GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7751 - 7775** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
84461	neuralized E3 ubiquitin protein ligase 4	NEURL4
84465	multiple EGF like domains 11	MEGF11
84466	multiple EGF like domains 10	MEGF10
84467	fibrillin 3	FBN3
84501	spire type actin nucleation factor 2	SPIRE2
84502	junctophilin 4	JPH4
84513	phospholipid phosphatase 5	PLPP5 DPPL1 HTPAP diacylglycerol pyrophosphate phosphatase-like 1	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer depressive disorder hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma major depressive disorder melancholic depression obsolete melancholia pancreatic adenocarcinoma
84514	GH3 domain containing	GHDC
84532	acyl-CoA synthetase short chain family member 1	ACSS1 AceCS2L MGC33843 dJ568C11.3	acute myocardial infarction bladder carcinoma cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis embryoma lung cancer lung non-small cell carcinoma myocardial infarction papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction urinary bladder cancer
84539	melanin concentrating hormone receptor 2	MCHR2
84542	SANT and BTB domain regulator of CSR	SANBR
84561	solute carrier family 12 member 8	SLC12A8
84569	lysozyme like 1	LYZL1 LYC2 MGC33408
84570	collagen type XXV alpha 1 chain	COL25A1
84572	N-acetylglucosamine-1-phosphate transferase subunit gamma	GNPTG CAB56184 GlcNAc-phosphotransferase gamma-subunit c316G12.3	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis III gamma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
84614	zinc finger and BTB domain containing 37	ZBTB37
84617	tubulin beta 6 class V	TUBB6
84620	ST6 beta-galactoside alpha-2,6-sialyltransferase 2	ST6GAL2 KIAA1877 St6GalII	breast cancer esophageal cancer esophageal carcinoma thyroid gland follicular carcinoma
84622	zinc finger protein 594	ZNF594
84623	kirre like nephrin family adhesion molecule 3	KIRREL3
84624	fibronectin type III domain containing 1	FNDC1
84628	netrin G2	NTNG2
84629	trinucleotide repeat containing 18	TNRC18
84630	tau tubulin kinase 1	TTBK1
84631	SLIT and NTRK like family member 2	SLITRK2

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