GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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	July 8, 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 **1276 - 1300** of **1582** in total

« First

‹ Prev

…

48

49

50

51

52

53

54

55

56

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
3628	inositol polyphosphate-1-phosphatase	INPP1	Homo sapiens (human)	bipolar disorder cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer obsolete major affective disorder 2
1591	cytochrome P450 family 24 subfamily A member 1	CYP24A1 Aliases: CP24 P450-CC24 lncBCAS1-4_1	Homo sapiens (human)	Alport syndrome B-cell lymphoma Behcet's disease Langerhans-cell histiocytosis Vogt-Koyanagi-Harada disease X-linked dominant hypophosphatemic rickets abdominal obesity-metabolic syndrome 1 actinic keratosis acute pancreatitis adenocarcinoma adenoma age related macular degeneration aggressive systemic mastocytosis allergic asthma ankylosing spondylitis aortic valve disease 2 aortic valve stenosis asthma atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cartilage disease cerebral infarction cerebral palsy cerebrovascular disease cholangiocarcinoma chromophobe renal cell carcinoma chronic kidney disease ciliary body disease clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal adenocarcinoma colorectal adenoma colorectal cancer colorectal carcinoma connective tissue disease craniosynostosis cribriform carcinoma cutaneous fibrous histiocytoma degeneration of macula and posterior pole dermatitis diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma diffuse large B-cell lymphoma embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial hypocalciuric hypercalcemia 1 familial hypocalciuric hypercalcemia 2 familial hypocalciuric hypercalcemia 3 familial hypocalciuric hypercalcemia follicular adenoma generalized atherosclerosis gestational diabetes glomerulonephritis granular cell carcinoma hemiplegia hepatitis C hepatocellular carcinoma hidradenoma hypercalcemia hyperphosphatemia hypertension immune system disease intellectual disability intrahepatic cholangiocarcinoma intrinsic asthma inverted follicular keratosis iris disease isolated cleft palate keratoacanthoma kidney disease kidney failure large intestine cancer learning disability leiomyoma leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphadenitis lymphoma macular degeneration mast-cell sarcoma mastitis melanoacanthoma melanoma microcystic adenoma multiple endocrine neoplasia type 1 multiple sclerosis myofibroma nephritis nephrocalcinosis nephrolithiasis nephrosis nodular goiter non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ocular melanoma oral squamous cell carcinoma osteomalacia osteoporosis ovary adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis panuveitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis phosphorus metabolism disease pre-eclampsia prostate cancer prostate carcinoma psoriasis psoriatic arthritis pulmonary valve stenosis pustulosis of palm and sole pyoureter rectum cancer reflex sympathetic dystrophy relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma renal tubular acidosis reticulosarcoma retinoblastoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis secondary hyperparathyroidism skin benign neoplasm skin cancer skin disease skin melanoma skin papilloma skin tag spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy squamous cell carcinoma syringoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma 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 ulcerative colitis uremia uric acid nephrolithiasis uterine corpus cancer uterine fibroid uveitis
55768	N-glycanase 1	NGLY1 Aliases: FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	Homo sapiens (human)	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
23553	hyaluronidase 4	HYAL4	Homo sapiens (human)	oxyphilic adenoma renal oncocytoma
123099	delta 4-desaturase, sphingolipid 2	DEGS2 Aliases: DES2 FADS8 dihydroceramide desaturase 2 sphingolipid delta(4)-desaturase 2	Homo sapiens (human)	acquired immunodeficiency syndrome colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis disease of mental health human immunodeficiency virus infectious disease large intestine cancer neurodegenerative disease obesity psychotic disorder schizophrenia type 2 diabetes mellitus
5950	retinol binding protein 4	RBP4	Homo sapiens (human)	acute pyelonephritis atherosclerosis cerebral infarction chronic kidney disease colon adenoma congestive heart failure coronary artery disease diabetic angiopathy diabetic retinopathy dilated cardiomyopathy essential hypertension familial hypercholesterolemia gallbladder cancer gestational diabetes hyperinsulinism hypertension liver cirrhosis myocardial infarction obesity pre-eclampsia proliferative diabetic retinopathy psoriasis severe pre-eclampsia systemic scleroderma type 2 diabetes mellitus
117145	thioesterase superfamily member 4	THEM4 Aliases: C-terminal modulator protein CTMP	Homo sapiens (human)	amyotrophic lateral sclerosis attention deficit hyperactivity disorder breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma liver cancer lung benign neoplasm lung cancer lung carcinoma mixed glioma pancreatic adenocarcinoma progressive muscular atrophy type 2 diabetes mellitus
