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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 4676 - 4700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10534 stomach cancer HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:2316 brain ischemia HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:1824 status epilepticus HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:17664290
DOID:1059 intellectual disability HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • PMID:26416544
DOID:0081221 autosomal recessive intellectual developmental disorder 59 HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • RGD:7240710
DOID:3312 bipolar disorder HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11673796
  • PMID:14699425
  • PMID:9322233
DOID:5419 schizophrenia HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11317223
DOID:5408 Paget's disease of bone HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:10763 hypertension HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9970 obesity HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9352 type 2 diabetes mellitus HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:12086927
  • PMID:15220217
DOID:9352 type 2 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:1569197
  • PMID:3322910
DOID:11717 neonatal diabetes HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • RGD:7240710
DOID:0050524 maturity-onset diabetes of the young HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
DOID:0110741 type 1 diabetes mellitus 2 HGNC:6081 Homo sapiens (human) 3630 INS
  • RGD:7240710
DOID:3892 insulinoma HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:2565624
  • PMID:8175958
DOID:9452 steatotic liver disease HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:18713300
DOID:0014667 disease of metabolism HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:22151886
DOID:10763 hypertension HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:16113600
  • PMID:16382177
  • PMID:16552513
  • PMID:17284223
  • PMID:17284779
  • PMID:18824271
  • PMID:20535137
  • PMID:21765853
  • PMID:26783749
DOID:3587 pancreatic ductal carcinoma HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19571666

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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