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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5501 - 5525** of **5716** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:8866	actinic keratosis Aliases: SK - Solar keratosis Senile hyperkeratosis Solar keratosis actinic (Solar) Keratosis	KNSTRN OCA2	4948 90417	Homo sapiens (human)	Alliance of Genome Resources
DOID:8869	neuromyelitis optica Aliases: Devic's disease Devic's syndrome	Cd59b	25407	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8869	neuromyelitis optica Aliases: Devic's disease Devic's syndrome	AQP4 HLA-DQB1 HLA-DRB1	3119 3123 361	Homo sapiens (human)	Alliance of Genome Resources
DOID:8886	chorioretinitis Aliases: retinochoroiditis	COL2A1	1280	Homo sapiens (human)	Alliance of Genome Resources
DOID:8893	psoriasis	ADRB2 AGER ALB APOE C2 CADM2 CAST CD40 CFB COMT CTLA4 CYP1A1 HLA-DQA1 HLA-DQB1 ICAM1 IL10 IL13 IL17A IL20 IL23R LTA MBL2 NAT2 STAT3 STAT4 TAP1 TNF VEGFA	10 1312 149233 1493 154 1543 177 213 253559 3117 3119 3383 348 3586 3596 3605 4049 4153 50604 629 6774 6775 6890 7124 717 7422 831 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:8893	psoriasis	Itgb2 Sptlc2 Stat3 Vegfa	16414 20773 20848 22339	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:890	mitochondrial encephalomyopathy	TYMP	1890	Homo sapiens (human)	Alliance of Genome Resources
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	EPM2A SEMA6B	10501 7957	Homo sapiens (human)	Alliance of Genome Resources
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	Scarb2	12492	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8923	skin melanoma Aliases: Cutaneous Malignant Melanoma cutaneous melanoma malignant ear melanoma malignant lip melanoma malignant lower limb melanoma malignant melanoma of ear and/or external auricular canal malignant melanoma of skin of lower limb malignant melanoma of skin of trunk except scrotum malignant melanoma of skin of upper limb malignant neck melanoma malignant scalp melanoma malignant trunk melanoma malignant upper limb melanoma	BRCA2 CCL2 CTCF DDR1 ICAM1 MMP1 MMP9 OCA2 TYR	10664 3383 4312 4318 4948 6347 675 7299 780	Homo sapiens (human)	Alliance of Genome Resources
DOID:8923	skin melanoma Aliases: Cutaneous Malignant Melanoma cutaneous melanoma malignant ear melanoma malignant lip melanoma malignant lower limb melanoma malignant melanoma of ear and/or external auricular canal malignant melanoma of skin of lower limb malignant melanoma of skin of trunk except scrotum malignant melanoma of skin of upper limb malignant neck melanoma malignant scalp melanoma malignant trunk melanoma malignant upper limb melanoma	Grm1	14816	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8924	autoimmune thrombocytopenic purpura Aliases: Immune thrombocytopenic purpura idiopathic thrombocytopenic purpura primary thrombocytopenic purpura	CD40LG CD86 FCGR2A FCGR2B FCGR3A HLA-DQB1 HLA-DRB1 IL10 IL1A IL1RN IL2 IL4 ITGB3	2212 2213 2214 3119 3123 3552 3557 3558 3565 3586 3690 942 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:8927	learning disability Aliases: Academic skill disorder learning disorder	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:8929	atrophic gastritis Aliases: gastric atrophy	ATP4B HLA-DQB1 HLA-DRB1 PTPN11	3119 3123 496 5781	Homo sapiens (human)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	Hmgcr	25675	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	ATP7B	540	Homo sapiens (human)	Alliance of Genome Resources
DOID:8946	severe nonproliferative diabetic retinopathy Aliases: High risk non proliferative diabetic retinopathy Severe NPDR	Pdgfrb	18596	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	Insr	16337	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	ACE2 ACE ADIPOQ ADRB3 AGER AGT AKR1B1 ANGPT1 APOB APOE CDKAL1 CFB CFH CLU EDN1 ELN EPO FLT1 GLO1 HFE HLA-B HLA-DQB1 HLA-DRB1 ICAM1 IL10 IL6 INS ITGA2 LTA MMP2 MMP9 NOS3 PON1 SERPINE1 SERPINF1 SGF29 SOD1 SOD3 TLR4 TNF VEGFA VPS26A WFS1 XRCC1	112869 1191 155 1636 177 183 1906 2006 2056 231 2321 2739 284 3075 3077 3106 3119 3123 338 3383 348 3569 3586 3630 3673 4049 4313 4318 4846 5054 5176 5444 54901 59272 629 6647 6649 7099 7124 7422 7466 7515 9370 9559	Homo sapiens (human)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	Agt Akr1b1 Angpt2 Aqp4 Nfe2l2 Ngf Nos3 Ppargc1a	24179 24192 24600 25293 310738 83516 83619 89805	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8955	sideroblastic anemia Aliases: ANEMIA SIDEROBLASTIC Anemia, hypochromic with iron loading	CALR	811	Homo sapiens (human)	Alliance of Genome Resources
DOID:896	metal metabolism disorder Aliases: inborn metal metabolism disorder	TRPM6	140803	Homo sapiens (human)	Alliance of Genome Resources
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:898	autosomal dominant polycystic kidney disease Aliases: ADPKD Congenital biliary ectasias POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1	pkd2	432387	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:898	autosomal dominant polycystic kidney disease Aliases: ADPKD Congenital biliary ectasias POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1	LRP5 MTOR PKD1 PKD2	2475 4041 5310 5311	Homo sapiens (human)	Alliance of Genome Resources

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