GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **5126 - 5150** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
11343	monoglyceride lipase	MGLL HU-K5 MAGL MGL monoacylglycerol lipase	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 Balo concentric sclerosis Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adenosquamous carcinoma adrenoleukodystrophy agnosia alcohol dependence alcohol use disorder alternating hemiplegia of childhood amyotrophic lateral sclerosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascending cholangitis atherosclerosis atopic dermatitis autonomic neuropathy bacterial sepsis bone cancer bone disease bone osteosarcoma brain stem infarction breast cancer breast carcinoma breast medullary carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cardiac arrest cardiovascular system disease cartilage disease central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood osteosarcoma cholangitis cholesteatoma cholinergic urticaria chronic fatigue syndrome chronic interstitial cystitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma dermatitis diabetes mellitus embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma epilepsy follicular adenoma gastric ulcer gastrointestinal stromal tumor generalized anxiety disorder gestational diabetes glaucoma granular cell carcinoma heart disease hepatitis hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease interstitial cystitis invasive ductal carcinoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma microcystic adenoma middle cerebral artery infarction migraine myelitis myocardial infarction narcolepsy nervous system disease neuroblastoma neurodegenerative disease neuropathy obesity osteoporosis osteosarcoma papillary adenoma peripheral nervous system disease phobic disorder polyneuropathy polyp of middle ear primary sclerosing cholangitis progressive muscular atrophy prostate cancer prostate carcinoma reflex sympathetic dystrophy sclerosing cholangitis silent myocardial infarction skin melanoma squamous cell carcinoma status epilepticus steatotic liver disease substance abuse substance-related disorder suppurative cholangitis thrombophilia tongue squamous cell carcinoma tropical sprue tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uterine corpus cancer varicocele visual epilepsy
11342	ring finger protein 13	RNF13
11341	stimulator of chondrogenesis 1	SCRG1
11340	exosome component 8	EXOSC8
11339	Opa interacting protein 5	OIP5
11338	U2 small nuclear RNA auxiliary factor 2	U2AF2
11332	acyl-CoA thioesterase 7	ACOT7 ACH1 ACT BACH CTE-II LACH1 Long chain acyl-CoA thioester hydrolase MGC1126 brain acyl CoA hydrolase hBACH	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 Clouston syndrome Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium vivax malaria Reye syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation bacterial infectious disease beta thalassemia blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health distal arthrogryposis dysentery dysthymic disorder eating disorder embryoma epilepsy esophagus squamous cell carcinoma female stress incontinence gallbladder disease gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inclusion body myositis infertility intrinsic asthma kwashiorkor large intestine cancer leprosy liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malaria marasmus melancholic depression mixed glioma multiple sclerosis muscular dystrophy myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nonpapillary renal cell carcinoma nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease osteomyelitis ovarian cancer ovarian carcinoma papillary renal cell carcinoma peripheral nervous system disease peroxisome biogenesis disorder 7A pertussis polyneuropathy postpartum depression pre-eclampsia prediabetes syndrome primary open angle glaucoma primary ovarian insufficiency primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition psychotic disorder pulmonary tuberculosis renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma sick sinus syndrome silent myocardial infarction spermatic cord torsion systemic scleroderma temporal lobe epilepsy thalassemia tuberculosis 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 urethral intrinsic sphincter deficiency viral infectious disease visual epilepsy
11331	prohibitin 2	PHB2
11330	chymotrypsin C	CTRC
11328	FKBP prolyl isomerase 9	FKBP9
11326	V-set and immunoglobulin domain containing 4	VSIG4
11325	DEAD-box helicase 42	DDX42
11322	transmembrane channel like 6	TMC6
11320	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A	MGAT4A GnT-4a GnT-Iva	bipolar disorder cancer colorectal cancer diabetes mellitus disease of metabolism embryoma gestational trophoblastic neoplasm hypoplastic left heart syndrome large intestine cancer pancreatic cancer type 2 diabetes mellitus
11318	G protein-coupled receptor 182	GPR182
11315	Parkinsonism associated deglycase	PARK7
11314	CD300a molecule	CD300A
11313	lysophospholipase 2	LYPLA2 APT-2 acyl-protein thioesterase 2	familial combined hyperlipidemia melanoma skin melanoma
11309	solute carrier organic anion transporter family member 2B1	SLCO2B1
11285	beta-1,4-galactosyltransferase 7	B4GALT7 XGALT-1 beta4Gal-T7 galactosyltransferase I	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type 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 Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy 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 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 bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
11283	cytochrome P450 family 4 subfamily F member 8	CYP4F8	colorectal adenocarcinoma hypertension prostate cancer prostate carcinoma
11282	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	MGAT4B GnT-Ivb	cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
11280	sodium voltage-gated channel alpha subunit 11	SCN11A
11278	KLF transcription factor 12	KLF12
11276	synergin gamma	SYNRG

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