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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P04217	Alpha-1B-glycoprotein	A1BG	8	29
Q5UIP0	Telomere-associated protein RIF1	RIF1	10	29
Q6P4A8	Phospholipase B-like 1	PLBD1	6	29
O00300	Tumor necrosis factor receptor superfamily member 11B	TNFRSF11B OCIF OPG	6	29
Q6UXI9	Nephronectin	NPNT EGFL6L POEM	10	29
Q9NUM4	Transmembrane protein 106B	TMEM106B	8	29
P06870	Kallikrein-1	KLK1	6	28
P04003	C4b-binding protein alpha chain	C4BPA C4BP	9	28
Q92859	Neogenin	NEO1 IGDCC2 NGN	14	28
Q8IXL6	Extracellular serine/threonine protein kinase FAM20C	FAM20C DMP4	14	28
P04180	Phosphatidylcholine-sterol acyltransferase	LCAT	7	28	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 Bloom syndrome Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Norum disease Pick's disease Reye syndrome Tangier disease abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acute chest syndrome acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anemia aortic atherosclerosis arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness brain stem infarction cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chylomicron retention disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis disease of metabolism dry eye syndrome familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome gallbladder disease glomerulonephritis granular corneal dystrophy heart disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hyperalphalipoproteinemia 1 hyperlipoproteinemia type V hypolipoproteinemia inherited metabolic disorder kidney disease kidney failure lipoid nephrosis liver cancer liver disease macrocytic anemia macular corneal dystrophy motor peripheral neuropathy myocardial infarction nephritis nephrosis nephrotic syndrome nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum ovarian cancer ovarian carcinoma proteinuria pyoureter recurrent corneal erosion renal osteodystrophy rheumatoid arthritis sickle cell anemia silent myocardial infarction steatotic liver disease uremia xerophthalmia
Q9HCU4	Cadherin EGF LAG seven-pass G-type receptor 2	CELSR2 CDHF10 EGFL2 KIAA0279 MEGF3	21	28
P17936	Insulin-like growth factor-binding protein 3	IGFBP3 IBP3	17	28
P15289	Arylsulfatase A	ARSA	4	28	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 Behcet's disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Clostridium difficile colitis Clouston syndrome Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease DiGeorge syndrome Down syndrome Dubowitz syndrome Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease Klatskin's tumor Krabbe disease Landau-Kleffner syndrome Lynch syndrome Niemann-Pick disease 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 Phelan-McDermid syndrome Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Sandhoff disease Seckel syndrome Silver-Russell syndrome Sneddon syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Tay-Sachs disease Unverricht-Lundborg syndrome Wilson disease X-linked Aarskog syndrome X-linked ichthyosis X-linked nonsyndromic deafness abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acoustic neuroma acute chest syndrome acute intermittent porphyria acute interstitial pneumonia acute kidney tubular necrosis acute myocardial infarction adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia alcohol dependence alcohol use disorder allergic asthma alternating hemiplegia of childhood amnestic disorder amyloidosis anemia angioedema ankylosing spondylitis anterior spinal artery syndrome anxiety disorder argininosuccinic aciduria arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autism spectrum disorder autistic disorder autoimmune hepatitis autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal dominant osteopetrosis 2 autosomal recessive Robinow syndrome autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness autosomal recessive osteopetrosis 7 bacterial sepsis benign epilepsy with centrotemporal spikes blood coagulation disease brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cataract cellular schwannoma central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood T-cell acute lymphoblastic leukemia cholangiocarcinoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome choreatic disease chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism coronary artery disease coronary thrombosis craniosynostosis critical illness polyneuropathy dementia demyelinating disease demyelinating polyneuropathy dentatorubral-pallidoluysian atrophy depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism diverticulitis dysthymic disorder dystonia early myoclonic encephalopathy embryoma encephalitis encephalomyelitis enterocele epilepsy esophageal cancer esophageal carcinoma esophagitis essential hypertension essential thrombocythemia familial hyperlipidemia female stress incontinence follicular