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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 70126 - 70150 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0110818 hereditary spastic paraplegia 73 HGNC:18540 Homo sapiens (human) 126129 CPT1C
  • RGD:7240710
DOID:0080337 mitochondrial DNA depletion syndrome 15 HGNC:11741 Homo sapiens (human) 7019 TFAM
  • RGD:7240710
DOID:13909 red-green color blindness HGNC:4206 Homo sapiens (human) 2652 OPN1MW
  • RGD:7240710
DOID:0111333 early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome HGNC:29634 Homo sapiens (human) 84466 MEGF10
  • RGD:7240710
DOID:0060720 autosomal recessive congenital ichthyosis 11 HGNC:11344 Homo sapiens (human) 6768 ST14
  • RGD:7240710
DOID:0080224 autosomal dominant dystrophic epidermolysis bullosa HGNC:2214 Homo sapiens (human) 1294 COL7A1
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:3690 Homo sapiens (human) 2261 FGFR3
  • RGD:7240710
DOID:0060777 congenital secretory sodium diarrhea 8 HGNC:11073 Homo sapiens (human) 6550 SLC9A3
  • RGD:7240710
DOID:0110347 osteogenesis imperfecta type 15 HGNC:12774 Homo sapiens (human) 7471 WNT1
  • RGD:7240710
DOID:4465 papillary renal cell carcinoma HGNC:7029 Homo sapiens (human) 4233 MET
  • RGD:7240710
DOID:0080620 familial glucocorticoid deficiency HGNC:7863 Homo sapiens (human) 23530 NNT
  • RGD:7240710
DOID:0050676 Birt-Hogg-Dube syndrome HGNC:13995 Homo sapiens (human) 56980 PRDM10
  • RGD:7240710
DOID:676 juvenile rheumatoid arthritis HGNC:26789 Homo sapiens (human) 144811 LACC1
  • RGD:7240710
DOID:5426 primary ovarian insufficiency HGNC:28569 Homo sapiens (human) 254528 MEIOB
  • RGD:7240710
DOID:0110774 hereditary spastic paraplegia 23 HGNC:29043 Homo sapiens (human) 25778 DSTYK
  • RGD:7240710
DOID:0110411 retinitis pigmentosa 60 HGNC:15860 Homo sapiens (human) 24148 PRPF6
  • RGD:7240710
DOID:0111436 optic atrophy 11 HGNC:12843 Homo sapiens (human) 10730 YME1L1
  • RGD:7240710
DOID:1612 breast cancer HGNC:1748 Homo sapiens (human) 999 CDH1
  • RGD:7240710
DOID:0080530 granular corneal dystrophy 1 HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:10595 Charcot-Marie-Tooth disease HGNC:6182 Homo sapiens (human) 3710 ITPR3
  • RGD:7240710
DOID:11713 diabetic angiopathy HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • RGD:7240710
DOID:0112163 spermatogenic failure 45 HGNC:2948 Homo sapiens (human) 146754 DNAH2
  • RGD:7240710
DOID:0110361 retinitis pigmentosa 75 HGNC:26147 Homo sapiens (human) 60509 AGBL5
  • RGD:7240710
DOID:1270 hereditary hemorrhagic telangiectasia HGNC:4217 Homo sapiens (human) 2658 GDF2
  • RGD:7240710
DOID:0080037 Worth syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • 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