GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **12726 - 12750** of **15957** in total

« First

‹ Prev

…

506

507

508

509

510

511

512

513

514

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0111693	familial adult myoclonic epilepsy 4 Aliases: FAME4 FCMTE4 familial cortical myoclonic tremor and epilepsy 4	YEATS2	55689	Homo sapiens (human)	Alliance of Genome Resources
DOID:13359	Ehlers-Danlos syndrome Aliases: Cutis hyperelastica elastic skin	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080739	Ehlers-Danlos syndrome spondylodysplastic type 3	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081141	agammaglobulinemia 9	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:557	kidney disease Aliases: impaired renal function disease nephropathy	YLR001C ZWF1	850687 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060444	granular corneal dystrophy 2 Aliases: CGD2 avellino corneal dystrophy combined granular-lattice corneal dystrophy corneal dystrophy, Avellino type granular corneal dystrophy type 2	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1474	aggressive periodontitis Aliases: juvenile periodontitis	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080530	granular corneal dystrophy 1 Aliases: corneal dystrophy, Groenouw type I	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060447	epithelial basement membrane dystrophy Aliases: Cogan corneal dystrophy EBMD microcystic corneal dystrophy	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080010	bone structure disease	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060453	Reis-Bucklers corneal dystrophy Aliases: RBCD anterior limiting membrane dystrophy type I corneal dystrophy of Bowman layer type I geographic corneal dystrophy granular corneal dystrophy type III	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:824	periodontitis Aliases: chronic pericementitis	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:90	degenerative disc disease Aliases: cervical disc degenerative disease intervertebral disc degeneration lumbar disc degeneration vertebral disc disease	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:971	tendinitis	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060455	Thiel-Behnke corneal dystrophy Aliases: TBCD Waardenburg-Jonker corneal dystrophy anterior limiting membrane dystrophy type II corneal dystrophy honeycomb-shaped corneal dystrophy of Bowman layer type II	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111436	optic atrophy 11 Aliases: OPA11	YME1L1	10730	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090019	sitosterolemia Aliases: phytosterolemia	YOL075C	854080	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	YPR1	851974	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9255	frontotemporal dementia Aliases: Wilhemsen-Lynch disease frontotemporal lobar degeneration multiple system tauopathy with presenile dementia pallidopontonigral degeneration	YPS3 YPS7	850812 851950	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080282	developmental and epileptic encephalopathy 56 Aliases: DEE56 early infantile epileptic encephalopathy 56	YWHAG	7532	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050795	cone dystrophy Aliases: retinal cone dystrophy	Yap1	22601	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111249	uveal coloboma-cleft lip and palate-intellectual disability Aliases: COB1 Uveal coloboma-cleft lip/palate-mental retardation syndrome coloboma-microphthalmos syndrome coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation	Yap1	22601	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:070355	multisystem proteinopathy	Yars1	107271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C Aliases: CMTDIC Charcot-Marie-Tooth neuropathy dominant intermediate C DI-CMTC autosomal dominant intermediate Charcot-Marie-Tooth disease type C	Yars1	107271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111693	familial adult myoclonic epilepsy 4 Aliases: FAME4 FCMTE4 familial cortical myoclonic tremor and epilepsy 4	Yeats2	208146	Mus musculus (house mouse)	Alliance of Genome Resources

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

International Collaboration

Acknowledgements