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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 4026 - 4050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9452 steatotic liver disease HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:19670414
DOID:11714 gestational diabetes HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:18937705
DOID:0060363 glycerol kinase deficiency HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238
  • PMID:9719371
  • RGD:7240710
DOID:13810 familial hypercholesterolemia HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:14532840
DOID:9970 obesity HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:8893 psoriasis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:8304420
DOID:4450 renal cell carcinoma HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:14654968
DOID:1612 breast cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:19282568
DOID:9352 type 2 diabetes mellitus HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:9500559
DOID:10283 prostate cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7624992
DOID:10763 hypertension HGNC:429 Homo sapiens (human) 239 ALOX12
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:8577 ulcerative colitis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:0060363 glycerol kinase deficiency HGNC:4291 Homo sapiens (human) 2712 GK2
  • MGI:6194238
DOID:14499 Fabry disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
  • PMID:2539398
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
DOID:12804 mucopolysaccharidosis IV HGNC:4298 Homo sapiens (human) 2720 GLB1
  • PMID:11511921
  • PMID:19091613
DOID:0080502 GM1 gangliosidosis type 1 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0111392 mucopolysaccharidosis type IVB HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0080501 GM1 gangliosidosis type 2 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:3322 GM1 gangliosidosis HGNC:4298 Homo sapiens (human) 2720 GLB1
  • MGI:6194238
  • PMID:10737981
  • PMID:17309651
DOID:0080489 GM1 gangliosidosis type 3 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0060710 autosomal recessive congenital ichthyosis 2 HGNC:430 Homo sapiens (human) 242 ALOX12B
  • RGD:7240710

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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