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 **3976 - 4000** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A2H4FZ21	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A386NI95	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
P12821	Angiotensin-converting enzyme	ACE DCP DCP1	Homo sapiens (human)	23	115	Alport 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 B-cell lymphoma Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Becker muscular dystrophy Behcet's disease Burkitt lymphoma CAKUT Chagas 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 Cowden syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Goodpasture syndrome Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 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 Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Kawasaki disease Keshan disease Kuhnt-Junius degeneration Langerhans-cell histiocytosis Leber hereditary optic neuropathy Lewy body dementia Marfan syndrome Meckel syndrome 8 Meckel syndrome Mycoplasma pneumoniae pneumonia Netherton syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Potter's syndrome Prinzmetal angina Raynaud disease Reye syndrome Richter's syndrome Senior-Loken syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia Takayasu's arteritis Werner syndrome Wilson disease X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 ablepharon macrostomia syndrome acne acquired immunodeficiency syndrome acrodermatitis acromegaly actinic keratosis acute biphenotypic leukemia acute chest syndrome acute kidney failure acute leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute pyelonephritis adenocarcinoma adenoma adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy adult fibrosarcoma adult lymphoma adult respiratory distress syndrome age related macular degeneration agenesis of the corpus callosum with peripheral neuropathy agnosia agoraphobia agranulocytosis alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic contact dermatitis allergic rhinitis alopecia areata alopecia alpha 1-antitrypsin deficiency alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anemia angioedema angioma serpiginosum ankylosing spondylitis anterolateral myocardial infarction anteroseptal myocardial infarction anthracosilicosis antisocial personality disorder antithrombin III deficiency anuria anxiety disorder aortic aneurysm aortic atherosclerosis aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy asbestosis aseptic meningitis aspiration pneumonia aspiration pneumonitis asthma atherosclerosis atrial fibrillation atrioventricular block atrioventricular septal defect autistic disorder autoimmune disease autoimmune hepatitis 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 dominant polycystic kidney disease autosomal recessive congenital ichthyosis 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 autosomal recessive polycystic kidney disease background diabetic retinopathy bacterial infectious disease bacterial sepsis basal cell carcinoma berylliosis bestrophinopathy bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone cancer bone disease bone marrow cancer borderline personality disorder brain disease brain infarction brain ischemia brain stem infarction breast cancer breast carcinoma breast fibrocystic disease bronchiolitis obliterans bronchus cancer bronchus carcinoma burning mouth syndrome campomelic dysplasia cancer cannabis abuse cannabis dependence capillary disease capillary hemangioma carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis carpal tunnel syndrome cartilage disease cataract 32 multiple types cataract catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cavernous hemangioma celiac disease central gyrate choroidal dystrophy central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral atherosclerosis cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood lymphoma childhood type dermatomyositis cholangiocarcinoma cholera cholestasis chondrocalcinosis chorioretinitis choroiditis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease ciliary body disease clear cell renal cell carcinoma colitis collagen disease collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency complex partial epilepsy cone-rod dystrophy congenital central hypoventilation syndrome congenital diaphragmatic hernia congenital heart disease congenital hypothyroidism congenital muscular dystrophy congenital nongoitrous hypothyroidism 4 congestive heart failure connective tissue disease coronary aneurysm coronary artery disease coronary artery vasospasm coronary restenosis coronary stenosis coronary thrombosis craniometaphyseal dysplasia crescentic glomerulonephritis cribriform carcinoma critical illness polyneuropathy cystic fibrosis cystoid macular edema degeneration of macula and posterior pole dementia dental caries dentin caries depressive disorder dermatitis dermatomyositis diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diastolic heart failure diastrophic dysplasia dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of mental health disease of metabolism distal myopathy drug psychosis dry eye syndrome duodenum cancer dyschromatosis symmetrica hereditaria dysgerminoma of ovary dysthymic disorder eclampsia embryoma embryonal cancer encephalitis encephalomyelitis endocarditis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis enterocele epilepsy episodic kinesigenic dyskinesia 1 esophageal cancer esophageal carcinoma esophagitis essential hypertension essential thrombocythemia exudative vitreoretinopathy 1 exudative vitreoretinopathy facioscapulohumeral muscular dystrophy familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial mediterranean fever familial nephrotic syndrome familial periodic paralysis fibromyalgia fibrosarcoma focal segmental glomerulosclerosis 1 focal segmental