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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 7726 - 7750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11832 visual epilepsy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:23333565
DOID:9743 diabetic neuropathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:3526 cerebral infarction HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:17122425
  • PMID:20946167
  • PMID:25126700
DOID:4231 histiocytoma HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • MGI:6194238
DOID:5199 ureteral obstruction HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12306 vitiligo HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19439879
  • PMID:20613769
  • PMID:23868633
DOID:0060050 autoimmune disease of blood HGNC:24337 Homo sapiens (human) 56913 C1GALT1
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:12009 Homo sapiens (human) 7167 TPI1
  • PMID:9338582
DOID:684 hepatocellular carcinoma HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • PMID:28867541
DOID:11476 osteoporosis HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • MGI:6194238
DOID:552 pneumonia HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0050807 Kahrizi syndrome HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0060575 3MC syndrome 1 HGNC:6901 Homo sapiens (human) 5648 MASP1
  • RGD:7240710
DOID:0080197 congenital muscular dystrophy with cataracts and intellectual disability HGNC:33882 Homo sapiens (human) 51763 INPP5K
  • MGI:6194238
  • RGD:7240710
DOID:104 bacterial infectious disease HGNC:30242 Homo sapiens (human) 7991 TUSC3
  • MGI:6194238
DOID:8618 oral cavity cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:16721740
DOID:11723 Duchenne muscular dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:22934738
DOID:9256 colorectal cancer HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • RGD:7240710
DOID:0060589 Yunis-Varon syndrome HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:0070384 developmental and epileptic encephalopathy 98 HGNC:800 Homo sapiens (human) 477 ATP1A2
  • RGD:7240710
DOID:13452 scleritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:23177360
DOID:1612 breast cancer HGNC:9376 Homo sapiens (human) 5562 PRKAA1
  • PMID:22562547
DOID:0112182 mismatch repair cancer syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28218421
DOID:0090001 Fraser syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238

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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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Last updated: August 19, 2024