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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 13751 - 13775 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0080218 primary spontaneous pneumothorax HGNC:27310 Homo sapiens (human) 201163 FLCN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070164 spermatogenic failure 2 HGNC:7327 Homo sapiens (human) 4438 MSH4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050998 nonprogressive cerebellar ataxia with mental retardation HGNC:18806 Homo sapiens (human) 23261 CAMTA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060790 hypomyelinating leukodystrophy 3 HGNC:10648 Homo sapiens (human) 9255 AIMP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080382 nephrotic syndrome type 3 HGNC:17175 Homo sapiens (human) 51196 PLCE1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080944 familial Behcet-like autoinflammatory syndrome HGNC:11896 Homo sapiens (human) 7128 TNFAIP3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080422 Dravet syndrome HGNC:10585 Homo sapiens (human) 6323 SCN1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6039 uveal melanoma HGNC:950 Homo sapiens (human) 8314 BAP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111958 immunodeficiency 11B HGNC:16393 Homo sapiens (human) 84433 CARD11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050778 Meckel syndrome HGNC:20652 Homo sapiens (human) 79770 TXNDC15 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080254 orofaciodigital syndrome XVI HGNC:28128 Homo sapiens (human) 84314 TMEM107 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112373 autosomal dominant auditory neuropathy 3 HGNC:28472 Homo sapiens (human) 79188 TMEM43 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112277 immunodeficiency 79 HGNC:1678 Homo sapiens (human) 920 CD4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080776 partial androgen insensitivity syndrome HGNC:644 Homo sapiens (human) 367 AR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060826 syndromic X-linked intellectual disability Shashi type HGNC:9910 Homo sapiens (human) 27316 RBMX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090124 neurogenic-type arthrogryposis multiplex congenita-2 HGNC:29205 Homo sapiens (human) 57222 ERGIC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070062 Arboleda-Tham syndrome HGNC:13013 Homo sapiens (human) 7994 KAT6A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0061001 glycine encephalopathy 2 HGNC:473 Homo sapiens (human) 275 AMT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111506 palmoplantar keratoderma-esophageal carcinoma syndrome HGNC:20788 Homo sapiens (human) 79651 RHBDF2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070068 autosomal dominant intellectual developmental disorder 38 HGNC:3192 Homo sapiens (human) 1917 EEF1A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080054 achondrogenesis type IA HGNC:12305 Homo sapiens (human) 9321 TRIP11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112162 autosomal recessive nonsyndromic deafness 116 HGNC:2051 Homo sapiens (human) 9080 CLDN9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070005 Seckel syndrome 9 HGNC:30764 Homo sapiens (human) 10293 TRAIP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060895 Parkinson's disease 4 HGNC:11138 Homo sapiens (human) 6622 SNCA inference by association of genotype from phenotype used in manual assertion
  • 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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Last updated: December 8, 2025