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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **51 - 75** of **1582** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
6996	thymine DNA glycosylase	TDG Aliases: G/T mismatch-specific thymine DNA glycosylase	Homo sapiens (human)	adult medulloblastoma benign ependymoma breast cancer breast carcinoma cancer cellular ependymoma childhood medulloblastoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer hepatitis B high grade glioma large intestine cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma multiple myeloma myxopapillary ependymoma pancreatic cancer pancreatic carcinoma papillary ependymoma rectal benign neoplasm rectum adenocarcinoma rectum cancer skin benign neoplasm skin cancer stomach cancer stomach carcinoma tanycytic ependymoma
1890	thymidine phosphorylase	TYMP Aliases: gliostatin	Homo sapiens (human)	Barrett's esophagus Kallmann syndrome Leigh disease Sheehan syndrome adenocarcinoma adenoma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis basal cell carcinoma benign mesothelioma bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer cervical cancer cervical squamous cell carcinoma cervix carcinoma childhood cerebral astrocytoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common bile duct neoplasm congenital ptosis coronary artery disease cribriform carcinoma diabetes mellitus diarrhea ductal carcinoma in situ embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis esophagus adenocarcinoma esophagus squamous cell carcinoma fibrillary astrocytoma gallbladder cancer gallbladder carcinoma gastrointestinal system cancer gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatic veno-occlusive disease hepatocellular carcinoma high grade glioma hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism inherited metabolic disorder intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor large intestine cancer learning disability leukodystrophy liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma malignant astrocytoma malignant mesothelioma marasmus mitochondrial DNA depletion syndrome 1 mitochondrial DNA depletion syndrome 4b mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 8a mitochondrial DNA depletion syndrome 8b mitochondrial encephalomyopathy mitochondrial metabolism disease mitochondrial myopathy mixed glioma multiple myeloma nasopharynx carcinoma neuroblastoma neuropathy nonpapillary renal cell carcinoma nutrition disease ophthalmoplegia oropharynx cancer ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma paraganglioma peripheral nervous system disease peritoneal carcinoma pilocytic astrocytoma polyneuropathy prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma ptosis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma teratoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tropical sprue tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer
6916	thromboxane A synthase 1	TBXAS1 Aliases: CYP5 CYP5A1 THAS TS TXAS TXS cytochrome P450, family 5, subfamily A, polypeptide 1	Homo sapiens (human)	Camurati-Engelmann disease Ghosal hematodiaphyseal syndrome acute myocardial infarction acute necrotizing pancreatitis alcoholic hepatitis alcoholic liver cirrhosis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxia telangiectasia atherosclerosis autosomal recessive osteopetrosis 7 benign mesothelioma brain infarction brain stem infarction breast cancer breast carcinoma cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis essential hypertension glomerulonephritis heart disease hydronephrosis hypertension inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease liver cirrhosis lung benign neoplasm macrocytic anemia malignant mesothelioma malignant pleural mesothelioma membranous glomerulonephritis myelofibrosis myocardial infarction nephritis osteopetrosis osteosclerosis pancytopenia pituitary adenoma pituitary cancer pituitary carcinoma platelet-type bleeding disorder 14 prostate cancer prostate carcinoma pulmonary embolism schizophrenia silent myocardial infarction speech disorder thrombocytopenia thrombosis ulcerative colitis urinary bladder cancer
100131187	thiosulfate sulfurtransferase like domain containing 1	TSTD1	Homo sapiens (human)
284486	thioesterase superfamily member 5	THEM5 Aliases: FLJ37964	Homo sapiens (human)	catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia steatotic liver disease
117145	thioesterase superfamily member 4	THEM4 Aliases: C-terminal modulator protein CTMP	Homo sapiens (human)	amyotrophic lateral sclerosis attention deficit hyperactivity disorder breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma liver cancer lung benign neoplasm lung cancer lung carcinoma mixed glioma pancreatic adenocarcinoma progressive muscular atrophy type 2 diabetes mellitus
83639	testis expressed 101	TEX101 Aliases: CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
6975	tectorin beta	TECTB	Homo sapiens (human)
7007	tectorin alpha	TECTA	Homo sapiens (human)	Stickler syndrome X-linked nonsyndromic deafness 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 breast cancer herpes zoster obsolete autosomal recessive nonsyndromic deafness 105 sensorineural hearing loss trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
80351	tankyrase 2	TNKS2 Aliases: ARTD6 PARP-5b PARP-5c PARP5B PARP5C TANK2 TNKL TRF1-interacting ankyrin-related ADP-ribose polymerase 2 pART6	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma cleft lip cribriform carcinoma depressive disorder diabetes mellitus endometrial cancer endometrial carcinoma granular cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia osteosarcoma skin benign neoplasm skin cancer squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer
