GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2801 - 2825** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
6407	semenogelin 2	SEMG2
6414	selenoprotein P	SELENOP
6416	mitogen-activated protein kinase kinase 4	MAP2K4
6418	SET nuclear proto-oncogene	SET
6419	SET domain and mariner transposase fusion gene	SETMAR
6421	splicing factor proline and glutamine rich	SFPQ
6422	secreted frizzled related protein 1	SFRP1
6424	secreted frizzled related protein 4	SFRP4
6428	serine and arginine rich splicing factor 3	SRSF3
6429	serine and arginine rich splicing factor 4	SRSF4
6430	serine and arginine rich splicing factor 5	SRSF5
6431	serine and arginine rich splicing factor 6	SRSF6
6432	serine and arginine rich splicing factor 7	SRSF7
6433	splicing factor SWAP	SFSWAP
6434	transformer 2 beta homolog	TRA2B
6439	surfactant protein B	SFTPB
6440	surfactant protein C	SFTPC BRICD6 BRICHOS domain containing 6 PSP-C SMDP2 SP-C	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clostridium difficile colitis Hermansky-Pudlak syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome asthma bacterial pneumonia breast cancer breast carcinoma bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral degeneration chondrosarcoma chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia cribriform carcinoma cystadenoma cystic fibrosis dementia desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential hypertension familial periodic paralysis gastroesophageal reflux disease gestational diabetes granular cell carcinoma herpes simplex hiatus hernia hydrocephalus hyperinsulinism hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease intrinsic asthma lipoid proteinosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma myopathy neonatal respiratory failure newborn respiratory distress syndrome nonspecific interstitial pneumonia obstructive hydrocephalus obstructive lung disease obstructive sleep apnea peptic esophagitis perinatal necrotizing enterocolitis pneumonia polycystic ovary syndrome postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pulmonary valve insufficiency respiratory syncytial virus infectious disease sarcomatoid carcinoma secondary hypertrophic osteoarthropathy senile degeneration of brain tubular adenocarcinoma
6441	surfactant protein D	SFTPD COLEC7 SP-D	Bloch-Sulzberger syndrome Coronavirus infectious disease Crohn's colitis Crohn's disease Ebola hemorrhagic fever Fabry disease Wolman disease acquired immunodeficiency syndrome acute interstitial pneumonia acute lymphoblastic leukemia acute pancreatitis adenocarcinoma adenoid hypertrophy adenoma adult acute lymphocytic leukemia adult respiratory distress syndrome allergic asthma allergic disease allergic rhinitis anthracosilicosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis bacterial pneumonia bacterial sepsis blastomycosis brain stem infarction breast cancer bronchiectasis bronchiolitis obliterans bronchiolitis bronchitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer cardiovascular system disease cataract 32 multiple types cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chronic ethmoiditis chronic interstitial cystitis chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease colitis communicating hydrocephalus cone-rod dystrophy congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary stenosis craniosynostosis cribriform carcinoma cystic fibrosis diabetes mellitus diabetic ketoacidosis disease of metabolism dry eye syndrome embryoma fundus albipunctatus gastroenteritis glomerulonephritis granular cell carcinoma heart disease herpes simplex virus keratitis human immunodeficiency virus infectious disease hydrocephalus hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease influenza interstitial cystitis interstitial lung disease interstitial nephritis intrinsic asthma kidney disease leprosy leukopenia lipid storage disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis lymphoblastic lymphoma middle cerebral artery infarction mixed connective tissue disease nephritis nephrosis neurogenic arthropathy newborn respiratory distress syndrome nutmeg liver obesity obstructive hydrocephalus obstructive lung disease osteoarthritis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis paracoccidioidomycosis parapsoriasis periodontitis peripheral artery disease periventricular leukomalacia pneumocystosis pneumonia postinflammatory pulmonary fibrosis pre-malignant neoplasm prostate adenocarcinoma prostate cancer prostate carcinoma prune belly syndrome psoriasis pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pustulosis of palm and sole pyelitis pyelonephritis pyoureter renal infectious disease respiratory failure respiratory syncytial virus infectious disease retinitis pigmentosa rheumatoid arthritis rhinitis sarcoidosis scleroderma senile degeneration of brain sickle cell anemia silicosis sinusitis squamous cell carcinoma sudden infant death syndrome systemic lupus erythematosus systemic primary carnitine deficiency disease systemic scleroderma tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis viral infectious disease xerophthalmia
6442	sarcoglycan alpha	SGCA
6443	sarcoglycan beta	SGCB
6444	sarcoglycan delta	SGCD
6445	sarcoglycan gamma	SGCG
6448	N-sulfoglucosamine sulfohydrolase	SGSH HSS MPS3A SFMD mucopolysaccharidosis type IIIA sulfamidase	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Kearns-Sayre syndrome Kluver-Bucy syndrome Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome adrenoleukodystrophy ankylosing spondylitis anorexia nervosa arthritis arthropathy beta-mannosidosis cancer cardiomyopathy central nervous system disease central nervous system origin vertigo cerebral degeneration chronic obstructive pulmonary disease cone-rod dystrophy congenital nystagmus depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dissociated nystagmus embryoma endomyocardial fibrosis eosinophilic esophagitis epilepsy fundus albipunctatus fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease major depressive disorder melancholic depression movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis mucosulfatidosis multiple epiphyseal dysplasia narcolepsy nervous system disease neurodegeneration with brain iron accumulation neurodegenerative disease obsolete melancholia osteoarthritis osteochondrodysplasia pathologic nystagmus retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus visual epilepsy
6449	small glutamine rich tetratricopeptide repeat co-chaperone alpha	SGTA
6452	SH3 domain binding protein 2	SH3BP2

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