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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 6976 - 7000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9970 obesity HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16772345
DOID:0050873 follicular lymphoma HGNC:4021 Homo sapiens (human) 2531 KDSR
  • PMID:8417785
DOID:6432 pulmonary hypertension HGNC:4820 Homo sapiens (human) 3038 HAS3
  • MGI:6194238
DOID:557 kidney disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:25142320
DOID:1793 pancreatic cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:9452 steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:4852 pleomorphic xanthoastrocytoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25346165
DOID:2986 IgA glomerulonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12220450
DOID:3770 pulmonary fibrosis HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:10543276
  • PMID:13680361
  • PMID:19347046
DOID:11396 pulmonary edema HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9628235
DOID:114 heart disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:4699 Homo sapiens (human) 2992 GYG1
  • RGD:7240710
DOID:162 cancer HGNC:8896 Homo sapiens (human) 5230 PGK1
  • MGI:6194238
DOID:9268 glycine encephalopathy HGNC:4208 Homo sapiens (human) 2653 GCSH
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19207313
DOID:4450 renal cell carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11369057
DOID:11335 sarcoidosis HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • PMID:20151281
DOID:10024 migraine with aura HGNC:800 Homo sapiens (human) 477 ATP1A2
  • PMID:12953268
DOID:0112223 developmental and epileptic encephalopathy 89 HGNC:4092 Homo sapiens (human) 2571 GAD1
  • RGD:7240710
DOID:0110184 Charcot-Marie-Tooth disease type 4J HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19199550
DOID:783 end stage renal disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:17033970
  • PMID:19138334

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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