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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 68626 - 68650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0080631 Elsahy-Waters syndrome HGNC:1750 Homo sapiens (human) 1009 CDH11
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:7173 Homo sapiens (human) 4314 MMP3
  • PMID:15467919
DOID:583 hemolytic anemia HGNC:10006 Homo sapiens (human) 6005 RHAG
  • PMID:10467273
DOID:0110357 retinitis pigmentosa 35 HGNC:10729 Homo sapiens (human) 64218 SEMA4A
  • RGD:7240710
DOID:0080065 autosomal recessive spinocerebellar ataxia 19 HGNC:11071 Homo sapiens (human) 6548 SLC9A1
  • RGD:7240710
DOID:0110217 Leber congenital amaurosis 17 HGNC:4221 Homo sapiens (human) 392255 GDF6
  • RGD:7240710
DOID:11650 bronchopulmonary dysplasia HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:17196572
DOID:0060496 respiratory allergy HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:18086269
DOID:1287 cardiovascular system disease HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16023652
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:15056512
DOID:809 cocaine abuse HGNC:1964 Homo sapiens (human) 1143 CHRNB4
  • PMID:32841724
DOID:5419 schizophrenia HGNC:4579 Homo sapiens (human) 2897 GRIK1
  • PMID:11702055
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:11842 Homo sapiens (human) 11011 TLK2
  • RGD:7240710
DOID:8725 vascular dementia HGNC:5232 Homo sapiens (human) 3303 HSPA1A
  • PMID:15832029
DOID:0080434 developmental and epileptic encephalopathy 61 HGNC:201 Homo sapiens (human) 53616 ADAM22
  • RGD:7240710
DOID:0111973 immunodeficiency 17 HGNC:1675 Homo sapiens (human) 917 CD3G
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:4583 Homo sapiens (human) 2901 GRIK5
  • PMID:28900078
DOID:11054 urinary bladder cancer HGNC:11920 Homo sapiens (human) 355 FAS
  • PMID:16538171
DOID:3969 thyroid gland papillary carcinoma HGNC:4798 Homo sapiens (human) 3026 HABP2
  • RGD:7240710
DOID:8632 Kaposi's sarcoma HGNC:3581 Homo sapiens (human) 2186 BPTF
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:26909998
  • PMID:27660094
DOID:2841 asthma HGNC:6998 Homo sapiens (human) 4210 MEFV
  • PMID:18219832
DOID:1574 alcohol use disorder HGNC:4076 Homo sapiens (human) 2555 GABRA2
  • PMID:15024690
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:7655856
DOID:526 human immunodeficiency virus infectious disease HGNC:69 Homo sapiens (human) 6059 ABCE1
  • PMID:19657357

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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