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 |
---|---|
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 |
---|---|---|---|---|---|---|---|---|
DOID:0070028 | APP-related cerebral amyloid angiopathy | HGNC:620 | Homo sapiens (human) | 351 | APP |
|
||
DOID:0070028 | APP-related cerebral amyloid angiopathy | MGI:88059 | Mus musculus (house mouse) | 11820 | App |
|
||
DOID:0070028 | APP-related cerebral amyloid angiopathy | WB:WBGene00000149 | Caenorhabditis elegans | 180783 | apl-1 |
|
||
DOID:0070028 | APP-related cerebral amyloid angiopathy | RGD:2139 | Rattus norvegicus (Norway rat) | 54226 | App |
|
||
DOID:0070027 | CST3-related cerebral amyloid angiopathy | WB:WBGene00000535 | Caenorhabditis elegans | 177372 | cpi-1 |
|
||
DOID:0070027 | CST3-related cerebral amyloid angiopathy | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
|
||
DOID:0070027 | CST3-related cerebral amyloid angiopathy | RGD:2432 | Rattus norvegicus (Norway rat) | 25307 | Cst3 |
|
||
DOID:0070025 | X-linked dyskeratosis congenita | RGD:621780 | Rattus norvegicus (Norway rat) | 170944 | Dkc1 |
|
||
DOID:0070025 | X-linked dyskeratosis congenita | MGI:1861727 | Mus musculus (house mouse) | 245474 | Dkc1 |
|
||
DOID:0070025 | X-linked dyskeratosis congenita | HGNC:2890 | Homo sapiens (human) | 1736 | DKC1 |
|
||
DOID:0070024 | autosomal recessive dyskeratosis congenita 6 | HGNC:8609 | Homo sapiens (human) | 5073 | PARN |
|
||
DOID:0070016 | autosomal dominant dyskeratosis congenita 2 | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
|
||
DOID:0070013 | Seckel syndrome 2 | HGNC:9891 | Homo sapiens (human) | 5932 | RBBP8 |
|
||
DOID:0070013 | Seckel syndrome 2 | MGI:2442995 | Mus musculus (house mouse) | 225182 | Rbbp8 |
|
||
DOID:0070012 | Seckel syndrome 5 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
|
||
DOID:0070011 | Seckel syndrome 7 | HGNC:14906 | Homo sapiens (human) | 51199 | NIN |
|
||
DOID:0070010 | Seckel syndrome 4 | FB:FBgn0011020 | Drosophila melanogaster (fruit fly) | 40859 | Sas-4 |
|
||
DOID:0070007 | Seckel syndrome 1 | HGNC:882 | Homo sapiens (human) | 545 | ATR |
|
||
DOID:0070005 | Seckel syndrome 9 | HGNC:30764 | Homo sapiens (human) | 10293 | TRAIP |
|
||
DOID:0070004 | myeloid neoplasm | Xenbase:XB-GENE-1018562 | Xenopus laevis (African clawed frog) | 399444 | fgfr1.L |
|
||
DOID:0070004 | myeloid neoplasm | FB:FBgn0010389 | Drosophila melanogaster (fruit fly) | 42160 | htl |
|
||
DOID:0070004 | myeloid neoplasm | MGI:107899 | Mus musculus (house mouse) | 12491 | Cd36 |
|
||
DOID:0070004 | myeloid neoplasm | WB:WBGene00007517 | Caenorhabditis elegans | 182513 | gpx-3 |
|
||
DOID:0070004 | myeloid neoplasm | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
|
||
DOID:0070004 | myeloid neoplasm | FB:FBgn0035815 | Drosophila melanogaster (fruit fly) | 38868 | Snmp2 |
|
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