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:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
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DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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DOID:0060060 | non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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DOID:13375 | temporal arteritis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:1926 | Gaucher's disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:10534 | stomach cancer | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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DOID:0111936 | immunodeficiency 14 | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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DOID:14115 | toxic shock syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:3132 | porphyria cutanea tarda | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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DOID:1070 | primary open angle glaucoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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DOID:1742 | drug psychosis | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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DOID:12930 | dilated cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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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