148789	beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2 Aliases: MGC39558	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
5260	phosphorylase kinase catalytic subunit gamma 1	PHKG1	Homo sapiens (human)
1634	decorin	DCN Aliases: DSPG2 SLRR1B decorin proteoglycan	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 CADASIL 1 CADASIL Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Kaposi's sarcoma Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Lyme disease Marfan syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peyronie's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Rothmund-Thomson syndrome SADDAN Seckel syndrome Silver-Russell syndrome Werner syndrome X-linked Aarskog syndrome abdominal aortic aneurysm achondrogenesis type IB achondroplasia actinic keratosis acute interstitial pneumonia acute myocardial infarction adult respiratory distress syndrome allergic asthma alopecia amyloidosis angiokeratoma angiosarcoma angle-closure glaucoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrophic gastritis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy balanitis xerotica obliterans basal cell carcinoma benign breast phyllodes tumor bladder carcinoma bladder neck obstruction bone disease bone giant cell tumor bone osteosarcoma brain cancer breast cancer breast carcinoma breast fibroadenoma breast fibrocystic disease breast malignant phyllodes tumor breast metaplastic carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cartilage disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cherubism childhood angiosarcoma childhood osteosarcoma cholestasis chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic interstitial cystitis chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin clear cell renal cell carcinoma collagen disease collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital disorder of glycosylation congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy congenital stromal corneal dystrophy congestive heart failure connective tissue disease cornea plana corneal neovascularization coronary artery disease coronary thrombosis crescentic glomerulonephritis cutis laxa cystic fibrosis diabetes mellitus diabetic ketoacidosis distal myopathy embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epidermolysis bullosa dystrophica epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exostosis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis female stress incontinence gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance heart disease hepatocellular carcinoma hiatus hernia high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy hypochondroplasia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inclusion body myositis intellectual disability interstitial cystitis interstitial nephritis intestinal benign neoplasm intestinal cancer intrinsic asthma invasive ductal carcinoma kidney disease kidney failure kidney hypertrophy large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer learning disability limb-girdle muscular dystrophy lipoma liver cancer liver carcinoma liver cirrhosis localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma mal de Meleda malignant peripheral nerve sheath tumor mesangial proliferative glomerulonephritis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microglandular adenosis mixed glioma multiple myeloma multiple sclerosis multiple symmetric lipomatosis muscular dystrophy myeloproliferative disorder with eosinophilia myocardial infarction myocarditis myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myxofibrosarcoma neovascular inflammatory vitreoretinopathy nephritis nephrosclerosis nephrosis neurilemmoma neuroblastoma neurofibrosarcoma neurogenic arthropathy newborn respiratory distress syndrome nonpapillary renal cell carcinoma obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma papilloma periarthritis placental insufficiency pleomorphic lipoma polycystic kidney disease 1 polycystic ovary syndrome posterior amorphous corneal dystrophy postinflammatory pulmonary fibrosis prediabetes syndrome primary angle-closure glaucoma primary open angle glaucoma primary pulmonary hypertension progeria prostate cancer prostate carcinoma proteinuria pseudoachondroplasia pseudosarcomatous fibromatosis pulmonary fibrosis pulmonary hypertension pyelitis pyelonephritis pyoureter rapidly progressive glomerulonephritis recessive dystrophic epidermolysis bullosa renal carcinoma renal cell carcinoma renal infectious disease restrictive dermopathy retinal disease retinitis rippling muscle disease 2 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma seborrheic keratosis silent myocardial infarction situs inversus skin atrophy skin disease spindle cell sarcoma squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tendinitis thrombosis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease transitional cell carcinoma tuberous sclerosis 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 urinary bladder cancer uterine corpus cancer vascular cancer vascular disease vulva carcinoma vulvar dystrophy
