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:0080199 | colorectal carcinoma | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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DOID:299 | adenocarcinoma | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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DOID:3168 | squamous cell neoplasm | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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DOID:4552 | large cell carcinoma | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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DOID:3905 | lung carcinoma | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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DOID:4947 | cholangiocarcinoma | HGNC:23170 | Homo sapiens (human) | 11169 | WDHD1 |
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DOID:9675 | pulmonary emphysema | HGNC:3972 | Homo sapiens (human) | 11167 | FSTL1 |
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DOID:0110771 | hereditary spastic paraplegia 18 | HGNC:1356 | Homo sapiens (human) | 11160 | ERLIN2 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:1356 | Homo sapiens (human) | 11160 | ERLIN2 |
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DOID:11650 | bronchopulmonary dysplasia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:1909 | melanoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:2394 | ovarian cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:13375 | temporal arteritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:0080199 | colorectal carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:7148 | rheumatoid arthritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:0050685 | small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:3770 | pulmonary fibrosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:6000 | congestive heart failure | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:3083 | chronic obstructive pulmonary disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:1380 | endometrial cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:10763 | hypertension | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:10591 | pre-eclampsia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:9119 | acute myeloid leukemia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:9470 | bacterial meningitis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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DOID:3068 | glioblastoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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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