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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 70851 - 70875 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0070519 early-onset vitamin B6-dependent epilepsy 4 HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • RGD:7240710
DOID:1094 attention deficit hyperactivity disorder HGNC:644 Homo sapiens (human) 367 AR
  • PMID:10380986
DOID:5082 liver cirrhosis HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:24758241
DOID:0080582 hypotrichosis 14 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:11365 Homo sapiens (human) 6775 STAT4
  • PMID:18516230
  • PMID:18803832
  • PMID:20479942
  • PMID:22729903
  • PMID:23049788
  • RGD:7240710
DOID:0080609 anterior segment dysgenesis 4 HGNC:9005 Homo sapiens (human) 5308 PITX2
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:6600 Homo sapiens (human) 3980 LIG3
  • PMID:19147782
DOID:0060060 non-Hodgkin lymphoma HGNC:7132 Homo sapiens (human) 4297 KMT2A
  • PMID:8361504
DOID:1287 cardiovascular system disease HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:21282363
DOID:0111744 cerebellar ataxia type 41 HGNC:12335 Homo sapiens (human) 7222 TRPC3
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:19100 Homo sapiens (human) 149233 IL23R
  • PMID:23093364
DOID:6364 migraine HGNC:3179 Homo sapiens (human) 1909 EDNRA
  • PMID:11376172
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:17588142
DOID:10933 obsessive-compulsive disorder HGNC:11050 Homo sapiens (human) 6532 SLC6A4
  • PMID:14593431
  • RGD:7240710
DOID:5614 eye disease HGNC:2200 Homo sapiens (human) 1280 COL2A1
  • PMID:19430638
DOID:10283 prostate cancer HGNC:6859 Homo sapiens (human) 6885 MAP3K7
  • PMID:17785553
DOID:0111813 syndactyly type 8 HGNC:3672 Homo sapiens (human) 8823 FGF16
  • RGD:7240710
DOID:0112001 immunodeficiency 50 HGNC:7373 Homo sapiens (human) 4478 MSN
  • RGD:7240710
DOID:1727 retinal vein occlusion HGNC:7166 Homo sapiens (human) 4313 MMP2
  • PMID:23791966
DOID:9119 acute myeloid leukemia HGNC:23019 Homo sapiens (human) 8233 ZRSR2
  • PMID:25550361
  • PMID:32027246
DOID:0110446 dilated cardiomyopathy 1W HGNC:12665 Homo sapiens (human) 7414 VCL
  • RGD:7240710
DOID:13714 anodontia HGNC:7176 Homo sapiens (human) 4318 MMP9
  • PMID:24351915
DOID:9155 mucocutaneous leishmaniasis HGNC:6709 Homo sapiens (human) 4049 LTA
  • PMID:7595196
DOID:0060444 granular corneal dystrophy 2 HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:8986 narcolepsy HGNC:4940 Homo sapiens (human) 3115 HLA-DPB1
  • PMID:25574827

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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: December 9, 2024