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:1612 | breast cancer | HGNC:1508 | Homo sapiens (human) | 840 | CASP7 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:1508 | Homo sapiens (human) | 840 | CASP7 |
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DOID:0060074 | ductal carcinoma in situ | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:1824 | status epilepticus | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:2316 | brain ischemia | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:11132 | prostatic hypertrophy | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:1002 | endometritis | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:4001 | ovarian carcinoma | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:3525 | middle cerebral artery infarction | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:10652 | Alzheimer's disease | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:8552 | chronic myeloid leukemia | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:3908 | lung non-small cell carcinoma | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:10286 | prostate carcinoma | HGNC:1507 | Homo sapiens (human) | 839 | CASP6 |
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DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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DOID:3525 | middle cerebral artery infarction | HGNC:14986 | Homo sapiens (human) | 9892 | SNAP91 |
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DOID:10652 | Alzheimer's disease | HGNC:14986 | Homo sapiens (human) | 9892 | SNAP91 |
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DOID:2835 | polycythemia due to hypoxia | HGNC:14980 | Homo sapiens (human) | 64089 | SNX16 |
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DOID:0060309 | syndromic X-linked intellectual disability | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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DOID:14711 | FG syndrome | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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DOID:0060041 | autism spectrum disorder | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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DOID:0060807 | syndromic X-linked intellectual disability Najm type | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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DOID:0080612 | anterior segment dysgenesis 7 | HGNC:14966 | Homo sapiens (human) | 7837 | PXDN |
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DOID:0112007 | growth hormone secreting pituitary adenoma 2 | HGNC:14963 | Homo sapiens (human) | 83550 | GPR101 |
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DOID:9970 | obesity | HGNC:14958 | Homo sapiens (human) | 23369 | PUM2 |
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DOID:0111743 | cerebellar ataxia type 47 | HGNC:14957 | Homo sapiens (human) | 9698 | PUM1 |
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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