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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
91373	UDP-N-acetylglucosamine pyrophosphorylase 1 like 1	UAP1L1	Homo sapiens (human)	hepatocellular carcinoma liver cancer
6675	UDP-N-acetylglucosamine pyrophosphorylase 1	UAP1 Aliases: AGX1 AgX UDP-N-acetylglucosamine diphosphorylase 1 UDP-N-acetylhexosamine pyrophosphorylase 1	Homo sapiens (human)	hepatitis B hepatocellular carcinoma liver cancer pneumocystosis
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
7991	tumor suppressor candidate 3	TUSC3 Aliases: MGC13453 MRT7 MagT2 Magnesium uptake/transporter TUSC3 N33 OST3A SLC58A2 oligosaccharyltransferase 3 homolog A (S. cerevisiae)	Homo sapiens (human)	Peutz-Jeghers syndrome agnosia autosomal recessive intellectual developmental disorder 7 autosomal recessive intellectual developmental disorder bacterial infectious disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration childhood osteosarcoma chondrosarcoma choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression microcephaly mixed glioma neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma partial motor epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tongue squamous cell carcinoma ulcerative colitis visual epilepsy von Hippel-Lindau disease
100131187	thiosulfate sulfurtransferase like domain containing 1	TSTD1	Homo sapiens (human)
11181	trehalase	TREH Aliases: MGC129621 TRE TREA alpha,alpha-trehalase alpha,alpha-trehalose glucohydrolase	Homo sapiens (human)	adult medulloblastoma autosomal dominant cerebellar ataxia bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood medulloblastoma diabetes mellitus diabetic ketoacidosis diarrhea embryoma familial nephrotic syndrome giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma herpes simplex high grade glioma kidney disease lipoid nephrosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma medulloblastoma medullomyoblastoma melanotic medulloblastoma mixed glioma nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome optic atrophy 1 optic atrophy pyoureter rheumatoid arthritis spinal cancer steatotic liver disease type 2 diabetes mellitus
8459	tyrosylprotein sulfotransferase 2	TPST2 Aliases: TANGO13B protein-tyrosine sulfotransferase 2 transport and golgi organization 13 homolog B (Drosophila)	Homo sapiens (human)
8460	tyrosylprotein sulfotransferase 1	TPST1 Aliases: TANGO13A transport and golgi organization 13 homolog A (Drosophila)	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer colorectal adenocarcinoma colorectal cancer colorectal carcinoma gout large intestine cancer lung benign neoplasm lung cancer lung carcinoma
7167	triosephosphate isomerase 1	TPI1	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 Behcet's disease Chagas disease Creutzfeldt-Jakob disease Ebola hemorrhagic fever Goodpasture syndrome Japanese encephalitis Pick's disease Reye syndrome Takayasu's arteritis adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aseptic meningitis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bipolar disorder blastomycosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carbohydrate metabolic disorder cardiomyopathy central nervous system cancer central nervous system disease cerebral degeneration cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chronic fatigue syndrome chronic myeloid leukemia colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia congestive heart failure coronary artery disease cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia dengue disease dermatitis diaphragm disease diarrhea disease of metabolism dystonia embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma exanthem familial hypertrophic cardiomyopathy familial periodic paralysis favism giant cell glioblastoma giardiasis glioblastoma gliosarcoma granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypertrophic cardiomyopathy immune system disease inherited metabolic disorder intellectual disability intrinsic asthma kwashiorkor large intestine cancer learning disability leech infestation lingual-facial-buccal dyskinesia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma malignant pleural mesothelioma marasmus melanoma microsporidiosis mixed glioma multiple sclerosis myelitis myiasis myopathy nervous system disease neuroblastoma neurodegenerative disease neuromuscular disease neuropathy newborn respiratory distress syndrome nodular goiter normocytic anemia nutrition disease ocular hypertension