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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 6376 - 6400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0111953 immunodeficiency 23 SGD:S000000784 Saccharomyces cerevisiae S288C 856652 PCM1
  • MGI:6194238
DOID:127 leiomyoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
  • PMID:18000229
DOID:4440 seminoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:7474604
DOID:12217 Lewy body dementia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:20665591
DOID:4450 renal cell carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11369057
DOID:0080178 mucositis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:2316 brain ischemia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:11476 osteoporosis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:10534 stomach cancer HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:26432329
DOID:3008 invasive ductal carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:8102204
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: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

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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