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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 5626 - 5650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12377 spinal muscular atrophy HGNC:4879 Homo sapiens (human) 3074 HEXB
  • PMID:1720305
DOID:3211 lysosomal storage disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
DOID:2565 macular corneal dystrophy RGD:1561144 Rattus norvegicus (Norway rat) 307859 Chst5
  • MGI:6194238
DOID:10873 Kuhnt-Junius degeneration HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:19684010
DOID:2921 glomerulonephritis HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:10584677
DOID:1459 hypothyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:11383 cryptorchidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:893 Wilson disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:20648654
DOID:438 autoimmune disease of the nervous system HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:15486486
DOID:418 systemic scleroderma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:21124692
DOID:7998 hyperthyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:0080379 nephrotic syndrome type 2 HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:17999093
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
  • PMID:12200370
  • PMID:16025836
  • PMID:8814351
DOID:12217 Lewy body dementia HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:23576984
DOID:3587 pancreatic ductal carcinoma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:19488907
DOID:635 acquired immunodeficiency syndrome HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:17530998
DOID:0050598 extrapulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:24874302
DOID:6432 pulmonary hypertension HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:17107989
DOID:11650 bronchopulmonary dysplasia HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20050784
DOID:2957 pulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:19126442
  • PMID:24874302
DOID:12205 dengue disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:16274635
  • RGD:7240710
DOID:12206 dengue hemorrhagic fever HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:15838506
  • PMID:21245921
DOID:2841 asthma HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21471959

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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