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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 69826 - 69850 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0111870 nonphotosensitive trichothiodystrophy 7 HGNC:11572 Homo sapiens (human) 6897 TARS1
  • RGD:7240710
DOID:0080379 nephrotic syndrome type 2 HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • RGD:7240710
DOID:0112274 X-linked spermatogenic failure 3 HGNC:26708 Homo sapiens (human) 286464 CFAP47
  • RGD:7240710
DOID:3827 congenital diaphragmatic hernia HGNC:15472 Homo sapiens (human) 8854 ALDH1A2
  • RGD:7240710
DOID:0050449 pachyonychia congenita HGNC:6427 Homo sapiens (human) 3872 KRT17
  • RGD:7240710
DOID:0081371 lacrimoauriculodentodigital syndrome 2 HGNC:3690 Homo sapiens (human) 2261 FGFR3
  • RGD:7240710
DOID:0060259 renal-hepatic-pancreatic dysplasia HGNC:7907 Homo sapiens (human) 27031 NPHP3
  • RGD:7240710
DOID:0112210 developmental and epileptic encephalopathy 74 HGNC:4087 Homo sapiens (human) 2566 GABRG2
  • RGD:7240710
DOID:0080493 ovarian dysgenesis 1 HGNC:3969 Homo sapiens (human) 2492 FSHR
  • RGD:7240710
DOID:0080581 hyperekplexia 4 HGNC:25903 Homo sapiens (human) 84896 ATAD1
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:15632 Homo sapiens (human) 51311 TLR8
  • RGD:7240710
DOID:0080107 microcephaly and chorioretinopathy 3 HGNC:16691 Homo sapiens (human) 27229 TUBGCP4
  • RGD:7240710
DOID:0111332 Pitt-Hopkins-like syndrome 2 HGNC:8008 Homo sapiens (human) 9378 NRXN1
  • RGD:7240710
DOID:0112147 retinitis pigmentosa 90 HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • RGD:7240710
DOID:0090011 immunodeficiency-centromeric instability-facial anomalies syndrome 4 HGNC:4861 Homo sapiens (human) 3070 HELLS
  • RGD:7240710
DOID:0070292 primary autosomal recessive microcephaly 9 HGNC:29298 Homo sapiens (human) 22995 CEP152
  • RGD:7240710
DOID:0081360 spastic quadriplegic cerebral palsy 2 HGNC:19309 Homo sapiens (human) 23189 KANK1
  • RGD:7240710
DOID:0081372 lacrimoauriculodentodigital syndrome 3 HGNC:3666 Homo sapiens (human) 2255 FGF10
  • RGD:7240710
DOID:0111607 distal arthrogryposis type 3 HGNC:26270 Homo sapiens (human) 63895 PIEZO2
  • RGD:7240710
DOID:0110202 Charcot-Marie-Tooth disease dominant intermediate A HGNC:4181 Homo sapiens (human) 8729 GBF1
  • RGD:7240710
DOID:1700 X-linked ichthyosis HGNC:11425 Homo sapiens (human) 412 STS
  • RGD:7240710
DOID:0070249 autosomal dominant Emery-Dreifuss muscular dystrophy 4 HGNC:17089 Homo sapiens (human) 23345 SYNE1
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:0081017 congenital fibrosis of the extraocular muscles 3A HGNC:20772 Homo sapiens (human) 10381 TUBB3
  • RGD:7240710
DOID:0110082 arrhythmogenic right ventricular dysplasia 11 HGNC:3036 Homo sapiens (human) 1824 DSC2
  • RGD:7240710

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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: December 9, 2024