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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol ▲	Evidence	References
DOID:684	hepatocellular carcinoma	HGNC:20456	Homo sapiens (human)	84231	TRAF7	mutant phenotype evidence used in manual assertion	PMID:31730901
DOID:1788	peritoneal mesothelioma	HGNC:20456	Homo sapiens (human)	84231	TRAF7	inference by association of genotype from phenotype used in manual assertion	PMID:30171198
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:0112204	developmental and epileptic encephalopathy 68	HGNC:29947	Homo sapiens (human)	22906	TRAK1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070296	primary autosomal recessive microcephaly	HGNC:25604	Homo sapiens (human)	55262	TRAPPC14	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060674	catecholaminergic polymorphic ventricular tachycardia	HGNC:12261	Homo sapiens (human)	10345	TRDN	inference by association of genotype from phenotype used in manual assertion	PMID:22422768
DOID:0060679	catecholaminergic polymorphic ventricular tachycardia 5	HGNC:12261	Homo sapiens (human)	10345	TRDN	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:12365	malaria	HGNC:17760	Homo sapiens (human)	54210	TREM1	inference by association of genotype from phenotype used in manual assertion	PMID:27671831
DOID:0040085	bacterial sepsis	HGNC:17760	Homo sapiens (human)	54210	TREM1	direct assay evidence used in manual assertion	PMID:21507332
DOID:0110049	Alzheimer's disease 17	HGNC:17761	Homo sapiens (human)	54209	TREM2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111836	congenital nongoitrous hypothyroidism 7	HGNC:12299	Homo sapiens (human)	7201	TRHR	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10763	hypertension	HGNC:12299	Homo sapiens (human)	7201	TRHR	inference by association of genotype from phenotype used in manual assertion	PMID:11566956
DOID:0050436	mulibrey nanism	HGNC:7523	Homo sapiens (human)	4591	TRIM37	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060307	autosomal dominant intellectual developmental disorder	HGNC:12303	Homo sapiens (human)	7204	TRIO	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070074	autosomal dominant intellectual developmental disorder 44	HGNC:12303	Homo sapiens (human)	7204	TRIO	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0110486	autosomal recessive nonsyndromic deafness 28	HGNC:17009	Homo sapiens (human)	11078	TRIOBP	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:0080234	Clark-Baraitser syndrome	HGNC:12306	Homo sapiens (human)	9320	TRIP12	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080689	mosaic variegated aneuploidy syndrome 3	HGNC:12307	Homo sapiens (human)	9319	TRIP13	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111464	combined oxidative phosphorylation deficiency 35	HGNC:20286	Homo sapiens (human)	54802	TRIT1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050776	non-syndromic X-linked intellectual disability	SGD:S000004872	Saccharomyces cerevisiae S288C	855301	TRM732	genetic interaction evidence used in manual assertion	PMID:25404562
DOID:0050776	non-syndromic X-linked intellectual disability	SGD:S000004872	Saccharomyces cerevisiae S288C	855301	TRM732	sequence similarity evidence used in manual assertion	PMID:25404562
DOID:0111471	combined oxidative phosphorylation deficiency 30	HGNC:26022	Homo sapiens (human)	54931	TRMT10C	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080209	sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay	HGNC:17341	Homo sapiens (human)	51095	TRNT1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111729	familial episodic pain syndrome 1	HGNC:497	Homo sapiens (human)	8989	TRPA1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710

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