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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 10626 - 10650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:6432 pulmonary hypertension HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:21034646
DOID:11204 allergic conjunctivitis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:21042565
DOID:13241 Behcet's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21044750
DOID:0050083 Keshan disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:21055077
DOID:0080178 mucositis RGD:3269 Rattus norvegicus (Norway rat) 25737 Pcna
  • PMID:21080177
DOID:2986 IgA glomerulonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:21108742
DOID:9452 steatotic liver disease RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:21114362
DOID:8778 Crohn's disease HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21114432
DOID:0080322 polycystic kidney disease RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • PMID:21119215
DOID:7147 ankylosing spondylitis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21122270
DOID:676 juvenile rheumatoid arthritis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21124648
DOID:418 systemic scleroderma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:21124692
DOID:9352 type 2 diabetes mellitus HGNC:8971 Homo sapiens (human) 5286 PIK3C2A
  • PMID:21127054
DOID:10763 hypertension HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21130083
DOID:0060326 myelomeningocele HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:21135204
  • PMID:23427181
DOID:9352 type 2 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:21143859
DOID:0050581 brachydactyly HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:21155763
DOID:8805 intermediate coronary syndrome HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21162967
DOID:13608 biliary atresia HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:21172039
DOID:10591 pre-eclampsia HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:21173508
  • PMID:21299359
DOID:3083 chronic obstructive pulmonary disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21179920
  • PMID:22207678
DOID:3068 glioblastoma HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:21188471
  • PMID:26956052
DOID:3770 pulmonary fibrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:21190578
DOID:1459 hypothyroidism RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:21190599
DOID:3068 glioblastoma HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:21195542

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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