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 | July 29, 2024 |
Disease ID ▲ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
---|---|---|---|---|---|---|---|---|
DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
|
||
DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
|
||
DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000212 | Caenorhabditis elegans | 181323 | asm-2 |
|
||
DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
|
||
DOID:0070112 | Niemann-Pick disease type B | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
|
||
DOID:0070113 | Niemann-Pick disease type C1 | MGI:1097712 | Mus musculus (house mouse) | 18145 | Npc1 |
|
||
DOID:0070113 | Niemann-Pick disease type C1 | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
|
||
DOID:0070129 | autosomal recessive cutis laxa type IID | Xenbase:XB-GENE-990439 | Xenopus tropicalis (tropical clawed frog) | 407846 | st6gal2 |
|
||
DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
|
||
DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
|
||
DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
|
||
DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
|
||
DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
|
||
DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:16253 | Homo sapiens (human) | 55304 | SPTLC3 |
|
||
DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
|
||
DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
|
||
DOID:0070199 | Miyoshi muscular dystrophy 1 | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
|
||
DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | RGD:2670 | Rattus norvegicus (Norway rat) | 24385 | Gck |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | FB:FBgn0042711 | Drosophila melanogaster (fruit fly) | 117364 | Hex-t1 |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
|
||
DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
|
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 v4.0.0
Last updated: August 19, 2024