8658	tankyrase	TNKS Aliases: ARTD5 PARP-5a PARP5A TIN1 TINF1 TNKS1 TRF1-interacting ankyrin-related ADP-ribose polymerase 1 pART5	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome 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 Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acoustic neuroma acute myeloid leukemia adenocarcinoma adenoma adult hepatocellular carcinoma adult medulloblastoma amyotrophic lateral sclerosis anaplastic astrocytoma angiomatous meningioma arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome benign meningioma bladder carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma cerebral infarction cerebrovascular disease cherubism childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood medulloblastoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome clear cell meningioma cleft lip colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma depressive disorder embryoma exostosis familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma granular cell carcinoma hepatocellular carcinoma herpes simplex high grade glioma inflammatory liposarcoma inherited metabolic disorder insulinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer liver cancer lung acinar adenocarcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma major depressive disorder malignant astrocytoma medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma monoclonal gammopathy of uncertain significance multiple myeloma neuroblastoma neurotic disorder obesity obsolete melancholia olfactory groove meningioma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma parasagittal meningioma pilocytic astrocytoma pituitary adenoma progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma sarcomatoid carcinoma sclerosing liposarcoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tarsal-carpal coalition syndrome transitional cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma urinary bladder cancer well-differentiated liposarcoma
27111	syndecan binding protein 2	SDCBP2 Aliases: SITAC18 ST-2 syntenin-2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cancer cerebral degeneration colorectal cancer colorectal carcinoma congestive heart failure diarrhea epidermodysplasia verruciformis large intestine cancer
6385	syndecan 4	SDC4 Aliases: SYND4 amphiglycan ryudocan syndecan proteoglycan 4	Homo sapiens (human)	Chagas disease Sezary's disease actinic keratosis acute interstitial pneumonia acute myeloid leukemia acute myocardial infarction allergic asthma anaplastic astrocytoma aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autism spectrum disorder autistic disorder bacterial infectious disease bone osteosarcoma breast cancer breast carcinoma cancer cataract 32 multiple types cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood osteosarcoma chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometriosis of uterus endometriosis fibrillary astrocytoma fibrodysplasia ossificans progressiva gastroenteritis gemistocytic astrocytoma glomerulonephritis hepatitis C high grade glioma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis intrinsic asthma juvenile pilocytic astrocytoma kidney disease large intestine cancer leprosy liver cirrhosis lung cancer lung non-small cell carcinoma malignant astrocytoma melanoma myocardial infarction myositis ossificans nephritis nephrosis osteoarthritis osteosarcoma papillary adenocarcinoma papillary renal cell carcinoma pilocytic astrocytoma pneumonia postinflammatory pulmonary fibrosis primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma pulmonary fibrosis pyoureter rheumatoid arthritis seborrheic keratosis silent myocardial infarction skin disease skin melanoma subependymal giant cell astrocytoma synovitis tenosynovitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma trypanosomiasis type 2 diabetes mellitus ureteral obstruction
9672	syndecan 3	SDC3 Aliases: N-syndecan SYND3 syndecan proteoglycan 3	Homo sapiens (human)	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 Creutzfeldt-Jakob disease Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 breast fibrocystic disease cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis C hepatocellular carcinoma liver cancer microglandular adenosis muscular dystrophy nonpapillary renal cell carcinoma obesity pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma
6383	syndecan 2	SDC2 Aliases: CD362 SYND2 fibroglycan syndecan proteoglycan 2	Homo sapiens (human)	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 CST3-related cerebral amyloid angiopathy Duchenne muscular dystrophy Joubert syndrome Klatskin's tumor Marfan syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome adenocarcinoma adenoma adult fibrosarcoma ameloblastoma anthracosilicosis asbestosis autistic disorder 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 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 benign mesothelioma bone cancer bone osteosarcoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral amyloid angiopathy cerebral degeneration childhood osteosarcoma cholangiocarcinoma chondrosarcoma cleft lip cleft palate colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy congestive heart failure diabetes mellitus diabetic ketoacidosis disease of mental health distal myopathy dysplastic nevus syndrome embryoma epidermolysis bullosa esophagus squamous cell carcinoma facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome fibrodysplasia ossificans progressiva fibrosarcoma