GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **401 - 425** of **18496** in total

« First

‹ Prev

…

13

14

15

16

17

18

19

20

21

…

Next ›

Last »
UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NR19	Acetyl-coenzyme A synthetase, cytoplasmic	ACSS2 ACAS2	Homo sapiens (human)	0	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 Crohn's colitis Crohn's disease Ewing sarcoma Klippel-Feil syndrome Marfan syndrome McCune Albright syndrome Pick's disease Reye syndrome Stevens-Johnson syndrome abdominal aortic aneurysm acquired immunodeficiency syndrome acute chest syndrome acute lymphoblastic leukemia acute myocardial infarction adult acute lymphocytic leukemia alcohol dependence alcohol use disorder aortic valve insufficiency appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthropathy atherosclerosis atrial fibrillation bacterial sepsis bladder carcinoma breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congestive heart failure coronary aneurysm coronary artery disease coronary thrombosis decubitus ulcer depressive disorder diabetes insipidus diabetes mellitus diabetic ketoacidosis disease of mental health distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma erythema multiforme esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension familial adenomatous polyposis familial hypercholesterolemia gastroschisis giant cell glioblastoma glioblastoma gliosarcoma head and neck cancer heart disease hepatocellular carcinoma hiatus hernia high grade glioma human immunodeficiency virus infectious disease hypertension hypoplastic left heart syndrome impotence inflammatory bowel disease 1 inflammatory bowel disease insulinoma islet cell tumor kidney failure large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leishmaniasis liver cancer liver carcinoma lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression mixed glioma myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neurohypophyseal diabetes insipidus neurotic disorder nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obstructive sleep apnea omphalocele pancreatic adenocarcinoma pancreatic cancer papillary renal cell carcinoma peripheral artery disease pneumonia premature ejaculation primary hypertrophic osteoarthropathy prostate cancer prostate carcinoma prostatic adenoma psychologic dyspareunia psychotic disorder rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retroperitoneal sarcoma sarcomatoid renal cell carcinoma septic arthritis silent myocardial infarction situs inversus spinal cancer spindle cell sarcoma spondylolisthesis steatotic liver disease stomach cancer stomach carcinoma stomach disease subacute delirium substance abuse substance-related disorder synovitis tenosynovitis thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus ulcerative colitis umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer visceral leishmaniasis
O00400	Acetyl-coenzyme A transporter 1	SLC33A1 ACATN AT1	Homo sapiens (human)	1	0	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 Bartter disease Charcot-Marie-Tooth disease type 5 Conn's syndrome Henoch-Schoenlein purpura MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome Waterhouse-Friderichsen syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation autism spectrum disorder autistic disorder bestrophinopathy brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chronic kidney disease colitis colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma essential hypertension familial hypertrophic cardiomyopathy focal epilepsy follicular adenoma gastroenteritis generalized anxiety disorder glomerulonephritis granular cell carcinoma heart disease hepatoblastoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hyperhomocysteinemia hypersensitivity vasculitis hypertension hypertensive heart disease hypertrophic cardiomyopathy ileitis ileocolitis intellectual disability intrinsic asthma kidney disease large intestine cancer learning disability leiomyosarcoma liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant hypertension melancholic depression melanoma microcystic adenoma myocardial infarction myxoid leiomyosarcoma nephritis nephrosis neurodegenerative disease neurotic disorder nodular prostate nutmeg liver obesity obsolete melancholia obstructive sleep apnea papillary adenoma paraplegia partial motor epilepsy pathologic nystagmus periodontitis phobic disorder placental insufficiency polycystic ovary syndrome primary hyperaldosteronism progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pyoureter renovascular hypertension scleroderma secondary hypertension sensorineural hearing loss sensory peripheral neuropathy sick sinus syndrome silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus systemic scleroderma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus vesicoureteral reflux visual epilepsy
P02708	Acetylcholine receptor subunit alpha	CHRNA1 ACHRA CHNRA	Homo sapiens (human)	1	0
P11230	Acetylcholine receptor subunit beta	CHRNB1 ACHRB CHRNB	Homo sapiens (human)	1	0
Q07001	Acetylcholine receptor subunit delta	CHRND ACHRD	Homo sapiens (human)	2	0
Q04844	Acetylcholine receptor subunit epsilon	CHRNE ACHRE	Homo sapiens (human)	2	0
P07510	Acetylcholine receptor subunit gamma	CHRNG ACHRG	Homo sapiens (human)	2	0
