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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 7976 - 8000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L HGNC:3622 Homo sapiens (human) 2218 FKTN
  • PMID:17044012
DOID:12930 dilated cardiomyopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:2679 dysembryoplastic neuroepithelial tumor HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25346165
DOID:3572 intracranial sinus thrombosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:20946167
DOID:6406 double outlet right ventricle HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:8577 ulcerative colitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:28120341
DOID:332 amyotrophic lateral sclerosis HGNC:4616 Homo sapiens (human) 2931 GSK3A
  • PMID:12675919
DOID:10608 celiac disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18728522
DOID:1909 melanoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:9758419
DOID:7998 hyperthyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
  • RGD:7240710
DOID:8893 psoriasis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:8304420
DOID:8947 diabetic retinopathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:10003 sensorineural hearing loss HGNC:9592 Homo sapiens (human) 5730 PTGDS
  • MGI:6194238
DOID:0050709 early infantile epileptic encephalopathy HGNC:5385 Homo sapiens (human) 3420 IDH3B
  • MGI:6194238
DOID:13580 cholestasis HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • MGI:6194238
DOID:1588 thrombocytopenia HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
DOID:893 Wilson disease HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:11212 hydrophthalmos HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:9097971
DOID:11714 gestational diabetes HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19269197
DOID:12858 Huntington's disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:5022 aflatoxins-related hepatocellular carcinoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • 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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Last updated: August 19, 2024