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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 January 28, 2025
Displaying entries 13201 - 13225 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0110384 retinitis pigmentosa 25 HGNC:21555 Homo sapiens (human) 346007 EYS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:11849 Homo sapiens (human) 7098 TLR3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110158 Charcot-Marie-Tooth disease type 2I HGNC:7225 Homo sapiens (human) 4359 MPZ inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070489 classic dopamine transporter deficiency syndrome HGNC:11049 Homo sapiens (human) 6531 SLC6A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081153 common variable immunodeficiency 11 HGNC:6005 Homo sapiens (human) 59067 IL21 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080628 alopecia-mental retardation syndrome 1 HGNC:349 Homo sapiens (human) 197 AHSG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080337 mitochondrial DNA depletion syndrome 15 HGNC:11741 Homo sapiens (human) 7019 TFAM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:6055 Homo sapiens (human) 3617 IMPG1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112196 spondylometaepiphyseal dysplasia, short limb-hand type HGNC:2731 Homo sapiens (human) 4921 DDR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050579 glycogen storage disease XV HGNC:4699 Homo sapiens (human) 2992 GYG1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050633 ocular albinism 1 HGNC:20145 Homo sapiens (human) 4935 GPR143 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081179 autosomal recessive intellectual developmental disorder 3 HGNC:30237 Homo sapiens (human) 54862 CC2D1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111936 immunodeficiency 14 HGNC:8977 Homo sapiens (human) 5293 PIK3CD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:13829 Homo sapiens (human) 80326 WNT10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110728 neuronal ceroid lipofuscinosis 5 HGNC:2076 Homo sapiens (human) 1203 CLN5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070277 primary autosomal recessive microcephaly 15 HGNC:25897 Homo sapiens (human) 84879 MFSD2A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110148 Charcot-Marie-Tooth disease type 1A HGNC:9118 Homo sapiens (human) 5376 PMP22 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050628 advanced sleep phase syndrome HGNC:11813 Homo sapiens (human) 8914 TIMELESS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13929 lacrimal duct obstruction HGNC:5950 Homo sapiens (human) 3321 IGSF3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070555 Nagashima-type palmoplantar keratosis HGNC:13902 Homo sapiens (human) 8710 SERPINB7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060010 Omenn syndrome HGNC:17642 Homo sapiens (human) 64421 DCLRE1C inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050887 Townes-Brocks syndrome HGNC:17748 Homo sapiens (human) 51339 DACT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110171 Charcot-Marie-Tooth disease axonal type 2S HGNC:5542 Homo sapiens (human) 3508 IGHMBP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080235 autosomal dominant intellectual developmental disorder 48 HGNC:9801 Homo sapiens (human) 5879 RAC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110713 Oguchi disease-2 HGNC:10013 Homo sapiens (human) 6011 GRK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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Supported by JST NBDC Grant Number JPMJND2204

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