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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 **1101 - 1125** 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:10763	hypertension Aliases: HTN hyperpiesia vascular hypertensive disorder	CDC19 CTS2 EMI2 ENO1 ENO2 ERR1 ERR2 ERR3 GLK1 GLR1 HXK1 HXK2 OGG1 PEP4 PYK2 RHO1 TIF4631 TIF4632 VVS1 YBT1 YLR001C	850317 850614 850678 850687 851193 851977 852128 852543 852639 852833 853071 853169 854529 854575 854942 855373 855848 855949 856014 856294 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	BPT1 BUD2 CTS2 EMI2 GLK1 GLR1 HMG1 HMG2 HXK1 HXK2 OGG1 VVS1	850317 850614 850645 851171 851977 852128 852543 852639 853770 854900 854942 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	BPT1 DGA1 ECM38 EMI2 GLK1 HFA1 HXK1 HXK2 KAR2 LAG1 PHO8 POX1	850317 850614 850645 851006 852092 852128 852639 852667 853418 854419 855247 856386	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9993	hypoglycemia Aliases: Hypoglycaemia	EMI2 ERS1 GAC1 GIP2 GLK1 HXK1 HXK2	850317 850438 850614 852128 852639 854350 856781	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9970	obesity	CNE1 DPL1 ECM14 EMI2 GCY1 GLK1 HFA1 HXK1 HXK2 IZH1 KEX2 NPP1 NPP2 PEP4 POX1 PUF3 RHO1 SEC16 SLA1 SRB8 SSN2 TDH1 TDH2 TDH3 TRM732 VVS1 YOL075C YPR1 ZWF1	850317 850391 850442 850614 850647 851241 851888 851974 852053 852102 852128 852276 852543 852639 852667 853106 853395 853465 854080 854287 855247 855301 855480 855483 855949 856020 856294 856533 856699	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9351	diabetes mellitus Aliases: diabetes	ADP1 ECM14 ECM38 EMI2 GIT1 GLK1 GLR1 HMG1 HMG2 HXK1 HXK2 NFT1 VVS1 ZWF1	850317 850369 850462 850614 851006 851171 852128 852543 852639 853978 854900 855480 856014 856533	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	ADP1 ATG26 BPT1 CTS2 DAP2 ECM14 ECM38 EMI2 GAC1 GCY1 GIP2 GLC7 GLK1 GLO1 GUT2 HMG1 HMG2 HXK1 HXK2 IRC21 KEX2 LAG1 NPP1 NPP2 OGG1 PIG1 PYK2 STE6 VVS1 YBT1 YPR1 ZWF1	850317 850369 850391 850614 850645 850678 850886 850979 851006 851171 851974 851977 852128 852543 852639 853671 854287 854350 854529 854651 854900 854942 855009 855095 855480 855483 856386 856423 856533 856699 856781 856870	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2048	autoimmune hepatitis Aliases: Autoimmune chronic active hepatitis autoimmune hepatitis with centrilobular necrosis	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11088	asphyxia neonatorum Aliases: Asphyxia - birth Asphyxia, in liveborn infant Birth asphyxia postnatal asphyxia	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060438	Cole-Carpenter syndrome	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9778	irritable bowel syndrome Aliases: IBD Irritable colon	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2055	post-traumatic stress disorder Aliases: PTSD traumatic neurosis	EUG1 KAR2 PDI1	850314 852130 853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	ECM38 EUG1 PDI1 STE6	850314 851006 852130 853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:6432	pulmonary hypertension	EUG1 HMG1 HMG2 HXK1 PDI1 RHO1 VVS1	850314 850614 851171 852130 852543 854900 856294	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10155	intestinal cancer Aliases: malignant intestinal tumors malignant neoplasm of intestine	EMC1	850312	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081276	cerebellar atrophy, visual impairment, and psychomotor retardation Aliases: CAVIPMR	EMC1	850312	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070437	hyperphosphatasia with impaired intellectual development syndrome 6 Aliases: GPIBD40 HPMRS4 glycosylphosphatidylinositol biosynthesis defect 40 hyperphosphatasia with mental retardation syndrome 4	PIGY	84992	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111722	amelogenesis imperfecta type 3C Aliases: AI3C amelogenesis imperfecta type IIIC autosomal recessive amelogenesis imperfecta hypocalcification type	RELT	84957	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081177	autosomal recessive intellectual developmental disorder 1	PRSS12	8492	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080581	hyperekplexia 4	ATAD1	84896	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081225	autosomal recessive intellectual developmental disorder 64	LINGO1	84894	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112382	muscular dystrophy-dystroglycanopathy type C8 Aliases: LGMDR24 MDDGC2 autosomal recessive limb-girdle muscular dystrophy 24 muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8 muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related	POMGNT2	84892	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111231	congenital muscular dystrophy-dystroglycanopathy type A8 Aliases: MDDGA8 Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8	POMGNT2	84892	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070277	primary autosomal recessive microcephaly 15 Aliases: MCPH15 NEDMISBA neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities	MFSD2A	84879	Homo sapiens (human)	Alliance of Genome Resources

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