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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

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Disease ID	Disease Name ▼	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References
DOID:10652	Alzheimer's disease	HGNC:6619	Homo sapiens (human)	3990	LIPC	inference by association of genotype from phenotype used in manual assertion	PMID:17175070
DOID:10652	Alzheimer's disease	FB:FBgn0030522	Drosophila melanogaster (fruit fly)	32342	amrt	combinatorial experimental and author inference evidence used in manual assertion	PMID:34905536
DOID:0050473	Alstrom syndrome	MGI:1934606	Mus musculus (house mouse)	236266	Alms1	author statement supported by traceable reference	MGI:6197902 MGI:6197907 PMID:16000322 PMID:16516152 PMID:17206865 PMID:28859131
DOID:0050473	Alstrom syndrome	HGNC:428	Homo sapiens (human)	7840	ALMS1	inference by association of genotype from phenotype used in manual assertion	PMID:11941369 PMID:16720663 PMID:22876109 RGD:7240710
DOID:10983	Alport syndrome	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:15182324
DOID:10983	Alport syndrome	HGNC:2204	Homo sapiens (human)	1285	COL4A3	inference by association of genotype from phenotype used in manual assertion	PMID:7987301
DOID:10983	Alport syndrome	HGNC:2207	Homo sapiens (human)	1287	COL4A5	inference by association of genotype from phenotype used in manual assertion	PMID:2349482
DOID:0111555	Alkuraya-Kucinskas syndrome	HGNC:26953	Homo sapiens (human)	84162	BLTP1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:4252	Alexander disease	HGNC:4235	Homo sapiens (human)	2670	GFAP	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:4252	Alexander disease	MGI:95697	Mus musculus (house mouse)	14580	Gfap	author statement supported by traceable reference	PMID:17065456
DOID:0050630	Aland Island eye disease	HGNC:1393	Homo sapiens (human)	778	CACNA1F	inference by association of genotype from phenotype used in manual assertion	PMID:17525176 RGD:7240710
DOID:9245	Alagille syndrome	HGNC:7882	Homo sapiens (human)	4853	NOTCH2	inference by association of genotype from phenotype used in manual assertion	PMID:16773578 RGD:7240710
DOID:9245	Alagille syndrome	HGNC:6188	Homo sapiens (human)	182	JAG1	inference by association of genotype from phenotype used in manual assertion	PMID:21714972 RGD:7240710
DOID:9245	Alagille syndrome	MGI:1095416	Mus musculus (house mouse)	16449	Jag1	author statement supported by traceable reference	PMID:11259677 PMID:21062863 PMID:22156581 PMID:23095891 PMID:29162437
DOID:0050629	Aicardi-Goutieres syndrome	MGI:1889575	Mus musculus (house mouse)	56417	Adar	author statement supported by traceable reference	PMID:34332594 PMID:34343497
DOID:0050629	Aicardi-Goutieres syndrome	HGNC:225	Homo sapiens (human)	103	ADAR	inference by association of genotype from phenotype used in manual assertion	PMID:23001123 RGD:7240710
DOID:0050629	Aicardi-Goutieres syndrome	HGNC:15925	Homo sapiens (human)	25939	SAMHD1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:13774	Addison's disease	HGNC:29013	Homo sapiens (human)	23274	CLEC16A	inference by association of genotype from phenotype used in manual assertion	PMID:18593762
DOID:13774	Addison's disease	HGNC:7067	Homo sapiens (human)	4261	CIITA	inference by association of genotype from phenotype used in manual assertion	PMID:18593762
DOID:13774	Addison's disease	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:12072047 PMID:20455895
DOID:13774	Addison's disease	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:19858318 PMID:21816777
DOID:0060227	Adams-Oliver syndrome	HGNC:29216	Homo sapiens (human)	57514	ARHGAP31	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060227	Adams-Oliver syndrome	HGNC:2910	Homo sapiens (human)	54567	DLL4	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060227	Adams-Oliver syndrome	HGNC:5724	Homo sapiens (human)	3516	RBPJ	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060227	Adams-Oliver syndrome	HGNC:19189	Homo sapiens (human)	57572	DOCK6	inference by association of genotype from phenotype used in manual assertion	PMID:25824905 RGD:7240710

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