GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7176 - 7200** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
54899	PX domain containing serine/threonine kinase like	PXK
11264	peroxisomal membrane protein 4	PXMP4
5829	paxillin	PXN
92370	2-phosphoxylose phosphatase 1	PXYLP1 FLJ23751	myopia
5831	pyrroline-5-carboxylate reductase 1	PYCR1
29920	pyrroline-5-carboxylate reductase 2	PYCR2
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
5837	glycogen phosphorylase, muscle associated	PYGM GSD5 McArdle syndrome glycogen phosphorylase, muscle form glycogen storage disease type V myophosphorylase	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Peutz-Jeghers syndrome X-linked myopathy with excessive autophagy 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 bacterial sepsis breast cancer breast carcinoma cancer carcinoma cholestasis coronary artery disease cystinuria disease of metabolism distal myopathy facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis galactosemia gastrinoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout head and neck squamous cell carcinoma insulinoma invasive lobular carcinoma islet cell tumor isolated elevated serum creatine phosphokinase levels kidney failure limb-girdle muscular dystrophy lipoma melanoma multiple endocrine neoplasia type 1 multiple symmetric lipomatosis muscular dystrophy myoglobinuria myopathy 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 pleomorphic lipoma pre-eclampsia pseudosarcomatous fibromatosis sarcomatoid carcinoma skin melanoma vitelliform macular dystrophy von Hippel-Lindau disease
90780	pygopus family PHD finger 2	PYGO2
149628	pyrin and HIN domain family member 1	PYHIN1
84795	pyridine nucleotide-disulphide oxidoreductase domain 2	PYROXD2
5859	glutaminyl-tRNA synthetase 1	QARS1
9444	QKI, KH domain containing RNA binding	QKI
25797	glutaminyl-peptide cyclotransferase	QPCT
23475	quinolinate phosphoribosyltransferase	QPRT QPRTase nicotinate-nucleotide pyrophosphorylase (carboxylating)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute myeloid leukemia adenoma adenosarcoma endemic goiter follicular adenoma gliosarcoma hepatitis C high grade glioma microcystic adenoma mixed glioma nephroblastoma neuroblastoma neurodegenerative disease papillary adenoma substernal goiter thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma
84109	pyroglutamylated RFamide peptide receptor	QRFPR
54870	glutamine rich 1	QRICH1
79832	glutamine and serine rich 1	QSER1
5768	quiescin sulfhydryl oxidase 1	QSOX1
169714	quiescin sulfhydryl oxidase 2	QSOX2
81890	queuine tRNA-ribosyltransferase catalytic subunit 1	QTRT1 TGT tRNA-guanine transglycosylase	IgA glomerulonephritis acute pancreatitis breast cancer bronchus cancer bronchus carcinoma cancer carcinoma cerebral infarction cerebrovascular disease essential thrombocythemia functionless pituitary adenoma hepatocellular carcinoma liver angiosarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma multiple sclerosis myotonic dystrophy type 2 pancreatitis parapsoriasis parietal foramina prolactinoma psoriasis pulmonary embolism pustulosis of palm and sole sarcomatoid carcinoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation
79691	queuine tRNA-ribosyltransferase accessory subunit 2	QTRT2 FLJ12960
23518	R3H domain containing 1	R3HDM1
22864	R3H domain containing 2	R3HDM2

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