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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 October 9, 2024
Displaying entries 69326 - 69350 of 71927 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:5173 Homo sapiens (human) 3265 HRAS
  • PMID:9195373
DOID:8545 malignant hyperthermia HGNC:1397 Homo sapiens (human) 779 CACNA1S
  • PMID:9199552
  • RGD:7240710
DOID:1389 polyneuropathy HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • PMID:9201602
DOID:0050830 peripheral artery disease HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • PMID:9201602
DOID:8997 polycythemia vera HGNC:3416 Homo sapiens (human) 2057 EPOR
  • PMID:9207443
DOID:10247 pleurisy RGD:2201 Rattus norvegicus (Norway rat) 25245 Bdkrb2
  • PMID:9208140
DOID:11832 visual epilepsy RGD:3199 Rattus norvegicus (Norway rat) 25340 Npy5r
  • PMID:9212103
DOID:11132 prostatic hypertrophy HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:9215294
DOID:12930 dilated cardiomyopathy HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:9220309
DOID:0080365 endometrial hyperplasia HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:2871 endometrial carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:332 amyotrophic lateral sclerosis HGNC:3581 Homo sapiens (human) 2186 BPTF
  • PMID:9225734
DOID:4947 cholangiocarcinoma HGNC:12541 Homo sapiens (human) 54600 UGT1A9
  • PMID:9230212
DOID:1338 congenital dyserythropoietic anemia MGI:104669 Mus musculus (house mouse) 17158 Man2a1
  • PMID:9230311
DOID:5844 myocardial infarction RGD:3648 Rattus norvegicus (Norway rat) 25216 Sdc1
  • PMID:9237025
DOID:0060856 right atrial isomerism MGI:87912 Mus musculus (house mouse) 11481 Acvr2b
  • PMID:9242489
DOID:6195 conjunctivitis HGNC:9071 Homo sapiens (human) 5340 PLG
  • PMID:9242524
DOID:9952 acute lymphoblastic leukemia HGNC:2438 Homo sapiens (human) 1440 CSF3
  • PMID:9250830
DOID:1825 childhood absence epilepsy HGNC:4579 Homo sapiens (human) 2897 GRIK1
  • PMID:9259378
DOID:1596 depressive disorder HGNC:4079 Homo sapiens (human) 2558 GABRA5
  • PMID:9267853
DOID:11984 hypertrophic cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:12930 dilated cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:0060738 junctional epidermolysis bullosa non-Herlitz type MGI:99915 Mus musculus (house mouse) 16780 Lamb3
  • PMID:9271670
DOID:8866 actinic keratosis HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • PMID:9274625
DOID:2871 endometrial carcinoma HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:9276029

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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: December 9, 2024