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 **451 - 475** of **14279** in total

« First

‹ Prev

…

15

16

17

18

19

20

21

22

23

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References ▲
DOID:0111061	familial hypobetalipoproteinemia 2	MGI:88052	Mus musculus (house mouse)	238055	Apob	author statement supported by traceable reference	PMID:10705993 PMID:8921909
DOID:4440	seminoma	HGNC:6770	Homo sapiens (human)	4089	SMAD4	inference by association of genotype from phenotype used in manual assertion	PMID:10706106
DOID:1612	breast cancer	HGNC:7553	Homo sapiens (human)	4609	MYC	inference by association of genotype from phenotype used in manual assertion	PMID:10706127
DOID:2217	Bernard-Soulier syndrome	MGI:1333744	Mus musculus (house mouse)	14723	Gp1ba	author statement supported by traceable reference	PMID:10706630
DOID:2229	factor XI deficiency	HGNC:3529	Homo sapiens (human)	2160	F11	inference by association of genotype from phenotype used in manual assertion	PMID:10706758 PMID:11127865 PMID:2813350 RGD:7240710
DOID:13359	Ehlers-Danlos syndrome	HGNC:2201	Homo sapiens (human)	1281	COL3A1	inference by association of genotype from phenotype used in manual assertion	PMID:10706896 PMID:1370809 PMID:16012458
DOID:0060367	Parkinson's disease 1	MGI:1277151	Mus musculus (house mouse)	20617	Snca	author statement supported by traceable reference	PMID:10707987 PMID:18622040
DOID:0060001	withdrawal disorder	RGD:3435	Rattus norvegicus (Norway rat)	24929	Ptger3	mutant phenotype evidence used in manual assertion	PMID:10708732
DOID:4780	anti-basement membrane glomerulonephritis	HGNC:2505	Homo sapiens (human)	1493	CTLA4	mutant phenotype evidence used in manual assertion	PMID:10712436
DOID:3343	glycoproteinosis	HGNC:23026	Homo sapiens (human)	84572	GNPTG	inference by association of genotype from phenotype used in manual assertion	PMID:10712439
DOID:1612	breast cancer	MGI:98953	Mus musculus (house mouse)	22408	Wnt1	author statement supported by traceable reference	PMID:10713683
DOID:10652	Alzheimer's disease	HGNC:5991	Homo sapiens (human)	3552	IL1A	inference by association of genotype from phenotype used in manual assertion	PMID:10716257 PMID:11402127
DOID:7148	rheumatoid arthritis	HGNC:10907	Homo sapiens (human)	6556	SLC11A1	inference by association of genotype from phenotype used in manual assertion	PMID:10719815 PMID:12135431
DOID:0111008	X-linked cone-rod dystrophy 1	MGI:1344037	Mus musculus (house mouse)	19893	Rpgr	author statement supported by traceable reference	PMID:10725384 PMID:14691151
DOID:0110414	retinitis pigmentosa 3	MGI:1344037	Mus musculus (house mouse)	19893	Rpgr	author statement supported by traceable reference	PMID:10725384 PMID:21546531 PMID:22563472
DOID:0110741	type 1 diabetes mellitus 2	MGI:96434	Mus musculus (house mouse)	16002	Igf2	author statement supported by traceable reference	PMID:10727441
DOID:10762	portal hypertension	RGD:3184	Rattus norvegicus (Norway rat)	24598	Nos1	direct assay evidence used in manual assertion	PMID:10727442
DOID:0110838	Usher syndrome type 2A	HGNC:12601	Homo sapiens (human)	7399	USH2A	inference by association of genotype from phenotype used in manual assertion	PMID:10729113 PMID:9624053 RGD:7240710
DOID:3393	coronary artery disease	HGNC:9204	Homo sapiens (human)	5444	PON1	inference by association of genotype from phenotype used in manual assertion	PMID:10729395 PMID:11917194
DOID:3526	cerebral infarction	HGNC:9204	Homo sapiens (human)	5444	PON1	inference by association of genotype from phenotype used in manual assertion	PMID:10729395
DOID:10976	membranous glomerulonephritis	RGD:2232	Rattus norvegicus (Norway rat)	24232	C3	direct assay evidence used in manual assertion	PMID:10729746
DOID:2841	asthma	HGNC:9040	Homo sapiens (human)	7941	PLA2G7	inference by association of genotype from phenotype used in manual assertion	PMID:10733466
DOID:583	hemolytic anemia	HGNC:4311	Homo sapiens (human)	2729	GCLC	inference by association of genotype from phenotype used in manual assertion	PMID:10733484
DOID:0060334	transient neonatal diabetes mellitus	MGI:1352629	Mus musculus (house mouse)	20927	Abcc8	author statement supported by traceable reference	PMID:10734066
DOID:12960	acrocephalosyndactylia	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	PMID:10735635 PMID:23532954 PMID:7668257 PMID:9677057 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