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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 2726 - 2750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081215 autosomal recessive intellectual developmental disorder 52 HGNC:19263 Homo sapiens (human) 81562 LMAN2L
  • RGD:7240710
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:19263 Homo sapiens (human) 81562 LMAN2L
  • RGD:7240710
DOID:0050771 pheochromocytoma HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:2189303
DOID:10763 hypertension HGNC:1929 Homo sapiens (human) 1113 CHGA
  • MGI:6194238
  • PMID:20113265
  • PMID:21061160
DOID:2986 IgA glomerulonephritis HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:20113265
DOID:783 end stage renal disease HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:18235090
  • PMID:20730520
DOID:10283 prostate cancer HGNC:1929 Homo sapiens (human) 1113 CHGA
  • PMID:20663522
DOID:1909 melanoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16456816
DOID:2349 arteriosclerosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10073974
DOID:3083 chronic obstructive pulmonary disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20656949
DOID:13406 pulmonary sarcoidosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15763444
DOID:0080199 colorectal carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12124825
DOID:11650 bronchopulmonary dysplasia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20558631
DOID:6000 congestive heart failure HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:19961288
DOID:0050685 small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15541818
DOID:5419 schizophrenia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • RGD:7240710
DOID:3770 pulmonary fibrosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20888745
DOID:1612 breast cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12889595
DOID:3068 glioblastoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:11161003
DOID:10763 hypertension HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • MGI:6194238
DOID:9470 bacterial meningitis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:11986266
DOID:2394 ovarian cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12883737
DOID:9744 type 1 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18957531
DOID:3393 coronary artery disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17627189
DOID:9352 type 2 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:21143859

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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