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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 5326 - 5350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:3571 liver cancer HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:13603 obstructive jaundice HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:0081385 ataxia-telangiectasia-like disorder-2 HGNC:8729 Homo sapiens (human) 5111 PCNA
  • RGD:7240710
DOID:2154 nephroblastoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11869017
DOID:0050585 congenital generalized lipodystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A
  • RGD:7240710
DOID:0112300 spondylometaphyseal dysplasia with cone-rod dystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A
  • RGD:7240710
DOID:0112343 hereditary spastic paraplegia 82 HGNC:8756 Homo sapiens (human) 5833 PCYT2
  • RGD:7240710
DOID:1826 epilepsy HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • MGI:6194238
DOID:0080768 pyridoxine-dependent epilepsy HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • MGI:6194238
DOID:0070519 early-onset vitamin B6-dependent epilepsy 4 HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • PMID:30901224
DOID:0080155 very long chain acyl-CoA dehydrogenase deficiency HGNC:88 Homo sapiens (human) 33 ACADL
  • MGI:6194238
DOID:0112072 nuclear type mitochondrial complex I deficiency 20 HGNC:88 Homo sapiens (human) 33 ACADL
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:8806 Homo sapiens (human) 5160 PDHA1
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency HGNC:8806 Homo sapiens (human) 5160 PDHA1
  • MGI:6194238
  • PMID:10679936
  • PMID:20002461
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:8806 Homo sapiens (human) 5160 PDHA1
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • MGI:6194238
DOID:0111910 spermatogenic failure HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency HGNC:8808 Homo sapiens (human) 5162 PDHB
  • PMID:15138885
  • RGD:7240710
DOID:0110011 advanced sleep phase syndrome 1 HGNC:8846 Homo sapiens (human) 8864 PER2
  • MGI:6194238
  • RGD:7240710

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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