GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **351 - 375** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
79868	ALG13 UDP-N-acetylglucosaminyltransferase subunit	ALG13 CDG1S FLJ23018 MDS031 N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase TDRD13 YGL047W tudor domain containing 13	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
79837	phosphatidylinositol-5-phosphate 4-kinase type 2 gamma	PIP4K2C FLJ22055	bipolar disorder breast cancer cancer diabetic ketoacidosis embryoma lingual-facial-buccal dyskinesia obsolete type 1 diabetes mellitus 9 schizophrenia 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
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 FLJ21934
79796	ALG9 alpha-1,2-mannosyltransferase	ALG9 dol-P-Man dependent alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
79748	lectin, mannose binding 1 like	LMAN1L ERGIC-53L ERGL
79712	glycosyltransferase like domain containing 1	GTDC1 FLJ11753 Hmat-Xa mannosyltransferase-like	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 aphthous stomatitis cerebral degeneration schizophrenia
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
79695	polypeptide N-acetylgalactosaminyltransferase 12	GALNT12 GalNAc-T12 polypeptide GalNAc transferase 12	adenocarcinoma adenoma bilateral breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma
79694	mannosidase endo-alpha	MANEA FLJ12838 endomannosidase glycoprotein endo-alpha-1,2-mannosidase mandaselin	anxiety disorder autoimmune disease autoimmune lymphoproliferative syndrome breast cancer cancer cocaine abuse cocaine dependence delusional disorder disease of mental health embryoma endocarditis immune system disease infective endocarditis morphine dependence panic disorder paranoid schizophrenia phobic disorder polycystic ovary syndrome psychotic disorder social phobia subacute bacterial endocarditis
79691	queuine tRNA-ribosyltransferase accessory subunit 2	QTRT2 FLJ12960
79690	galactose-3-O-sulfotransferase 4	GAL3ST4 FLJ12116	leprosy
79679	V-set domain containing T cell activation inhibitor 1	VTCN1 B7 family member, H4 B7 superfamily member 1 B7-H4 B7H4 B7S1 B7x FLJ22418	B-cell lymphoma IgA glomerulonephritis Langerhans-cell histiocytosis Sjogren's syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy atrophic gastritis autoimmune disease autoimmune lymphoproliferative syndrome benign breast phyllodes tumor bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma celiac disease central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma ciliary body disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma common wart complement deficiency cribriform carcinoma cutaneous Paget's disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma gastritis gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease intrahepatic cholangiocarcinoma invasive ductal carcinoma iris disease juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoma melanoma membranous glomerulonephritis microphthalmia myeloproliferative disorder with eosinophilia nephritis nephrosis neurogenic arthropathy non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma panuveitis papillary carcinoma papillary renal cell carcinoma placental insufficiency pleural tuberculosis primary biliary cholangitis primary immunodeficiency disease pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma synovial sarcoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tuberculosis 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 urinary bladder cancer uterine corpus cancer uveitis uveoparotid fever
79668	poly(ADP-ribose) polymerase family member 8	PARP8 ARTD16 FLJ21308 pART16	colorectal cancer colorectal carcinoma large intestine cancer
79661	nei like DNA glycosylase 1	NEIL1 DNA endonuclease eight-like glycosylase 1 FLJ22402 FPG1 NEI1 hFPG1	Alzheimer's disease Behcet's disease Chandler syndrome Fanconi anemia complementation group A Fanconi anemia Fuchs' endothelial dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acquired immunodeficiency syndrome bile duct adenocarcinoma bile duct carcinoma cancer carcinoma cerebral infarction cerebrovascular disease cholangiocarcinoma chromosome 15q24 deletion syndrome colorectal cancer common variable immunodeficiency corneal disease depressive disorder diabetes mellitus distal arthrogryposis dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hyperlipidemia gallbladder disease glucose intolerance head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease hyperinsulinism intrahepatic cholangiocarcinoma keratoconus large intestine cancer liver cancer liver disease lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression multiple myeloma neurotic disorder obesity obsolete melancholia prediabetes syndrome primary sclerosing cholangitis progeria sarcomatoid carcinoma sclerosing cholangitis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus
79660	protein phosphatase 1 regulatory subunit 3B	PPP1R3B FLJ14005 GL PP1 subunit R4 PPP1R4 hepatic glycogen-targeting subunit, G(L)	Lafora disease alcohol use disorder antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer major depressive disorder maturity-onset diabetes of the young melancholic depression melanoma neurotic disorder obesity obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency skin melanoma steatotic liver disease thrombophilia type 2 diabetes mellitus
79644	steroid 5 alpha-reductase 3	SRD5A3 3-oxo-5-alpha-steroid 4-dehydrogenase (NADP(+)) FLJ13352 SRD5A2L SRD5A2L1 polyprenol reductase	Creutzfeldt-Jakob disease Hailey-Hailey disease Kahrizi syndrome Marfan syndrome Rothmund-Thomson syndrome acquired hyperkeratosis agnosia angioma serpiginosum antithrombin III deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 bilateral optic nerve hypoplasia blindness capillary hemangioma cataract cavernous hemangioma cerebellar ataxia cerebellar disease coloboma congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cutis laxa dermatitis developmental coordination disorder dissociated nystagmus epilepsy eye disease fundus dystrophy glaucoma hypertrichosis hypothyroidism ichthyosis inguinal hernia intellectual disability isolated cleft palate isolated growth hormone deficiency learning disability mal de Meleda microcytic anemia microphthalmia myxedema nonepidermolytic palmoplantar keratoderma obsolete infantile epileptic encephalopathy optic atrophy palmoplantar keratosis pathologic nystagmus pituitary hypoplasia prostate cancer prostate carcinoma protein C deficiency protein S deficiency recurrent corneal erosion restrictive dermopathy situs inversus spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 thrombophilia tuberous sclerosis visual epilepsy
79642	arylsulfatase family member J	ARSJ FLJ23548
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz 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 Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
79611	acyl-CoA synthetase short chain family member 3	ACSS3 FLJ21963	cancer embryoma stomach cancer stomach carcinoma
79603	ceramide synthase 4	CERS4 FLJ12089 Trh1	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
79586	chondroitin polymerizing factor	CHPF CHSY2 CSS2 chondroitin sulfate synthase 2	IgA glomerulonephritis cancer central nervous system cancer depressive disorder dysthymic disorder embryoma gliosarcoma high grade glioma major depressive disorder melancholic depression mixed glioma neurotic disorder obsolete melancholia
79411	galactosidase beta 1 like	GLB1L MGC10771
79369	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4	B3GNT4 B3GN-T4 beta3Gn-T4
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB KIAA1208 MGC4170	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
79154	dehydrogenase/reductase 11	DHRS11 MGC4172 SDR24C1 short chain dehydrogenase/reductase family 24C, member 1	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adrenal gland cancer breast cancer breast carcinoma cancer cerebral degeneration choriocarcinoma colon adenocarcinoma colorectal cancer colorectal carcinoma disorder of sexual development duodenum cancer duodenum disease embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal disease heart cancer hereditary breast ovarian cancer syndrome hermaphroditism hypogonadotropic hypogonadism 23 with or without anosmia hypospadias invasive ductal carcinoma large intestine cancer multiple sclerosis peroxisomal disease pheochromocytoma placenta cancer polycystic ovary syndrome prostate cancer prostate carcinoma pseudohermaphroditism small intestine cancer sporadic breast cancer steatotic liver disease stomach cancer stomach carcinoma stomach disease uterine corpus cancer

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