homo sapiens (human) 242 ALOX12B
  • RGD:7240710
DOID:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:0111680 essential fructosuria HGNC:6315 Homo sapiens (human) 3795 KHK
  • RGD:7240710
DOID:0080537 hypermanganesemia with dystonia 2 HGNC:20858 Homo sapiens (human) 23516 SLC39A14
  • RGD:7240710
DOID:9970 obesity HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
DOID:13564 aspergillosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21381282
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238

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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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