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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 69476 - 69500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:3651 pyruvate carboxylase deficiency disease HGNC:8636 Homo sapiens (human) 5091 PC
  • PMID:9585612
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:7652 Homo sapiens (human) 4683 NBN
  • PMID:9590180
DOID:9074 systemic lupus erythematosus MGI:88223 Mus musculus (house mouse) 12259 C1qa
  • PMID:9590289
DOID:10003 sensorineural hearing loss HGNC:11720 Homo sapiens (human) 7007 TECTA
  • PMID:9590290
  • PMID:9949200
DOID:0080000 muscular disease HGNC:6143 Homo sapiens (human) 3679 ITGA7
  • PMID:9590299
DOID:576 proteinuria HGNC:9204 Homo sapiens (human) 5444 PON1
  • PMID:9591753
DOID:2799 bronchiolitis obliterans HGNC:3176 Homo sapiens (human) 1906 EDN1
  • PMID:9595474
DOID:10003 sensorineural hearing loss HGNC:7594 Homo sapiens (human) 51168 MYO15A
  • PMID:9603736
DOID:14720 Ehlers-Danlos syndrome classic type 1 MGI:109347 Mus musculus (house mouse) 17022 Lum
  • PMID:9606218
DOID:5844 myocardial infarction HGNC:3146 Homo sapiens (human) 1889 ECE1
  • PMID:9607404
DOID:0080016 spina bifida HGNC:7432 Homo sapiens (human) 4522 MTHFD1
  • PMID:9611072
DOID:285 hairy cell leukemia HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:9613675
DOID:11339 pneumocystosis HGNC:7508 Homo sapiens (human) 4582 MUC1
  • PMID:9617869
DOID:0050741 alcohol dependence HGNC:1569 Homo sapiens (human) 885 CCK
  • PMID:9622381
DOID:0050185 erythema multiforme HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:9627123
DOID:11396 pulmonary edema HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9628235
DOID:9884 muscular dystrophy HGNC:10806 Homo sapiens (human) 6443 SGCB
  • PMID:9631401
DOID:1574 alcohol use disorder RGD:2845 Rattus norvegicus (Norway rat) 24473 Htr1a
  • PMID:9631953
DOID:1574 alcohol use disorder FB:FBgn0003301 Drosophila melanogaster (fruit fly) 32406 rut
  • PMID:9635429
DOID:2355 anemia HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:9635949
DOID:1591 renovascular hypertension RGD:2071 Rattus norvegicus (Norway rat) 81638 Agtr1b
  • PMID:9644212
DOID:11476 osteoporosis MGI:109587 Mus musculus (house mouse) 18383 Tnfrsf11b
  • PMID:9647741
DOID:1074 kidney failure HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:9650354
DOID:11335 sarcoidosis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:9659531
DOID:4450 renal cell carcinoma HGNC:7849 Homo sapiens (human) 4830 NME1
  • PMID:9663430

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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