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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 2876 - 2900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1496 echinococcosis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:2142987
DOID:0050453 lissencephaly HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:2476 hereditary spastic paraplegia HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12124825
DOID:2043 hepatitis B HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:29239247
DOID:9146 visceral leishmaniasis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17357060
  • PMID:22995279
  • PMID:26297290
DOID:14067 Plasmodium falciparum malaria HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24943486
DOID:8536 herpes zoster HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:21954956
DOID:83 cataract HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
DOID:0050777 Joubert syndrome HGNC:21474 Homo sapiens (human) 56623 INPP5E
  • MGI:6194238
  • PMID:23386033
DOID:3962 thyroid gland follicular carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:594 panic disorder HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:24473444
DOID:0080108 myoglobinuria HGNC:8889 Homo sapiens (human) 5224 PGAM2
  • PMID:8447317
DOID:3319 lymphangioleiomyomatosis HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • PMID:29885404
DOID:9975 cocaine dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:18704099
DOID:5517 stomach carcinoma HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:15273732
DOID:9744 type 1 diabetes mellitus HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:15914531
DOID:9970 obesity HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:0050598 extrapulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:24874302
DOID:0081120 Graves ophthalmopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:15158621
  • PMID:20394549
DOID:0080572 congenital disorder of glycosylation Iw HGNC:30611 Homo sapiens (human) 201595 STT3B
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18936159
  • PMID:24102912
DOID:10763 hypertension HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:18619052
DOID:10763 hypertension HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:3454 brain infarction HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • 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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Last updated: August 19, 2024