osteoarthritis osteochondritis dissecans osteoporosis papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis peripheral nervous system disease periventricular leukomalacia pleurisy polyarteritis nodosa polyneuropathy progressive supranuclear palsy proliferative type fibrocystic change of breast protein-energy malnutrition reflex sympathetic dystrophy rheumatoid arthritis schizophrenia scleroderma skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma systemic lupus erythematosus systemic scleroderma thyroid gland papillary carcinoma tongue squamous cell carcinoma toxoplasmosis triosephosphate isomerase deficiency trypanosomiasis tuberculosis tubular adenocarcinoma uveal melanoma viral infectious disease viral meningitis visual epilepsy yellow fever
7165	TPD52 like 2	TPD52L2	Homo sapiens (human)
7157	tumor protein p53	TP53	Homo sapiens (human)	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
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
8794	TNF receptor superfamily member 10c	TNFRSF10C Aliases: CD263 DcR1 LIT TRAILR3 TRID	Homo sapiens (human)	Churg-Strauss syndrome Coffin-Siris syndrome 1 Coffin-Siris syndrome Crohn's colitis Crohn's disease Down syndrome Richter's syndrome acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma adult lymphoma agranulocytosis benign ependymoma benign mesothelioma bladder carcinoma breast cancer breast carcinoma cancer cellular ependymoma central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood lymphoma chronic lymphocytic leukemia chronic obstructive pulmonary disease colon cancer congenital heart disease cribriform carcinoma cystadenoma distal arthrogryposis embryoma endometrial cancer endometrial carcinoma essential thrombocythemia familial hypercholesterolemia giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inflammatory bowel disease 1 inflammatory bowel disease intellectual disability juvenile rheumatoid arthritis learning disability leukemia leukopenia liver cancer lung cancer lung non-small cell carcinoma lymphoma malignant mesothelioma melanoma mixed glioma multiple myeloma multiple sclerosis myelodysplastic syndrome myxopapillary ependymoma neuroblastoma neutropenia obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary ependymoma periodontitis post-traumatic stress disorder prostate cancer prostate carcinoma severe congenital neutropenia skin melanoma systemic lupus erythematosus tanycytic ependymoma tongue squamous cell carcinoma tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer uveal melanoma
7124	tumor necrosis factor	TNF	Homo sapiens (human)	Alzheimer's disease Behcet's disease COVID-19 Cor pulmonale Crohn's disease Fanconi anemia Gaucher's disease Graves ophthalmopathy Graves' disease IgA glomerulonephritis Kawasaki disease Mycobacterium avium complex disease Mycoplasma pneumoniae pneumonia Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease Weill-Marchesani syndrome acne acquired immunodeficiency syndrome acute myocardial infarction adult respiratory distress syndrome alcoholic hepatitis amyloidosis anemia anogenital venereal wart anterior uveitis anti-basement membrane glomerulonephritis aortic valve stenosis aplastic anemia aspiration pneumonia asthma atopic dermatitis atrial fibrillation autistic disorder autoimmune hepatitis bacterial pneumonia beta thalassemia brain infarction breast adenocarcinoma breast cancer bronchiectasis bronchopulmonary dysplasia cardiac arrest cardiomyopathy cerebral infarction cervical cancer cholesteatoma of middle ear chorioamnionitis chronic obstructive pulmonary disease cicatricial pemphigoid cochlear disease congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary restenosis cryoglobulinemia cutaneous leishmaniasis cystic fibrosis cystitis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic neuropathy diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy disseminated intravascular coagulation encephalitis end stage renal disease endometriosis endophthalmitis epididymitis epilepsy erythema nodosum esophagitis extrinsic allergic alveolitis eye disease farmer's lung gastritis glaucoma heart valve disease hemochromatosis hepatitis A hepatitis B hepatocellular carcinoma hepatopulmonary syndrome hepatorenal syndrome hereditary hemorrhagic telangiectasia herpes zoster hidradenitis suppurativa high grade glioma human immunodeficiency virus infectious disease hypertension hypochromic microcytic anemia impotence inclusion body myopathy with Paget disease of bone