follicular adenoma fragile X syndrome gallbladder cancer gallbladder carcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatitis B hepatitis C hepatocellular carcinoma hereditary multiple exostoses high grade glioma hydranencephaly hypereosinophilic syndrome hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis interstitial nephritis intrahepatic cholangiocarcinoma kidney disease kidney failure large intestine cancer limb-girdle muscular dystrophy lipoid nephrosis lissencephaly liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lupus nephritis malignant mesothelioma melanoma membranous glomerulonephritis microcystic adenoma microphthalmia mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome obesity 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 hilar cholangiocellular carcinoma obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteosarcoma pancreatic adenocarcinoma papillary adenoma papillary carcinoma pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postinflammatory pulmonary fibrosis proximal symphalangism psychotic disorder pulmonary fibrosis pyelitis pyelonephritis pyoureter renal infectious disease rheumatoid arthritis rippling muscle disease 2 scleroderma short-rib thoracic dysplasia 14 with polydactyly silicosis situs inversus skin melanoma skin squamous cell carcinoma squamous cell carcinoma syndromic X-linked intellectual disability Najm type systemic lupus erythematosus systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia
6382	syndecan 1	SDC1 Aliases: CD138 SYND1 syndecan syndecan proteoglycan 1	Homo sapiens (human)	B-cell lymphoma Bannayan-Riley-Ruvalcaba syndrome Burkitt lymphoma Cowden syndrome Crohn's colitis Crohn's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma, nodular sclerosis Hodgkin's lymphoma IgG4-related disease Kaposi's sarcoma Kawasaki disease POEMS syndrome Richter's syndrome acquired hyperkeratosis acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adhesions of uterus adult fibrosarcoma adult liposarcoma adult medulloblastoma allergic contact dermatitis ameloblastoma amyloidosis antithrombin III deficiency aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bacterial sepsis basal cell carcinoma benign mesothelioma benign peritoneal mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma blood coagulation disease bone disease bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cartilage disease celiac disease central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood liposarcoma childhood medulloblastoma cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell adenocarcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common variable immunodeficiency common wart congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma dedifferentiated liposarcoma dermatitis dermoid cyst diabetes mellitus diabetic cataract diabetic retinopathy diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disseminated intravascular coagulation diverticulitis of colon embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma essential hypertension extramedullary plasmacytoma familial hyperlipidemia familial nephrotic syndrome fibrolamellar carcinoma fibrosarcoma follicular lymphoma gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gonorrhea granular cell carcinoma granular corneal dystrophy 2 hair follicle neoplasm head and neck squamous cell carcinoma heavy chain disease hematologic cancer hepatitis C hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunoglobulin alpha deficiency impotence inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza interstitial nephritis intrahepatic cholangiocarcinoma invasive ductal carcinoma keratoacanthoma kidney disease kidney failure large intestine cancer leukemia lipoid nephrosis liposarcoma liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malaria malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mesenchymal cell neoplasm microphthalmia mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia multiple myeloma multiple sclerosis myelitis myocardial infarction myoepithelioma nasopharynx carcinoma nephritis nephrosis nephrotic syndrome neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuromyelitis optica obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete inherited blood coagulation disease obsolete ymphosarcoma optic neuritis osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma papilloma parapsoriasis peritoneal mesothelioma pilomatrixoma placenta cancer placental insufficiency plasma cell neoplasm plasmacytoma pleomorphic liposarcoma pneumonia polycythemia vera polyp of corpus uteri postinflammatory pulmonary fibrosis pre-eclampsia premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease primary sclerosing cholangitis proliferative diabetic retinopathy prostate cancer prostate carcinoma protein C deficiency protein S deficiency proteinuria psoriasis psychologic dyspareunia pulmonary fibrosis purpura fulminans pustulosis of palm and sole pyelitis pyelonephritis pyoureter refractory plasma cell neoplasm relapsing-remitting multiple sclerosis renal cell carcinoma renal infectious disease renal oncocytoma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma sclerosing cholangitis sebaceous carcinoma selective IgA deficiency disease silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma subacute sclerosing panencephalitis sweat gland cancer systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma transitional cell carcinoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia urinary bladder cancer uterine corpus cancer uterus leiomyosarcoma
