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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 October 9, 2024
Displaying entries 70901 - 70925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0070529 Sifrim-Hitz-Weiss syndrome HGNC:1919 Homo sapiens (human) 1108 CHD4
  • RGD:7240710
DOID:0070210 hereditary lymphedema IA HGNC:3767 Homo sapiens (human) 2324 FLT4
  • RGD:7240710
DOID:0080289 orofaciodigital syndrome XVII HGNC:29239 Homo sapiens (human) 27152 INTU
  • RGD:7240710
DOID:0060706 X-linked lymphoproliferative syndrome 2 HGNC:592 Homo sapiens (human) 331 XIAP
  • RGD:7240710
DOID:0111584 dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome HGNC:6636 Homo sapiens (human) 4000 LMNA
  • RGD:7240710
DOID:0111162 epidermal nevus HGNC:5173 Homo sapiens (human) 3265 HRAS
  • RGD:7240710
DOID:0060892 late onset Parkinson's disease HGNC:10555 Homo sapiens (human) 6311 ATXN2
  • RGD:7240710
DOID:6846 familial melanoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • RGD:7240710
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:0111019 cone-rod dystrophy 12 HGNC:9454 Homo sapiens (human) 8842 PROM1
  • RGD:7240710
DOID:0081147 common variable immunodeficiency 4 HGNC:17755 Homo sapiens (human) 115650 TNFRSF13C
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:17967 Homo sapiens (human) 51135 IRAK4
  • RGD:7240710
DOID:0080379 nephrotic syndrome type 2 HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • RGD:7240710
DOID:0112181 Schinzel type phocomelia HGNC:12786 Homo sapiens (human) 7476 WNT7A
  • RGD:7240710
DOID:0070389 developmental and epileptic encephalopathy 103 HGNC:6234 Homo sapiens (human) 3747 KCNC2
  • RGD:7240710
DOID:0081203 autosomal recessive intellectual developmental disorder 38 HGNC:4868 Homo sapiens (human) 8924 HERC2
  • RGD:7240710
DOID:0110521 autosomal recessive nonsyndromic deafness 70 HGNC:23166 Homo sapiens (human) 87178 PNPT1
  • RGD:7240710
DOID:5419 schizophrenia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • RGD:7240710
DOID:0081150 common variable immunodeficiency 7 HGNC:2336 Homo sapiens (human) 1380 CR2
  • RGD:7240710
DOID:0050974 spinocerebellar ataxia type 25 HGNC:23166 Homo sapiens (human) 87178 PNPT1
  • RGD:7240710
DOID:0060765 autosomal dominant Robinow syndrome 2 HGNC:3084 Homo sapiens (human) 1855 DVL1
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:7865 Homo sapiens (human) 4838 NODAL
  • RGD:7240710
DOID:0111608 distal arthrogryposis type 5 HGNC:26270 Homo sapiens (human) 63895 PIEZO2
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0112213 multiple congenital anomalies-hypotonia-seizures syndrome 4 HGNC:14135 Homo sapiens (human) 9091 PIGQ
  • RGD:7240710

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

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Supported by JST NBDC Grant Number JPMJND2204

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


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