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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 65376 - 65400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0070062 Arboleda-Tham syndrome HGNC:13013 Homo sapiens (human) 7994 KAT6A
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:6522 Homo sapiens (human) 3931 LCAT
  • PMID:12673583
DOID:0050827 rheumatic heart disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:16426242
  • PMID:17578051
DOID:9074 systemic lupus erythematosus HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:12651073
  • PMID:18552411
  • PMID:21658414
DOID:9620 vesicoureteral reflux HGNC:11976 Homo sapiens (human) 7148 TNXB
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:3432 Homo sapiens (human) 2066 ERBB4
  • PMID:22294845
DOID:0110794 hereditary spastic paraplegia 42 HGNC:95 Homo sapiens (human) 9197 SLC33A1
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:932 Homo sapiens (human) 570 BAAT
  • PMID:12704386
DOID:8552 chronic myeloid leukemia HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:20305143
DOID:2280 hidradenitis suppurativa HGNC:17091 Homo sapiens (human) 23385 NCSTN
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:20103627
DOID:2513 basal cell carcinoma HGNC:950 Homo sapiens (human) 8314 BAP1
  • PMID:25080371
DOID:2513 basal cell carcinoma HGNC:8101 Homo sapiens (human) 4948 OCA2
  • PMID:19384953
  • PMID:21270109
DOID:0080716 infantile liver failure syndrome HGNC:15625 Homo sapiens (human) 51594 NBAS
  • RGD:7240710
DOID:13949 interstitial cystitis HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:12442007
DOID:9415 allergic asthma HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:22397267
DOID:2436 glomangioma HGNC:14373 Homo sapiens (human) 11146 GLMN
  • RGD:7240710
DOID:1682 congenital heart disease HGNC:11843 Homo sapiens (human) 7092 TLL1
  • PMID:22883091
DOID:1588 thrombocytopenia HGNC:132 Homo sapiens (human) 60 ACTB
  • RGD:7240710
DOID:1380 endometrial cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:18318428
DOID:2986 IgA glomerulonephritis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:12484505
DOID:9119 acute myeloid leukemia HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:17983459
DOID:3908 lung non-small cell carcinoma HGNC:3438 Homo sapiens (human) 2074 ERCC6
  • PMID:28924235
DOID:3393 coronary artery disease HGNC:12828 Homo sapiens (human) 7515 XRCC1
  • PMID:24315498
DOID:0112192 tetraamelia syndrome 1 HGNC:12782 Homo sapiens (human) 7473 WNT3
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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