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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 **7651 - 7675** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
5033	prolyl 4-hydroxylase subunit alpha 1	P4HA1	Homo sapiens (human)
8974	prolyl 4-hydroxylase subunit alpha 2	P4HA2	Homo sapiens (human)
283208	prolyl 4-hydroxylase subunit alpha 3	P4HA3	Homo sapiens (human)
5034	prolyl 4-hydroxylase subunit beta	P4HB	Homo sapiens (human)
54681	prolyl 4-hydroxylase, transmembrane	P4HTM	Homo sapiens (human)
5547	prolylcarboxypeptidase	PRCP	Homo sapiens (human)
8842	prominin 1	PROM1	Homo sapiens (human)
150696	prominin 2	PROM2	Homo sapiens (human)
5443	proopiomelanocortin	POMC	Homo sapiens (human)
5095	propionyl-CoA carboxylase subunit alpha	PCCA	Homo sapiens (human)	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia nicotine dependence obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis refractive error severe congenital neutropenia sick sinus syndrome stomach cancer stomach carcinoma thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
5096	propionyl-CoA carboxylase subunit beta	PCCB	Homo sapiens (human)	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia anxiety disorder cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy generalized anxiety disorder granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis schizophrenia severe congenital neutropenia sick sinus syndrome thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
5122	proprotein convertase subtilisin/kexin type 1	PCSK1	Homo sapiens (human)
27344	proprotein convertase subtilisin/kexin type 1 inhibitor	PCSK1N	Homo sapiens (human)
5126	proprotein convertase subtilisin/kexin type 2	PCSK2	Homo sapiens (human)
54760	proprotein convertase subtilisin/kexin type 4	PCSK4	Homo sapiens (human)
5125	proprotein convertase subtilisin/kexin type 5	PCSK5	Homo sapiens (human)
5046	proprotein convertase subtilisin/kexin type 6	PCSK6	Homo sapiens (human)
9159	proprotein convertase subtilisin/kexin type 7	PCSK7	Homo sapiens (human)
255738	proprotein convertase subtilisin/kexin type 9	PCSK9	Homo sapiens (human)
5660	prosaposin	PSAP Aliases: saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy	Homo sapiens (human)	Farber lipogranulomatosis Gaucher's disease type I Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Unverricht-Lundborg syndrome X-linked nonsyndromic deafness acquired immunodeficiency syndrome adult fibrosarcoma agnosia allergic asthma amnestic disorder amyotrophic lateral sclerosis anemia aortic valve disease 2 aortic valve stenosis asthma atypical Gaucher's disease due to saposin c deficiency autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness bacterial sepsis blepharospasm breast cancer breast carcinoma cancer candidiasis central nervous system cancer central sleep apnea cholecystitis choreatic disease colitis combined saposin deficiency critical illness polyneuropathy cutaneous candidiasis dementia dental caries dentin caries denture stomatitis depressive disorder dysthymic disorder dystonia early myoclonic encephalopathy embryoma epilepsy fascioliasis fibrosarcoma focal hand dystonia frontotemporal dementia gallbladder cancer gallbladder carcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma hepatitis B hepatitis E hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease late onset Parkinson's disease leukodystrophy lingual-facial-buccal dyskinesia lipid storage disease liver cancer lysosomal storage disease macrocytic anemia major depressive disorder malaria melancholic depression meningoencephalitis metachromatic leukodystrophy mixed glioma movement disease multiple myeloma 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 neuropathy neurotic disorder obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia optic atrophy oral candidiasis ovarian cancer ovarian carcinoma panic disorder paraplegia parapsoriasis peripheral nervous system disease phobic disorder plasma cell neoplasm polyneuropathy progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole retrograde amnesia schizophrenia situs inversus social phobia sphingolipidosis stomach cancer stomach carcinoma stomatitis syndromic X-linked intellectual disability type 10 thrombocytopenia tuberous sclerosis ulcerative stomatitis visual epilepsy vulvovaginal candidiasis vulvovaginitis
768239	prosaposin like 1	PSAPL1	Homo sapiens (human)
5729	prostaglandin D2 receptor	PTGDR	Homo sapiens (human)
11251	prostaglandin D2 receptor 2	PTGDR2	Homo sapiens (human)
5730	prostaglandin D2 synthase	PTGDS Aliases: L-PGDS PGDS lipocalin-type prostaglandin D synthase	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 Axenfeld-Rieger syndrome Crohn's colitis Crohn's disease Fabry disease Graves' disease Guillain-Barre syndrome Loeffler syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome Parkinson's disease Pendred Syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acrodermatitis acute myocardial infarction acute promyelocytic leukemia adult lymphoma adult medulloblastoma allergic asthma alopecia anaplastic astrocytoma androgenic alopecia angiomatous meningioma aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atopic dermatitis attention deficit hyperactivity disorder autoimmune thyroiditis benign meningioma bipolar disorder brain cancer breast cancer breast carcinoma bronchiolitis bronchitis cancer carcinoma cardiovascular system disease carotid artery disease central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebrotendinous xanthomatosis childhood cerebral astrocytoma childhood lymphoma childhood medulloblastoma cholestasis chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniosynostosis cryptorchidism depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma disease of mental health dry eye syndrome dyshormonogenic goiter dysthymic disorder egg allergy embryoma encephalitis encephalomyelitis enterocele eosinophilic pneumonia essential hypertension fibrillary astrocytoma fibrous meningioma gastritis gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis goiter heart disease high grade glioma hypereosinophilic syndrome hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile pilocytic astrocytoma kidney disease large congenital melanocytic nevus large intestine cancer late onset Parkinson's disease lipid storage disease liver cirrhosis lung benign neoplasm lupus nephritis lymphoma lymphoplasmacyte-rich meningioma major depressive disorder malignant astrocytoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma myelitis myocardial infarction nephritis nephrosclerosis nephrosis neurofibromatosis neurotic disorder nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea olfactory groove meningioma open-angle glaucoma osteoarthritis ovarian cancer ovarian carcinoma pancytopenia papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma periodontitis pigment dispersion syndrome pilocytic astrocytoma pituitary adenoma pneumonia post-traumatic stress disorder pre-eclampsia prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psychotic disorder pyoureter respiratory syncytial virus infectious disease rhinitis sarcomatoid carcinoma schizophrenia secretory meningioma sensorineural hearing loss silent myocardial infarction sinusitis situs inversus skin melanoma skin squamous cell carcinoma spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma stuttering subependymal giant cell astrocytoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transitional meningioma tuberous sclerosis type 2 diabetes mellitus ulcerative colitis ureteral obstruction vestibular schwannomatosis xerophthalmia
5731	prostaglandin E receptor 1	PTGER1	Homo sapiens (human)

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