284541	cytochrome P450 family 4 subfamily A member 22	CYP4A22	Homo sapiens (human)	autosomal recessive polycystic kidney disease hepatocellular carcinoma hypertension liver cancer polycystic kidney disease 4
112817	4-hydroxy-2-oxoglutarate aldolase 1	HOGA1 Aliases: DHDPS2 FLJ37472 N-acetylneuraminate pyruvate lyase 2 (putative) NPL2 dihydrodipicolinate synthetase homolog 2 (E. coli)	Homo sapiens (human)	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 3 primary hyperoxaluria
929	CD14 molecule	CD14	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Behcet's disease Brucella melitensis brucellosis Clostridium difficile colitis Clouston syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Crohn's colitis Crohn's disease Down syndrome Gaucher's disease Graves' disease Hirschsprung's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis Lyme disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia West Nile fever X-linked agammaglobulinemia Zika fever Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute chest syndrome acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute pericementitis adenosarcoma adrenal cortical hypofunction adrenoleukodystrophy adult lymphoma adult respiratory distress syndrome aggressive periodontitis alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma allergic disease allergic rhinitis amyloidosis amyotrophic lateral sclerosis ankylosing spondylitis aortic valve disease 2 aortic valve stenosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis atrial fibrillation auditory system disease autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant familial periodic fever autosomal dominant polycystic kidney disease autosomal recessive hypercholesterolemia autosomal recessive polycystic kidney disease avian influenza bacterial infectious disease bacterial meningitis bacterial sepsis benign mesothelioma bile duct adenocarcinoma bile duct carcinoma biliary atresia biliary tract disease black piedra bladder carcinoma blood coagulation disease bone giant cell tumor bone osteosarcoma brain stem infarction breast cancer breast carcinoma bronchiolitis bronchus cancer bronchus carcinoma brucellosis burning mouth syndrome cancer carcinoma cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cataract cavernous hemangioma celiac disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma choledochal cyst cholestasis chorioamnionitis chorioangioma chromophobe renal cell carcinoma chromosome 5q deletion syndrome chronic apical periodontitis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease ciliary body disease clear cell renal cell carcinoma coccidioidomycosis cognitive disorder colitis collecting duct carcinoma colorectal cancer colorectal carcinoma common cold common variable immunodeficiency complement deficiency congenital hypogammaglobulinemia congestive heart failure conjunctivitis coronary artery disease coronary thrombosis croup cystic fibrosis dengue disease dengue hemorrhagic fever dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic macular edema diabetic retinopathy diarrhea disease of metabolism disseminated intravascular coagulation distal arthrogryposis dysgerminoma eclampsia eczema herpeticum embryoma encephalomyelitis enthesopathy epithelioid sarcoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exostosis fibrodysplasia ossificans progressiva food allergy galactosemia gallbladder disease gastroenteritis gastrointestinal stromal tumor giant cell glioblastoma glioblastoma glomus tumor glucose intolerance goiter gout heart disease hemangioma hemochromatosis type 1 hemochromatosis hepatic coma hepatic encephalopathy hepatitis B hepatitis C hepatitis hepatocellular carcinoma histiocytoid hemangioma histoplasmosis human immunodeficiency virus infectious disease hyperinsulinism hypertension hyperthyroidism ileitis ileocolitis immune system disease infertility inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome intermittent claudication interstitial lung disease intracranial aneurysm intrahepatic cholangiocarcinoma intramuscular hemangioma intrinsic asthma invasive ductal carcinoma iris disease irritable bowel syndrome juvenile myelomonocytic leukemia juvenile rheumatoid arthritis keratoconjunctivitis sicca kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leprosy leukemia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lymphangioma lymphoblastic lymphoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 major depressive disorder malaria malignant mesothelioma marasmus mastitis meconium aspiration syndrome melancholic depression melanoma melioidosis microscopic colitis middle cerebral artery infarction migraine mitral valve stenosis multiple myeloma multiple sclerosis myelodysplastic syndrome myocardial infarction myositis ossificans nephroblastoma nephrolithiasis neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibromatosis 1 neurofibromatosis neurogenic