GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Alliance of Genome Resources ID

Species

Gene ID

Gene Symbol

FlyGlycoDB

Evidence

References

Display
results per page.

Clear

Submissions

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 **5526 - 5550** of **14279** in total

« First

‹ Prev

…

218

219

220

221

222

223

224

225

226

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References ▲
DOID:2476	hereditary spastic paraplegia	SGD:S000005691	Saccharomyces cerevisiae S288C	854336	SEY1	mutant phenotype evidence used in manual assertion	PMID:19665976
DOID:10754	otitis media	MGI:2442062	Mus musculus (house mouse)	268396	Sh3pxd2b	author statement supported by traceable reference	PMID:19669234
DOID:10763	hypertension	HGNC:2623	Homo sapiens (human)	1559	CYP2C9	direct assay evidence used in manual assertion	PMID:19669737
DOID:3908	lung non-small cell carcinoma	HGNC:3148	Homo sapiens (human)	1890	TYMP	mutant phenotype evidence used in manual assertion	PMID:19671868
DOID:1793	pancreatic cancer	HGNC:3148	Homo sapiens (human)	1890	TYMP	mutant phenotype evidence used in manual assertion	PMID:19671868
DOID:326	ischemia	RGD:621861	Rattus norvegicus (Norway rat)	89805	Angpt2	direct assay evidence used in manual assertion	PMID:19672036
DOID:5520	head and neck squamous cell carcinoma	HGNC:9646	Homo sapiens (human)	5783	PTPN13	inference by association of genotype from phenotype used in manual assertion	PMID:19672627 PMID:19892796
DOID:9256	colorectal cancer	HGNC:9673	Homo sapiens (human)	5795	PTPRJ	inference by association of genotype from phenotype used in manual assertion	PMID:19672627 RGD:7240710
DOID:3910	lung adenocarcinoma	HGNC:9646	Homo sapiens (human)	5783	PTPN13	inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:3910	lung adenocarcinoma	HGNC:9673	Homo sapiens (human)	5795	PTPRJ	inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:9256	colorectal cancer	HGNC:9646	Homo sapiens (human)	5783	PTPN13	inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:3907	lung squamous cell carcinoma	HGNC:9646	Homo sapiens (human)	5783	PTPN13	inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:3907	lung squamous cell carcinoma	HGNC:9673	Homo sapiens (human)	5795	PTPRJ	inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:8534	gastroesophageal reflux disease	HGNC:9031	Homo sapiens (human)	5320	PLA2G2A	mutant phenotype evidence used in manual assertion	PMID:19672667
DOID:10534	stomach cancer	HGNC:9585	Homo sapiens (human)	5727	PTCH1	direct assay evidence used in manual assertion	PMID:19673023
DOID:4249	Gerstmann-Straussler-Scheinker syndrome	MGI:97769	Mus musculus (house mouse)	19122	Prnp	author statement supported by traceable reference	PMID:19675240 PMID:1980379 PMID:8698234
DOID:1074	kidney failure	HGNC:3020	Homo sapiens (human)	1812	DRD1	inference by association of genotype from phenotype used in manual assertion	PMID:19675531
DOID:2219	Glanzmann's thrombasthenia	HGNC:6156	Homo sapiens (human)	3690	ITGB3	inference by association of genotype from phenotype used in manual assertion	PMID:1967954 RGD:7240710
DOID:13406	pulmonary sarcoidosis	HGNC:5331	Homo sapiens (human)	64127	NOD2	inference by association of genotype from phenotype used in manual assertion	PMID:19679608
DOID:13406	pulmonary sarcoidosis	HGNC:1606	Homo sapiens (human)	1234	CCR5	inference by association of genotype from phenotype used in manual assertion	PMID:19679608
DOID:10763	hypertension	RGD:2072	Rattus norvegicus (Norway rat)	24182	Agtr2	mutant phenotype evidence used in manual assertion	PMID:19680135 PMID:21040717
DOID:0080998	acute necrotizing pancreatitis	RGD:2254	Rattus norvegicus (Norway rat)	24241	Calca	direct assay evidence used in manual assertion	PMID:19684430
DOID:3748	esophagus squamous cell carcinoma	HGNC:1455	Homo sapiens (human)	811	CALR	mutant phenotype evidence used in manual assertion	PMID:19684620 PMID:23814025
DOID:1824	status epilepticus	HGNC:1033	Homo sapiens (human)	627	BDNF	mutant phenotype evidence used in manual assertion	PMID:19686240
DOID:0060691	platelet-type bleeding disorder 16	HGNC:6138	Homo sapiens (human)	3674	ITGA2B	inference by association of genotype from phenotype used in manual assertion	PMID:19691478 PMID:21029361 PMID:22394243 RGD:7240710

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements