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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 **9826 - 9850** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	Homo sapiens (human)	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
56052	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 Aliases: CDG1K HMAT1 HMT-1 Mat-1	Homo sapiens (human)	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
27125	ALF transcription elongation factor 4	AFF4	Homo sapiens (human)
3899	ALF transcription elongation factor 3	AFF3	Homo sapiens (human)
2334	ALF transcription elongation factor 2	AFF2	Homo sapiens (human)
84335	AKT1 substrate 1	AKT1S1	Homo sapiens (human)
10000	AKT serine/threonine kinase 3	AKT3	Homo sapiens (human)
208	AKT serine/threonine kinase 2	AKT2	Homo sapiens (human)	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
207	AKT serine/threonine kinase 1	AKT1	Homo sapiens (human)	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
254268	AKNA domain containing 1	AKNAD1	Homo sapiens (human)
84883	AIF family member 2	AIFM2	Homo sapiens (human)
113146	AHNAK nucleoprotein 2	AHNAK2	Homo sapiens (human)
79026	AHNAK nucleoprotein	AHNAK	Homo sapiens (human)
60509	AGBL carboxypeptidase 5	AGBL5	Homo sapiens (human)
340351	AGBL carboxypeptidase 3	AGBL3	Homo sapiens (human)
123624	AGBL carboxypeptidase 1	AGBL1	Homo sapiens (human)
165	AE binding protein 1	AEBP1	Homo sapiens (human)
11047	ADRM1 26S proteasome ubiquitin receptor	ADRM1	Homo sapiens (human)
116969	ADP-ribosyltransferase 5	ART5 Aliases: ARTC5	Homo sapiens (human)	cholera
420	ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)	ART4 Aliases: ARTC4 CD297 DOK1 NAD(+)--protein-arginine ADP-ribosyltransferase 4	Homo sapiens (human)	carotid artery thrombosis carotid stenosis conjunctivitis
419	ADP-ribosyltransferase 3 (inactive)	ART3 Aliases: ARTC3	Homo sapiens (human)	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
417	ADP-ribosyltransferase 1	ART1 Aliases: ART2 ARTC1 CD296	Homo sapiens (human)	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
54936	ADP-ribosylserine hydrolase	ADPRS Aliases: ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	Homo sapiens (human)	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
113622	ADP-ribosylhydrolase like 1	ADPRHL1	Homo sapiens (human)
141	ADP-ribosylarginine hydrolase	ADPRH Aliases: ARH1 [Protein ADP-ribosylarginine] hydrolase	Homo sapiens (human)	autosomal recessive hypercholesterolemia cancer cardiomyopathy cholera endomyocardial fibrosis familial hypercholesterolemia hypertrophic cardiomyopathy ovarian cancer ovarian carcinoma

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