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 **13151 - 13175** of **14279** in total

« First

‹ Prev

…

523

524

525

526

527

528

529

530

531

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References
DOID:10487	Hirschsprung's disease	HGNC:12789	Homo sapiens (human)	7479	WNT8B	inference by association of genotype from phenotype used in manual assertion	PMID:20972907
DOID:10754	otitis media	MGI:96794	Mus musculus (house mouse)	16905	Lmna	author statement supported by traceable reference	PMID:22819531
DOID:9256	colorectal cancer	HGNC:3527	Homo sapiens (human)	2146	EZH2	inference by association of genotype from phenotype used in manual assertion	PMID:21926398
DOID:1245	vulva cancer	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:12543794
DOID:9074	systemic lupus erythematosus	HGNC:1910	Homo sapiens (human)	10036	CHAF1A	direct assay evidence used in manual assertion	PMID:24836587
DOID:0111363	Heinz body anemia	HGNC:4824	Homo sapiens (human)	3040	HBA2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10283	prostate cancer	SGD:S000000966	Saccharomyces cerevisiae S288C	856911	CHD1	sequence similarity evidence used in manual assertion	PMID:31222142
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:1993	rectum cancer	HGNC:12833	Homo sapiens (human)	7520	XRCC5	inference by association of genotype from phenotype used in manual assertion	PMID:26735576
DOID:1793	pancreatic cancer	HGNC:6001	Homo sapiens (human)	3558	IL2	direct assay evidence used in manual assertion	PMID:9080118
DOID:0111907	thrombophilia due to thrombin defect	HGNC:3535	Homo sapiens (human)	2147	F2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112045	non-syndromic X-linked intellectual disability 93	HGNC:17342	Homo sapiens (human)	254065	BRWD3	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:5419	schizophrenia	FB:FBgn0004509	Drosophila melanogaster (fruit fly)	47220	Fur1	combinatorial experimental and author inference evidence used in manual assertion	PMID:36028314
DOID:2043	hepatitis B	HGNC:5965	Homo sapiens (human)	3588	IL10RB	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070551	epidermolytic palmoplantar keratoderma 2	HGNC:6412	Homo sapiens (human)	3848	KRT1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:6432	pulmonary hypertension	HGNC:3542	Homo sapiens (human)	2153	F5	inference by association of genotype from phenotype used in manual assertion	PMID:20182352
DOID:9562	primary ciliary dyskinesia	HGNC:18661	Homo sapiens (human)	56171	DNAH7	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:2986	IgA glomerulonephritis	HGNC:6000	Homo sapiens (human)	3557	IL1RN	inference by association of genotype from phenotype used in manual assertion	PMID:10916103 PMID:19280228
DOID:3083	chronic obstructive pulmonary disease	HGNC:10798	Homo sapiens (human)	653509	SFTPA1	inference by association of genotype from phenotype used in manual assertion	PMID:11589345 PMID:19797132
DOID:0070283	primary autosomal recessive microcephaly 13	HGNC:1856	Homo sapiens (human)	1062	CENPE	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10283	prostate cancer	HGNC:7646	Homo sapiens (human)	10	NAT2	inference by association of genotype from phenotype used in manual assertion	PMID:12355549
DOID:10588	adrenoleukodystrophy	SGD:S000006068	Saccharomyces cerevisiae S288C	855956	PXA1	genetic interaction evidence used in manual assertion	PMID:18757502 PMID:21145416
DOID:5844	myocardial infarction	RGD:621320	Rattus norvegicus (Norway rat)	81687	Mmp9	direct assay evidence used in manual assertion	PMID:16845718
DOID:0050745	diffuse large B-cell lymphoma	HGNC:1643	Homo sapiens (human)	933	CD22	mutant phenotype evidence used in manual assertion	PMID:25708834
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	RGD:3017	Rattus norvegicus (Norway rat)	24539	Lpl	direct assay evidence used in manual assertion	PMID:30214514

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