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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 11276 - 11300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:3146 lipid metabolism disorder HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:10828087
DOID:3905 lung carcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:22797725
DOID:6543 acne HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18615253
DOID:3805 porokeratosis HGNC:3631 Homo sapiens (human) 2224 FDPS
  • RGD:7240710
DOID:61 mitral valve disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14765837
DOID:10892 hypospadias HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15579657
  • PMID:21300689
DOID:0110794 hereditary spastic paraplegia 42 HGNC:95 Homo sapiens (human) 9197 SLC33A1
  • RGD:7240710
DOID:2986 IgA glomerulonephritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:12220450
DOID:2394 ovarian cancer HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17611497
  • RGD:7240710
DOID:4372 intracranial embolism HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:16973281
DOID:1470 major depressive disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15714130
  • PMID:19068087
DOID:2043 hepatitis B HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16231358
DOID:1024 leprosy HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:17548585
  • RGD:7240710
DOID:5520 head and neck squamous cell carcinoma HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:19954746
DOID:9744 type 1 diabetes mellitus HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:12706323
DOID:2377 multiple sclerosis HGNC:4795 Homo sapiens (human) 9563 H6PD
  • PMID:19935835
DOID:3307 teratoma HGNC:8905 Homo sapiens (human) 5236 PGM1
  • PMID:5259759
DOID:684 hepatocellular carcinoma HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:23740135
DOID:0111258 pentosuria HGNC:18985 Homo sapiens (human) 51181 DCXR
  • RGD:7240710
DOID:0070403 hypomyelinating leukodystrophy 26 HGNC:16872 Homo sapiens (human) 347734 SLC35B2
  • RGD:7240710
DOID:0112198 spondyloepimetaphyseal dysplasia with joint laxity type 1 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:631 fibromyalgia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:24762091
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0080560 congenital disorder of glycosylation Ih HGNC:23161 Homo sapiens (human) 79053 ALG8
  • RGD:7240710

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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: August 19, 2024