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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **6926 - 6950** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
57223	protein phosphatase 4 regulatory subunit 3B	PPP4R3B	Homo sapiens (human)
57718	protein phosphatase 4 regulatory subunit 4	PPP4R4	Homo sapiens (human)
5537	protein phosphatase 6 catalytic subunit	PPP6C	Homo sapiens (human)
22870	protein phosphatase 6 regulatory subunit 1	PPP6R1	Homo sapiens (human)
9701	protein phosphatase 6 regulatory subunit 2	PPP6R2	Homo sapiens (human)
55291	protein phosphatase 6 regulatory subunit 3	PPP6R3	Homo sapiens (human)
23082	PPARG related coactivator 1	PPRC1	Homo sapiens (human)
5538	palmitoyl-protein thioesterase 1	PPT1 Aliases: CLN1 INCL ceroid-lipofuscinosis, neuronal 1, infantile	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Gaucher's disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Reye syndrome Stargardt disease Unverricht-Lundborg syndrome actinic keratosis age related macular degeneration alternating hemiplegia of childhood amnestic disorder autonomic neuropathy basal cell carcinoma blepharospasm blindness brain disease breast cancer breast carcinoma cancer cannabis abuse cannabis dependence central nervous system disease cerebral degeneration colorectal cancer congestive heart failure degeneration of macula and posterior pole denture stomatitis depressive disorder dysthymic disorder early myoclonic encephalopathy embryoma endometriosis of uterus endometriosis epilepsy eye disease focal hand dystonia giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma hyperthyroidism intellectual disability inverted follicular keratosis keratoacanthoma large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung cancer lung non-small cell carcinoma lysosomal storage disease macular degeneration major depressive disorder male infertility melancholic depression melanoacanthoma movement disease nervous system disease neuroblastoma neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder obsolete melancholia optic atrophy polycystic ovary syndrome primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma psychotic disorder retrograde amnesia schizoaffective disorder schizophrenia schizophreniform disorder seborrheic keratosis secondary Parkinson disease skin disease stomatitis syndromic X-linked intellectual disability 94 thyrotoxicosis ulcerative stomatitis visual epilepsy
9374	palmitoyl-protein thioesterase 2	PPT2	Homo sapiens (human)	cancer cerebellar ataxia cerebellar disease embryoma histiocytosis membranous glomerulonephritis multiple myeloma multiple sclerosis neuroblastoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis
23398	peptidylprolyl isomerase domain and WD repeat containing 1	PPWD1	Homo sapiens (human)
10084	polyglutamine binding protein 1	PQBP1	Homo sapiens (human)
84279	protease associated domain containing 1	PRADC1	Homo sapiens (human)
343068	PRAME family member 5	PRAMEF5	Homo sapiens (human)
118471	proline rich acidic protein 1	PRAP1	Homo sapiens (human)
5542	proline rich protein BstNI subfamily 1	PRB1	Homo sapiens (human)
653247	proline rich protein BstNI subfamily 2	PRB2	Homo sapiens (human)
9055	protein regulator of cytokinesis 1	PRC1	Homo sapiens (human)
5546	proline rich mitotic checkpoint control factor	PRCC	Homo sapiens (human)
5547	prolylcarboxypeptidase	PRCP	Homo sapiens (human)
639	PR/SET domain 1	PRDM1	Homo sapiens (human)
56980	PR/SET domain 10	PRDM10	Homo sapiens (human)
63977	PR/SET domain 15	PRDM15	Homo sapiens (human)
63976	PR/SET domain 16	PRDM16	Homo sapiens (human)
7799	PR/SET domain 2	PRDM2	Homo sapiens (human)
5052	peroxiredoxin 1	PRDX1	Homo sapiens (human)

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