glomerulosclerosis 2 focal segmental glomerulosclerosis 5 focal segmental glomerulosclerosis 6 focal segmental glomerulosclerosis 7 focal segmental glomerulosclerosis 8 focal segmental glomerulosclerosis 9 focal segmental glomerulosclerosis follicular adenoma frontotemporal dementia fundus albipunctatus gallbladder cancer gallbladder carcinoma gallbladder disease gastric ulcer gastritis gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gastrointestinal system disease generalized anxiety disorder generalized atherosclerosis germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance glycogen storage disease II glycogen storage disease V granular cell carcinoma granular corneal dystrophy 2 granulomatosis with polyangiitis heart cancer heart disease heart valve disease hematologic cancer hemochromatosis hemopericardium hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema hereditary hemorrhagic telangiectasia hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spherocytosis type 1 hereditary spherocytosis hiatus hernia high grade glioma human immunodeficiency virus infectious disease hydronephrosis hyperandrogenism hypercalcemia hyperglycemia hyperhomocysteinemia hyperinsulinism hyperparathyroidism hyperpituitarism hypersensitivity vasculitis hypertension hypertensive heart disease hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypoplastic left heart syndrome hypothyroidism ichthyosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis idiopathic scoliosis ileitis ileocolitis immune system disease impotence inappropriate ADH syndrome infective endocarditis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory myofibroblastic tumor intermediate coronary syndrome intermittent claudication intermittent explosive disorder interstitial lung disease interstitial nephritis intestinal disease intracranial aneurysm intracranial arteriosclerosis intrahepatic cholangiocarcinoma intrahepatic cholestasis of pregnancy intrinsic asthma iris disease iron metabolism disease irritable bowel syndrome keratoconjunctivitis sicca keratosis follicularis kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer left bundle branch hemiblock leiomyoma leukemia leukostasis limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphangioleiomyomatosis lymphoma lymphopenia macrocytic anemia macular degeneration macular retinal edema major depressive disorder malaria male infertility malignant hypertension marasmus megacystis-microcolon-intestinal hypoperistalsis syndrome melancholic depression melanoma membranous glomerulonephritis meningoencephalitis mevalonic aciduria microcephaly microcystic adenoma microglandular adenosis microinvasive gastric cancer microphthalmia middle cerebral artery infarction migraine with aura migraine without aura migraine mitral valve disease mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma mixed sleep apnea mongolian spot mood disorder morbid obesity motor peripheral neuropathy multiple endocrine neoplasia type 2A multiple myeloma multiple sclerosis multiple system atrophy muscular dystrophy musculoskeletal system disease myelitis myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction myocarditis myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma myopathy myositis myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema narcolepsy nasopharynx carcinoma neovascular inflammatory vitreoretinopathy nephritis nephrocalcinosis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome nervous system disease neurocirculatory asthenia neurodegenerative disease neuromuscular disease neuromyelitis optica neuropathy neurotic disorder neutropenia newborn respiratory distress syndrome nicotine dependence nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma normal pressure hydrocephalus nutmeg liver nutrition disease nutritional optic neuropathy obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome 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 chronobiology disease obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete eye and adnexa disease obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea ocular hypotension oculopharyngeal muscular dystrophy oligohydramnios open-angle glaucoma osteitis fibrosa osteoarthritis osteomalacia osteonecrosis osteoporosis otosclerosis ovarian cancer ovarian carcinoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis panic disorder panuveitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis patent ductus arteriosus pemphigus vulgaris pemphigus peptic esophagitis peptic ulcer disease pericardial effusion perinatal necrotizing enterocolitis periodontal disease periodontitis peripheral artery disease peripheral nervous system disease peripheral vascular disease periventricular leukomalacia personality disorder pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency plasmacytoma pneumonia polyarteritis nodosa polycystic kidney disease 1 polycystic kidney disease 4 polycystic ovary syndrome polycythemia vera polycythemia polyneuropathy portal hypertension post-traumatic stress disorder posterior uveitis postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome premature ejaculation primary biliary cholangitis primary hyperaldosteronism primary hyperparathyroidism primary open angle glaucoma primary ovarian insufficiency primary polycythemia primary pulmonary hypertension progeria progressive muscular atrophy progressive supranuclear palsy proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protein-energy malnutrition proteinuria pseudoxanthoma elasticum psoriasis psoriatic arthritis psychologic dyspareunia psychotic disorder pterygium pulmonary edema pulmonary embolism pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole pyelitis pyelonephritis pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rapidly progressive glomerulonephritis rectal benign