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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 4926 - 4950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:639 acute disseminated encephalomyelitis HGNC:4953 Homo sapiens (human) 3127 HLA-DRB5
  • PMID:15201511
DOID:1826 epilepsy HGNC:2295 Homo sapiens (human) 1356 CP
  • PMID:7914452
DOID:1584 acute chest syndrome HGNC:4827 Homo sapiens (human) 3043 HBB
  • PMID:23952145
DOID:9952 acute lymphoblastic leukemia HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:6958349
DOID:302 substance abuse HGNC:5286 Homo sapiens (human) 3350 HTR1A
  • PMID:26926882
DOID:0060450 Lisch epithelial corneal dystrophy HGNC:13356 Homo sapiens (human) 57192 MCOLN1
  • RGD:7240710
DOID:0111390 mucopolysaccharidosis Ih HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:12971 hereditary spherocytosis HGNC:11027 Homo sapiens (human) 6521 SLC4A1
  • PMID:8282779
  • PMID:8547122
  • PMID:9207478
  • PMID:9326249
DOID:0111626 D-glyceric aciduria HGNC:24247 Homo sapiens (human) 132158 GLYCTK
  • RGD:7240710
DOID:9975 cocaine dependence HGNC:29944 Homo sapiens (human) 55714 TENM3
  • PMID:18438686
DOID:0111800 syndromic microphthalmia 12 HGNC:9865 Homo sapiens (human) 5915 RARB
  • RGD:7240710
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:13054 Homo sapiens (human) 9203 ZMYM3
  • RGD:7240710
DOID:1586 rheumatic fever HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:17559688
DOID:0111492 combined oxidative phosphorylation deficiency 32 HGNC:16618 Homo sapiens (human) 65993 MRPS34
  • RGD:7240710
DOID:5517 stomach carcinoma HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:15273732
DOID:0080678 mucolipidosis III gamma HGNC:23026 Homo sapiens (human) 84572 GNPTG
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19286843
DOID:1799 islet cell tumor HGNC:2681 Homo sapiens (human) 1616 DAXX
  • PMID:21252315
DOID:0080290 familial erythrocytosis 5 HGNC:3415 Homo sapiens (human) 2056 EPO
  • RGD:7240710
DOID:9669 senile cataract HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:24868140
DOID:1474 aggressive periodontitis HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:28662328
DOID:0111286 psoriasis 1 HGNC:4933 Homo sapiens (human) 3107 HLA-C
  • RGD:7240710
DOID:0081082 acute myelomonocytic leukemia HGNC:1539 Homo sapiens (human) 865 CBFB
  • PMID:8351518
DOID:13543 hyperparathyroidism HGNC:14006 Homo sapiens (human) 55503 TRPV6
  • RGD:7240710
DOID:9952 acute lymphoblastic leukemia HGNC:959 Homo sapiens (human) 581 BAX
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

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