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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 70826 - 70850 of 71927 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:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:13207 proliferative diabetic retinopathy HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:16364297
DOID:10646 schizotypal personality disorder HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22146151
DOID:2508 Takayasu's arteritis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:20579752
DOID:2841 asthma HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:21920897
DOID:9744 type 1 diabetes mellitus HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:10553500
  • PMID:16969646
  • PMID:21870072
DOID:0080199 colorectal carcinoma HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:824 periodontitis HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:22795565
DOID:11394 adult respiratory distress syndrome HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:8893 psoriasis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:12029499
DOID:11981 morbid obesity HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22828946
DOID:1508 candidiasis SGD:S000001306 Saccharomyces cerevisiae S288C 854767 AGE2
  • MGI:6194238
DOID:0110361 retinitis pigmentosa 75 HGNC:26147 Homo sapiens (human) 60509 AGBL5
  • RGD:7240710
DOID:11555 Fuchs' endothelial dystrophy HGNC:26504 Homo sapiens (human) 123624 AGBL1
  • RGD:7240710
DOID:0050888 syndromic intellectual disability HGNC:23463 Homo sapiens (human) 642517 AGAP9
  • MGI:6194238
DOID:1969 cerebral palsy HGNC:23463 Homo sapiens (human) 642517 AGAP9
  • MGI:6194238
DOID:0050888 syndromic intellectual disability HGNC:23467 Homo sapiens (human) 729092 AGAP5
  • MGI:6194238
DOID:1969 cerebral palsy HGNC:23467 Homo sapiens (human) 729092 AGAP5
  • MGI:6194238
DOID:0050888 syndromic intellectual disability HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • PMID:26464646
DOID:10283 prostate cancer HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • PMID:19176382
DOID:1969 cerebral palsy HGNC:16922 Homo sapiens (human) 116987 AGAP1
  • MGI:6194238
DOID:0050888 syndromic intellectual disability HGNC:16922 Homo sapiens (human) 116987 AGAP1
  • MGI:6194238
DOID:0050461 aspartylglucosaminuria HGNC:318 Homo sapiens (human) 175 AGA
  • MGI:6194238
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA
  • PMID:1703489

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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: December 9, 2024