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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 4001 - 4025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1324 lung cancer HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:26767034
  • PMID:33255360
DOID:2476 hereditary spastic paraplegia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:783 end stage renal disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:18809976
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:10547581
DOID:6432 pulmonary hypertension HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238
DOID:3307 teratoma HGNC:8905 Homo sapiens (human) 5236 PGM1
  • PMID:5259759
DOID:631 fibromyalgia HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:22532869
DOID:0080556 congenital disorder of glycosylation Id HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
  • RGD:7240710
DOID:1586 rheumatic fever HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:14567831
DOID:684 hepatocellular carcinoma HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:23740135
DOID:5844 myocardial infarction HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:0111258 pentosuria HGNC:18985 Homo sapiens (human) 51181 DCXR
  • RGD:7240710
DOID:784 chronic kidney disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:21111939
DOID:0050563 nonsyndromic deafness HGNC:31088 Homo sapiens (human) 144245 ALG10B
  • MGI:6194238
DOID:12549 hepatitis A HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:0070403 hypomyelinating leukodystrophy 26 HGNC:16872 Homo sapiens (human) 347734 SLC35B2
  • RGD:7240710
DOID:0112198 spondyloepimetaphyseal dysplasia with joint laxity type 1 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:631 fibromyalgia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:24762091
DOID:10591 pre-eclampsia HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18852388
  • PMID:20303587
  • PMID:28705740
DOID:6713 cerebrovascular disease HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:26072930
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:12402217
  • PMID:16984965
  • PMID:19881467
  • PMID:26255563

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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