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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 **14926 - 14950** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:219	colon cancer	ERS1 GPX1 GPX2 PBS2	850438 852546 853313 853842	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070214	familial hyperinsulinemic hypoglycemia 7 Aliases: EIHI HHF7 exercise-induced hyperinsulinemic hypoglycemia exercise-induced hyperinsulinism hyperinsulinism due to SLC16A1 deficiency hyperinsulinism due to monocarboxylate transporter 1 deficiency	ERS1 ESBP6	850438 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070262	congenital disorder of glycosylation type IIj Aliases: CDG IIj CDG syndrome type IIj CDG2J CDGIIdj COG4-CDG Carbohydrate deficient glycoprotein syndrome type IIj Congenital disorder of glycosylation type 2j	COG4 ERS1	850438 856220	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:299	adenocarcinoma	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1062	Fanconi syndrome Aliases: Congenital Fanconi syndrome De Toni-Fanconi syndrome Fanconi-de Toni syndrome Fanconi-de-Toni syndrome Infantile nephropathic cystinosis Lignac-Fanconi syndrome adult Fanconi Anemia adult Fanconi syndrome deToni Fanconi syndrome	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110934	nemaline myopathy 7 Aliases: NEM7 nemaline myopathy 7, autosomal recessive	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1064	cystinosis Aliases: cystine storage disease	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1100	ovarian disease	PAT1	850440	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080985	syndromic X-linked intellectual disorder Lujan-Fryns-type	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1967	leiomyosarcoma Aliases: Leiomyosarcomas	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14711	FG syndrome Aliases: Keller syndrome Opitz-Kaveggia syndrome	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:591	phobic disorder	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1470	major depressive disorder Aliases: clinical depression major depression recurrent major depression single major depressive episode unipolar depression	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8778	Crohn's disease Aliases: Crohn disease Crohn's disease of colon Crohn's disease of large bowel Granulomatous Colitis Pediatric Crohn's disease	ATG26 FAB1 GIT1 PHO8 SMF3 STE6	850462 850574 850721 850886 852092 853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:7148	rheumatoid arthritis Aliases: Arthritis or polyarthritis, rheumatic atrophic Arthritis	CTS2 GIT1 KAR2 SMF3	850462 850721 851977 853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050908	myelodysplastic syndrome	GIT1 IDP1 IDP2 IDP3	850462 850871 851493 855723	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2841	asthma Aliases: bronchial hyperreactivity chronic obstructive asthma chronic obstructive asthma with acute exacerbation chronic obstructive asthma with status asthmaticus	CTS2 GIT1 HMG1 HMG2 NFT1 RHO1 STE13 STE6	850462 851171 851977 853671 853978 854394 854900 856294	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3021	acute kidney failure	GIT1 GLR1 GPX1 GPX2 PEP4	850462 852546 853842 855949 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050700	cardiomyopathy Aliases: Cardiomyopathies	GIT1 PMT4	850462 853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1852	intrahepatic cholestasis Aliases: neonatal intrahepatic cholestasis	GIT1 STE6	850462 853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1074	kidney failure Aliases: renal failure	GIT1 MEP2	850462 855580	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3883	Lynch syndrome Aliases: COCA 1 HNPCC - hereditary nonpolyposis colon cancer Hereditary Defective Mismatch Repair syndrome Hereditary non-polyposis colon cancer Hereditary non-polyposis colon cancer syndrome Hereditary non-polyposis colorectal cancer Hereditary non-polyposis colorectal cancer syndrome Hereditary nonpolyposis colon cancer Hereditary nonpolyposis colon cancer syndrome Hereditary nonpolyposis colorectal cancer syndrome hereditary nonpolyposis colorectal cancer hereditary nonpolyposis colorectal neoplasm	GIT1 RNY1	850462 855980	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112182	mismatch repair cancer syndrome Aliases: BTP1 syndrome BTPS1 CMMR-D syndrome CMMRDS MMR deficiency Turcot syndrome brain tumor-polyposis syndrome 1 childhood cancer syndrome constitutional mismatch repair deficiency syndrome	GIT1 RNY1	850462 855980	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14365	systemic primary carnitine deficiency disease Aliases: carnitine transporter deficiency carnitine uptake defect deficiency of plasma-membrane carnitine transporter primary carnitine deficiency renal carnitine transport defect	GIT1	850462	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:655	inherited metabolic disorder Aliases: Inborn Errors of Metabolism Metabolic hereditary disorder inborn metabolism disorder	GIT1	850462	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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