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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 10426 - 10450 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3393 coronary artery disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29482350
DOID:13544 low tension glaucoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:20357201
DOID:5773 oral submucous fibrosis HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:23776093
DOID:1115 sarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:31089155
DOID:9119 acute myeloid leukemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:24836762
  • PMID:25412846
  • PMID:25573287
DOID:0060071 pre-malignant neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:4467 clear cell renal cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28551630
DOID:10283 prostate cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18225585
DOID:10964 cholesteatoma of middle ear HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:9455944
DOID:10811 nasal cavity cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19950227
DOID:10534 stomach cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:27323394
  • PMID:28387921
DOID:4926 bronchiolo-alveolar adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0050834 CHARGE syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:9351 diabetes mellitus MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:14500 fucosidosis MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
  • PMID:27491075
DOID:162 cancer HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0050884 triosephosphate isomerase deficiency HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
  • RGD:7240710
DOID:2978 carbohydrate metabolic disorder HGNC:12009 Homo sapiens (human) 7167 TPI1
  • PMID:9338582
DOID:9282 ocular hypertension HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0070238 primary coenzyme Q10 deficiency 1 MGI:1919133 Mus musculus (house mouse) 71883 Coq2
  • 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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