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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 3076 - 3100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:326 ischemia HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:2526 prostate adenocarcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:20638364
DOID:0112263 hypoinsulinemic hypoglycemia with hemihypertrophy HGNC:392 Homo sapiens (human) 208 AKT2
  • RGD:7240710
DOID:3070 high grade glioma HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:19330838
DOID:10286 prostate carcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:24838891
DOID:162 cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:22815832
DOID:9993 hypoglycemia HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:21979934
DOID:11612 polycystic ovary syndrome HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:10763 hypertension HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:22146979
DOID:9256 colorectal cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:11756242
DOID:4001 ovarian carcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:16721043
DOID:684 hepatocellular carcinoma HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:3069 malignant astrocytoma HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:20167810
DOID:1574 alcohol use disorder HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:9970 obesity HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:12663464
DOID:9352 type 2 diabetes mellitus HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:15166380
  • PMID:18204829
  • PMID:18972094
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I MGI:2384774 Mus musculus (house mouse) 208211 Alg1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation MGI:2384774 Mus musculus (house mouse) 208211 Alg1
  • MGI:6194238
DOID:0080563 congenital disorder of glycosylation Ik MGI:2384774 Mus musculus (house mouse) 208211 Alg1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation MGI:1098592 Mus musculus (house mouse) 208624 Alg3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id MGI:1098592 Mus musculus (house mouse) 208624 Alg3
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1
  • MGI:6194238
  • PMID:29661920
  • PMID:32169121

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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