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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 3601 - 3625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1793 pancreatic cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:3744 cervical squamous cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:16803522
DOID:1380 endometrial cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18348659
DOID:2671 transitional cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:15841086
DOID:4608 common bile duct neoplasm HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10760693
DOID:11054 urinary bladder cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:16937303
DOID:3908 lung non-small cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:2394 ovarian cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:15262124
  • PMID:15628771
DOID:4450 renal cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:12614261
  • PMID:16861722
DOID:890 mitochondrial encephalomyopathy HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9924029
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA
  • PMID:1703489
DOID:0050461 aspartylglucosaminuria HGNC:318 Homo sapiens (human) 175 AGA
  • MGI:6194238
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:11764092
DOID:6000 congestive heart failure HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:1824 status epilepticus HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:4480 achondroplasia HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16507130
DOID:0112282 spondyloepiphyseal dysplasia Kimberley type HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16080123
  • RGD:7240710
DOID:2748 glycogen storage disease III HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
  • PMID:16705713
  • RGD:7240710
DOID:4676 uremia HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
DOID:0060668 anencephaly HGNC:3225 Homo sapiens (human) 1946 EFNA5
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip HGNC:32456 Homo sapiens (human) 440138 ALG11
  • RGD:7240710
DOID:0080759 Fanconi renotubular syndrome 3 HGNC:3247 Homo sapiens (human) 1962 EHHADH
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

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