GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8476 - 8500** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
55768	N-glycanase 1	NGLY1 FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	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
64579	N-deacetylase and N-sulfotransferase 4	NDST4	arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder azoospermia cancer colorectal cancer colorectal carcinoma coronary artery disease embryoma intellectual disability large intestine cancer nutmeg liver prostate cancer prostate carcinoma
9348	N-deacetylase and N-sulfotransferase 3	NDST3 HSST3	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder autism spectrum disorder azoospermia central nervous system disease depressive disorder generalized anxiety disorder intellectual disability major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia
8509	N-deacetylase and N-sulfotransferase 2	NDST2 HSST2 NST2	autism spectrum disorder azoospermia intellectual disability prostate cancer prostate carcinoma
3340	N-deacetylase and N-sulfotransferase 1	NDST1 N-Deacetylase-N-sulfotransferase 1 NST1 [Heparan sulfate]-glucosamine N-sulfotransferase 1 heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase 1	DiGeorge syndrome Treacher Collins syndrome acute myocardial infarction adult respiratory distress syndrome agnosia autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia breast cancer breast carcinoma cancer cerebral degeneration chikungunya choreatic disease chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma congenital diaphragmatic hernia coronary thrombosis dengue hemorrhagic fever depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia embryoma encephalitis encephalomyelitis epilepsy focal epilepsy gastrointestinal stromal tumor giant cell glioblastoma glioblastoma glomerulonephritis hiatus hernia high grade glioma hypereosinophilic syndrome intellectual disability kidney disease learning disability lingual-facial-buccal dyskinesia liver cirrhosis major depressive disorder melancholic depression microcephaly microphthalmia myelitis myocardial infarction nephritis nephrosis neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary renal cell carcinoma partial motor epilepsy pyoureter renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma silent myocardial infarction stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus velocardiofacial syndrome visual epilepsy
60560	N-alpha-acetyltransferase 35, NatC auxiliary subunit	NAA35
80018	N-alpha-acetyltransferase 25, NatB auxiliary subunit	NAA25
79612	N-alpha-acetyltransferase 16, NatA auxiliary subunit	NAA16
80155	N-alpha-acetyltransferase 15, NatA auxiliary subunit	NAA15
653308	N-acylsphingosine amidohydrolase 2B	ASAH2B ASAH2L bA449O16.3 bA98I6.3	breast cancer breast carcinoma
56624	N-acylsphingosine amidohydrolase 2	ASAH2 neutral ceramidase non-lysosomal ceramidase	Alzheimer's disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cardiomyopathy celiac disease colorectal cancer congenital diaphragmatic hernia cystic fibrosis dementia diabetes mellitus diabetic ketoacidosis gallbladder disease gamma heavy chain disease glaucoma heavy chain disease inflammatory bowel disease large intestine cancer liver disease lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neuroblastoma obesity systemic Epstein-Barr virus positive T-cell lymphoma of childhood type 2 diabetes mellitus
427	N-acylsphingosine amidohydrolase 1	ASAH1 AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase	Albright's hereditary osteodystrophy 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 Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder sphingolipidosis spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
27163	N-acylethanolamine acid amidase	NAAA	Alagille syndrome 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 Burkitt lymphoma DiGeorge syndrome Glanzmann's thrombasthenia Goodpasture syndrome Hantavirus hemorrhagic fever with renal syndrome Henoch-Schoenlein purpura 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 Japanese encephalitis Marfan syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis abdominal obesity-metabolic syndrome 1 acrodermatitis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia adult respiratory distress syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis bacterial sepsis bladder carcinoma blood coagulation disease bone marrow cancer cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia colorectal cancer colorectal carcinoma coronary artery disease craniosynostosis dengue disease dermatitis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia granulomatosis with polyangiitis gray platelet syndrome heart disease hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma hypersensitivity vasculitis inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer leukopenia liver cancer liver cirrhosis macrocytic anemia myelodysplastic syndrome myeloproliferative neoplasm newborn respiratory distress syndrome nicotine dependence obesity obsolete inherited blood coagulation disease obsolete type 1 diabetes mellitus 9 osteoarthritis platelet-type bleeding disorder 10 platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pneumonia polyarteritis nodosa portal hypertension portal vein thrombosis primary pulmonary hypertension prostate cancer prostate carcinoma qualitative platelet defect situs inversus steatotic liver disease thalassemia thrombocytopenia thrombocytosis 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 ulcerative colitis urinary bladder cancer velocardiofacial syndrome viral infectious disease yellow fever
