GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7776 - 7800** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
84632	actin filament associated protein 1 like 2	AFAP1L2
84634	KISS1 receptor	KISS1R
84636	G protein-coupled receptor 174	GPR174
84640	ubiquitin specific peptidase 38	USP38
84641	major facilitator superfamily domain containing 14B	MFSD14B
84647	phospholipase A2 group XIIB	PLA2G12B	membranous glomerulonephritis
84649	diacylglycerol O-acyltransferase 2	DGAT2	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 agenesis of the corpus callosum with peripheral neuropathy androgen insensitivity syndrome cancer cholestasis chronic kidney disease generalized atherosclerosis hepatitis B hepatitis C hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 liver cancer metabolic dysfunction-associated steatotic liver disease motor peripheral neuropathy neuropathy obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy premature menopause prostate cancer prostate carcinoma steatotic liver disease
84654	spermatogenic leucine zipper 1	SPZ1
84658	adhesion G protein-coupled receptor E3	ADGRE3
84659	ribonuclease A family member 7	RNASE7
84660	coiled-coil domain containing 62	CCDC62
84665	myopalladin	MYPN
84668	hyccin PI4KA lipid kinase complex subunit 1	HYCC1
84674	caspase recruitment domain family member 6	CARD6
84675	tripartite motif containing 55	TRIM55
84676	tripartite motif containing 63	TRIM63
84678	lysine demethylase 2B	KDM2B
84679	solute carrier family 9 member A7	SLC9A7
84687	protein phosphatase 1 regulatory subunit 9B	PPP1R9B
84693	methylmalonyl-CoA epimerase	MCEE GLOD2 MCE MMCE glyoxalase domain containing 2 methylmalonyl CoA isomerase	disease of metabolism esophagitis gastroesophageal reflux disease lactic acidosis methylmalonic acidemia peptic esophagitis pneumonia sepiapterin reductase deficiency
84695	lysyl oxidase like 3	LOXL3
84696	abhydrolase domain containing 1	ABHD1
84699	cAMP responsive element binding protein 3 like 3	CREB3L3
84700	myosin XVIIIB	MYO18B
84701	cytochrome c oxidase subunit 4I2	COX4I2

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