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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 **10076 - 10100** of **14279** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol ▲	Evidence	References
DOID:3565	meningioma	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:12236	primary biliary cholangitis	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0110914	infantile hypophosphatasia	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:3347	osteosarcoma	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:10609	rickets	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0112347	hereditary spastic paraplegia 84	HGNC:8983	Homo sapiens (human)	5297	PI4KA	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070606	autosomal dominant nonsyndromic deafness 87	HGNC:8984	Homo sapiens (human)	5298	PI4KB	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:9119	acute myeloid leukemia	HGNC:15514	Homo sapiens (human)	8301	PICALM	inference by association of genotype from phenotype used in manual assertion	PMID:12461747 RGD:7240710
DOID:0081234	autosomal recessive intellectual developmental disorder 75	HGNC:16491	Homo sapiens (human)	55367	PIDD1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050580	hereditary lymphedema	HGNC:28993	Homo sapiens (human)	9780	PIEZO1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111576	dehydrated hereditary stomatocytosis 1	HGNC:28993	Homo sapiens (human)	9780	PIEZO1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111607	distal arthrogryposis type 3	HGNC:26270	Homo sapiens (human)	63895	PIEZO2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111608	distal arthrogryposis type 5	HGNC:26270	Homo sapiens (human)	63895	PIEZO2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2	FB:FBgn0034270	Drosophila melanogaster (fruit fly)	37020	PIG-A	combinatorial experimental and curator inference evidence used in manual assertion	PMID:38124489
DOID:0060284	paroxysmal nocturnal hemoglobinuria	HGNC:8957	Homo sapiens (human)	5277	PIGA	inference by association of genotype from phenotype used in manual assertion	PMID:12424196 RGD:7240710
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2	HGNC:8957	Homo sapiens (human)	5277	PIGA	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112216	developmental and epileptic encephalopathy 80	HGNC:8959	Homo sapiens (human)	9488	PIGB	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16	HGNC:8960	Homo sapiens (human)	5279	PIGC	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112152	CHIME syndrome	HGNC:8966	Homo sapiens (human)	9487	PIGL	inference by association of genotype from phenotype used in manual assertion	PMID:22444671 RGD:7240710
DOID:0080138	multiple congenital anomalies-hypotonia-seizures syndrome 1	HGNC:8967	Homo sapiens (human)	23556	PIGN	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070434	hyperphosphatasia with impaired intellectual development syndrome 2	HGNC:23215	Homo sapiens (human)	84720	PIGO	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080283	developmental and epileptic encephalopathy 55	HGNC:3046	Homo sapiens (human)	51227	PIGP	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112213	multiple congenital anomalies-hypotonia-seizures syndrome 4	HGNC:14135	Homo sapiens (human)	9091	PIGQ	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070382	developmental and epileptic encephalopathy 95	HGNC:14937	Homo sapiens (human)	94005	PIGS	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060284	paroxysmal nocturnal hemoglobinuria	HGNC:14938	Homo sapiens (human)	51604	PIGT	inference by association of genotype from phenotype used in manual assertion	RGD:7240710

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