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Repository for lectin-assisted multimodality data
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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 326 - 350 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:0080322 polycystic kidney disease ZFIN:ZDB-GENE-040827-4 Danio rerio (zebrafish) 432387 pkd2 author statement supported by traceable reference used in manual assertion
  • PMID:19966229
  • PMID:32159259
DOID:0060340 ciliopathy ZFIN:ZDB-GENE-040827-4 Danio rerio (zebrafish) 432387 pkd2 author statement supported by traceable reference used in manual assertion
  • PMID:30582331
DOID:898 autosomal dominant polycystic kidney disease ZFIN:ZDB-GENE-040827-4 Danio rerio (zebrafish) 432387 pkd2 author statement supported by traceable reference used in manual assertion
  • PMID:24627348
  • PMID:26432887
  • PMID:28769124
  • PMID:31183407
  • PMID:31330507
  • PMID:31919453
  • PMID:34551202
DOID:6419 tetralogy of Fallot ZFIN:ZDB-GENE-040624-11 Danio rerio (zebrafish) 415107 popdc1 author statement supported by traceable reference used in manual assertion
  • PMID:32843646
DOID:0112184 thyroid dyshormonogenesis 5 HGNC:32698 Homo sapiens (human) 405753 DUOXA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:83 cataract ZFIN:ZDB-GENE-040312-2 Danio rerio (zebrafish) 404210 crim1 author statement supported by traceable reference used in manual assertion
  • PMID:30979021
DOID:10629 microphthalmia ZFIN:ZDB-GENE-040312-2 Danio rerio (zebrafish) 404210 crim1 author statement supported by traceable reference used in manual assertion
  • PMID:30979021
DOID:5419 schizophrenia ZFIN:ZDB-GENE-030616-135 Danio rerio (zebrafish) 403310 cacna1da curator inference used in manual assertion
  • PMID:33057948
DOID:9975 cocaine dependence HGNC:29349 Homo sapiens (human) 401145 CCSER1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:0111911 spermatogenic failure 34 HGNC:21675 Homo sapiens (human) 401024 FSIP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10003 sensorineural hearing loss ZFIN:ZDB-GENE-040426-1371 Danio rerio (zebrafish) 393385 slc44a4 author statement supported by traceable reference used in manual assertion
  • PMID:28013291
DOID:0110217 Leber congenital amaurosis 17 HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060836 isolated microphthalmia 4 HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080589 Klippel-Feil syndrome 1 HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081320 multiple synostoses syndrome 4 HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:674 cleft palate HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18716610
DOID:9296 cleft lip HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18716610
DOID:0090081 hypogonadotropic hypogonadism 22 with or without anosmia HGNC:22788 Homo sapiens (human) 389549 FEZF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070525 peeling skin syndrome 6 HGNC:33276 Homo sapiens (human) 388698 FLG2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081212 autosomal recessive intellectual developmental disorder 48 HGNC:31399 Homo sapiens (human) 388662 SLC6A17 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060546 Hermansky-Pudlak syndrome 8 HGNC:20914 Homo sapiens (human) 388552 BLOC1S3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110574 autosomal dominant nonsyndromic deafness 4B HGNC:31948 Homo sapiens (human) 388551 CEACAM16 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111636 autosomal recessive nonsyndromic deafness 113 HGNC:31948 Homo sapiens (human) 388551 CEACAM16 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8986 narcolepsy MGI:2680765 Mus musculus (house mouse) 387285 Hcrtr2 author statement supported by traceable reference
  • PMID:12797957
  • PMID:21368172
DOID:12716 newborn respiratory distress syndrome HGNC:23631 Homo sapiens (human) 387129 NPSR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16938805
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