neoplasm rectum adenocarcinoma rectum cancer red-green color blindness reflex sympathetic dystrophy renal artery disease renal artery obstruction renal carcinoma renal cell carcinoma renal hypertension renal infectious disease renal osteodystrophy renovascular hypertension respiratory syncytial virus infectious disease restrictive cardiomyopathy 1 restrictive cardiomyopathy reticulosarcoma retinal disease retinal vein occlusion retinitis pigmentosa retinitis retinopathy of prematurity rheumatoid arthritis rhinitis rickets rippling muscle disease 2 sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleritis scleroderma seasonal affective disorder seborrheic keratosis seminoma sensorineural hearing loss severe acute respiratory syndrome severe congenital neutropenia sexual dysfunction sick sinus syndrome sickle cell anemia silent myocardial infarction silicosis situs inversus skin atrophy skin benign neoplasm skin cancer skin disease skin melanoma sleep apnea small intestine cancer somatization disorder somatoform disorder speech-language disorder-1 spondyloarthropathy spondylosis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis subacute sclerosing panencephalitis substance abuse substance-related disorder synovial sarcoma systemic lupus erythematosus systemic scleroderma systolic heart failure telangiectasis temporal lobe epilepsy testicular cancer testicular germ cell cancer testis seminoma tetralogy of Fallot thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue trypanosomiasis tuberculosis tuberculous pneumothorax tuberous sclerosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis uremia ureteral obstruction urinary system benign neoplasm urinary system cancer urinary tract obstruction urticaria uterine corpus cancer uterine fibroid uveitis uveoparotid fever vascular dementia vascular disease vasculitis vasomotor rhinitis vertebrobasilar insufficiency vesicoureteral reflux viral infectious disease viral meningitis viral pneumonia visual epilepsy vitiligo xerophthalmia
E2GJM2	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P04000	Long-wave-sensitive opsin 1	OPN1LW RCP	Homo sapiens (human)	2	0
P46095	G-protein coupled receptor 6	GPR6	Homo sapiens (human)	3	0
C0M124	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q68BL8	Olfactomedin-like protein 2B	OLFML2B	Homo sapiens (human)	12	5
B7Z2R9	cDNA FLJ52540, highly similar to Lysosome-associated membrane glycoprotein 2	LAMP2	Homo sapiens (human)	2	0
Q8NGE8	Olfactory receptor 4D9	OR4D9	Homo sapiens (human)	1	0
Q8WTQ7	Rhodopsin kinase GRK7	GRK7 GPRK7	Homo sapiens (human)	1	1
C9JZT5	Butyrophilin subfamily 3 member A3 (Fragment)	BTN3A3	Homo sapiens (human)	1	0
A0A5J6VAR0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9BW92	Threonine--tRNA ligase, mitochondrial	TARS2 TARSL1	Homo sapiens (human)	2	2
P50391	Neuropeptide Y receptor type 4	NPY4R PPYR1	Homo sapiens (human)	4	0
P07602	Prosaposin	PSAP GLBA SAP1	Homo sapiens (human)	22	299	Farber lipogranulomatosis Gaucher's disease type I Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Unverricht-Lundborg syndrome X-linked nonsyndromic deafness acquired immunodeficiency syndrome adult fibrosarcoma agnosia allergic asthma amnestic disorder amyotrophic lateral sclerosis anemia aortic valve disease 2 aortic valve stenosis asthma atypical Gaucher's disease due to saposin c deficiency 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 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 bacterial sepsis blepharospasm breast cancer breast carcinoma cancer candidiasis central nervous system cancer central sleep apnea cholecystitis choreatic disease colitis combined saposin deficiency critical illness polyneuropathy cutaneous candidiasis dementia dental caries dentin caries denture stomatitis depressive disorder dysthymic disorder dystonia early myoclonic encephalopathy embryoma epilepsy fascioliasis fibrosarcoma focal hand dystonia frontotemporal dementia gallbladder cancer gallbladder carcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma hepatitis B hepatitis E hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease leukodystrophy lingual-facial-buccal dyskinesia liver cancer lysosomal storage disease macrocytic anemia major depressive disorder malaria melancholic depression meningoencephalitis metachromatic leukodystrophy mixed glioma movement disease multiple myeloma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neuropathy neurotic disorder obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia optic atrophy oral candidiasis ovarian cancer ovarian carcinoma panic disorder paraplegia parapsoriasis peripheral nervous system disease phobic disorder plasma cell neoplasm polyneuropathy progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole retrograde amnesia schizophrenia situs inversus social phobia sphingolipidosis stomach cancer stomach carcinoma stomatitis syndromic X-linked intellectual disability type 10 thrombocytopenia tuberous sclerosis ulcerative stomatitis visual epilepsy vulvovaginal candidiasis vulvovaginitis
F5H061	TNF receptor superfamily member 1A	TNFRSF1A	Homo sapiens (human)	1	0
Q9P2I0	Cleavage and polyadenylation specificity factor subunit 2	CPSF2 CPSF100 KIAA1367	Homo sapiens (human)	1	1
Q86X02	Cerebellar degeneration-related protein 2-like	CDR2L HUMPPA	Homo sapiens (human)	0	1
Q14156	Protein EFR3 homolog A	EFR3A KIAA0143	Homo sapiens (human)	0	1
O78075	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q7Z692	Carcinoembryonic antigen-related cell adhesion molecule 19	CEACAM19 CEAL1	Homo sapiens (human)	1	0
Q8IWR0	Zinc finger CCCH domain-containing protein 7A	ZC3H7A ZC3H7 ZC3HDC7	Homo sapiens (human)	2	1
D2DKF7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9HAV4	Exportin-5	XPO5 KIAA1291 RANBP21	Homo sapiens (human)	0	1

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