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Alliance of Genome Resources

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
Displaying entries 1276 - 1300 of 12216 in total
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
  • RGD:7240710
DOID:0070112 Niemann-Pick disease type B WB:WBGene00000211 Caenorhabditis elegans 174131 asm-1
  • MGI:6194238
DOID:0070112 Niemann-Pick disease type B WB:WBGene00000212 Caenorhabditis elegans 181323 asm-2
  • MGI:6194238
DOID:0070112 Niemann-Pick disease type B WB:WBGene00000213 Caenorhabditis elegans 176879 asm-3
  • MGI:6194238
DOID:0070112 Niemann-Pick disease type B MGI:98325 Mus musculus (house mouse) 20597 Smpd1
  • MGI:6194238
DOID:0070113 Niemann-Pick disease type C1 MGI:1097712 Mus musculus (house mouse) 18145 Npc1
  • MGI:6194238
  • PMID:28167839
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
  • RGD:7240710
DOID:0070129 autosomal recessive cutis laxa type IID Xenbase:XB-GENE-990439 Xenopus tropicalis (tropical clawed frog) 407846 st6gal2
  • MGI:6194238
DOID:0070129 autosomal recessive cutis laxa type IID HGNC:851 Homo sapiens (human) 523 ATP6V1A
  • RGD:7240710
DOID:0070134 autosomal recessive cutis laxa type IIA HGNC:18481 Homo sapiens (human) 23545 ATP6V0A2
  • RGD:7240710
DOID:0070152 hereditary sensory and autonomic neuropathy type 1A HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
  • RGD:7240710
DOID:0070157 hereditary sensory and autonomic neuropathy type 1C HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • RGD:7240710
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • MGI:6194238
DOID:0070174 spermatogenic failure 17 HGNC:19218 Homo sapiens (human) 89869 PLCZ1
  • RGD:7240710
DOID:0070199 Miyoshi muscular dystrophy 1 MGI:1349385 Mus musculus (house mouse) 26903 Dysf
  • MGI:6194238
DOID:0070215 familial hyperinsulinemic hypoglycemia 4 HGNC:4799 Homo sapiens (human) 3033 HADH
  • RGD:7240710
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck
  • MGI:6194238
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 FB:FBgn0042711 Drosophila melanogaster (fruit fly) 117364 Hex-t1
  • MGI:6194238
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 SGD:S000000545 Saccharomyces cerevisiae S288C 850317 GLK1
  • MGI:6194238
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:33558985
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024