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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 11626 - 11650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG
  • RGD:7240710
DOID:12798 mucopolysaccharidosis HGNC:24102 Homo sapiens (human) 22901 ARSG
  • MGI:6194238
DOID:12800 mucopolysaccharidosis VI HGNC:714 Homo sapiens (human) 411 ARSB
  • MGI:6194238
  • PMID:1550123
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:0060350 adenine phosphoribosyltransferase deficiency SGD:S000002849 Saccharomyces cerevisiae S288C 852051 APT2
  • MGI:6194238
DOID:684 hepatocellular carcinoma SGD:S000002849 Saccharomyces cerevisiae S288C 852051 APT2
  • MGI:6194238
DOID:684 hepatocellular carcinoma SGD:S000004484 Saccharomyces cerevisiae S288C 854986 APT1
  • MGI:6194238
DOID:0060350 adenine phosphoribosyltransferase deficiency SGD:S000004484 Saccharomyces cerevisiae S288C 854986 APT1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:626 Homo sapiens (human) 353 APRT
  • MGI:6194238
DOID:0060350 adenine phosphoribosyltransferase deficiency HGNC:626 Homo sapiens (human) 353 APRT
  • MGI:6194238
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:9751198
DOID:11714 gestational diabetes HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:6828336
DOID:1824 status epilepticus HGNC:612 Homo sapiens (human) 347 APOD
  • MGI:6194238
DOID:4762 vasculogenic impotence HGNC:612 Homo sapiens (human) 347 APOD
  • MGI:6194238
DOID:9970 obesity HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:7913935
DOID:9352 type 2 diabetes mellitus HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:15369805
  • PMID:7895459
DOID:2316 brain ischemia HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:13129 severe pre-eclampsia HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:24619222
DOID:684 hepatocellular carcinoma HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18712175
DOID:3459 breast carcinoma HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:11748448
DOID:2394 ovarian cancer HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:17974506
  • PMID:19787261
DOID:4362 cervical cancer HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18503157
  • PMID:19292061

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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