8871	synaptojanin 2	SYNJ2 Aliases: INPP5H inositol polyphosphate-5-phosphatase H phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 2	Homo sapiens (human)	Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Parkinson's disease amyotrophic lateral sclerosis 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 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 breast cancer bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital muscular dystrophy depressive disorder distal myopathy early-onset Parkinson's disease facioscapulohumeral muscular dystrophy giant cell glioblastoma glioblastoma large intestine cancer limb-girdle muscular dystrophy lung cancer lung carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
8867	synaptojanin 1	SYNJ1 Aliases: INPP5G PARK20 inositol polyphosphate-5-phosphatase G phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1	Homo sapiens (human)	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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease 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 infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
6441	surfactant protein D	SFTPD Aliases: COLEC7 SP-D	Homo sapiens (human)	Bloch-Sulzberger syndrome Coronavirus infectious disease Crohn's colitis Crohn's disease Ebola hemorrhagic fever Fabry disease Wolman disease acquired immunodeficiency syndrome acute interstitial pneumonia acute lymphoblastic leukemia acute pancreatitis adenocarcinoma adenoid hypertrophy adenoma adult acute lymphocytic leukemia adult respiratory distress syndrome allergic asthma allergic disease allergic rhinitis anthracosilicosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis bacterial pneumonia bacterial sepsis blastomycosis brain stem infarction breast cancer bronchiectasis bronchiolitis obliterans bronchiolitis bronchitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer cardiovascular system disease cataract 32 multiple types cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chronic ethmoiditis chronic interstitial cystitis chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease colitis communicating hydrocephalus cone-rod dystrophy congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary stenosis craniosynostosis cribriform carcinoma cystic fibrosis diabetes mellitus diabetic ketoacidosis disease of metabolism dry eye syndrome embryoma fundus albipunctatus gastroenteritis glomerulonephritis granular cell carcinoma heart disease herpes simplex virus keratitis human immunodeficiency virus infectious disease hydrocephalus hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease influenza interstitial cystitis interstitial lung disease interstitial nephritis intrinsic asthma kidney disease leprosy leukopenia lipid storage disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis lymphoblastic lymphoma middle cerebral artery infarction mixed connective tissue disease nephritis nephrosis neurogenic arthropathy newborn respiratory distress syndrome nutmeg liver obesity obstructive hydrocephalus obstructive lung disease osteoarthritis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis paracoccidioidomycosis parapsoriasis periodontitis peripheral artery disease periventricular leukomalacia pneumocystosis pneumonia postinflammatory pulmonary fibrosis pre-malignant neoplasm prostate adenocarcinoma prostate cancer prostate carcinoma prune belly syndrome psoriasis pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pustulosis of palm and sole pyelitis pyelonephritis pyoureter renal infectious disease respiratory failure respiratory syncytial virus infectious disease retinitis pigmentosa rheumatoid arthritis rhinitis sarcoidosis scleroderma senile degeneration of brain sickle cell anemia silicosis sinusitis squamous cell carcinoma sudden infant death syndrome systemic lupus erythematosus systemic primary carnitine deficiency disease systemic scleroderma tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis viral infectious disease xerophthalmia
6440	surfactant protein C	SFTPC Aliases: BRICD6 BRICHOS domain containing 6 PSP-C SMDP2 SP-C	Homo sapiens (human)	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 Clostridium difficile colitis Hermansky-Pudlak syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome asthma bacterial pneumonia breast cancer breast carcinoma bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral degeneration chondrosarcoma chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia cribriform carcinoma cystadenoma cystic fibrosis dementia desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential hypertension familial periodic paralysis gastroesophageal reflux disease gestational diabetes granular cell carcinoma herpes simplex hiatus hernia hydrocephalus hyperinsulinism hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease intrinsic asthma lipoid proteinosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma myopathy neonatal respiratory failure newborn respiratory distress syndrome nonspecific interstitial pneumonia obstructive hydrocephalus obstructive lung disease obstructive sleep apnea peptic esophagitis perinatal necrotizing enterocolitis pneumonia polycystic ovary syndrome postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pulmonary valve insufficiency respiratory syncytial virus infectious disease sarcomatoid carcinoma secondary hypertrophic osteoarthropathy senile degeneration of brain tubular adenocarcinoma
