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 |
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Alliance of Genome Resources | July 29, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▲ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
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DOID:684 | hepatocellular carcinoma | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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DOID:2957 | pulmonary tuberculosis | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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DOID:10591 | pre-eclampsia | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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DOID:2272 | vulvovaginal candidiasis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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DOID:9409 | diabetes insipidus | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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DOID:0110389 | retinitis pigmentosa 73 | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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DOID:10763 | hypertension | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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DOID:4448 | macular degeneration | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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DOID:0111257 | gamma-glutamyl transpeptidase deficiency | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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DOID:3429 | inclusion body myositis | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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DOID:11984 | hypertrophic cardiomyopathy | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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DOID:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
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DOID:4195 | hyperglycemia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:1380 | endometrial cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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DOID:8549 | chronic ulcer of skin | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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DOID:936 | brain disease | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024