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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 9401 - 9425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10923 sickle cell anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:5686464
DOID:3457 invasive lobular carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:11245336
DOID:9952 acute lymphoblastic leukemia HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:8562939
DOID:1793 pancreatic cancer HGNC:7047 Homo sapiens (human) 11320 MGAT4A
  • PMID:16434023
DOID:9279 hyperhomocysteinemia HGNC:800 Homo sapiens (human) 477 ATP1A2
  • MGI:6194238
DOID:1508 candidiasis HGNC:4020 Homo sapiens (human) 10690 FUT9
  • MGI:6194238
DOID:3717 gastric adenocarcinoma HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:24796667
DOID:2384 Wernicke encephalopathy HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0050773 paraganglioma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:0110644 long QT syndrome 1 HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:18008256
  • PMID:19575238
  • PMID:20403143
DOID:0111141 delayed sleep phase syndrome HGNC:2384 Homo sapiens (human) 1407 CRY1
  • RGD:7240710
DOID:0050866 oral squamous cell carcinoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:24706327
DOID:1907 malignant fibrous histiocytoma HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23166610
DOID:3070 high grade glioma HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0050156 idiopathic pulmonary fibrosis HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • RGD:7240710
DOID:0060887 ossification of the posterior longitudinal ligament of spine HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:15834329
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia HGNC:5201 Homo sapiens (human) 9394 HS6ST1
  • RGD:7240710
DOID:162 cancer HGNC:5382 Homo sapiens (human) 3417 IDH1
  • MGI:6194238
DOID:10325 silicosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:0080566 congenital disorder of glycosylation In HGNC:30220 Homo sapiens (human) 91869 RFT1
  • RGD:7240710
DOID:7998 hyperthyroidism HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease HGNC:7454 Homo sapiens (human) 9108 MTMR7
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:22095073
DOID:3827 congenital diaphragmatic hernia HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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