GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7376 - 7400** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
79905	transmembrane channel like 7	TMC7
79908	butyrophilin like 8	BTNL8
79915	ATPase family AAA domain containing 5	ATAD5
79925	sperm flagellar 2	SPEF2
79930	docking protein 3	DOK3
79932	KIAA0319 like	KIAA0319L
79933	synaptopodin 2 like	SYNPO2L
79935	cyclin P	CCNP
79937	contactin associated protein family member 3	CNTNAP3
79944	L-2-hydroxyglutarate dehydrogenase	L2HGDH 2-hydroxyglutarate dehydrogenase FLJ12618	2-hydroxyglutaric aciduria D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria L-2-hydroxyglutaric aciduria brain cancer cerebellar ataxia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital nystagmus disease of metabolism dissociated nystagmus dystonia encephalitis encephalomyelitis epilepsy giant cell glioblastoma glioblastoma hereditary spastic paraplegia high grade glioma hypertropia intellectual disability learning disability mechanical strabismus myelitis nervous system cancer neurodegenerative disease nonpapillary renal cell carcinoma ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 vascular dementia visual epilepsy
79947	dehydrodolichyl diphosphate synthase subunit	DHDDS DS FLJ13102 HDS RP59 hCIT	Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Dubowitz syndrome Ehrlich tumor carcinoma Laron 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 Patau syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome Weissenbacher-Zweymuller syndrome X-linked Aarskog syndrome Zollinger-Ellison syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult medulloblastoma adult oligodendroglioma agranulocytosis amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bladder carcinoma blepharospasm blindness bone osteosarcoma brain stem glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carnitine palmitoyltransferase II deficiency cataract central nervous system cancer central nervous system lymphoma cerebral degeneration cervical squamous cell carcinoma childhood medulloblastoma childhood oligodendroglioma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital diaphragmatic hernia corneal disease cribriform carcinoma cryptorchidism decubitus ulcer dementia depressive disorder developmental delay and seizures with or without movement abnormalities diarrhea dysthymic disorder dystonia early myoclonic encephalopathy embryoma endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma focal hand dystonia fundus albipunctatus giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma hiatus hernia high grade glioma hyperinsulinism hypoglycemia hypogonadism inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor keratoconus kidney failure large intestine cancer leukopenia lingual-facial-buccal dyskinesia liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma neuroblastoma neurofibromatosis 1 neurofibromatosis neurotic disorder neutropenia obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma oligodendroglioma ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic endocrine carcinoma papillary renal cell carcinoma pathological gambling progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal degeneration retinitis pigmentosa 59 retinitis pigmentosa rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe congenital neutropenia squamous cell carcinoma squamous cell neoplasm status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder thyroid gland medullary carcinoma tooth agenesis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer varicocele visual epilepsy
79948	phospholipid phosphatase related 3	PLPPR3
79955	PDZ domain containing 7	PDZD7
79956	endoplasmic reticulum metallopeptidase 1	ERMP1
79960	jade family PHD finger 1	JADE1
79966	stearoyl-CoA desaturase 5	SCD5 ACOD4 FADS4 FLJ21032 HSCD5	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 T-cell acute lymphoblastic leukemia acquired immunodeficiency syndrome age related macular degeneration ankylosing spondylitis arthritis arthropathy autosomal dominant nonsyndromic deafness 79 breast cancer cancer cardiomyopathy cerebral degeneration degeneration of macula and posterior pole depressive disorder diabetes mellitus embryoma endomyocardial fibrosis familial hypertrophic cardiomyopathy hepatocellular carcinoma human immunodeficiency virus infectious disease hypertrophic cardiomyopathy liver cancer macular degeneration melanoma osteoarthritis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease restrictive cardiomyopathy rheumatoid arthritis sickle cell anemia skin melanoma systemic lupus erythematosus systemic primary carnitine deficiency disease type 2 diabetes mellitus
79971	Wnt ligand secretion mediator	WLS
79974	cadherin like and PC-esterase domain containing 1	CPED1
79977	grainyhead like transcription factor 2	GRHL2
79980	DSN1 component of MIS12 kinetochore complex	DSN1
79987	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	SVEP1
79993	ELOVL fatty acid elongase 7	ELOVL7 FLJ23563	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy cancer hidradenitis suppurativa hidradenitis inflammatory bowel disease multiple system atrophy pompholyx prostate cancer prostate carcinoma
80000	GREB1 like retinoic acid receptor coactivator	GREB1L
80003	pecanex 2	PCNX2
80005	dedicator of cytokinesis 5	DOCK5

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