GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6076 - 6100** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
54209	triggering receptor expressed on myeloid cells 2	TREM2
54210	triggering receptor expressed on myeloid cells 1	TREM1
54221	syntrophin gamma 2	SNTG2
54328	G protein-coupled receptor 173	GPR173
54329	G protein-coupled receptor 85	GPR85
54344	dolichyl-phosphate mannosyltransferase subunit 3, regulatory	DPM3 DPM synthase complex subunit MGC125904 MGC125905 MGC34275	Duchenne muscular dystrophy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B15 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy rippling muscle disease 2
54346	unc-93 homolog A	UNC93A
54361	Wnt family member 4	WNT4
54363	hydroxyacid oxidase 1	HAO1 GOX glycolate oxidase 1	familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 hyperinsulinemic hypoglycemia inherited metabolic disorder nephrolithiasis primary hyperoxaluria prostate cancer prostate carcinoma uric acid nephrolithiasis
54386	TERF2 interacting protein	TERF2IP
54407	solute carrier family 38 member 2	SLC38A2
54413	neuroligin 3	NLGN3
54414	sialic acid acetylesterase	SIAE	autoimmune disease
54429	taste 2 receptor member 5	TAS2R5
54431	DnaJ heat shock protein family (Hsp40) member C10	DNAJC10
54432	Yip1 domain family member 1	YIPF1
54437	semaphorin 5B	SEMA5B
54439	RNA binding motif protein 27	RBM27
54443	anillin, actin binding protein	ANLN
54455	F-box protein 42	FBXO42
54456	Mov10 like RNA helicase 1	MOV10L1
54461	F-box and WD repeat domain containing 5	FBXW5
54462	coiled-coil serine rich protein 2	CCSER2
54463	reticulophagy regulator 1	RETREG1
54464	5'-3' exoribonuclease 1	XRN1

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