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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 11826 - 11850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9970 obesity HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • PMID:14569040
DOID:0060778 congenital diarrhea 7 with exudative enteropathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • RGD:7240710
DOID:784 chronic kidney disease HGNC:1548 Homo sapiens (human) 873 CBR1
  • MGI:6194238
DOID:162 cancer HGNC:1801 Homo sapiens (human) 8760 CDS2
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:423 myopathy HGNC:7449 Homo sapiens (human) 8776 MTMR1
  • MGI:6194238
DOID:219 colon cancer HGNC:11906 Homo sapiens (human) 8794 TNFRSF10C
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:11906 Homo sapiens (human) 8794 TNFRSF10C
  • MGI:6194238
DOID:0080128 mitochondrial DNA depletion syndrome 9 HGNC:11449 Homo sapiens (human) 8802 SUCLG1
  • RGD:7240710
DOID:0080124 mitochondrial DNA depletion syndrome 5 HGNC:11448 Homo sapiens (human) 8803 SUCLA2
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:26893476
DOID:850 lung disease HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:19265174
DOID:13406 pulmonary sarcoidosis HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:14641797
DOID:3770 pulmonary fibrosis HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:15308504
DOID:2841 asthma HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:18382474
  • PMID:18774397
  • PMID:19910030
  • PMID:20860503
DOID:0050570 congenital disorder of glycosylation type I HGNC:3005 Homo sapiens (human) 8813 DPM1
  • MGI:6194238
DOID:0080557 congenital disorder of glycosylation Ie HGNC:3005 Homo sapiens (human) 8813 DPM1
  • RGD:7240710
DOID:0080571 congenital disorder of glycosylation Iu HGNC:3006 Homo sapiens (human) 8818 DPM2
  • RGD:7240710
DOID:114 heart disease HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:19525977
DOID:7148 rheumatoid arthritis HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:36104638
DOID:684 hepatocellular carcinoma HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:23643089
DOID:1612 breast cancer HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:22199269
DOID:557 kidney disease HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • 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