GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6101 - 6125** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
3356	5-hydroxytryptamine receptor 2A	HTR2A	Alzheimer's disease alcohol dependence alcohol use disorder alcoholic psychosis anorexia nervosa autism spectrum disorder bladder neck obstruction chronic obstructive pulmonary disease cocaine abuse cocaine dependence congenital diaphragmatic hernia congestive heart failure depressive disorder hyperglycemia hypertension inflammatory and toxic neuropathy major depressive disorder nicotine dependence non-alcoholic fatty liver obesity obsessive-compulsive disorder pancreatitis pathological gambling schizophrenia steatotic liver disease withdrawal disorder
3355	5-hydroxytryptamine receptor 1F	HTR1F
3354	5-hydroxytryptamine receptor 1E	HTR1E
3352	5-hydroxytryptamine receptor 1D	HTR1D
3351	5-hydroxytryptamine receptor 1B	HTR1B
3350	5-hydroxytryptamine receptor 1A	HTR1A
109703458	hydroxyacyl-thioester dehydratase type 2	HTD2	rheumatoid arthritis
27336	HIV-1 Tat specific factor 1	HTATSF1
10553	HIV-1 Tat interactive protein 2	HTATIP2
10808	heat shock protein family H (Hsp110) member 1	HSPH1
3339	heparan sulfate proteoglycan 2	HSPG2 PRCAN endorepellin perlecan perlecan proteoglycan	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 Balkan nephropathy Bethlem myopathy Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 HELLP syndrome IgA glomerulonephritis Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Norum disease Ollier disease Peters anomaly Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Schwartz-Jampel syndrome 1 Seckel syndrome Silver-Russell syndrome Silverman-Handmaker type dyssegmental dysplasia Stevens-Johnson syndrome Tangier disease Werdnig-Hoffmann disease X-linked Aarskog syndrome X-linked spondyloepiphyseal dysplasia tarda abdominal obesity-metabolic syndrome 1 abetalipoproteinemia achondroplasia acute promyelocytic leukemia adenoid cystic carcinoma adenoma adrenoleukodystrophy adult fibrosarcoma adult oligodendroglioma age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis ameloblastoma amyloidosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 Robinow syndrome 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 autosomal recessive osteopetrosis 7 benign mastocytoma bipolar disorder blepharophimosis blepharospasm blindness brain stem infarction breast cancer bronchus cancer bronchus carcinoma cancer carcinoma carotid artery disease cataract central nervous system cancer cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood oligodendroglioma childhood spinal muscular atrophy cholangiocarcinoma chondrocalcinosis chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma choreaacanthocytosis chronic lymphocytic leukemia chronic myeloid leukemia cleft palate cleidocranial dysplasia clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cornea plana coronary artery disease cystic fibrosis degeneration of macula and posterior pole dextro-looped transposition of the great arteries diabetes mellitus diabetic ketoacidosis disease of mental health distal myopathy embryoma enthesopathy epidermolysis bullosa epilepsy erythema multiforme esophageal cancer esophageal carcinoma exostosis extracutaneous mastocytoma facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome fibromyalgia fibrosarcoma focal hand dystonia follicular adenoma fragile X syndrome gallbladder cancer gallbladder carcinoma gas gangrene generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatitis B hepatitis C hepatitis E hepatoblastoma hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydranencephaly hypereosinophilic syndrome hyperglycemia hypertension hypolipoproteinemia immune system disease in situ carcinoma interstitial nephritis intracranial aneurysm intrahepatic cholangiocarcinoma isolated cleft palate isolated ectopia lentis isolated elevated serum creatine phosphokinase levels juvenile spinal muscular atrophy kidney disease kidney failure large intestine cancer leech infestation limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis low compliance bladder lung cancer lung carcinoma lupus erythematosus lupus nephritis macular degeneration malignant epithelial mesothelioma malignant hyperthermia mast cell neoplasm mastocytosis melanoma membranous glomerulonephritis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microcystic adenoma mixed glioma mixed oligodendroglioma-astrocytoma mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple types of congenital heart defects 6 muscular dystrophy musculoskeletal system disease myiasis myopia myositis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephritis nephrolithiasis nephrosis nephrotic syndrome type 1 nephrotic syndrome nutmeg liver obesity 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 obsolete dextro-looped transposition of the great arteries 1 obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy oligodendroglioma osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary carcinoma periarthritis polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pre-eclampsia primary pulmonary hypertension progressive muscular atrophy prostate cancer prostate carcinoma proximal symphalangism pseudosarcomatous fibromatosis psychotic disorder pyelitis pyelonephritis pyoureter radioulnar synostosis renal infectious disease salivary gland adenoid cystic carcinoma sarcomatoid carcinoma schizophrenia scleroderma scoliosis short-rib thoracic dysplasia 14 with polydactyly sick sinus syndrome skin melanoma spermatic cord torsion spinal muscular atrophy squamous cell carcinoma steatotic liver disease syndromic X-linked intellectual disability Najm type systemic lupus erythematosus systemic scleroderma tendinitis thanatophoric dysplasia thrombocytopenia thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxic shock syndrome toxoplasmosis tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia uric acid nephrolithiasis urticaria pigmentosa uveal melanoma
3336	heat shock protein family E (Hsp10) member 1	HSPE1
3329	heat shock protein family D (Hsp60) member 1	HSPD1
23640	HSPA (Hsp70) binding protein 1	HSPBP1
26353	heat shock protein family B (small) member 8	HSPB8
3315	heat shock protein family B (small) member 1	HSPB1
3313	heat shock protein family A (Hsp70) member 9	HSPA9
3312	heat shock protein family A (Hsp70) member 8	HSPA8 HSC70 HSC71 HSP73
3310	heat shock protein family A (Hsp70) member 6	HSPA6
3309	heat shock protein family A (Hsp70) member 5	HSPA5 BiP glucose-regulated protein, 78kDa
22824	heat shock protein family A (Hsp70) member 4 like	HSPA4L
3308	heat shock protein family A (Hsp70) member 4	HSPA4
3306	heat shock protein family A (Hsp70) member 2	HSPA2
3305	heat shock protein family A (Hsp70) member 1 like	HSPA1L
3304	heat shock protein family A (Hsp70) member 1B	HSPA1B