P22303	Acetylcholinesterase	ACHE	Homo sapiens (human)	3	2	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 Balo concentric sclerosis Chagas disease Clostridium difficile colitis Creutzfeldt-Jakob disease Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IGSF1 deficiency syndrome Japanese encephalitis Kawasaki disease Lafora disease Lambert-Eaton myasthenic syndrome Lewy body dementia Marfan syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Noonan syndrome 1 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Schwartz-Jampel syndrome 1 Wilson-Turner syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute stress disorder adrenoleukodystrophy adult medulloblastoma allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy 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 distal hereditary motor neuronopathy 1 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 bacterial sepsis bipolar disorder bladder carcinoma blood platelet disease brain cancer brain disease breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease carotid artery disease cauda equina neoplasm central nervous system disease central nervous system origin vertigo centronuclear myopathy X-linked centronuclear myopathy cerebellar ataxia cerebellar disease cerebral atherosclerosis cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease chancroid childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cognitive disorder collecting duct carcinoma colon cancer colonic benign neoplasm colonic pseudo-obstruction colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myasthenic syndrome 5 congenital myasthenic syndrome congenital myopathy 1A 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 structural myopathy congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome conversion disorder coronary artery disease coronary thrombosis cystic fibrosis dementia dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism dissociative amnesia dissociative disorder distal myopathy dysthymic disorder dystonia embryoma endocrine exophthalmos endometritis enophthalmos epilepsy episodic ataxia type 1 essential thrombocythemia facioscapulohumeral muscular dystrophy familial hyperlipidemia fibrillary astrocytoma fibromyalgia focal epilepsy frontotemporal dementia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder glaucoma head and neck squamous cell carcinoma heart disease hemiplegia hepatocellular carcinoma high grade glioma hyperglycemia hypothyroidism idiopathic scoliosis immune system disease impotence inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intracranial arteriosclerosis intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma kidney cancer large intestine cancer laryngeal squamous cell carcinoma lateral sclerosis learning disability leptospirosis leukemia limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis liver disease lower respiratory tract disease lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphogranuloma venereum major depressive disorder malaria malignant astrocytoma medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy melancholic depression melanoma melanotic medulloblastoma migraine morbid obesity motor neuron disease movement disease multiple epiphyseal dysplasia multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myasthenia gravis myelodysplastic syndrome myelomeningocele myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myotonic dystrophy type 2 myxedema narcolepsy nasal cavity disease necrotizing ulcerative gingivitis nemaline myopathy nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibroma neuromuscular disease neuromuscular junction disease neurotic disorder nonpapillary renal cell carcinoma normocytic anemia nutmeg liver 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 constipation obsolete exophthalmos obsolete melancholia obsolete ymphosarcoma oculopharyngeal muscular dystrophy orbital disease osteochondrodysplasia osteoporosis ovarian cancer overnutrition papillary adenocarcinoma papillary renal cell carcinoma paranasal sinus disease partial motor epilepsy perineurioma peripheral nerve sheath neoplasm peripheral nervous system neoplasm persian gulf syndrome phobic disorder pilocytic astrocytoma polydactyly premature ejaculation primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psychologic dyspareunia psychotic disorder renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma sleeping sickness spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy sporadic breast cancer status epilepticus stomach cancer stomach carcinoma subacute delirium subependymal giant cell astrocytoma substance abuse substance-related disorder temporal arteritis teratocarcinoma tethered spinal cord syndrome thanatophoric dysplasia thrombocytopenia thyroid gland papillary carcinoma trypanosomiasis tuberous sclerosis type 2 diabetes mellitus typhus ulcerative colitis upper respiratory tract disease urinary bladder cancer varicose veins vascular dementia viral infectious disease visual epilepsy vitiligo von Hippel-Lindau disease yaws yellow fever
Q6ZMB0	Acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase	B3GNT6	Homo sapiens (human)	3	1	cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis islet cell tumor large intestine cancer pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma
A0A1B0GUA4	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GUG1	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GVG2	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GW68	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GTZ5	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
Q13510	Acid ceramidase	ASAH1 ASAH	Homo sapiens (human)	8	123	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 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
A0A1B0GUH5	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GTM3	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
E7EMM4	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
Q6ZNF0	Acid phosphatase type 7	ACP7 PAPL PAPL1	Homo sapiens (human)	3	0
Q92485	Acid sphingomyelinase-like phosphodiesterase 3b	SMPDL3B ASML3B ASMLPD	Homo sapiens (human)	3	0	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
P78348	Acid-sensing ion channel 1	ASIC1 ACCN2 BNAC2	Homo sapiens (human)	2	0
Q16515	Acid-sensing ion channel 2	ASIC2 ACCN ACCN1 BNAC1 MDEG	Homo sapiens (human)	6	0
Q9UHC3	Acid-sensing ion channel 3	ASIC3 ACCN3 SLNAC1 TNAC1	Homo sapiens (human)	2	1
Q96FT7	Acid-sensing ion channel 4	ASIC4 ACCN4	Homo sapiens (human)	3	0
Q9NY37	Acid-sensing ion channel 5	ASIC5 ACCN5 HINAC	Homo sapiens (human)	2	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements