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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 9526 - 9550 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:2841 asthma HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:15266299
  • PMID:18547625
DOID:1485 cystic fibrosis HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • PMID:15271694
DOID:1485 cystic fibrosis HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:15271694
DOID:5517 stomach carcinoma HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:15273732
DOID:670 amphetamine abuse HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15274053
  • PMID:17187009
  • PMID:21934638
  • PMID:33544778
DOID:1612 breast cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15285606
  • PMID:17429315
  • PMID:17507616
  • PMID:17562079
DOID:11650 bronchopulmonary dysplasia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15286263
DOID:8029 sporadic breast cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:15287024
DOID:3146 lipid metabolism disorder HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:1528846
DOID:3587 pancreatic ductal carcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:15289361
DOID:9351 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15292329
DOID:341 peripheral vascular disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15295097
DOID:0060713 autosomal recessive congenital ichthyosis 4B MGI:99461 Mus musculus (house mouse) 18700 Piga
  • PMID:15304084
DOID:3770 pulmonary fibrosis HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:15308504
DOID:11123 Henoch-Schoenlein purpura HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15315169
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:15318095
DOID:9743 diabetic neuropathy HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15318096
DOID:3407 carotid artery disease HGNC:9592 Homo sapiens (human) 5730 PTGDS
  • PMID:15325247
DOID:1287 cardiovascular system disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:15331559
DOID:8398 osteoarthritis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15334463
DOID:3328 temporal lobe epilepsy HGNC:7956 Homo sapiens (human) 4886 NPY1R
  • PMID:15337376
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:15346351
DOID:9352 type 2 diabetes mellitus RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:15356383
  • PMID:18344121
DOID:2841 asthma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15356557
  • PMID:16266379
  • PMID:19067129
  • PMID:19159017
  • PMID:20685742
DOID:9352 type 2 diabetes mellitus HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:15369805
  • PMID:7895459

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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


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