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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 9926 - 9950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3492 mixed connective tissue disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19684145
DOID:13252 mesenteric vascular occlusion HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:14213 hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:8406453
DOID:3371 chondrosarcoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12598313
DOID:10159 osteonecrosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:9253 gastrointestinal stromal tumor HGNC:10681 Homo sapiens (human) 6390 SDHB
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:8896 Homo sapiens (human) 5230 PGK1
  • MGI:6194238
DOID:8481 rheumatic myocarditis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:22987107
DOID:9452 steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:2671 transitional cell carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:10022688
DOID:1920 hyperuricemia HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19033255
DOID:0111237 congenital muscular dystrophy-dystroglycanopathy type A1 HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • RGD:7240710
DOID:1184 nephrotic syndrome HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy HGNC:22954 Homo sapiens (human) 56983 POGLUT1
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:22173044
DOID:0050700 cardiomyopathy HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
DOID:557 kidney disease HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • MGI:6194238
DOID:10534 stomach cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:27572739
DOID:12662 paracoccidioidomycosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:17145373
DOID:0080821 exercise-induced bronchoconstriction HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10984370
DOID:13042 persistent fetal circulation syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:0050933 ovarian serous carcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:25455994
DOID:1184 nephrotic syndrome HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:16088202
DOID:1380 endometrial cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • 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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