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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 71876 - 71900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0110401 retinitis pigmentosa 74 HGNC:967 Homo sapiens (human) 583 BBS2
  • RGD:7240710
DOID:0070155 hereditary sensory and autonomic neuropathy type 2A HGNC:14540 Homo sapiens (human) 65125 WNK1
  • RGD:7240710
DOID:0080696 Winchester syndrome HGNC:7160 Homo sapiens (human) 4323 MMP14
  • RGD:7240710
DOID:0111847 osteogenesis imperfecta type 19 HGNC:15455 Homo sapiens (human) 51360 MBTPS2
  • RGD:7240710
DOID:0111769 46,XY sex reversal 6 HGNC:6848 Homo sapiens (human) 4214 MAP3K1
  • RGD:7240710
DOID:0111876 linear skin defects with multiple congenital anomalies 3 HGNC:20372 Homo sapiens (human) 54539 NDUFB11
  • RGD:7240710
DOID:0070177 spermatogenic failure 22 HGNC:28569 Homo sapiens (human) 254528 MEIOB
  • RGD:7240710
DOID:0111970 immunodeficiency 10 HGNC:11386 Homo sapiens (human) 6786 STIM1
  • RGD:7240710
DOID:0070149 hereditary sensory and autonomic neuropathy type 7 HGNC:10583 Homo sapiens (human) 11280 SCN11A
  • RGD:7240710
DOID:0080286 spinocerebellar ataxia 44 HGNC:4593 Homo sapiens (human) 2911 GRM1
  • RGD:7240710
DOID:0112202 developmental and epileptic encephalopathy HGNC:11018 Homo sapiens (human) 140679 SLC32A1
  • RGD:7240710
DOID:0111292 idiopathic generalized epilepsy 10 HGNC:4084 Homo sapiens (human) 2563 GABRD
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:10589 Homo sapiens (human) 6327 SCN2B
  • RGD:7240710
DOID:0111992 immunodeficiency 53 HGNC:9956 Homo sapiens (human) 5971 RELB
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:5438 Homo sapiens (human) 3458 IFNG
  • RGD:7240710
DOID:0111574 autosomal recessive woolly hair 3 HGNC:30839 Homo sapiens (human) 147183 KRT25
  • RGD:7240710
DOID:0060751 familial temporal lobe epilepsy 7 HGNC:9957 Homo sapiens (human) 5649 RELN
  • RGD:7240710
DOID:0111584 dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome HGNC:6636 Homo sapiens (human) 4000 LMNA
  • RGD:7240710
DOID:0080537 hypermanganesemia with dystonia 2 HGNC:20858 Homo sapiens (human) 23516 SLC39A14
  • RGD:7240710
DOID:0090127 camptodactyly-arthropathy-coxa vara-pericarditis syndrome HGNC:9364 Homo sapiens (human) 10216 PRG4
  • RGD:7240710
DOID:0070223 progressive familial intrahepatic cholestasis 3 HGNC:45 Homo sapiens (human) 5244 ABCB4
  • RGD:7240710
DOID:0111835 congenital nongoitrous hypothyroidism 9 HGNC:6128 Homo sapiens (human) 8471 IRS4
  • RGD:7240710
DOID:0112185 thyroid dyshormonogenesis 1 HGNC:11040 Homo sapiens (human) 6528 SLC5A5
  • RGD:7240710
DOID:14080 glucocorticoid-remediable aldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • RGD:7240710
DOID:0070066 autosomal dominant intellectual developmental disorder 36 HGNC:9302 Homo sapiens (human) 5518 PPP2R1A
  • 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