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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 1126 - 1150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0050753 cerebellar ataxia HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24573090
DOID:2476 hereditary spastic paraplegia HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24573090
DOID:10283 prostate cancer HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:24571686
DOID:3068 glioblastoma HGNC:8977 Homo sapiens (human) 5293 PIK3CD
  • PMID:24523440
DOID:0050861 colorectal adenocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:24500602
DOID:0110861 autosomal recessive polycystic kidney disease RGD:620916 Rattus norvegicus (Norway rat) 170911 Pik3ca
  • PMID:24498161
DOID:0110861 autosomal recessive polycystic kidney disease RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:24498161
DOID:10762 portal hypertension RGD:628827 Rattus norvegicus (Norway rat) 252917 Nr1d1
  • PMID:24497272
DOID:14018 alcoholic liver cirrhosis HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • PMID:24497272
DOID:2224 essential thrombocythemia HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24496303
  • PMID:25860380
  • RGD:7240710
DOID:9281 phenylketonuria RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • PMID:24488205
DOID:594 panic disorder HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:24473444
DOID:2030 anxiety disorder HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:24473444
DOID:1875 impotence RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:24467772
DOID:2383 neonatal jaundice HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24460025
DOID:9974 drug dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:24455721
DOID:104 bacterial infectious disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24453114
DOID:9352 type 2 diabetes mellitus HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:24452036
DOID:0050700 cardiomyopathy RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:24441175
DOID:2224 essential thrombocythemia HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:24434346
DOID:12399 pathological gambling HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:24390676
DOID:10808 gastric ulcer RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad
  • PMID:24378970
DOID:11716 prediabetes syndrome RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • PMID:24361842
DOID:3827 congenital diaphragmatic hernia MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • PMID:24355925
DOID:3827 congenital diaphragmatic hernia RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • PMID:24352370

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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