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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	October 29, 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 **526 - 550** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
10941	UDP glucuronosyltransferase family 2 member A1 complex locus	UGT2A1	Homo sapiens (human)	cancer embryoma laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
54600	UDP glucuronosyltransferase family 1 member A9	UGT1A9 Aliases: HLUGP4 LUGP4 UGT1AI	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Plasmodium falciparum malaria abdominal obesity-metabolic syndrome 1 acute kidney failure adult hepatocellular carcinoma agranulocytosis atopic dermatitis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer cancer carcinoma childhood hepatocellular carcinoma cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis dermatitis diabetes mellitus diarrhea embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D hepatocellular carcinoma influenza kidney disease large intestine cancer leukopenia liver cancer liver disease lung cancer lung non-small cell carcinoma neonatal jaundice neutropenia obesity obsolete constipation obsolete dyspepsia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma stomach cancer thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
54576	UDP glucuronosyltransferase family 1 member A8	UGT1A8 Aliases: UGT1H	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leiomyoma leukopenia liver disease myofibroma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy xeroderma pigmentosum group D
54577	UDP glucuronosyltransferase family 1 member A7	UGT1A7 Aliases: UGT1G	Homo sapiens (human)	Crigler-Najjar syndrome Crohn's colitis Crohn's disease Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 acute pancreatitis adult hepatocellular carcinoma agranulocytosis alcoholic pancreatitis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest childhood hepatocellular carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma hemoglobin H disease hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis inflammatory bowel disease 1 inflammatory bowel disease influenza kernicterus due to isoimmunization kernicterus large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer leukopenia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma tracheal disease type 2 diabetes mellitus ulcerative colitis urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
54578	UDP glucuronosyltransferase family 1 member A6	UGT1A6 Aliases: GNT1 HLUGP UGT1F	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia arteriosclerotic cardiovascular disease asthma atherosclerosis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease childhood acute lymphocytic leukemia cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma contact dermatitis coronary artery disease cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastritis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin H disease hepatitis B hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrinsic asthma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcystic adenoma neonatal jaundice neutropenia nodular prostate nutmeg liver obesity occupational dermatitis papillary adenoma prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
54579	UDP glucuronosyltransferase family 1 member A5	UGT1A5 Aliases: UGT1E	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis diabetes mellitus embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D influenza leukopenia liver disease neonatal jaundice neutropenia obesity prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54657	UDP glucuronosyltransferase family 1 member A4	UGT1A4 Aliases: HUG-BR2 UGT1D	Homo sapiens (human)	Crigler-Najjar syndrome Fleck corneal dystrophy Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cardiac arrest celiac disease cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hematologic cancer hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver disease neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54659	UDP glucuronosyltransferase family 1 member A3	UGT1A3 Aliases: UGT1C	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis allergic asthma asthma beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis cryptococcosis diabetes mellitus differentiated thyroid gland carcinoma embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis gallbladder disease glycogen storage disease II hepatitis D influenza intrinsic asthma islet cell tumor leukopenia liver disease lung adenocarcinoma lung cancer neonatal jaundice neutropenia obesity pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54575	UDP glucuronosyltransferase family 1 member A10	UGT1A10 Aliases: UGT1J	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrahepatic cholangiocarcinoma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung carcinoma lung small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
54658	UDP glucuronosyltransferase family 1 member A1	UGT1A1 Aliases: UGT1A	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 Carney complex Crigler-Najjar syndrome Crohn's colitis Crohn's disease Fabry disease Gaucher's disease Gilbert syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute kidney failure acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pyelonephritis adenocarcinoma adenoma adult respiratory distress syndrome agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amnestic disorder anemia arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder bacterial sepsis beta thalassemia biliary tract cancer bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical squamous cell carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic myeloid leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diarrhea 6 congenital hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis