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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 8601 - 8625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:289 endometriosis HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:3742 bladder squamous cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:26916953
DOID:3770 pulmonary fibrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:21190578
DOID:10763 hypertension HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:19204185
DOID:397 restrictive cardiomyopathy HGNC:21088 Homo sapiens (human) 79966 SCD5
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:16868149
DOID:3068 glioblastoma HGNC:5382 Homo sapiens (human) 3417 IDH1
  • PMID:19765000
  • PMID:25495392
DOID:9744 type 1 diabetes mellitus HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18361935
DOID:8893 psoriasis HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554
DOID:1612 breast cancer HGNC:2637 Homo sapiens (human) 1576 CYP3A4
  • PMID:15180491
DOID:10534 stomach cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:3560 Homo sapiens (human) 2171 FABP5
  • PMID:16489065
DOID:5679 retinal disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
  • PMID:16115302
  • PMID:20714777
DOID:10591 pre-eclampsia HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
DOID:12700 hyperprolactinemia HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • MGI:6194238
DOID:2526 prostate adenocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:19079609
DOID:8955 sideroblastic anemia HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24325359
DOID:684 hepatocellular carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:4480 achondroplasia HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:0050709 early infantile epileptic encephalopathy HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:17086182
DOID:0111953 immunodeficiency 23 HGNC:8907 Homo sapiens (human) 5238 PGM3
  • RGD:7240710
DOID:10763 hypertension HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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


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