GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3226 - 3250** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
7290	histone cell cycle regulator	HIRA
7291	twist family bHLH transcription factor 1	TWIST1
7292	TNF superfamily member 4	TNFSF4
7293	TNF receptor superfamily member 4	TNFRSF4
7297	tyrosine kinase 2	TYK2
7298	thymidylate synthetase	TYMS
7299	tyrosinase	TYR
7301	TYRO3 protein tyrosine kinase	TYRO3
7306	tyrosinase related protein 1	TYRP1
7311	ubiquitin A-52 residue ribosomal protein fusion product 1	UBA52
7317	ubiquitin like modifier activating enzyme 1	UBA1
7337	ubiquitin protein ligase E3A	UBE3A
7341	small ubiquitin like modifier 1	SUMO1
7343	upstream binding transcription factor	UBTF
7348	uroplakin 1B	UPK1B
7351	uncoupling protein 2	UCP2	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
7352	uncoupling protein 3	UCP3
7353	ubiquitin recognition factor in ER associated degradation 1	UFD1
7355	solute carrier family 35 member A2	SLC35A2 UDP-Gal-Tr UDP-galactose translocator UGAT UGT UGT1 UGT2 UGTL	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 Barrett's esophagus Crigler-Najjar syndrome Dandy-Walker syndrome Gilbert syndrome Laron syndrome Pick's disease Reye syndrome West syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adult lymphoma agranulocytosis alternating exotropia anisometropia aromatase excess syndrome autosomal recessive chronic granulomatous disease 1 bacterial infectious disease beta thalassemia bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma cancer carcinoma central nervous system lymphoma central sleep apnea cerebral degeneration childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis chronic granulomatous disease clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIm congenital disorder of glycosylation congenital nystagmus craniosynostosis cryptococcosis cyclic hematopoiesis cystinuria developmental and epileptic encephalopathy 36 diarrhea dissociated nystagmus embryoma epilepsy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esotropia exotropia galactosemia gallbladder disease gastroesophageal reflux disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatitis B hepatitis C hepatitis D hyperopia hypertropia hypoglycemia intellectual disability large intestine cancer learning disability leukopenia liver disease lymphoma macular corneal dystrophy mechanical strabismus microcephaly monocular esotropia monocular exotropia neonatal jaundice neutropenia obsolete constipation obsolete infantile epileptic encephalopathy obsolete ymphosarcoma obstructive sleep apnea ophthalmoplegia ovarian cancer ovarian carcinoma pathologic nystagmus peptic esophagitis placental insufficiency primary cutaneous amyloidosis prostate cancer prostate carcinoma pyloric stenosis sarcomatoid carcinoma scoliosis sensorineural hearing loss severe congenital neutropenia sickle cell anemia spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tetralogy of Fallot thalassemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
7357	UDP-glucose ceramide glucosyltransferase	UGCG GCS ceramide glucosyltransferase glucosylceramide synthase	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
7358	UDP-glucose 6-dehydrogenase	UGDH GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	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
7360	UDP-glucose pyrophosphorylase 2	UGP2 SVUGP2 UGPP1 UTP--glucose-1-phosphate uridylyltransferase	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
7363	UDP glucuronosyltransferase family 2 member B4	UGT2B4 UGT2B11	breast cancer cancer cerebral infarction cerebrovascular disease cholestasis embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma hepatocellular carcinoma liver cancer primary biliary cholangitis steatotic liver disease
7364	UDP glucuronosyltransferase family 2 member B7	UGT2B7 UGT2B9	agnosia bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardia cancer cardiovascular system disease clear cell renal cell carcinoma colorectal cancer colorectal carcinoma congestive heart failure diarrhea embryoma endometrial cancer endometrial carcinoma epilepsy gallbladder disease heart disease hepatitis hepatocellular carcinoma kidney cancer large intestine cancer leukopenia liver cancer liver carcinoma liver disease renal carcinoma renal cell carcinoma sarcomatoid carcinoma sickle cell anemia transitional cell carcinoma tuberculosis urinary bladder cancer uterine corpus cancer visual epilepsy
7365	UDP glucuronosyltransferase family 2 member B10	UGT2B10	cancer embryoma prostate cancer prostate carcinoma

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