55226	N-acetyltransferase 10	NAT10
140838	N-acetylneuraminic acid phosphatase	NANP MGC26833 dJ694B14.3	cancer cerebral degeneration colorectal cancer esophageal cancer esophageal carcinoma large intestine cancer malaria
54187	N-acetylneuraminate synthase	NANS	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 abdominal obesity-metabolic syndrome 1 acute myocardial infarction anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder bone cancer bone osteosarcoma breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma communicating hydrocephalus congenital central hypoventilation syndrome congenital nystagmus congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis craniosynostosis depressive disorder diabetes mellitus dissociated nystagmus dysthymic disorder embryoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma essential thrombocythemia generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma hydrocephalus hypertrichosis inflammatory liposarcoma intellectual disability learning disability liposarcoma liver cancer liver cirrhosis major depressive disorder malignant fibrous histiocytoma melancholic depression microcephaly mixed glioma mixed sleep apnea mucopolysaccharidosis IV multiple epiphyseal dysplasia myelodysplastic syndrome myocardial infarction neuroblastoma neurotic disorder obesity obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteomyelitis osteosarcoma parapsoriasis pathologic nystagmus peripheral osteosarcoma phobic disorder pleomorphic adenoma pleomorphic liposarcoma polycystic ovary syndrome premenstrual tension prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole restless legs syndrome rhabdomyosarcoma sarcoma sclerosing liposarcoma silent myocardial infarction skin disease sleep apnea social phobia spindle cell sarcoma spondyloepimetaphyseal dysplasia, Genevieve-type spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 synovial sarcoma tongue cancer tongue squamous cell carcinoma type 2 diabetes mellitus well-differentiated liposarcoma
80896	N-acetylneuraminate pyruvate lyase	NPL DHDPS1 NPL1 dihydrodipicolinate synthetase homolog 1 (E. coli)	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 Crohn's colitis Crohn's disease Ewing sarcoma Pick's disease Reye syndrome alcohol dependence alcohol use disorder atopic dermatitis bipolar disorder cerebral degeneration cholestasis congestive heart failure dermatitis epilepsy essential hypertension generalized epilepsy with febrile seizures plus hypertension idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease influenza juvenile myoclonic epilepsy myopathy obsolete major affective disorder 1 obsolete major affective disorder 2 panic disorder prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss ulcerative colitis visual epilepsy
51172	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA APAA UCE	Fabry disease alexia chylomicron retention disease dyslexia glycoproteinosis lipid storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis III mucopolysaccharidosis type IIIB neurodegenerative disease stuttering
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
84572	N-acetylglucosamine-1-phosphate transferase subunit gamma	GNPTG CAB56184 GlcNAc-phosphotransferase gamma-subunit c316G12.3	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis III gamma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
55577	N-acetylglucosamine kinase	NAGK	prostate cancer prostate carcinoma
254827	N-acetylated alpha-linked acidic dipeptidase like 2	NAALADL2
10004	N-acetylated alpha-linked acidic dipeptidase like 1	NAALADL1
10003	N-acetylated alpha-linked acidic dipeptidase 2	NAALAD2
4669	N-acetyl-alpha-glucosaminidase	NAGLU NAG Sanfilippo disease IIIB	Alzheimer's disease Burkitt lymphoma Charcot-Marie-Tooth disease axonal type 2V Clouston syndrome Dent disease Fanconi syndrome Glanzmann's thrombasthenia Kluver-Bucy syndrome Legg-Calve-Perthes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma amnestic disorder amyloidosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autistic disorder cancer cardiovascular system disease cholera chronic kidney disease chronic pyelonephritis cone-rod dystrophy congestive heart failure coronary artery disease cribriform carcinoma cystinosis cystitis dementia dentatorubral-pallidoluysian atrophy diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy essential thrombocythemia focal segmental glomerulosclerosis follicular adenoma fundus albipunctatus glomerulonephritis granular cell carcinoma gray platelet syndrome heart disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability kidney disease kidney failure learning disability lipoid nephrosis liver cirrhosis lysosomal storage disease malignant pleural mesothelioma microcystic adenoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma myelodysplastic syndrome nephritis nephrosis neuroblastoma neurodegenerative disease oculocerebrorenal syndrome oculocutaneous albinism type IA osteochondrodysplasia otitis media panic disorder papillary adenoma parapsoriasis platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 progressive familial intrahepatic cholestasis 1 progressive myoclonus epilepsy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole pyoureter qualitative platelet defect renal osteodystrophy retinitis pigmentosa retrograde amnesia sensorineural hearing loss spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 trigonitis tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease visual epilepsy

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