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:4928 | intrahepatic cholangiocarcinoma | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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DOID:0110124 | Bardet-Biedl syndrome 2 | HGNC:967 | Homo sapiens (human) | 583 | BBS2 |
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DOID:0070113 | Niemann-Pick disease type C1 | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
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DOID:0110827 | Usher syndrome type 2 | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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DOID:0050994 | episodic ataxia type 6 | HGNC:10941 | Homo sapiens (human) | 6507 | SLC1A3 |
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DOID:10763 | hypertension | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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DOID:10587 | Krabbe disease | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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DOID:0060903 | thrombosis | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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DOID:3633 | beta-mannosidosis | HGNC:6831 | Homo sapiens (human) | 4126 | MANBA |
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DOID:0060933 | developmental delay, dysmorphic facies, and brain anomalies | HGNC:23156 | Homo sapiens (human) | 11338 | U2AF2 |
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DOID:9279 | hyperhomocysteinemia | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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DOID:0111078 | tibial muscular dystrophy | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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DOID:0050660 | Beare-Stevenson cutis gyrata syndrome | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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DOID:409 | liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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DOID:2736 | Hajdu-Cheney syndrome | HGNC:7882 | Homo sapiens (human) | 4853 | NOTCH2 |
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DOID:0110454 | dilated cardiomyopathy 1S | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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DOID:0060556 | Kufor-Rakeb syndrome | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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DOID:0050887 | Townes-Brocks syndrome | HGNC:10524 | Homo sapiens (human) | 6299 | SALL1 |
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DOID:0110869 | congenital stationary night blindness 1E | HGNC:31371 | Homo sapiens (human) | 440435 | GPR179 |
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DOID:10763 | hypertension | HGNC:3146 | Homo sapiens (human) | 1889 | ECE1 |
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DOID:0111385 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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DOID:0060878 | hypoparathyroidism-deafness-renal disease syndrome | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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DOID:0080887 | vitamin D-dependent rickets type 1B | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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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