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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 8526 - 8550 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10763 hypertension HGNC:3574 Homo sapiens (human) 3992 FADS1
  • MGI:6194238
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
  • RGD:7240710
DOID:1059 intellectual disability HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • PMID:11889465
DOID:14501 Sjogren-Larsson syndrome HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
DOID:1324 lung cancer HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • PMID:23936004
DOID:1612 breast cancer HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • PMID:23512947
  • PMID:28977883
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:14501 Sjogren-Larsson syndrome HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:10283 prostate cancer HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • PMID:27270436
DOID:2841 asthma HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • PMID:19221603
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:9970 obesity HGNC:3569 Homo sapiens (human) 2180 ACSL1
  • MGI:6194238
  • PMID:16788709
DOID:10283 prostate cancer HGNC:3560 Homo sapiens (human) 2171 FABP5
  • PMID:16489065
DOID:8893 psoriasis HGNC:3560 Homo sapiens (human) 2171 FABP5
  • PMID:16283139
DOID:206 hereditary multiple exostoses HGNC:3518 Homo sapiens (human) 2137 EXTL3
  • MGI:6194238
DOID:206 hereditary multiple exostoses HGNC:3515 Homo sapiens (human) 2134 EXTL1
  • MGI:6194238
DOID:206 hereditary multiple exostoses HGNC:3513 Homo sapiens (human) 2132 EXT2
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:3512 Homo sapiens (human) 2131 EXT1
  • MGI:6194238
DOID:206 hereditary multiple exostoses HGNC:3512 Homo sapiens (human) 2131 EXT1
  • MGI:6194238
  • PMID:12490068
  • PMID:17767039
  • PMID:18330718
  • PMID:24297320
  • PMID:25421355
  • PMID:26839764
  • PMID:8981950
DOID:3371 chondrosarcoma HGNC:3512 Homo sapiens (human) 2131 EXT1
  • PMID:17226760
  • RGD:7240710
DOID:891 progressive myoclonus epilepsy HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • PMID:9771710
DOID:3534 Lafora disease HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • MGI:6194238
DOID:0111670 primary hyperoxaluria type 1 HGNC:341 Homo sapiens (human) 189 AGXT
  • MGI:6194238
  • RGD:7240710
DOID:2977 primary hyperoxaluria HGNC:341 Homo sapiens (human) 189 AGXT
  • 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