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:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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DOID:0080337 | mitochondrial DNA depletion syndrome 15 | HGNC:11741 | Homo sapiens (human) | 7019 | TFAM |
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DOID:13909 | red-green color blindness | HGNC:4206 | Homo sapiens (human) | 2652 | OPN1MW |
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DOID:0111333 | early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
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DOID:0060720 | autosomal recessive congenital ichthyosis 11 | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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DOID:0080224 | autosomal dominant dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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DOID:9256 | colorectal cancer | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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DOID:0060777 | congenital secretory sodium diarrhea 8 | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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DOID:0110347 | osteogenesis imperfecta type 15 | HGNC:12774 | Homo sapiens (human) | 7471 | WNT1 |
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DOID:4465 | papillary renal cell carcinoma | HGNC:7029 | Homo sapiens (human) | 4233 | MET |
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DOID:0080620 | familial glucocorticoid deficiency | HGNC:7863 | Homo sapiens (human) | 23530 | NNT |
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DOID:0050676 | Birt-Hogg-Dube syndrome | HGNC:13995 | Homo sapiens (human) | 56980 | PRDM10 |
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DOID:676 | juvenile rheumatoid arthritis | HGNC:26789 | Homo sapiens (human) | 144811 | LACC1 |
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DOID:5426 | primary ovarian insufficiency | HGNC:28569 | Homo sapiens (human) | 254528 | MEIOB |
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DOID:0110774 | hereditary spastic paraplegia 23 | HGNC:29043 | Homo sapiens (human) | 25778 | DSTYK |
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DOID:0110411 | retinitis pigmentosa 60 | HGNC:15860 | Homo sapiens (human) | 24148 | PRPF6 |
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DOID:0111436 | optic atrophy 11 | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
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DOID:1612 | breast cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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DOID:0080530 | granular corneal dystrophy 1 | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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DOID:11713 | diabetic angiopathy | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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DOID:0112163 | spermatogenic failure 45 | HGNC:2948 | Homo sapiens (human) | 146754 | DNAH2 |
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DOID:0110361 | retinitis pigmentosa 75 | HGNC:26147 | Homo sapiens (human) | 60509 | AGBL5 |
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DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:4217 | Homo sapiens (human) | 2658 | GDF2 |
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DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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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