GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2576 - 2600** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
5792	protein tyrosine phosphatase receptor type F	PTPRF
5793	protein tyrosine phosphatase receptor type G	PTPRG
5794	protein tyrosine phosphatase receptor type H	PTPRH
5795	protein tyrosine phosphatase receptor type J	PTPRJ
5796	protein tyrosine phosphatase receptor type K	PTPRK
5797	protein tyrosine phosphatase receptor type M	PTPRM
5798	protein tyrosine phosphatase receptor type N	PTPRN
5799	protein tyrosine phosphatase receptor type N2	PTPRN2
5800	protein tyrosine phosphatase receptor type O	PTPRO
5801	protein tyrosine phosphatase receptor type R	PTPRR
5802	protein tyrosine phosphatase receptor type S	PTPRS
5803	protein tyrosine phosphatase receptor type Z1	PTPRZ1
5806	pentraxin 3	PTX3
5817	PVR cell adhesion molecule	PVR
5818	nectin cell adhesion molecule 1	NECTIN1
5819	nectin cell adhesion molecule 2	NECTIN2
5822	PWP2 small subunit processome component	PWP2
5824	peroxisomal biogenesis factor 19	PEX19
5825	ATP binding cassette subfamily D member 3	ABCD3 PMP70 ZWS2 peroxisomal membrane protein 70 kDa
5829	paxillin	PXN
5831	pyrroline-5-carboxylate reductase 1	PYCR1
5832	aldehyde dehydrogenase 18 family member A1	ALDH18A1
5833	phosphate cytidylyltransferase 2, ethanolamine	PCYT2 CTP:phosphoethanolamine cytidylyltransferase ET ethanolamine-phosphate cytidylyltransferase: phosphorylethanolamine transferase	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cerebral degeneration embryoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 82 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia
5834	glycogen phosphorylase B	PYGB glycogen phosphorylase, brain form	acute myocardial infarction adenoid cystic carcinoma breast cancer cancer coronary artery disease coronary thrombosis diabetes mellitus embryoma lung cancer lung non-small cell carcinoma myocardial infarction salivary gland adenoid cystic carcinoma salivary gland cancer silent myocardial infarction type 2 diabetes mellitus
5836	glycogen phosphorylase L	PYGL GSD6 Hers disease glycogen phosphorylase, liver form glycogen storage disease type VI	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IV glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease hepatocellular carcinoma hypoglycemia lactic acidosis liver cancer

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