729238	surfactant protein A2	SFTPA2 Aliases: COLEC5 SP-A2 surfactant, pulmonary-associated protein A2A	Homo sapiens (human)	Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cystic fibrosis embryoma esophagitis gastroesophageal reflux disease granular cell carcinoma heart disease hydrocephalus hypereosinophilic syndrome hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease interstitial nephritis intrinsic asthma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis newborn respiratory distress syndrome obesity obstructive hydrocephalus obstructive lung disease otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory failure respiratory syncytial virus infectious disease rheumatoid arthritis secondary hypertrophic osteoarthropathy senile degeneration of brain spondyloarthropathy spondylosis squamous cell carcinoma tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis
653509	surfactant protein A1	SFTPA1 Aliases: COLEC4 SP-A SP-A1 surfactant, pulmonary-associated protein A1A	Homo sapiens (human)	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 Hermansky-Pudlak syndrome Pick's disease Reye syndrome T cell deficiency X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amnestic disorder amyloidosis anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolitis obliterans bronchiolitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types cerebral degeneration cerebral infarction cerebrovascular disease chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cryptogenic organizing pneumonia cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential thrombocythemia extrinsic allergic alveolitis familial periodic paralysis gastroesophageal reflux disease granular cell carcinoma heart disease hematologic cancer hydrocephalus hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease interstitial lung disease interstitial nephritis intrinsic asthma keratoconus liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis macrocytic anemia mastitis myelodysplastic syndrome myopathy neurodegenerative disease newborn respiratory distress syndrome obesity obsolete T lymphocyte deficiency obstructive hydrocephalus obstructive lung disease osteomalacia otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis pulmonary alveolar proteinosis pulmonary edema pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory syncytial virus infectious disease retrograde amnesia rickets secondary hypertrophic osteoarthropathy senile degeneration of brain shigellosis sinusitis squamous cell carcinoma staphyloenterotoxemia systolic heart failure tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis viral infectious disease
6820	sulfotransferase family 2B member 1	SULT2B1 Aliases: HSST2	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome achondroplasia acquired hyperkeratosis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 14 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis bacterial sepsis cholestasis ectropion endometrial cancer endometrial carcinoma gallbladder cancer gallbladder carcinoma granuloma annulare hepatocellular carcinoma hypotrichosis ichthyosis keratosis follicularis kidney failure liver cancer mongolian spot obsolete congenital ichthyosiform erythroderma otitis media prostate cancer prostate carcinoma pseudoxanthoma elasticum uterine corpus cancer
6783	sulfotransferase family 1E member 1	SULT1E1 Aliases: EST	Homo sapiens (human)	Alzheimer's disease Axenfeld-Rieger syndrome type 2 Creutzfeldt-Jakob disease DiGeorge syndrome Down syndrome Laron syndrome Marfan syndrome Richter's syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction acute myocarditis adult lymphoma adult medulloblastoma adult oligodendroglioma alcoholic hepatitis amyotrophic lateral sclerosis androgen insensitivity syndrome ankylosing spondylitis aortic disease arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autosomal recessive limb-girdle muscular dystrophy type 2C bacterial sepsis bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cardiovascular system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic fatigue syndrome chronic lymphocytic leukemia colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis coronary thrombosis craniosynostosis cystic fibrosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysentery dysthymic disorder embryoma encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis essential hypertension eye disease familial hypertrophic cardiomyopathy gallbladder disease gastric adenocarcinoma glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy inferior myocardial infarction inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermediate coronary syndrome kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mitochondrial metabolism disease mitral valve stenosis mixed oligodendroglioma-astrocytoma multiple endocrine neoplasia type 1 myocardial infarction nephritis nephrosis neurotic disorder nodular prostate obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma peripheral artery disease polycystic ovary syndrome pompholyx primary hyperoxaluria primary open angle glaucoma primary pulmonary hypertension progressive muscular atrophy proliferative type fibrocystic change of breast prostate cancer prostate carcinoma prostatic adenoma pyoureter retinal disease retinitis schizophrenia 1 schizophrenia scleroderma severe acute respiratory syndrome silent myocardial infarction situs inversus steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tetralogy of Fallot thymic carcinoma thymoma transient cerebral ischemia tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis uterine corpus cancer velocardiofacial syndrome vertebrobasilar insufficiency
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy

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