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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 **8501 - 8525** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
91012	ceramide synthase 5	CERS5 Aliases: FLJ25304 MGC45411 Trh4	Homo sapiens (human)	cancer colon cancer colonic benign neoplasm colorectal cancer congestive heart failure embryoma essential hypertension hypertension large intestine cancer rectal benign neoplasm rectum adenocarcinoma rectum cancer
79603	ceramide synthase 4	CERS4 Aliases: FLJ12089 Trh1	Homo sapiens (human)	atopic dermatitis breast cancer breast carcinoma cancer chronic kidney disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatitis embryoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer
204219	ceramide synthase 3	CERS3 Aliases: MGC27091	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome Weill-Marchesani syndrome achondroplasia acrodermatitis alopecia anhidrosis atopic dermatitis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis dermatitis ectropion hypohidrosis ichthyosis keratitis keratoconjunctivitis keratosis follicularis mongolian spot nonepidermolytic palmoplantar keratoderma obsolete congenital ichthyosiform erythroderma palmoplantar keratosis pseudoxanthoma elasticum sensorineural hearing loss
29956	ceramide synthase 2	CERS2 Aliases: FLJ10243 SP260	Homo sapiens (human)	bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chronic fatigue syndrome chronic kidney disease colitis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis gastroenteritis giant cell glioblastoma glioblastoma heart disease high grade glioma hyperglycemia ileitis ileocolitis inflammatory bowel disease melanoma multiple sclerosis myelitis papillary adenocarcinoma papillary renal cell carcinoma primary cutaneous amyloidosis prostate cancer prostate carcinoma sarcomatoid carcinoma sciatic neuropathy skin melanoma steatotic liver disease thyroid gland papillary carcinoma type 2 diabetes mellitus urinary bladder cancer
10715	ceramide synthase 1	CERS1 Aliases: LAG1 UOG1	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis blepharospasm cancer central nervous system cancer congestive heart failure coronary artery disease dementia dengue disease dentatorubral-pallidoluysian atrophy double outlet right ventricle early myoclonic encephalopathy embryoma focal hand dystonia gliosarcoma hand, foot and mouth disease head and neck squamous cell carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability learning disability malaria mixed glioma multiple types of congenital heart defects 6 neuroblastoma papillary adenocarcinoma papillary renal cell carcinoma primary spontaneous pneumothorax progressive myoclonus epilepsy 4 progressive myoclonus epilepsy 8 progressive myoclonus epilepsy steatotic liver disease tetralogy of Fallot thyroid gland papillary carcinoma ulcerative colitis viral infectious disease visceral heterotaxy visual epilepsy yellow fever
64781	ceramide kinase	CERK Aliases: DKFZp434E0211 FLJ21430 FLJ23239 KIAA1646 LK4 dA59H18.2 dA59H18.3 hCERK	Homo sapiens (human)	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
51148	cerebral endothelial cell adhesion molecule	CERCAM	Homo sapiens (human)
9350	cerberus 1, DAN family BMP antagonist	CER1	Homo sapiens (human)
10390	choline/ethanolamine phosphotransferase 1	CEPT1	Homo sapiens (human)	diabetic ketoacidosis obesity obsolete type 1 diabetes mellitus 9 retinal disease systemic lupus erythematosus 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
64793	centrosomal protein 85	CEP85	Homo sapiens (human)
84131	centrosomal protein 78	CEP78	Homo sapiens (human)
23177	centrosomal protein 68	CEP68	Homo sapiens (human)
9702	centrosomal protein 57	CEP57	Homo sapiens (human)
80817	centrosomal protein 44	CEP44	Homo sapiens (human)
11116	centrosomal protein 43	CEP43	Homo sapiens (human)
95681	centrosomal protein 41	CEP41	Homo sapiens (human)
9857	centrosomal protein 350	CEP350	Homo sapiens (human)
85459	centrosomal protein 295	CEP295	Homo sapiens (human)
55125	centrosomal protein 192	CEP192	Homo sapiens (human)
283638	centrosomal protein 170B	CEP170B	Homo sapiens (human)
9859	centrosomal protein 170	CEP170	Homo sapiens (human)
22897	centrosomal protein 164	CEP164	Homo sapiens (human)
22995	centrosomal protein 152	CEP152	Homo sapiens (human)
9662	centrosomal protein 135	CEP135	Homo sapiens (human)
22994	centrosomal protein 131	CEP131	Homo sapiens (human)

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