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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 **5551 - 5575** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:2018	hyperinsulinism Aliases: hyperinsulinemia	EMI2 FBP26 GLK1 HXK1 HXK2 IZH1 YBT1	850317 850614 850678 852102 852128 852639 853286	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060639	permanent neonatal diabetes mellitus Aliases: PDMI PNDM permanent diabetes mellitus of infancy	EMI2 GLK1 HXK1 HXK2 YBT1	850317 850614 850678 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10584	retinitis pigmentosa Aliases: pericentral pigmentary retinopathy	EMI2 GLK1 HXK1 HXK2	850317 850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111100	maturity-onset diabetes of the young type 2 Aliases: MODY glucokinase-related MODY type 2 MODY2	EMI2 GLK1 HXK1 HXK2	850317 850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070216	familial hyperinsulinemic hypoglycemia 3 Aliases: HHF3 hyperinsulinemic hypoglycemia due to glucokinase deficiency hyperinsulinism due to glucokinase deficiency	EMI2 GLK1 HXK1 HXK2	850317 850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13317	hyperinsulinemic hypoglycemia Aliases: Islet cell hyperplasia nesidioblastosis persistent hyperinsulinemia hypoglycemia of infancy	EMI2 GLK1 HXK1 HXK2	850317 850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	EMI2 HXK1 HXK2	850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081399	autosomal dominant distal hereditary motor neuronopathy 10	EMILIN1	11117	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080386	nephrotic syndrome type 10	EMP2	2013	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110056	amelogenesis imperfecta type 1C Aliases: AI1C amelogenesis imperfecta type IC autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion autosomal recessive amelogenesis imperfecta local hypoplastic type	ENAM	10117	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110052	amelogenesis imperfecta type 1B Aliases: AI1B AIH2 amelogenesis imperfecta type IB autosomal dominant hypoplastic local amelogenesis imperfecta hereditary localized enamel hypoplasia	ENAM	10117	Homo sapiens (human)	Alliance of Genome Resources
DOID:1037	lymphoid leukemia Aliases: lymphoblastic leukaemia lymphoblastic leukemia lymphocytic leukaemia	ENG FCGR2A FCGR2B FCGR3A	2022 2212 2213 2214	Homo sapiens (human)	Alliance of Genome Resources
DOID:10652	Alzheimer's disease Aliases: Alzheimer disease Alzheimers dementia	ENO1 ENO2 ERR1 ERR2 ERR3 GLR1 HMG1 HMG2 HRR25 HSF1 NFT1 PEP1 PEP4 STE20 TDH1 TDH2 TDH3 VPS1 VTH1 VTH2 VVS1 XRN1 YNR065C YPS3 YPS7	850812 851171 851950 852264 852543 852702 852806 853106 853169 853233 853395 853465 853870 853978 854575 854634 854900 855373 855802 855848 855897 855949 856014 856382 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080855	Parkinsonism	ENO1 ENO2 ERR1 ERR2 ERR3 GLR1 SMF3 YCT1	850671 850721 853169 854575 855373 855848 856014 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	ENO1 ENO2 ERR1 ERR2 ERR3 PEP4	853169 854575 855373 855848 855949 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11054	urinary bladder cancer Aliases: bladder cancer tumor of the bladder	ENO1 ENO2 GIS1 HXK1 PBS2 RHO1 SMF3	850614 850721 851670 853169 853313 856294 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:936	brain disease Aliases: encephalopathy	ENO1 ENO2 HRR25	853169 855897 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1800	neuroendocrine carcinoma	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12783	migraine without aura Aliases: common migraine	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12783	migraine without aura Aliases: common migraine	ENO2 LDLR TNF	2026 3949 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:1800	neuroendocrine carcinoma	ENO2	2026	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080333	aortic valve disease 1	ENPP1 IL6 NOTCH1	3569 4851 5167	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110815	hereditary spastic paraplegia 64 Aliases: SPG64 autosomal recessive spastic paraplegia 64 autosomal recessive spastic paraplegia type 64	ENTPD1	953	Homo sapiens (human)	Alliance of Genome Resources
DOID:705	Leber hereditary optic neuropathy Aliases: Leber's hereditary optic neuropathy Leber's optic atrophy	ENV9	854420	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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