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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 **8101 - 8125** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
60559	signal peptidase complex subunit 3	SPCS3	Homo sapiens (human)
149954	BPI fold containing family B member 4	BPIFB4	Homo sapiens (human)
347468	olfactory receptor family 13 subfamily H member 1	OR13H1	Homo sapiens (human)
5167	ectonucleotide pyrophosphatase/phosphodiesterase 1	ENPP1 Aliases: PC-1 PCA1	Homo sapiens (human)	Ehlers-Danlos syndrome HCL-V Laron syndrome McCune Albright syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired hyperkeratosis acute myocardial infarction adult astrocytic tumor allergic asthma amelogenesis imperfecta anaplastic astrocytoma anemia angioid streaks ankylosing spondylitis ankylosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autosomal dominant hypophosphatemic rickets autosomal recessive hypophosphatemic rickets autosomal recessive osteopetrosis 7 bicuspid aortic valve disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile duct disease blindness bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease carotid artery disease cartilage disease cerebral infarction cerebrovascular disease childhood astrocytic tumor childhood cerebral astrocytoma cholangiocarcinoma chondrocalcinosis chronic kidney disease colorectal cancer colorectal carcinoma congenital hypothyroidism congenital toxoplasmosis congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis end stage renal disease endometriosis of ovary endometriosis of uterus endometriosis enthesopathy essential hypertension exanthem fibrillary astrocytoma gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance hairy cell leukemia heart disease hepatitis C hepatocellular carcinoma hereditary elliptocytosis herpes simplex high grade glioma hypercalcemia hypercementosis hyperglycemia hyperinsulinism hyperphosphatemic familial tumoral calcinosis hypertension hypophosphatemia hypothyroidism insulinoma intermittent claudication intrinsic asthma juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer linear nevus sebaceous syndrome liver cancer lung benign neoplasm lung cancer lung carcinoma macrocytic anemia malignant astrocytoma melanoma mitral valve insufficiency mitral valve prolapse mongolian spot monoclonal gammopathy of uncertain significance morbid obesity mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple myeloma musculoskeletal system disease myelitis myocardial infarction myopia myxedema nephritis nephrocalcinosis nephrosis neurogenic arthropathy nodular prostate nonepidermolytic palmoplantar keratoderma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosclerosis otitis media palmoplantar keratosis pancreatic cancer pancreatic carcinoma periarthritis perinatal intestinal perforation peripheral artery disease peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma plasmacytoma pneumocystosis polycystic ovary syndrome polycythemia vera polycythemia postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pseudoxanthoma elasticum pulmonary valve stenosis pyoureter restrictive cardiomyopathy retinal disease retinitis rheumatoid arthritis rickets sarcomatoid carcinoma scoliosis sensorineural hearing loss silent myocardial infarction skin melanoma spondyloarthropathy spondylosis steatotic liver disease subependymal giant cell astrocytoma suppurative periapical periodontitis tendinitis tropical sprue tympanosclerosis 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 uremia viral infectious disease
5408	pancreatic lipase related protein 2 (gene/pseudogene)	PNLIPRP2 Aliases: PLRP2	Homo sapiens (human)	acute pancreatitis pancreatitis
10591	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	DNPH1 Aliases: dJ330M21.3 rcl	Homo sapiens (human)
26339	olfactory receptor family 5 subfamily K member 1	OR5K1	Homo sapiens (human)
57510	exportin 5	XPO5	Homo sapiens (human)
79736	transcription elongation factor, mitochondrial	TEFM	Homo sapiens (human)
29123	ankyrin repeat domain containing 11	ANKRD11	Homo sapiens (human)
64101	leucine rich repeat containing 4	LRRC4	Homo sapiens (human)
55107	anoctamin 1	ANO1	Homo sapiens (human)
80124	valosin containing protein interacting protein 1	VCPIP1	Homo sapiens (human)
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
54949	succinate dehydrogenase complex assembly factor 2	SDHAF2	Homo sapiens (human)
23547	leukocyte immunoglobulin like receptor A4	LILRA4	Homo sapiens (human)
23705	cell adhesion molecule 1	CADM1	Homo sapiens (human)
51384	Wnt family member 16	WNT16	Homo sapiens (human)
85459	centrosomal protein 295	CEP295	Homo sapiens (human)
3292	hydroxysteroid 17-beta dehydrogenase 1	HSD17B1 Aliases: Estradiol 17-beta-dehydrogenase-1 HSD17 MGC138140 SDR28C1 short chain dehydrogenase/reductase family 28CE, member 1	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 Pick's disease Reye syndrome Sertoli-Leydig cell tumor T-cell acute lymphoblastic leukemia adenocarcinoma adenoma breast cancer breast carcinoma breast disease breast fibrocystic disease bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera choriocarcinoma colorectal cancer colorectal carcinoma congenital adrenal hyperplasia cribriform carcinoma cystic kidney disease embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis follicular adenoma granular cell carcinoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome infertility invasive ductal carcinoma lactocele large intestine cancer leiomyoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease male breast cancer microcystic adenoma microglandular adenosis myofibroma nodular prostate non-congenital cyst of kidney obesity osteoporosis ovarian cancer ovarian carcinoma papillary adenoma placenta cancer placental insufficiency polycystic ovary syndrome prostate cancer prostate carcinoma prostatic adenoma sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer uterine disease uterine fibroid
160851	diacylglycerol kinase eta	DGKH Aliases: DGKeta	Homo sapiens (human)	allergic asthma asthma attention deficit hyperactivity disorder bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma disease of mental health esophageal cancer esophageal carcinoma intermittent explosive disorder intrinsic asthma lung benign neoplasm lung cancer lung carcinoma melancholic depression mood disorder nephrolithiasis neurotic disorder obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia panic disorder psychotic disorder schizophrenia uric acid nephrolithiasis
654346	galectin 9C	LGALS9C	Homo sapiens (human)	cancer
9942	xylulokinase	XYLB	Homo sapiens (human)	cerebral infarction cerebrovascular disease
93986	forkhead box P2	FOXP2	Homo sapiens (human)
5360	phospholipid transfer protein	PLTP	Homo sapiens (human)

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