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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 October 9, 2024
Displaying entries 68401 - 68425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050733 methylmalonic aciduria and homocystinuria type cblG HGNC:7468 Homo sapiens (human) 4548 MTR
  • RGD:7240710
DOID:9970 obesity HGNC:4392 Homo sapiens (human) 2778 GNAS
  • PMID:17062894
DOID:13564 aspergillosis HGNC:14558 Homo sapiens (human) 64581 CLEC7A
  • RGD:7240710
DOID:10159 osteonecrosis HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:28422712
DOID:0050866 oral squamous cell carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21393552
DOID:12849 autistic disorder HGNC:4091 Homo sapiens (human) 2570 GABRR2
  • PMID:16080114
DOID:10283 prostate cancer HGNC:7376 Homo sapiens (human) 4481 MSR1
  • PMID:17903305
DOID:9146 visceral leishmaniasis HGNC:6009 Homo sapiens (human) 3560 IL2RB
  • PMID:17108990
DOID:0070490 infantile parkinsonism-dystonia 2 HGNC:10935 Homo sapiens (human) 6571 SLC18A2
  • RGD:7240710
DOID:8778 Crohn's disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:19212205
DOID:0081331 glycogen storage disease Ic HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:1067 open-angle glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20357201
DOID:3910 lung adenocarcinoma HGNC:6407 Homo sapiens (human) 3845 KRAS
  • PMID:11745231
DOID:14735 hereditary angioedema HGNC:14178 Homo sapiens (human) 64711 HS3ST6
  • RGD:7240710
DOID:13544 low tension glaucoma HGNC:285 Homo sapiens (human) 153 ADRB1
  • PMID:16785856
DOID:2320 obstructive lung disease HGNC:7 Homo sapiens (human) 2 A2M
  • PMID:2475424
DOID:848 arthritis HGNC:19100 Homo sapiens (human) 149233 IL23R
  • PMID:19035472
DOID:2058 chronic mucocutaneous candidiasis HGNC:18358 Homo sapiens (human) 84818 IL17RC
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • PMID:16759312
DOID:12401 intermittent explosive disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:11204347
DOID:0070031 autosomal dominant intellectual developmental disorder 1 HGNC:20444 Homo sapiens (human) 55777 MBD5
  • RGD:7240710
DOID:3312 bipolar disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15050861
DOID:0110967 brachydactyly type A4 HGNC:5136 Homo sapiens (human) 3239 HOXD13
  • PMID:17236141
DOID:9952 acute lymphoblastic leukemia HGNC:3765 Homo sapiens (human) 2322 FLT3
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:6015 Homo sapiens (human) 3566 IL4R
  • PMID:14712310

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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: December 9, 2024