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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 70026 - 70050 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060037 developmental disorder of mental health HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:35642741
DOID:2394 ovarian cancer HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:26175272
DOID:684 hepatocellular carcinoma HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:17094378
DOID:3908 lung non-small cell carcinoma HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:18349282
DOID:2841 asthma HGNC:10473 Homo sapiens (human) 864 RUNX3
  • MGI:6194238
DOID:9970 obesity HGNC:13681 Homo sapiens (human) 8642 DCHS1
  • MGI:6194238
DOID:988 mitral valve prolapse HGNC:13681 Homo sapiens (human) 8642 DCHS1
  • MGI:6194238
  • RGD:7240710
DOID:0080585 Van Maldergem syndrome 1 HGNC:13681 Homo sapiens (human) 8642 DCHS1
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:9586 Homo sapiens (human) 8643 PTCH2
  • MGI:6194238
DOID:2513 basal cell carcinoma HGNC:9586 Homo sapiens (human) 8643 PTCH2
  • RGD:7240710
DOID:12270 coloboma HGNC:9586 Homo sapiens (human) 8643 PTCH2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:9586 Homo sapiens (human) 8643 PTCH2
  • MGI:6194238
DOID:0050902 medulloblastoma HGNC:9586 Homo sapiens (human) 8643 PTCH2
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
  • PMID:19681734
DOID:11612 polycystic ovary syndrome HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:16735089
DOID:1240 leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:18339682
DOID:0080909 castration-resistant prostate carcinoma HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:23196782
DOID:10283 prostate cancer HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:24571686
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:10273 heart conduction disease HGNC:6280 Homo sapiens (human) 8645 KCNK5
  • MGI:6194238
DOID:12583 velocardiofacial syndrome HGNC:1949 Homo sapiens (human) 8646 CHRD
  • MGI:6194238
DOID:11198 DiGeorge syndrome HGNC:1949 Homo sapiens (human) 8646 CHRD
  • MGI:6194238
DOID:0070232 benign recurrent intrahepatic cholestasis 2 HGNC:42 Homo sapiens (human) 8647 ABCB11
  • RGD:7240710

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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