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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 10576 - 10600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:3310 atopic dermatitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20642202
DOID:3083 chronic obstructive pulmonary disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20646456
DOID:5082 liver cirrhosis HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:20648474
  • PMID:29674183
  • PMID:31377187
DOID:10652 Alzheimer's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:20648654
DOID:1824 status epilepticus RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:20649973
DOID:10887 lepromatous leprosy HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20650301
DOID:1024 leprosy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20650301
DOID:3770 pulmonary fibrosis HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • PMID:20656946
DOID:3083 chronic obstructive pulmonary disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20656949
DOID:10283 prostate cancer HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:20663522
DOID:12217 Lewy body dementia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:20665591
DOID:8515 Cor pulmonale HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20669672
DOID:9427 hypertensive encephalopathy RGD:3369 Rattus norvegicus (Norway rat) 25747 Ppara
  • PMID:20671072
DOID:7148 rheumatoid arthritis HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:20676650
  • PMID:22505706
DOID:4752 multiple system atrophy HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:20683839
DOID:2527 nephrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20685819
DOID:3042 allergic contact dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20711192
DOID:2377 multiple sclerosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:20714168
DOID:1485 cystic fibrosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20717938
DOID:5016 hepatocellular clear cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20723213
DOID:5016 hepatocellular clear cell carcinoma HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:20723213
DOID:10652 Alzheimer's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:20727007
  • PMID:22213409
DOID:783 end stage renal disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20729266
DOID:783 end stage renal disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20729266
DOID:3083 chronic obstructive pulmonary disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:20732852

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Supported by JST NBDC Grant Number JPMJND2204

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


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