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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 7226 - 7250 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518
DOID:557 kidney disease HGNC:15527 Homo sapiens (human) 152831 KLB
  • MGI:6194238
DOID:162 cancer HGNC:1769 Homo sapiens (human) 10423 CDIPT
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:12675919
DOID:9282 ocular hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
DOID:11383 cryptorchidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:5199 ureteral obstruction HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:5419 schizophrenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15927374
DOID:11714 gestational diabetes HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:6828336
DOID:4362 cervical cancer HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19823053
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:4801 Homo sapiens (human) 3030 HADHA
  • MGI:6194238
DOID:0111234 congenital muscular dystrophy-dystroglycanopathy A7 HGNC:37276 Homo sapiens (human) 729920 CRPPA
  • RGD:7240710
DOID:162 cancer HGNC:19980 Homo sapiens (human) 64841 GNPNAT1
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238
DOID:13141 uveitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:229083
DOID:0080162 lupus nephritis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:22788914
DOID:13025 retinopathy of prematurity HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:21173508
  • PMID:21299359
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:10413701
DOID:0111254 glutaric acidemia I HGNC:4189 Homo sapiens (human) 2639 GCDH
  • MGI:6194238
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17016617
DOID:12205 dengue disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:16274635
  • RGD:7240710
DOID:9970 obesity HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17618961
DOID:11266 Hantavirus hemorrhagic fever with renal syndrome HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:25658420

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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