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:3021 | acute kidney failure | HGNC:6526 | Homo sapiens (human) | 3934 | LCN2 |
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DOID:11832 | visual epilepsy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:11832 | visual epilepsy | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:3021 | acute kidney failure | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:2055 | post-traumatic stress disorder | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:13271 | cutaneous porphyria | HGNC:12592 | Homo sapiens (human) | 7390 | UROS |
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DOID:12143 | neurogenic bladder | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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DOID:0080181 | PHARC syndrome | MGI:1923442 | Mus musculus (house mouse) | 76192 | Abhd12 |
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DOID:5419 | schizophrenia | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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DOID:0050778 | Meckel syndrome | MGI:1923928 | Mus musculus (house mouse) | 329795 | Tmem67 |
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DOID:0111001 | Joubert syndrome 6 | MGI:1923928 | Mus musculus (house mouse) | 329795 | Tmem67 |
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DOID:10140 | dry eye syndrome | MGI:104697 | Mus musculus (house mouse) | 17833 | Muc5ac |
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DOID:2355 | anemia | RGD:3845 | Rattus norvegicus (Norway rat) | 24825 | Tf |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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DOID:0050730 | coenzyme Q10 deficiency disease | MGI:1915164 | Mus musculus (house mouse) | 67914 | Coq9 |
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DOID:10591 | pre-eclampsia | HGNC:11935 | Homo sapiens (human) | 959 | CD40LG |
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DOID:9975 | cocaine dependence | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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DOID:9119 | acute myeloid leukemia | MGI:106184 | Mus musculus (house mouse) | 18148 | Npm1 |
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DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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DOID:3827 | congenital diaphragmatic hernia | MGI:2670972 | Mus musculus (house mouse) | 329872 | Frem1 |
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DOID:0060776 | congenital diarrhea 5 with tufting enteropathy | MGI:106653 | Mus musculus (house mouse) | 17075 | Epcam |
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DOID:9352 | type 2 diabetes mellitus | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:3021 | acute kidney failure | HGNC:7940 | Homo sapiens (human) | 4879 | NPPB |
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DOID:14452 | hypokalemic periodic paralysis | MGI:88294 | Mus musculus (house mouse) | 12292 | Cacna1s |
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DOID:10591 | pre-eclampsia | HGNC:2634 | Homo sapiens (human) | 1573 | CYP2J2 |
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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