GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4001 - 4025** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
9498	solute carrier family 4 member 8	SLC4A8
9500	MAGE family member D1	MAGED1
9507	ADAM metallopeptidase with thrombospondin type 1 motif 4	ADAMTS4
9508	ADAM metallopeptidase with thrombospondin type 1 motif 3	ADAMTS3
9509	ADAM metallopeptidase with thrombospondin type 1 motif 2	ADAMTS2
9510	ADAM metallopeptidase with thrombospondin type 1 motif 1	ADAMTS1
9512	peptidase, mitochondrial processing subunit beta	PMPCB
9513	FMR1 autosomal homolog 2	FXR2
9514	galactose-3-O-sulfotransferase 1	GAL3ST1 CST cerebroside (3' phosphoadenylylsulfate:galactosylceramide 3') sulfotransferase	Behcet's disease Marfan syndrome Papillon-Lefevre disease acute myocardial infarction adenocarcinoma adenoma amyotrophic lateral sclerosis anhidrosis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis diabetic macular edema embryoma episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma granular cell carcinoma heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza invasive ductal carcinoma lateral sclerosis liver cancer mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 osteoarthritis papillary renal cell carcinoma progressive bulbar palsy progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction situs inversus stomach cancer stomach carcinoma substance abuse substance-related disorder tuberous sclerosis tubular adenocarcinoma 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
9516	lipopolysaccharide induced TNF factor	LITAF
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 KIAA0526 LCB2 LCB2A hLCB2a	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
9518	growth differentiation factor 15	GDF15
9520	aminopeptidase puromycin sensitive	NPEPPS
9521	eukaryotic translation elongation factor 1 epsilon 1	EEF1E1
9522	secretory carrier membrane protein 1	SCAMP1
9524	trans-2,3-enoyl-CoA reductase	TECR MRT14 TER very-long-chain enoyl-CoA reductase	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
9526	mannose-P-dolichol utilization defect 1	MPDU1 CDGIf Lec35 PQLC5 SL15 SLC66A5	IgA glomerulonephritis acquired hyperkeratosis autosomal recessive congenital ichthyosis 1 blindness cancer cerebral degeneration congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cystinuria dissociated nystagmus galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hypertropia hypothyroidism ichthyosis keratosis follicularis mechanical strabismus microcephaly mongolian spot myxedema obsolete congenital ichthyosiform erythroderma ophthalmoplegia optic atrophy pathologic nystagmus pseudoxanthoma elasticum spontaneous ocular nystagmus strabismus
9528	transmembrane protein 59	TMEM59
9530	BAG cochaperone 4	BAG4
9531	BAG cochaperone 3	BAG3
9532	BAG cochaperone 2	BAG2
9536	prostaglandin E synthase	PTGES MGST-IV MGST1-L1 MGST1-like 1 PIG12 TP53I12 glutathione S-transferase 1-like 1 microsomal glutathione S-transferase 1-like 1 microsomal prostaglandin E synthase-1 p53-induced gene 12 tumor protein p53 inducible protein 12	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 Hirschsprung's disease Leydig cell tumor Marinesco-Sjogren syndrome 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 abdominal aortic aneurysm acute myocardial infarction adenocarcinoma adenoma adult lymphoma allergic asthma amyotrophic lateral sclerosis anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autism spectrum disorder autistic disorder bile duct adenocarcinoma bile duct carcinoma brain disease breast cancer breast carcinoma breast disease bronchus cancer bronchus carcinoma cancer carcinoma carotid artery disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood lymphoma cholangiocarcinoma chronic fatigue syndrome chronic kidney disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma disease of metabolism distal arthrogryposis ductal carcinoma in situ embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma gastroenteritis gastroesophageal reflux disease gemistocytic astrocytoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis hepatocellular carcinoma high grade glioma hydronephrosis hypertension ileitis ileocolitis ileus in situ carcinoma inflammatory bowel disease intestinal obstruction intracranial aneurysm intrahepatic cholangiocarcinoma intrinsic asthma ischemia islet cell tumor isovaleric acidemia juvenile pilocytic astrocytoma kidney disease lactocele large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma malignant astrocytoma melanoma mixed glioma multiple sclerosis myelitis myocardial infarction nephritis nephrosis neuroblastoma neurodegenerative disease obesity obsolete ymphosarcoma osteoarthritis ovary epithelial cancer pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma papilloma patent ductus arteriosus penile benign neoplasm peptic esophagitis periodontitis pilocytic astrocytoma pneumonia primary cerebellar degeneration primary ovarian insufficiency primary sclerosing cholangitis progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma pyoureter rheumatoid arthritis sarcomatoid carcinoma sclerosing cholangitis silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma squamous cell papilloma squamous papillomatosis status epilepticus subependymal giant cell astrocytoma thymic carcinoma thymoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma type C thymoma ureteral obstruction visual epilepsy
9540	tumor protein p53 inducible protein 3	TP53I3
9541	corepressor interacting with RBPJ, CIR1	CIR1
9542	neuregulin 2	NRG2

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