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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 8726 - 8750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:0111680 essential fructosuria HGNC:6315 Homo sapiens (human) 3795 KHK
  • RGD:7240710
DOID:0080537 hypermanganesemia with dystonia 2 HGNC:20858 Homo sapiens (human) 23516 SLC39A14
  • RGD:7240710
DOID:9970 obesity HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
DOID:13564 aspergillosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21381282
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238
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

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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