GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P35348	Alpha-1A adrenergic receptor	ADRA1A ADRA1C	4	1
Q8NI22	Multiple coagulation factor deficiency protein 2	MCFD2 SDNSF	4	3	arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease embryoma factor V deficiency factor VII deficiency factor VIII deficiency hematopoietic system disease nutmeg liver obsolete inherited blood coagulation disease seminoma testicular cancer testicular germ cell cancer testis seminoma transient cerebral ischemia vertebrobasilar insufficiency vitamin K deficiency bleeding
Q86SQ0	Pleckstrin homology-like domain family B member 2	PHLDB2 LL5B	4	1
Q9NPF5	DNA methyltransferase 1-associated protein 1	DMAP1 KIAA1425	4	2
P30926	Neuronal acetylcholine receptor subunit beta-4	CHRNB4	4	0
P22003	Bone morphogenetic protein 5	BMP5	4	0
Q9HC07	Putative divalent cation/proton antiporter TMEM165	TMEM165 TPARL	4	3	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
P31948	Stress-induced-phosphoprotein 1	STIP1	4	2
Q6ZUB1	Spermatogenesis-associated protein 31E1	SPATA31E1 C9orf79 FAM75E1	4	0
P29016	T-cell surface glycoprotein CD1b	CD1B	4	0
Q8NGJ8	Olfactory receptor 51S1	OR51S1	4	1
O14798	Tumor necrosis factor receptor superfamily member 10C	TNFRSF10C DCR1 LIT TRAILR3 TRID	4	1	Churg-Strauss syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Crohn's colitis Crohn's disease Down syndrome Richter's syndrome acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma adult lymphoma agranulocytosis benign ependymoma benign mesothelioma bladder carcinoma breast cancer breast carcinoma cancer cellular ependymoma central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood lymphoma chronic lymphocytic leukemia chronic obstructive pulmonary disease congenital heart disease cribriform carcinoma cystadenoma distal arthrogryposis embryoma endometrial cancer endometrial carcinoma essential thrombocythemia familial hypercholesterolemia giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inflammatory bowel disease 1 inflammatory bowel disease intellectual disability juvenile rheumatoid arthritis learning disability leukemia leukopenia liver cancer lung cancer lung non-small cell carcinoma lymphoma malignant mesothelioma melanoma mixed glioma multiple myeloma multiple sclerosis myelodysplastic syndrome myxopapillary ependymoma neuroblastoma neutropenia obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary ependymoma periodontitis post-traumatic stress disorder prostate cancer prostate carcinoma severe congenital neutropenia skin melanoma systemic lupus erythematosus tanycytic ependymoma tongue squamous cell carcinoma tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer uveal melanoma
Q8TDS7	Mas-related G-protein coupled receptor member D	MRGPRD MRGD	4	0
P30414	NK-tumor recognition protein	NKTR	4	1
Q9Y314	Nitric oxide synthase-interacting protein	NOSIP	4	3
Q8IZH2	5'-3' exoribonuclease 1	XRN1 SEP1	4	1
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
Q96AD5	Patatin-like phospholipase domain-containing protein 2	PNPLA2 ATGL	4	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 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Barth syndrome Chanarin-Dorfman syndrome Ehlers-Danlos syndrome Kuhnt-Junius degeneration Laron syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acanthosis nigricans achondroplasia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult liposarcoma age related macular degeneration agnosia anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive congenital ichthyosis 1 bacterial sepsis bladder carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cartilage disease cavernous hemangioma celiac disease central nervous system cancer cerebral degeneration childhood liposarcoma childhood osteosarcoma cholecystitis chorioangioma chylomicron retention disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cone-rod dystrophy congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma endometrial hyperplasia endomyocardial fibrosis epithelioid leiomyosarcoma exudative vitreoretinopathy 1 exudative vitreoretinopathy eye disease familial combined hyperlipidemia familial hyperlipidemia familial lipoprotein lipase deficiency familial periodic paralysis familial retinoblastoma fibromyalgia fundus albipunctatus gestational diabetes gliosarcoma glomus tumor glucose intolerance glycogen storage disease II granular cell carcinoma heart disease hemangioma hepatoblastoma hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperinsulinism hyperlipoproteinemia type V hypertrophic cardiomyopathy ichthyosis impotence intramuscular hemangioma isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leiomyosarcoma leukostasis lipoatrophic diabetes mellitus lipodystrophy liposarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma lymphangioma macular degeneration major depressive disorder melancholic depression melanoma microphthalmia mixed glioma mongolian spot myocardial infarction myopathy myositis myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuropathy neurotic disorder nicotine dependence obesity obsolete Matthew-Wood syndrome obsolete congenital ichthyosiform erythroderma obsolete melancholia ocular melanoma osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma peripheral nervous system disease pleomorphic liposarcoma polycystic ovary syndrome prediabetes syndrome premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia proliferative diabetic retinopathy prostate cancer prostate carcinoma pseudoxanthoma elasticum psychologic dyspareunia rectal benign neoplasm rectum adenocarcinoma rectum cancer retinal disease retinitis pigmentosa retinitis retinoblastoma retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis schizophrenia sensorineural hearing loss silent myocardial infarction skin melanoma steatotic liver disease stomach cancer stomach carcinoma systemic primary carnitine deficiency disease trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
Q15418	Ribosomal protein S6 kinase alpha-1	RPS6KA1 MAPKAPK1A RSK1	4	1
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	4	4
A0A087WXI2	Fc gamma binding protein	FCGBP	4	0
J3KQ66	Reelin	RELN	4	0
Q9C0F1	Centrosomal protein of 44 kDa	CEP44 KIAA1712	4	1
Q4AC94	C2 domain-containing protein 3	C2CD3	4	2
A8MVW0	Protein FAM171A2	FAM171A2	4	5

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