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:0050570 | congenital disorder of glycosylation type I | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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DOID:12700 | hyperprolactinemia | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:9351 | diabetes mellitus | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:10283 | prostate cancer | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:3459 | breast carcinoma | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:9970 | obesity | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:10283 | prostate cancer | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:1459 | hypothyroidism | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:3459 | breast carcinoma | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:12700 | hyperprolactinemia | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:162 | cancer | HGNC:11279 | Homo sapiens (human) | 6713 | SQLE |
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DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:16253 | Homo sapiens (human) | 55304 | SPTLC3 |
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DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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DOID:8893 | psoriasis | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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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