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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 **6126 - 6150** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
10284	Sin3A associated protein 18	SAP18	Homo sapiens (human)
10475	tripartite motif containing 38	TRIM38	Homo sapiens (human)
196513	decapping mRNA 1B	DCP1B Aliases: FLJ31638	Homo sapiens (human)
3115	major histocompatibility complex, class II, DP beta 1	HLA-DPB1	Homo sapiens (human)
440689	H2B clustered histone 18	H2BC18	Homo sapiens (human)
4247	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT2 Aliases: GNT-II	Homo sapiens (human)	Laron syndrome achondroplasia antithrombin III deficiency autosomal recessive chronic granulomatous disease 3 cancer chronic granulomatous disease clubfoot congenital disorder of glycosylation type II congenital disorder of glycosylation type IIa congenital disorder of glycosylation congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia craniosynostosis diabetes mellitus diabetic ketoacidosis disease of metabolism epilepsy factor XII deficiency gestational diabetes gingival hypertrophy gingival overgrowth microcephaly neuroblastoma obesity protein C deficiency protein S deficiency sensorineural hearing loss stereotypic movement disorder syndromic X-linked intellectual disability 94 thrombophilia type 2 diabetes mellitus ventricular septal defect visual epilepsy
131601	transmembrane protein adipocyte associated 1	TPRA1	Homo sapiens (human)
1233	C-C motif chemokine receptor 4	CCR4	Homo sapiens (human)
9034	C-C motif chemokine receptor like 2	CCRL2	Homo sapiens (human)
219865	olfactory receptor family 8 subfamily G member 5	OR8G5	Homo sapiens (human)
3290	hydroxysteroid 11-beta dehydrogenase 1	HSD11B1 Aliases: SDR26C1 short chain dehydrogenase/reductase family 26C, member 1	Homo sapiens (human)	ACTH-secreting pituitary adenoma Addison's disease 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 Clostridium difficile colitis Norum disease Pick's disease Reye syndrome Tangier disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acidophil adenoma acromegaly actinic keratosis acute myocardial infarction adamantinous craniopharyngioma adenocarcinoma adenoma adrenal cortical hypofunction adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy age related macular degeneration allergic contact dermatitis alopecia amnestic disorder amyloidosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis atrial fibrillation bone osteosarcoma breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma cancer cardiovascular system disease cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral degeneration cerebrotendinous xanthomatosis childhood osteosarcoma choreaacanthocytosis chronic ethmoiditis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cortisone reductase deficiency 2 cortisone reductase deficiency craniopharyngioma craniosynostosis cribriform carcinoma degeneration of macula and posterior pole dementia depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism dissociative amnesia dysthymic disorder embryoma essential hypertension familial hyperlipidemia fibromyalgia follicular adenoma functionless pituitary adenoma gallbladder disease gastrointestinal stromal tumor gestational diabetes glaucoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma hyperandrogenism hyperglycemia hyperhomocysteinemia hyperinsulinism hyperpituitarism hypertension hypolipoproteinemia inflammatory bowel disease irritable bowel syndrome large intestine cancer liver cancer liver disease lung cancer macular degeneration major depressive disorder malaria melancholic depression melanoma microcystic adenoma myocardial infarction myositis neurocirculatory asthenia neurotic disorder nutmeg liver obesity obsolete Cushing's syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis osteosarcoma papillary adenoma papillary craniopharyngioma pituitary-dependent Cushing's disease pleural tuberculosis pneumonia polycystic ovary syndrome postpartum depression pre-eclampsia prediabetes syndrome primary hyperaldosteronism prostate cancer prostate carcinoma psychotic disorder pulmonary tuberculosis retrograde amnesia rheumatoid arthritis seborrheic keratosis silent myocardial infarction skin benign neoplasm skin cancer skin disease skin melanoma status epilepticus steatotic liver disease synovitis systemic lupus erythematosus tenosynovitis tuberculous pneumothorax tubular adenocarcinoma 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 type 2 diabetes mellitus
84940	coronin 6	CORO6	Homo sapiens (human)
8493	protein phosphatase, Mg2+/Mn2+ dependent 1D	PPM1D	Homo sapiens (human)
9778	KIAA0232	KIAA0232	Homo sapiens (human)
10371	semaphorin 3A	SEMA3A	Homo sapiens (human)
2297	forkhead box D1	FOXD1	Homo sapiens (human)
284312	zinc finger and SCAN domain containing 1	ZSCAN1	Homo sapiens (human)
51101	zinc finger C2HC-type containing 1A	ZC2HC1A	Homo sapiens (human)
4193	MDM2 proto-oncogene	MDM2	Homo sapiens (human)
127343	diencephalon/mesencephalon homeobox 1	DMBX1	Homo sapiens (human)
4891	solute carrier family 11 member 2	SLC11A2	Homo sapiens (human)
6929	transcription factor 3	TCF3	Homo sapiens (human)
11322	transmembrane channel like 6	TMC6	Homo sapiens (human)
4957	outer dense fiber of sperm tails 2	ODF2	Homo sapiens (human)
170691	ADAM metallopeptidase with thrombospondin type 1 motif 17	ADAMTS17	Homo sapiens (human)

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