GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6626 - 6650** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
56547	matrix metallopeptidase 26	MMP26
56548	carbohydrate sulfotransferase 7	CHST7 C6ST-2 C6ST2	bronchus cancer bronchus carcinoma colorectal cancer colorectal carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma pneumonia
56605	endoplasmic reticulum oxidoreductase 1 beta	ERO1B
56606	solute carrier family 2 member 9	SLC2A9
56623	inositol polyphosphate-5-phosphatase E	INPP5E CORS1 PPI5PIV Phosphatidylinositol polyphosphate 5-phosphatase type IV pharbin	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
56624	N-acylsphingosine amidohydrolase 2	ASAH2 neutral ceramidase non-lysosomal ceramidase	Alzheimer's disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cardiomyopathy celiac disease colorectal cancer congenital diaphragmatic hernia cystic fibrosis dementia diabetes mellitus diabetic ketoacidosis gallbladder disease gamma heavy chain disease glaucoma heavy chain disease inflammatory bowel disease large intestine cancer liver disease lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neuroblastoma obesity systemic Epstein-Barr virus positive T-cell lymphoma of childhood type 2 diabetes mellitus
56647	BRCA2 and CDKN1A interacting protein	BCCIP
56649	transmembrane serine protease 4	TMPRSS4
56650	claudin domain containing 1	CLDND1
56654	neural proliferation, differentiation and control 1	NPDC1
56656	olfactory receptor family 2 subfamily S member 2	OR2S2
56658	tripartite motif containing 39	TRIM39
56659	potassium two pore domain channel subfamily K member 13	KCNK13
56660	potassium two pore domain channel subfamily K member 12	KCNK12
56666	pannexin 2	PANX2
56667	mucin 13, cell surface associated	MUC13
56670	succinate receptor 1	SUCNR1
56674	TMEM9 domain family member B	TMEM9B
56675	nuclear receptor interacting protein 3	NRIP3
56704	junctophilin 1	JPH1
56751	BarH like homeobox 1	BARHL1
56829	zinc finger CCCH-type containing, antiviral 1	ZC3HAV1
56833	SLAM family member 8	SLAMF8
56834	G protein-coupled receptor 137	GPR137
56848	sphingosine kinase 2	SPHK2	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 Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kaposi's sarcoma Pick's disease Reye syndrome actinic keratosis acute lymphoblastic leukemia acute pancreatitis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma alcoholic hepatitis alcoholic liver cirrhosis amnestic disorder anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bile duct adenocarcinoma bile duct carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cartilage disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease chikungunya childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma chondrosarcoma chronic fatigue syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma connective tissue disease coronary artery disease cystic fibrosis dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis essential hypertension fibrillary astrocytoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia immune system disease influenza intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia malignant astrocytoma malignant pleural mesothelioma metabolic dysfunction-associated steatohepatitis middle cerebral artery infarction mixed glioma multiple myeloma multiple sclerosis myelitis neuroblastoma neurodegenerative disease obesity obsolete asthenopia obsolete ymphosarcoma osteoarthritis osteoglophonic dysplasia osteosarcoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis pilocytic astrocytoma pneumonia postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary fibrosis pustulosis of palm and sole retinal disease retinitis retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma seborrheic keratosis skin disease skin squamous cell carcinoma steatotic liver disease subependymal giant cell astrocytoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia thyroid gland papillary carcinoma type 2 diabetes mellitus ureteral obstruction vascular disease viral infectious disease yellow fever

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