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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 5376 - 5400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:7998 hyperthyroidism HGNC:1027 Homo sapiens (human) 622 BDH1
  • MGI:6194238
DOID:0111646 congenital lactase deficiency HGNC:6530 Homo sapiens (human) 3938 LCT
  • RGD:7240710
DOID:11396 pulmonary edema HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:16162765
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:85 Homo sapiens (human) 32 ACACB
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
DOID:0050073 invasive aspergillosis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26861072
DOID:1324 lung cancer HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19959685
DOID:10652 Alzheimer's disease HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:18180323
DOID:1380 endometrial cancer HGNC:18185 Homo sapiens (human) 54206 ERRFI1
  • MGI:6194238
DOID:10763 hypertension HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
  • PMID:17143180
DOID:2986 IgA glomerulonephritis HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:11828340
  • PMID:17452405
DOID:4989 pancreatitis HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:2841 asthma HGNC:6710 Homo sapiens (human) 4048 LTA4H
  • MGI:6194238
DOID:8893 psoriasis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:22151390
DOID:0050866 oral squamous cell carcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:22612324
DOID:8725 vascular dementia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11273064
DOID:10286 prostate carcinoma HGNC:786 Homo sapiens (human) 468 ATF4
  • PMID:25680860
DOID:14687 diastrophic dysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • MGI:6194238
  • PMID:10482955
  • RGD:7240710
DOID:219 colon cancer HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:23027623
  • PMID:23859041
DOID:10762 portal hypertension HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:9669 senile cataract HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:24868140
DOID:3770 pulmonary fibrosis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:811 lipodystrophy HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • PMID:11967537
DOID:0111235 congenital muscular dystrophy-dystroglycanopathy type A12 HGNC:26267 Homo sapiens (human) 84197 POMK
  • RGD:7240710
DOID:14501 Sjogren-Larsson syndrome HGNC:405 Homo sapiens (human) 218 ALDH3A1
  • MGI:6194238

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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