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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 **7526 - 7550** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
5553	proteoglycan 2, pro eosinophil major basic protein	PRG2 Aliases: BMPG MBP eosinophil major basic protein proMBP	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 Chagas disease Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Pick's disease Reye syndrome allergic asthma asthma autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera colorectal cancer colorectal carcinoma congenital muscular dystrophy dermatophytosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma eosinophilic esophagitis facioscapulohumeral muscular dystrophy fungal infectious disease intrinsic asthma large intestine cancer limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma muscular dystrophy myelofibrosis myofibrillar myopathy 1 myofibrillar myopathy 3 nodular prostate obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy peritoneum cancer prostate cancer prostate carcinoma prostatic adenoma rippling muscle disease 2 uterine corpus cancer
5552	serglycin	SRGN Aliases: PPG serglycin proteoglycan	Homo sapiens (human)	MHC class II deficiency Sertoli cell-only syndrome Y-linked spermatogenic failure 1 acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adult respiratory distress syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer childhood type dermatomyositis cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis degenerative disc disease dental caries dentin caries dermatomyositis diabetes mellitus diabetic cataract diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health embryoma enterocele esophagus squamous cell carcinoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance gynecomastia hepatitis B hepatocellular carcinoma high grade glioma hypertension infant gynecomastia isolated cleft palate large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus male infertility malignant pleural mesothelioma mixed glioma multiple myeloma nasopharynx carcinoma newborn respiratory distress syndrome nutmeg liver oligospermia oral candidiasis osteoarthritis prediabetes syndrome psychotic disorder sarcomatoid carcinoma severe combined immunodeficiency type 2 diabetes mellitus
5551	perforin 1	PRF1	Homo sapiens (human)
5549	proline and arginine rich end leucine rich repeat protein	PRELP	Homo sapiens (human)
5547	prolylcarboxypeptidase	PRCP	Homo sapiens (human)
5546	proline rich mitotic checkpoint control factor	PRCC	Homo sapiens (human)
5542	proline rich protein BstNI subfamily 1	PRB1	Homo sapiens (human)
5540	neuropeptide Y receptor Y4	NPY4R	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
5537	protein phosphatase 6 catalytic subunit	PPP6C	Homo sapiens (human)
5531	protein phosphatase 4 catalytic subunit	PPP4C	Homo sapiens (human)
5530	protein phosphatase 3 catalytic subunit alpha	PPP3CA	Homo sapiens (human)
5528	protein phosphatase 2 regulatory subunit B'delta	PPP2R5D	Homo sapiens (human)
5524	protein phosphatase 2 phosphatase activator	PTPA	Homo sapiens (human)
5518	protein phosphatase 2 scaffold subunit Aalpha	PPP2R1A	Homo sapiens (human)
5514	protein phosphatase 1 regulatory subunit 10	PPP1R10	Homo sapiens (human)
5511	protein phosphatase 1 regulatory subunit 8	PPP1R8	Homo sapiens (human)
5510	protein phosphatase 1 regulatory subunit 7	PPP1R7	Homo sapiens (human)
5509	protein phosphatase 1 regulatory subunit 3D	PPP1R3D	Homo sapiens (human)
5507	protein phosphatase 1 regulatory subunit 3C	PPP1R3C Aliases: PTG Phosphatase 1, regulatory inhibitor subunit 5 protein targeting to glycogen	Homo sapiens (human)	alcohol use disorder antithrombin III deficiency breast cancer cancer colorectal cancer colorectal carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer hepatocellular carcinoma large intestine cancer liver cancer major depressive disorder melancholic depression neurotic disorder obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency steatotic liver disease thrombophilia type 2 diabetes mellitus
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer hypoglycemia language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
5504	protein phosphatase 1 regulatory inhibitor subunit 2	PPP1R2	Homo sapiens (human)
5502	protein phosphatase 1 regulatory inhibitor subunit 1A	PPP1R1A	Homo sapiens (human)
5501	protein phosphatase 1 catalytic subunit gamma	PPP1CC	Homo sapiens (human)	cancer congestive heart failure type 2 diabetes mellitus
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer

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