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 | October 9, 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:0111051 | platelet-type bleeding disorder 18 | HGNC:9879 | Homo sapiens (human) | 10235 | RASGRP2 |
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DOID:0110912 | leukocyte adhesion deficiency 3 | HGNC:9879 | Homo sapiens (human) | 10235 | RASGRP2 |
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DOID:4608 | common bile duct neoplasm | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:3587 | pancreatic ductal carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:1793 | pancreatic cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:4897 | bile duct carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:2394 | ovarian cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:26 | pancreas disease | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16893 | Homo sapiens (human) | 10226 | PLIN3 |
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DOID:9970 | obesity | HGNC:16893 | Homo sapiens (human) | 10226 | PLIN3 |
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DOID:0111581 | C syndrome | HGNC:16892 | Homo sapiens (human) | 10225 | CD96 |
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DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | HGNC:4216 | Homo sapiens (human) | 10220 | GDF11 |
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DOID:9993 | hypoglycemia | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:0050593 | primary congenital glaucoma | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:0110965 | brachydactyly type A2 | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:10652 | Alzheimer's disease | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:1612 | breast cancer | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:10825 | essential hypertension | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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DOID:1787 | pericarditis | HGNC:9364 | Homo sapiens (human) | 10216 | PRG4 |
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DOID:0090127 | camptodactyly-arthropathy-coxa vara-pericarditis syndrome | HGNC:9364 | Homo sapiens (human) | 10216 | PRG4 |
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DOID:1824 | status epilepticus | HGNC:9398 | Homo sapiens (human) | 10215 | OLIG2 |
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DOID:219 | colon cancer | MGI:2142572 | Mus musculus (house mouse) | 102103 | Mtus1 |
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DOID:3459 | breast carcinoma | MGI:2142572 | Mus musculus (house mouse) | 102103 | Mtus1 |
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DOID:4001 | ovarian carcinoma | MGI:2142572 | Mus musculus (house mouse) | 102103 | Mtus1 |
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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 v4.1.0
Last updated: December 9, 2024