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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 **7901 - 7925** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
56107	protocadherin gamma subfamily A, 9	PCDHGA9	Homo sapiens (human)
56104	protocadherin gamma subfamily B, 1	PCDHGB1	Homo sapiens (human)
56103	protocadherin gamma subfamily B, 2	PCDHGB2	Homo sapiens (human)
56102	protocadherin gamma subfamily B, 3	PCDHGB3	Homo sapiens (human)
8641	protocadherin gamma subfamily B, 4	PCDHGB4	Homo sapiens (human)
56101	protocadherin gamma subfamily B, 5	PCDHGB5	Homo sapiens (human)
56100	protocadherin gamma subfamily B, 6	PCDHGB6	Homo sapiens (human)
56099	protocadherin gamma subfamily B, 7	PCDHGB7	Homo sapiens (human)
5098	protocadherin gamma subfamily C, 3	PCDHGC3	Homo sapiens (human)
56098	protocadherin gamma subfamily C, 4	PCDHGC4	Homo sapiens (human)
56097	protocadherin gamma subfamily C, 5	PCDHGC5	Homo sapiens (human)
65217	protocadherin related 15	PCDH15	Homo sapiens (human)
283659	protogenin	PRTG	Homo sapiens (human)
55248	proton activated chloride channel 1	PACC1	Homo sapiens (human)
58497	prune exopolyphosphatase 1	PRUNE1 Aliases: DRES-17 H-PRUNE HTCD37	Homo sapiens (human)
79834	pseudopodium enriched atypical kinase 1	PEAK1	Homo sapiens (human)
150962	pseudouridine synthase 10	PUS10	Homo sapiens (human)
83480	pseudouridine synthase 3	PUS3	Homo sapiens (human)
54517	pseudouridine synthase 7	PUS7	Homo sapiens (human)
9698	pumilio RNA binding family member 1	PUM1	Homo sapiens (human)
23369	pumilio RNA binding family member 2	PUM2	Homo sapiens (human)
9933	pumilio RNA binding family member 3	PUM3	Homo sapiens (human)
4860	purine nucleoside phosphorylase	PNP Aliases: PUNP	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 Evans' syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lesch-Nyhan syndrome MELAS syndrome MHC class II deficiency Nezelof syndrome Omenn syndrome Pick's disease Reye syndrome Richter's syndrome T cell deficiency acute lymphoblastic leukemia adenosine deaminase deficiency adult lymphoma agammaglobulinemia agnosia alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma carotid artery disease central nervous system disease central nervous system lymphoma central nervous system vasculitis central retinal vein occlusion cerebral degeneration cerebral malaria cerebral palsy childhood acute lymphocytic leukemia childhood lymphoma chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer combined T cell and B cell immunodeficiency coronary artery disease critical illness polyneuropathy cutaneous leishmaniasis cyclic hematopoiesis developmental coordination disorder diabetic cataract diabetic retinopathy disease of metabolism embryoma esophageal cancer esophageal carcinoma fetal erythroblastosis gangliosidosis giant cell glioblastoma glioblastoma granulomatous angiitis head and neck squamous cell carcinoma hematologic cancer hepatocellular carcinoma herpes simplex high grade glioma hyperuricemia immune system disease inflammatory and toxic neuropathy intellectual disability large intestine cancer learning disability liver cancer locked-in syndrome lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia macrocytic anemia malaria maxillary sinus squamous cell carcinoma melanoma meningoencephalitis molybdenum cofactor deficiency type A monoclonal gammopathy of uncertain significance nervous system disease neuroblastoma neurodegenerative disease neuropathy obsolete T lymphocyte deficiency obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma periodontal disease periodontitis peripheral T-cell lymphoma peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pneumonia polyneuropathy primary immunodeficiency disease prostate cancer prostate carcinoma purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder quadriplegia reflex sympathetic dystrophy retinal vein occlusion sarcomatoid carcinoma severe combined immunodeficiency sinusitis skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy substance abuse substance-related disorder systemic lupus erythematosus thyroid gland medullary carcinoma trypanosomiasis tuberculosis urinary bladder cancer urinary tract obstruction vascular disease
5023	purinergic receptor P2X 1	P2RX1	Homo sapiens (human)
22953	purinergic receptor P2X 2	P2RX2	Homo sapiens (human)

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