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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 66026 - 66050 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:8991 cervix uteri carcinoma in situ HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:10073700
  • PMID:15458897
  • PMID:18351579
DOID:0111166 molybdenum cofactor deficiency type C HGNC:15465 Homo sapiens (human) 10243 GPHN
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:0080376 trichorhinophalangeal syndrome type III HGNC:12340 Homo sapiens (human) 7227 TRPS1
  • RGD:7240710
DOID:302 substance abuse HGNC:5287 Homo sapiens (human) 3351 HTR1B
  • PMID:12496953
  • PMID:28923721
DOID:0111071 congenital bile acid synthesis defect 1 HGNC:18324 Homo sapiens (human) 80270 HSD3B7
  • RGD:7240710
DOID:0080567 congenital disorder of glycosylation Ip HGNC:32456 Homo sapiens (human) 440138 ALG11
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15059615
DOID:9352 type 2 diabetes mellitus HGNC:5233 Homo sapiens (human) 3304 HSPA1B
  • PMID:15223990
DOID:11830 myopia HGNC:8547 Homo sapiens (human) 8974 P4HA2
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:16787 Homo sapiens (human) 80267 EDEM3
  • RGD:7240710
DOID:986 alopecia areata HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8077705
DOID:10907 microcephaly HGNC:14234 Homo sapiens (human) 64324 NSD1
  • PMID:23599694
DOID:3393 coronary artery disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:20602249
DOID:0110429 dilated cardiomyopathy 1H HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:10432437
  • PMID:15996167
DOID:0080839 X-linked warfarin sensitivity HGNC:3551 Homo sapiens (human) 2158 F9
  • RGD:7240710
DOID:0111086 Fanconi anemia complementation group G HGNC:3588 Homo sapiens (human) 2189 FANCG
  • RGD:7240710
DOID:4481 allergic rhinitis HGNC:3619 Homo sapiens (human) 2214 FCGR3A
  • PMID:18199088
DOID:0050811 congenital adrenal hyperplasia HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:2026124
DOID:12678 hypercalcemia HGNC:11019 Homo sapiens (human) 6569 SLC34A1
  • RGD:7240710
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:19263 Homo sapiens (human) 81562 LMAN2L
  • RGD:7240710
DOID:0050564 autosomal dominant nonsyndromic deafness HGNC:19987 Homo sapiens (human) 284656 EPHA10
  • RGD:7240710
DOID:0060892 late onset Parkinson's disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • RGD:7240710
DOID:2986 IgA glomerulonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2
  • PMID:21214373

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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