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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 7876 - 7900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080855 Parkinsonism HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:0110196 Charcot-Marie-Tooth disease type 4G HGNC:4922 Homo sapiens (human) 3098 HK1
  • RGD:7240710
DOID:4247 coronary restenosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16319143
DOID:10286 prostate carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16372331
DOID:0050700 cardiomyopathy HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:22549409
DOID:10534 stomach cancer HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:19050968
  • PMID:31725767
DOID:7147 ankylosing spondylitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22876137
DOID:1574 alcohol use disorder HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • MGI:6194238
DOID:162 cancer HGNC:30220 Homo sapiens (human) 91869 RFT1
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:17326817
DOID:9970 obesity HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy HGNC:11184 Homo sapiens (human) 6652 SORD
  • MGI:6194238
DOID:12306 vitiligo HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17337399
  • PMID:19416237
DOID:0050811 congenital adrenal hyperplasia HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
DOID:10579 leukodystrophy HGNC:16066 Homo sapiens (human) 55331 ACER3
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:2797 idiopathic interstitial pneumonia HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:19218648
DOID:0070259 congenital disorder of glycosylation type IIg HGNC:6545 Homo sapiens (human) 9382 COG1
  • RGD:7240710
DOID:5212 congenital disorder of glycosylation HGNC:37258 Homo sapiens (human) 644974 ALG1L2
  • MGI:6194238
DOID:2749 glycogen storage disease Ia HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
  • PMID:11851840
  • PMID:20389290
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
  • PMID:11030756
  • RGD:7240710
DOID:0060770 dextro-looped transposition of the great arteries HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:0050860 colorectal adenoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30469315
DOID:2316 brain ischemia HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238

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

Acknowledgements

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