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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 6451 - 6475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1287 cardiovascular system disease HGNC:4706 Homo sapiens (human) 2997 GYS1
  • PMID:17356695
DOID:0050700 cardiomyopathy HGNC:7150 Homo sapiens (human) 23417 MLYCD
  • PMID:10455107
DOID:0080489 GM1 gangliosidosis type 3 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0081385 ataxia-telangiectasia-like disorder-2 HGNC:8729 Homo sapiens (human) 5111 PCNA
  • RGD:7240710
DOID:114 heart disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:0081326 oxoglutarate dehydrogenase deficiency HGNC:25590 Homo sapiens (human) 55753 OGDHL
  • MGI:6194238
DOID:1324 lung cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16696009
DOID:1824 status epilepticus HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 HGNC:23719 Homo sapiens (human) 93210 PGAP3
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:2367 neuroaxonal dystrophy HGNC:7631 Homo sapiens (human) 4668 NAGA
  • PMID:2243144
DOID:0050560 Walker-Warburg syndrome HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • PMID:12369018
  • PMID:15637732
  • PMID:16575835
DOID:1612 breast cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:16875543
  • PMID:23643682
  • PMID:7053713
DOID:9406 hypopituitarism HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:8432 polycythemia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:18339134
DOID:3312 bipolar disorder HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • RGD:7240710
DOID:8552 chronic myeloid leukemia HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:17900686
DOID:8552 chronic myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25436036
DOID:824 periodontitis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:783 end stage renal disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:14654 prostatitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238

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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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