GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4901 - 4925** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
23215	proline rich coiled-coil 2C	PRRC2C
23214	exportin 6	XPO6
23213	sulfatase 1	SULF1 Extracellular sulfatase Sulf-1 KIAA1077 SULF-1 hSulf-1	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
23212	ribosome biogenesis regulator 1 homolog	RRS1
23211	zinc finger CCCH-type containing 4	ZC3H4
23205	acyl-CoA synthetase bubblegum family member 1	ACSBG1 BG1 BGM FLJ30320 KIAA0631 MGC14352 bubblegum hBG1 hsBG lipidosin very long-chain acyl-CoA synthetase	B-cell lymphoma Clostridium difficile colitis Crohn's colitis Crohn's disease Evans' syndrome HCL-V 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 Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome adrenoleukodystrophy autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma chronic kidney disease chronic lymphocytic leukemia colitis colon carcinoma colorectal cancer diffuse large B-cell lymphoma embryoma gastroenteritis gliosarcoma hairy cell leukemia hemophagocytic lymphohistiocytosis hepatocellular carcinoma high grade glioma ileitis ileocolitis ileus immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal obstruction irritable bowel syndrome kwashiorkor late onset Parkinson's disease liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia marasmus mixed glioma multiple myeloma mycosis fungoides neurocirculatory asthenia neurodegenerative disease non-Hodgkin lymphoma nutrition disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma primary immunodeficiency disease protein-energy malnutrition reticulosarcoma rheumatoid arthritis scleroderma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma ulcerative colitis viral infectious disease
23203	peptidase, mitochondrial processing subunit alpha	PMPCA
23201	family with sequence similarity 168 member A	FAM168A
23200	ATPase phospholipid transporting 11B (putative)	ATP11B
23199	Gse1 coiled-coil protein	GSE1
23198	proteasome activator subunit 4	PSME4
23197	Fas associated factor family member 2	FAF2
23196	family with sequence similarity 120 member A	FAM120A
23195	midasin AAA ATPase 1	MDN1
23194	F-box and leucine rich repeat protein 7	FBXL7
23193	glucosidase II alpha subunit	GANAB G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
23192	autophagy related 4B cysteine peptidase	ATG4B
23191	cytoplasmic FMR1 interacting protein 1	CYFIP1
23190	UBX domain protein 4	UBXN4
23189	KN motif and ankyrin repeat domains 1	KANK1
23187	pleckstrin homology like domain family B member 1	PHLDB1
23186	REST corepressor 1	RCOR1
23185	La ribonucleoprotein 4B	LARP4B
23184	mesoderm development LRP chaperone	MESD
23181	disco interacting protein 2 homolog A	DIP2A

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