cystinuria denture stomatitis diabetes mellitus diabetic ketoacidosis diarrhea differentiated thyroid gland carcinoma duodenum cancer embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematopoietic system disease hemiplegia hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemolytic anemia hepatitis A hepatitis B hepatitis C hepatitis D hepatitis hepatocellular carcinoma hereditary spherocytosis human immunodeficiency virus infectious disease hyperinsulinism hypertension hyperthyroidism hypertrophic pyloric stenosis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kernicterus due to isoimmunization kernicterus kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer leukopenia lipid storage disease liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoblastic lymphoma macrocytic anemia microcystic adenoma myeloid leukemia myocardial infarction neonatal jaundice nephrolithiasis neutropenia newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 occupational dermatitis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma peripheral artery disease prostate cancer prostate carcinoma prostatic adenoma rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retrograde amnesia sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma sensorineural hearing loss severe congenital neutropenia sickle cell anemia silent myocardial infarction small intestine adenocarcinoma small intestine cancer small intestine carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomatitis testicular cancer testis seminoma thalassemia thrombocytopenia thyrotoxicosis tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis 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 ulcerative stomatitis uric acid nephrolithiasis urinary bladder cancer uterine corpus cancer visual epilepsy xeroderma pigmentosum group D
7360	UDP-glucose pyrophosphorylase 2	UGP2 Aliases: SVUGP2 UGPP1 UTP--glucose-1-phosphate uridylyltransferase	Homo sapiens (human)	cancer central nervous system cancer classic galactosemia cystinuria developmental and epileptic encephalopathy 83 galactokinase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma paroxysmal nonkinesigenic dyskinesia 1
55757	UDP-glucose glycoprotein glucosyltransferase 2	UGGT2 Aliases: FLJ10873 FLJ11485 HUGT2 MGC117360 MGC150689 MGC87276 UDP-glucose:glycoprotein glucosyltransferase 2	Homo sapiens (human)	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma myocardial infarction silent myocardial infarction type 2 diabetes mellitus
56886	UDP-glucose glycoprotein glucosyltransferase 1	UGGT1 Aliases: HUGT1	Homo sapiens (human)	Crigler-Najjar syndrome Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha 1-antitrypsin deficiency beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis embryoma epilepsy gallbladder disease hepatitis C hepatitis D leukopenia liver disease neonatal jaundice neutropenia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia visual epilepsy xeroderma pigmentosum group D
7358	UDP-glucose 6-dehydrogenase	UGDH Aliases: GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	Homo sapiens (human)	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma developmental and epileptic encephalopathy 84 diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
7357	UDP-glucose ceramide glucosyltransferase	UGCG Aliases: GCS ceramide glucosyltransferase glucosylceramide synthase	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 Fabry disease Gaucher's disease type I Gaucher's disease Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Sandhoff disease acute myeloid leukemia aggressive NK-cell leukemia amyotrophic lateral sclerosis anemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus corneal disease coronary artery disease cystic kidney disease dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma double outlet right ventricle dysthymic disorder embryoma epilepsy essential hypertension giant cell glioblastoma glioblastoma glycine encephalopathy head and neck cancer head and neck squamous cell carcinoma hematologic cancer hemolytic anemia hepatocellular carcinoma high grade glioma hydrocephalus hyperglycemia hypertension intellectual disability invasive ductal carcinoma keratoconus kidney disease learning disability leukemia lipid storage disease liver cancer lung cancer lung non-small cell carcinoma macrocytic anemia major depressive disorder medulloblastoma medulloepithelioma melancholic depression multiple myeloma myelomeningocele narcolepsy neuroectodermal tumor neurotic disorder non-congenital cyst of kidney obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obstructive hydrocephalus ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma pharyngitis pneumonia post-traumatic stress disorder progressive muscular atrophy psoriatic arthritis rheumatoid arthritis senile degeneration of brain sick sinus syndrome status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute delirium supratentorial primitive neuroectodermal tumor tethered spinal cord syndrome thyroid gland papillary carcinoma type 2 diabetes mellitus visual epilepsy
23376	UFM1 specific ligase 1	UFL1	Homo sapiens (human)
7353	ubiquitin recognition factor in ER associated degradation 1	UFD1	Homo sapiens (human)
7352	uncoupling protein 3	UCP3	Homo sapiens (human)
7351	uncoupling protein 2	UCP2	Homo sapiens (human)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
54963	uridine-cytidine kinase 1 like 1	UCKL1	Homo sapiens (human)
7371	uridine-cytidine kinase 2	UCK2	Homo sapiens (human)
80700	UBX domain protein 6	UBXN6	Homo sapiens (human)
23190	UBX domain protein 4	UBXN4	Homo sapiens (human)
7343	upstream binding transcription factor	UBTF	Homo sapiens (human)
51366	ubiquitin protein ligase E3 component n-recognin 5	UBR5	Homo sapiens (human)

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