arthropathy neuropathy newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete dyspepsia obsolete inherited blood coagulation disease obsolete malignant histiocytosis obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive jaundice optic neuritis osteoarthritis osteonecrosis osteoporosis osteosarcoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis panuveitis papillary renal cell carcinoma parapsoriasis paroxysmal nocturnal hemoglobinuria paroxysmal nonkinesigenic dyskinesia 1 patent ductus arteriosus peptic ulcer disease periapical periodontitis periarthritis perinatal necrotizing enterocolitis periodontal disease periodontitis periodontosis peripheral artery disease peripheral nervous system disease peripheral vascular disease pituitary-dependent Cushing's disease pneumonia polyneuropathy prediabetes syndrome primary biliary cholangitis primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis prion disease progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma protein-energy malnutrition psoriasis psoriatic arthritis pulmonary sarcoidosis pulmonary tuberculosis purpura fulminans pustulosis of palm and sole relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease reticulosarcoma rheumatoid arthritis rhinitis sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma sclerosing cholangitis seborrheic keratosis secondary syphilis senile cataract severe acute respiratory syndrome sickle cell anemia silent myocardial infarction skin disease skin melanoma spindle cell sarcoma spondyloarthropathy spondylosis sporotrichosis status asthmaticus steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome superficial mycosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tendinitis thromboangiitis obliterans thrombophilia thyroid gland disease thyrotoxicosis tuberculosis tuberculous pneumothorax 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 ulcerative colitis uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction uveitis uveoparotid fever vasomotor rhinitis viral infectious disease viral meningitis visceral leishmaniasis white piedra yellow fever
23396	phosphatidylinositol-4-phosphate 5-kinase type 1 gamma	PIP5K1C Aliases: KIAA0589 LCCS3 PIP5Kgamma	Homo sapiens (human)	breast cancer breast carcinoma cancer invasive ductal carcinoma lethal congenital contracture syndrome 3 rabies
30	acetyl-CoA acyltransferase 1	ACAA1 Aliases: Lnc-Myd88 peroxisomal 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis Zellweger syndrome allergic asthma asthma beta-ketothiolase deficiency carotid artery disease hepatocellular carcinoma intrinsic asthma liver cancer lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma
1609	diacylglycerol kinase theta	DGKQ Aliases: DAGK DAGK7	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 Sjogren's syndrome cerebral degeneration diabetes mellitus diabetic ketoacidosis hepatocellular carcinoma keratoconjunctivitis sicca liver cancer myositis primary biliary cholangitis rheumatoid arthritis scleroderma systemic lupus erythematosus systemic scleroderma type 2 diabetes mellitus
51228	glycolipid transfer protein	GLTP	Homo sapiens (human)	colon carcinoma colorectal cancer colorectal carcinoma hepatitis C large intestine cancer
57134	mannosidase alpha class 1C member 1	MAN1C1 Aliases: HMIC	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
29880	ALG5 dolichyl-phosphate beta-glucosyltransferase	ALG5 Aliases: bA421P11.2	Homo sapiens (human)	congenital disorder of glycosylation type I polycystic kidney disease
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 Aliases: alpha2delta-4	Homo sapiens (human)	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
94005	phosphatidylinositol glycan anchor biosynthesis class S	PIGS Aliases: GPI transamidase component PIG-S GPI transamidase subunit PIG-S	Homo sapiens (human)	breast cancer cancer congenital nystagmus developmental and epileptic encephalopathy 95 dissociated nystagmus embryoma epilepsy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gingival hypertrophy gingival overgrowth hepatocellular carcinoma liver cancer microcephaly omphalocele pathologic nystagmus spontaneous ocular nystagmus umbilical hernia visual epilepsy
1727	cytochrome b5 reductase 3	CYB5R3 Aliases: B5R NADH-cytochrome b5 reductase 3	Homo sapiens (human)	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension estrogen-receptor negative breast cancer exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
341880	solute carrier family 35 member F4	SLC35F4 Aliases: FLJ37712	Homo sapiens (human)	acquired immunodeficiency syndrome bipolar disorder
114805	polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 Aliases: GalNAc-T13 KIAA1918 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 polypeptide GalNAc transferase 13	Homo sapiens (human)	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
166012	carbohydrate sulfotransferase 13	CHST13 Aliases: C4ST3 chondroitin 4-sulfotransferase 3	Homo sapiens (human)	arthritis arthropathy osteoarthritis primary pulmonary hypertension

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements