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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 6901 - 6925 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:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12883737
DOID:11446 sciatic neuropathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:162 cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:11460888
DOID:1070 primary open angle glaucoma HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22335808
DOID:0080159 Cryptococcal meningitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21592999
DOID:2377 multiple sclerosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8887999
  • PMID:8964914
  • PMID:9270614
DOID:3770 pulmonary fibrosis HGNC:921 Homo sapiens (human) 27087 B3GAT1
  • MGI:6194238
DOID:10763 hypertension HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • MGI:6194238
DOID:1612 breast cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:15102687
  • PMID:18676748
DOID:10787 premature menopause HGNC:2653 Homo sapiens (human) 1582 CYP8B1
  • MGI:6194238
DOID:3312 bipolar disorder HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:18430502
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19293779
DOID:10534 stomach cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16270381
DOID:0111233 congenital muscular dystrophy-dystroglycanopathy A14 HGNC:22932 Homo sapiens (human) 29925 GMPPB
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:2957 pulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:19126442
  • PMID:24874302
DOID:10763 hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip HGNC:32456 Homo sapiens (human) 440138 ALG11
  • RGD:7240710
DOID:10808 gastric ulcer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:162 cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238

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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