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:2394 | ovarian cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:3702 | cervical adenocarcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:0060180 | colitis | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:10283 | prostate cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:11054 | urinary bladder cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:10534 | stomach cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:0080365 | endometrial hyperplasia | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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DOID:13550 | angle-closure glaucoma | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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DOID:535 | sleep disorder | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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DOID:0060563 | Char syndrome | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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DOID:0050889 | non-syndromic intellectual disability | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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DOID:9970 | obesity | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:0050827 | rheumatic heart disease | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:10652 | Alzheimer's disease | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:8947 | diabetic retinopathy | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:1826 | epilepsy | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:0060108 | brain glioma | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:3525 | middle cerebral artery infarction | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:3319 | lymphangioleiomyomatosis | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:0050866 | oral squamous cell carcinoma | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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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