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:0111693 | familial adult myoclonic epilepsy 4 | HGNC:25489 | Homo sapiens (human) | 55689 | YEATS2 |
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DOID:11446 | sciatic neuropathy | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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DOID:0080109 | infantile myofibromatosis | HGNC:8804 | Homo sapiens (human) | 5159 | PDGFRB |
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DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | HGNC:13449 | Homo sapiens (human) | 84631 | SLITRK2 |
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DOID:0112341 | hereditary spastic paraplegia 80 | HGNC:12461 | Homo sapiens (human) | 51271 | UBAP1 |
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DOID:0110490 | autosomal recessive nonsyndromic deafness 31 | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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DOID:0110703 | hypotrichosis 6 | HGNC:21307 | Homo sapiens (human) | 147409 | DSG4 |
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DOID:0080240 | non-syndromic X-linked intellectual disability 106 | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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DOID:0111072 | myostatin-related muscle hypertrophy | HGNC:4223 | Homo sapiens (human) | 2660 | MSTN |
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DOID:0090030 | corticosteroid-binding globulin deficiency | HGNC:1540 | Homo sapiens (human) | 866 | SERPINA6 |
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DOID:9976 | heroin dependence | HGNC:8154 | Homo sapiens (human) | 4986 | OPRK1 |
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DOID:2843 | long QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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DOID:10763 | hypertension | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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DOID:14219 | renal tubular acidosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:30829 | Homo sapiens (human) | 347733 | TUBB2B |
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DOID:6000 | congestive heart failure | HGNC:285 | Homo sapiens (human) | 153 | ADRB1 |
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DOID:0080991 | congenital myopathy 1B | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
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DOID:0060812 | syndromic X-linked intellectual disability Siderius type | HGNC:20672 | Homo sapiens (human) | 23133 | PHF8 |
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DOID:1742 | drug psychosis | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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DOID:0110766 | hereditary spastic paraplegia 13 | HGNC:5261 | Homo sapiens (human) | 3329 | HSPD1 |
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DOID:988 | mitral valve prolapse | HGNC:20908 | Homo sapiens (human) | 22873 | DZIP1 |
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DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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DOID:0111628 | high myopia-sensorineural deafness syndrome | HGNC:23503 | Homo sapiens (human) | 84189 | SLITRK6 |
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DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:166 | Homo sapiens (human) | 81 | ACTN4 |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024