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:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:29284 | Homo sapiens (human) | 57609 | DIP2B |
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DOID:1588 | thrombocytopenia | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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DOID:0080444 | developmental and epileptic encephalopathy 27 | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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DOID:0050741 | alcohol dependence | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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DOID:0111485 | combined oxidative phosphorylation deficiency 24 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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DOID:0060882 | renal hypomagnesemia 4 | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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DOID:0081110 | keratosis palmoplantaris striata 3 | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:3969 | thyroid gland papillary carcinoma | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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DOID:0111707 | Bothnian type palmoplantar keratoderma | HGNC:638 | Homo sapiens (human) | 362 | AQP5 |
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DOID:0111222 | centronuclear myopathy 5 | HGNC:16901 | Homo sapiens (human) | 10290 | SPEG |
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DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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DOID:0050545 | visceral heterotaxy | HGNC:7865 | Homo sapiens (human) | 4838 | NODAL |
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DOID:0111069 | congenital bile acid synthesis defect 2 | HGNC:388 | Homo sapiens (human) | 6718 | AKR1D1 |
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DOID:0111776 | 46,XY sex reversal 5 | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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DOID:0110801 | hereditary spastic paraplegia 49 | HGNC:19957 | Homo sapiens (human) | 9895 | TECPR2 |
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DOID:0111354 | arthrogryposis, renal dysfunction, and cholestasis 2 | HGNC:20347 | Homo sapiens (human) | 63894 | VIPAS39 |
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DOID:0111450 | progressive myoclonus epilepsy 9 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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DOID:0070073 | autosomal dominant intellectual developmental disorder 43 | HGNC:4921 | Homo sapiens (human) | 3097 | HIVEP2 |
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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