Table Filtering
Other Information
Release Statistics Download
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 October 9, 2024
Displaying entries 71901 - 71925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10
  • RGD:7240710
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:29284 Homo sapiens (human) 57609 DIP2B
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:23657 Homo sapiens (human) 10020 GNE
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • RGD:7240710
DOID:0080444 developmental and epileptic encephalopathy 27 HGNC:4586 Homo sapiens (human) 2904 GRIN2B
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:4076 Homo sapiens (human) 2555 GABRA2
  • RGD:7240710
DOID:0080459 developmental and epileptic encephalopathy 12 HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • RGD:7240710
DOID:0112343 hereditary spastic paraplegia 82 HGNC:8756 Homo sapiens (human) 5833 PCYT2
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0111485 combined oxidative phosphorylation deficiency 24 HGNC:26274 Homo sapiens (human) 79731 NARS2
  • RGD:7240710
DOID:0060882 renal hypomagnesemia 4 HGNC:3229 Homo sapiens (human) 1950 EGF
  • RGD:7240710
DOID:0081110 keratosis palmoplantaris striata 3 HGNC:6412 Homo sapiens (human) 3848 KRT1
  • RGD:7240710
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0090045 childhood onset GLUT1 deficiency syndrome 2 HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:5173 Homo sapiens (human) 3265 HRAS
  • RGD:7240710
DOID:0111707 Bothnian type palmoplantar keratoderma HGNC:638 Homo sapiens (human) 362 AQP5
  • RGD:7240710
DOID:0111222 centronuclear myopathy 5 HGNC:16901 Homo sapiens (human) 10290 SPEG
  • RGD:7240710
DOID:0111234 congenital muscular dystrophy-dystroglycanopathy A7 HGNC:37276 Homo sapiens (human) 729920 CRPPA
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:7865 Homo sapiens (human) 4838 NODAL
  • RGD:7240710
DOID:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:0111776 46,XY sex reversal 5 HGNC:1552 Homo sapiens (human) 84733 CBX2
  • RGD:7240710
DOID:0110801 hereditary spastic paraplegia 49 HGNC:19957 Homo sapiens (human) 9895 TECPR2
  • RGD:7240710
DOID:0111354 arthrogryposis, renal dysfunction, and cholestasis 2 HGNC:20347 Homo sapiens (human) 63894 VIPAS39
  • RGD:7240710
DOID:0111450 progressive myoclonus epilepsy 9 HGNC:6638 Homo sapiens (human) 84823 LMNB2
  • RGD:7240710
DOID:0070073 autosomal dominant intellectual developmental disorder 43 HGNC:4921 Homo sapiens (human) 3097 HIVEP2
  • RGD:7240710

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024