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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 5651 - 5675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0111681 glutamate-cysteine ligase deficiency HGNC:4311 Homo sapiens (human) 2729 GCLC
  • RGD:7240710
DOID:0080759 Fanconi renotubular syndrome 3 HGNC:3247 Homo sapiens (human) 1962 EHHADH
  • RGD:7240710
DOID:0081221 autosomal recessive intellectual developmental disorder 59 HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:2316 brain ischemia HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:3717 gastric adenocarcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:31396300
DOID:12361 Graves' disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:18997483
  • PMID:20583542
DOID:874 bacterial pneumonia HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
DOID:0112381 muscular dystrophy-dystroglycanopathy type C12 HGNC:26267 Homo sapiens (human) 84197 POMK
  • RGD:7240710
DOID:0050742 nicotine dependence HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2658981
DOID:4195 hyperglycemia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:15056491
DOID:0050793 short QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • PMID:21115670
  • PMID:8554072
DOID:0081210 autosomal recessive intellectual developmental disorder 46 HGNC:7680 Homo sapiens (human) 3340 NDST1
  • RGD:7240710
DOID:12361 Graves' disease HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12919155
DOID:0060180 colitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:0050669 spastic cerebral palsy HGNC:4093 Homo sapiens (human) 2572 GAD2
  • MGI:6194238
DOID:1596 depressive disorder HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • MGI:6194238
DOID:700 mitochondrial metabolism disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • PMID:8651282
DOID:10140 dry eye syndrome HGNC:25531 Homo sapiens (human) 55711 FAR2
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:17018277
  • PMID:19133136
  • PMID:21211002
  • PMID:21595933
  • PMID:21757867
  • PMID:22589246
  • PMID:24383721
DOID:5082 liver cirrhosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
  • PMID:20006396

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

Acknowledgements

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