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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 **9001 - 9025** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
27286	sushi repeat containing protein X-linked 2	SRPX2	Homo sapiens (human)
83697	solute carrier family 4 member 9	SLC4A9	Homo sapiens (human)
2208	Fc epsilon receptor II	FCER2 Aliases: C-type lectin domain family 4 member J CD23 CLEC4J FCErII Fc epsilon RII FcepsilonRII	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma CD40 ligand deficiency Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kawasaki disease Langerhans cell sarcoma Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Wiskott-Aldrich syndrome X-linked agammaglobulinemia X-linked hyper IgM syndrome acquired immunodeficiency syndrome acute myeloid leukemia adult lymphoma agammaglobulinemia aggressive systemic mastocytosis allergic asthma asthma atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B cancer central nervous system lymphoma childhood T-cell acute lymphoblastic leukemia childhood leukemia childhood lymphoma chronic eosinophilic leukemia chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia chronic monocytic leukemia clonorchiasis congenital hypogammaglobulinemia dermatitis diabetic ketoacidosis encephalitis encephalomyelitis enterobiasis extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue follicular dendritic cell sarcoma follicular lymphoma food allergy gastric lymphoma gastritis human immunodeficiency virus infectious disease hyper IgM syndrome hyperthyroidism immunodeficiency with hyper IgM type 3 indolent systemic mastocytosis inflammatory bowel disease interdigitating dendritic cell sarcoma interstitial lung disease intestinal schistosomiasis intrinsic asthma leukemia lymphoid leukemia lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma mastocytosis mediastinal gray zone lymphoma multiple myeloma myelitis myeloid leukemia nasopharynx carcinoma obsolete congenital ichthyosiform erythroderma obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma parasitic helminthiasis infectious disease primary mediastinal B-cell lymphoma primary polycythemia prolymphocytic leukemia rheumatoid arthritis schistosomiasis severe acute respiratory syndrome squamous cell carcinoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic mastocytosis thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma trichinosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
3268	ArfGAP with FG repeats 2	AGFG2	Homo sapiens (human)
8808	interleukin 1 receptor like 2	IL1RL2 Aliases: IL-36R IL1R-rp2 IL1RRP2	Homo sapiens (human)	Hirschsprung's disease acrodermatitis allergic rhinitis arthritis arthropathy colitis craniosynostosis dermatitis gastroenteritis hepatitis C hidradenitis suppurativa hidradenitis ileitis ileocolitis impetigo herpetiformis inflammatory bowel disease 1 inflammatory bowel disease osteoarthritis parapsoriasis pompholyx psoriasis pustulosis of palm and sole ulcerative colitis vasomotor rhinitis
319100	trace amine associated receptor 6	TAAR6	Homo sapiens (human)
4647	myosin VIIA	MYO7A	Homo sapiens (human)
1665	DEAH-box helicase 15	DHX15	Homo sapiens (human)
8395	phosphatidylinositol-4-phosphate 5-kinase type 1 beta	PIP5K1B Aliases: MSS4 STM7	Homo sapiens (human)	Friedreich ataxia 1 Friedreich ataxia allergic asthma asthma cancer chronic kidney disease diabetes mellitus diabetic ketoacidosis embryoma intrinsic asthma osteoporosis pancreatic cancer pancreatic carcinoma type 2 diabetes mellitus
30837	suppressor of cytokine signaling 7	SOCS7	Homo sapiens (human)
11245	G protein-coupled receptor 176	GPR176	Homo sapiens (human)
26099	SUZ RNA binding domain containing 1	SZRD1	Homo sapiens (human)
3749	potassium voltage-gated channel subfamily C member 4	KCNC4	Homo sapiens (human)
85446	zinc finger homeobox 2	ZFHX2	Homo sapiens (human)
10468	follistatin	FST	Homo sapiens (human)
81873	actin related protein 2/3 complex subunit 5 like	ARPC5L	Homo sapiens (human)
9688	nucleoporin 93	NUP93	Homo sapiens (human)
100130361	chromosome X open reading frame 49	CXorf49	Homo sapiens (human)
1512	cathepsin H	CTSH	Homo sapiens (human)
23043	TRAF2 and NCK interacting kinase	TNIK	Homo sapiens (human)
989	septin 7	SEPTIN7	Homo sapiens (human)
1399	CRK like proto-oncogene, adaptor protein	CRKL	Homo sapiens (human)
131873	collagen type VI alpha 6 chain	COL6A6	Homo sapiens (human)
5310	polycystin 1, transient receptor potential channel interacting	PKD1 Aliases: PBP Pc-1 TRPP1 polycystin 1 transient receptor potential cation channel, subfamily P, member 1	Homo sapiens (human)	Alzheimer's disease Caroli disease Creutzfeldt-Jakob disease Duchenne muscular dystrophy Guillain-Barre syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Moyamoya disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Streptococcus pneumonia Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute interstitial pneumonia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia anaplastic astrocytoma angiomyolipoma arteriosclerotic cardiovascular disease atherosclerosis autoimmune pancreatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease azoospermia bacterial sepsis bone disease bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer cardiomyopathy cartilage disease cavernous hemangioma central nervous system cancer childhood cerebral astrocytoma chorioangioma chronic kidney disease clear cell renal cell carcinoma collagen disease colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cutaneous fibrous histiocytoma cystic fibrosis cystic kidney disease dermoid cyst dextrocardia diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endomyocardial fibrosis epilepsy episodic kinesigenic dyskinesia 1 essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor growth hormone secreting pituitary adenoma hemangioma hemoglobin H disease hidradenoma high grade glioma histiocytoid hemangioma hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza insulinoma intracranial aneurysm intramuscular hemangioma isolated elevated serum creatine phosphokinase levels juvenile pilocytic astrocytoma keratosis follicularis kidney cancer kidney disease kidney failure large intestine cancer lipoid nephrosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioma lymphopenia malignant astrocytoma melanoma mesangial proliferative glomerulonephritis mixed glioma mongolian spot muscular dystrophy myocardial infarction nephritis nephrolithiasis nephrosis nephrotic syndrome neurofibromatosis 1 neurofibromatosis 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 non-congenital cyst of kidney nutmeg liver obesity osteosarcoma pancreatic cancer pancreatic carcinoma papilloma parapsoriasis pilocytic astrocytoma pneumonia polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease 4 polycystic kidney disease polycystic liver disease polycystic ovary syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter red color blindness renal carcinoma renal cell carcinoma renovascular hypertension rheumatoid arthritis silent myocardial infarction situs inversus skin melanoma skin papilloma skin tag squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma thalassemia thoracic aortic aneurysm thyroid gland anaplastic carcinoma tuberous sclerosis 1 tuberous sclerosis 2 tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis visual epilepsy
23035	PH domain and leucine rich repeat protein phosphatase 2	PHLPP2	Homo sapiens (human)

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