adenoma gallbladder cancer gastroenteritis gastroesophageal reflux disease generalized anxiety disorder generalized atherosclerosis giant cell glioblastoma glioblastoma glomerulonephritis glycogen storage disease Ia heart disease hemiplegia hemochromatosis hepatitis B hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 herpes zoster high grade glioma hyperglycemia hypertension hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermediate coronary syndrome intrahepatic cholangiocarcinoma intrinsic asthma iron metabolism disease irritable bowel syndrome keratitis keratoconjunctivitis kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy lipid storage disease locked-in syndrome lung benign neoplasm lung cancer lung carcinoma lung disease lysosomal storage disease macrocytic anemia major depressive disorder malignant peripheral nerve sheath tumor malignant pleural mesothelioma mediastinitis medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanotic neurilemmoma meningoencephalitis metachromatic leukodystrophy microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia mitochondrial metabolism disease mitochondrial myopathy motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis multiple sclerosis myelitis myelomeningocele myocardial infarction myxedema nasopharynx carcinoma nephritis nephrosis nervous system disease neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete autosomal recessive nonsyndromic deafness 105 obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea optic atrophy osteoarthritis osteopetrosis osteoporosis osteosclerosis pancreatic adenocarcinoma pancreatic ductal adenocarcinoma papillary adenoma patent foramen ovale peptic esophagitis peripheral artery disease peripheral nervous system disease phobic disorder plexiform schwannoma pneumonia polyneuropathy primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis progressive bulbar palsy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy psychotic disorder pyoureter quadriplegia rectal benign neoplasm rectum adenocarcinoma rectum cancer red-green color blindness retrograde amnesia sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spina bifida spinal cancer superior mesenteric artery syndrome syndromic X-linked intellectual disability type 10 systemic lupus erythematosus tethered spinal cord syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis type 2 diabetes mellitus ulcerative colitis urethral stricture urticaria vascular dementia velocardiofacial syndrome ventricular septal defect visual epilepsy
P53801	Pituitary tumor-transforming gene 1 protein-interacting protein	PTTG1IP C21orf1 C21orf3	3	28
Q9Y2E5	Epididymis-specific alpha-mannosidase	MAN2B2 KIAA0935	13	28	cerebral infarction cerebrovascular disease primary immunodeficiency disease
P01225	Follitropin subunit beta	FSHB	2	28
Q96AP7	Endothelial cell-selective adhesion molecule	ESAM	5	28
P04439	HLA class I histocompatibility antigen, A alpha chain	HLA-A HLAA	3	28
P18084	Integrin beta-5	ITGB5	10	28
P13598	Intercellular adhesion molecule 2	ICAM2	8	28	Barrett's esophagus Hantavirus hemorrhagic fever with renal syndrome abdominal aortic aneurysm acquired immunodeficiency syndrome benign mesothelioma bronchus cancer bronchus carcinoma cancer embryoma esophageal cancer esophageal carcinoma human immunodeficiency virus infectious disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease lepromatous leprosy lung benign neoplasm lung cancer lung carcinoma malignant mesothelioma neuroblastoma pancreatic cancer pancreatic carcinoma pterygium scleroderma stomach cancer stomach carcinoma systemic scleroderma tuberculoid leprosy ulcerative colitis
Q12866	Tyrosine-protein kinase Mer	MERTK MER	18	28
Q12841	Follistatin-related protein 1	FSTL1 FRP	8	27
P06865	Beta-hexosaminidase subunit alpha	HEXA	7	27	GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Sandhoff disease Tay-Sachs disease Werdnig-Hoffmann disease acquired immunodeficiency syndrome adult lymphoma amyotrophic lateral sclerosis blindness cancer central nervous system cancer central nervous system lymphoma childhood lymphoma childhood spinal muscular atrophy cystic fibrosis dementia diffuse scleroderma embryoma epilepsy gangliosidosis gliosarcoma glycoproteinosis high grade glioma human immunodeficiency virus infectious disease inherited metabolic disorder intellectual disability juvenile spinal muscular atrophy learning disability lingual-facial-buccal dyskinesia lymphoma lysosomal storage disease mixed glioma movement disease mucolipidosis type IV neurodegenerative disease obesity obsolete ymphosarcoma progressive muscular atrophy rheumatoid arthritis sensorineural hearing loss sickle cell anemia spinal muscular atrophy visual epilepsy
Q9Y5Y7	Lymphatic vessel endothelial hyaluronic acid receptor 1	LYVE1 CRSBP1 HAR XLKD1	4	27

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