and frontotemporal dementia inflammatory bowel disease intermediate uveitis intracranial aneurysm iron deficiency anemia keratoconjunctivitis sicca kidney disease leprosy liver cirrhosis liver disease low tension glaucoma lung disease lung non-small cell carcinoma lupus nephritis lymphopenia malaria metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease mevalonic aciduria middle cerebral artery infarction migraine without aura migraine mixed connective tissue disease mucocutaneous leishmaniasis mucopolysaccharidosis VI multiple myeloma multiple sclerosis muscular dystrophy myelodysplastic syndrome myocardial infarction myositis neutropenia obesity obstructive sleep apnea open-angle glaucoma oral squamous cell carcinoma otitis media ovarian cancer paracoccidioidomycosis peptic esophagitis perinatal necrotizing enterocolitis periodontitis peritonitis periventricular leukomalacia pleurisy portal hypertension pre-eclampsia primary biliary cholangitis primary open angle glaucoma primary sclerosing cholangitis prostate cancer psoriasis psoriatic arthritis pulmonary edema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole radiculopathy renal cell carcinoma renal hypertension retinal detachment rheumatoid arthritis rhinitis root resorption schizophrenia sciatic neuropathy scleritis sensorineural hearing loss severe acute respiratory syndrome sickle cell anemia silicosis skin disease small cell carcinoma spondyloarthropathy status epilepticus systemic lupus erythematosus thalassemia thrombocytopenia toxic shock syndrome trachoma transient cerebral ischemia tuberculosis type 1 diabetes mellitus type 2 diabetes mellitus typhoid fever ulcerative colitis ureteral obstruction uveitis vascular dementia visceral leishmaniasis visual epilepsy vitiligo
84899	transmembrane O-mannosyltransferase targeting cadherins 4	TMTC4 Aliases: FLJ14624 FLJ22153	Homo sapiens (human)	autosomal recessive nonsyndromic deafness breast cancer idiopathic scoliosis
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
160335	transmembrane O-mannosyltransferase targeting cadherins 2	TMTC2 Aliases: DKFZp762A217	Homo sapiens (human)	allergic asthma asthma dermatitis glaucoma intrinsic asthma low tension glaucoma mutism primary open angle glaucoma sensorineural hearing loss
83857	transmembrane O-mannosyltransferase targeting cadherins 1	TMTC1 Aliases: ARG99 FLJ31400 FLJ41625 OLF	Homo sapiens (human)	bipolar disorder bone marrow disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health endometrial cancer endometrial carcinoma large intestine cancer psychotic disorder schizophrenia spinal cord disease syringomyelia
255043	transmembrane protein 86B	TMEM86B Aliases: MGC30208 alkenylglycerophosphocholine hydrolase alkenylglycerophosphoethanolamine hydrolase	Homo sapiens (human)
54916	transmembrane protein 260	TMEM260	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis T-cell non-Hodgkin lymphoma acute myeloid leukemia alcohol dependence alcohol use disorder cancer double outlet right ventricle embryoma kidney failure lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma stomach cancer ventricular septal defect
147007	transmembrane protein 199	TMEM199 Aliases: MGC45714 VMA12 VPH2	Homo sapiens (human)	breast cancer breast carcinoma candidiasis congenital disorder of glycosylation type IIp developmental and epileptic encephalopathy 36 gallbladder disease liver disease steatotic liver disease
55858	transmembrane protein 165	TMEM165 Aliases: GDT1 SLC64A1 TMPT27 TPA regulated locus TPARL	Homo sapiens (human)	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
54732	transmembrane p24 trafficking protein 9	TMED9 Aliases: HSGP25L2G p24a2 p24alpha2	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome adult T-cell leukemia/lymphoma alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 cancer central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy epilepsy frontotemporal dementia generalized anxiety disorder large intestine cancer lateral sclerosis malaria motor neuron disease nervous system disease neurodegenerative disease nonpapillary renal cell carcinoma obsolete T-cell lymphoblastic leukemia/lymphoma optic atrophy 1 optic atrophy papillary renal cell carcinoma phototoxic dermatitis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma status epilepticus tuberculosis visual epilepsy
283578	transmembrane p24 trafficking protein family member 8	TMED8	Homo sapiens (human)

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