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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 July 29, 2024
Displaying entries 5476 - 5500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9744 type 1 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38
  • MGI:6194238
  • PMID:12488956
  • PMID:16459468
DOID:8778 Crohn's disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:19212205
DOID:10652 Alzheimer's disease HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
  • PMID:15507493
  • PMID:17387692
  • PMID:18340469
  • PMID:20864222
  • PMID:28087189
DOID:11724 limb-girdle muscular dystrophy HGNC:17997 Homo sapiens (human) 79147 FKRP
  • PMID:14523375
DOID:3498 pancreatic ductal adenocarcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:29072694
  • PMID:33028359
DOID:3407 carotid artery disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17283255
DOID:2349 arteriosclerosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10073974
DOID:10763 hypertension HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • MGI:6194238
DOID:4500 hypokalemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:15668790
DOID:10914 amnestic disorder HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
DOID:326 ischemia HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:3007 Homo sapiens (human) 54344 DPM3
  • RGD:7240710
DOID:437 myasthenia gravis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:17986328
DOID:3083 chronic obstructive pulmonary disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:19927353
DOID:3310 atopic dermatitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20642202
DOID:2841 asthma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15356557
  • PMID:16266379
  • PMID:19067129
  • PMID:19159017
  • PMID:20685742
DOID:10763 hypertension HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:16180015
DOID:10283 prostate cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:21430300
DOID:0110937 autosomal dominant osteopetrosis 1 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0050852 limb ischemia HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:12586736
  • PMID:14568901
DOID:1168 familial hyperlipidemia HGNC:9989 Homo sapiens (human) 9104 RGN
  • MGI:6194238
DOID:576 proteinuria HGNC:7049 Homo sapiens (human) 4249 MGAT5
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:1569197
  • PMID:3322910

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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: August 19, 2024