GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **15926 - 15950** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96NU0	Contactin-associated protein-like 3B	CNTNAP3B CASPR3B	4	4
Q9BZ76	Contactin-associated protein-like 3	CNTNAP3 CASPR3 KIAA1714	9	1
Q9UHC6	Contactin-associated protein-like 2	CNTNAP2 CASPR2 KIAA0868	12	0
P78357	Contactin-associated protein 1	CNTNAP1 CASPR NRXN4	18	14
Q9UQ52	Contactin-6	CNTN6	14	4	Gilles de la Tourette syndrome Hirschsprung's disease Parkinson's disease 2 acquired immunodeficiency syndrome adenoid cystic carcinoma alcohol dependence alcohol use disorder anorexia nervosa attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder breast cancer communicating hydrocephalus cone-rod dystrophy 2 cone-rod dystrophy differentiated thyroid gland carcinoma epilepsy hydrocephalus intellectual disability learning disability obstructive hydrocephalus ovarian carcinoma salivary gland adenoid cystic carcinoma schizophrenia senile degeneration of brain systemic lupus erythematosus
O94779	Contactin-5	CNTN5	9	0	Behcet's disease Hirschsprung's disease Parkinson's disease 2 anorexia nervosa atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder communicating hydrocephalus congestive heart failure depressive disorder differentiated thyroid gland carcinoma essential hypertension gout hydrocephalus hypertension major depressive disorder melancholic depression neurotic disorder obsolete melancholia obstructive hydrocephalus primary biliary cholangitis schizophrenia senile degeneration of brain
Q8IWV2	Contactin-4	CNTN4	14	32	adrenal gland cancer alcohol dependence alcohol use disorder amyotrophic lateral sclerosis type 1 anorexia nervosa autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia autosomal recessive spinocerebellar ataxia 16 bilateral optic nerve hypoplasia bipolar disorder breast cancer breast carcinoma cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma disease of mental health duodenum cancer epilepsy essential hypertension gallbladder cancer gallbladder carcinoma heart cancer hypertension intellectual disability large intestine cancer learning disability obesity ovarian cancer ovarian carcinoma paraganglioma pheochromocytoma primary open angle glaucoma psychotic disorder schizophrenia small intestine cancer speech disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	13	12	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
Q02246	Contactin-2	CNTN2 AXT TAG1 TAX1	13	5	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 B-cell lymphoma Gamstorp-Wohlfart syndrome Guillain-Barre syndrome Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Unverricht-Lundborg syndrome Van der Woude syndrome Wolff-Parkinson-White syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis adult T-cell leukemia/lymphoma adult lymphoma adult oligodendroglioma anaplastic astrocytoma arthritis arthropathy atrial fibrillation atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bladder carcinoma blepharospasm bone marrow disease bone osteosarcoma cancer central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood oligodendroglioma childhood osteosarcoma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy early myoclonic encephalopathy embryoma epilepsy episodic ataxia type 1 fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma immune system disease intellectual disability juvenile pilocytic astrocytoma keratoconjunctivitis sicca learning disability leukemia lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma microcephaly mixed glioma mixed oligodendroglioma-astrocytoma myotonic dystrophy type 2 neurodegenerative disease neurofibroma neurofibromatosis 1 neurofibromatosis neurogenic arthropathy obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma partial motor epilepsy peripheral nervous system neoplasm pilocytic astrocytoma primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma retinal vascular occlusion rheumatoid arthritis schizophrenia spinal cord disease subependymal giant cell astrocytoma syringomyelia systemic Epstein-Barr virus positive T-cell lymphoma of childhood tropical spastic paraparesis urinary bladder cancer visual epilepsy
Q12860	Contactin-1	CNTN1	11	21	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 Compton-North congenital myopathy Guillain-Barre syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adenocarcinoma adenoma arthritis arthropathy attention deficit hyperactivity disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial nephrotic syndrome familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gliosarcoma granular cell carcinoma high grade glioma islet cell tumor large intestine cancer lipoid nephrosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma megaconial type congenital muscular dystrophy membranous glomerulonephritis mixed glioma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy nephrotic syndrome neuropathy peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma rigid spine muscular dystrophy 1 spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma
Q9NXG0	Centlein	CNTLN C9orf101 C9orf39	2	1
P26992	Ciliary neurotrophic factor receptor subunit alpha	CNTFR	4	0	acute lymphoblastic leukemia adult acute lymphocytic leukemia amyotrophic lateral sclerosis attention deficit hyperactivity disorder cancer central nervous system cancer childhood acute lymphocytic leukemia childhood acute myeloid leukemia cold-induced sweating syndrome 1 cold-induced sweating syndrome gliosarcoma high grade glioma idiopathic scoliosis mixed glioma myasthenia gravis progressive muscular atrophy rheumatoid arthritis
Q8N815	Cyclin N-terminal domain-containing protein 1	CNTD1 CNTD	0	1
P34972	Cannabinoid receptor 2	CNR2 CB2A CB2B	1	0
P21554	Cannabinoid receptor 1	CNR1 CNR	2	0
Q9BT09	Protein canopy homolog 3	CNPY3 CTG4A ERDA5 PRAT4A TNRC5	6	14
Q9Y2B0	Protein canopy homolog 2	CNPY2 MSAP TMEM4 ZSIG9	0	1
P09543	2',3'-cyclic-nucleotide 3'-phosphodiesterase	CNP	0	1
Q92600	CCR4-NOT transcription complex subunit 9	CNOT9 RCD1 RQCD1	0	1
Q9UFF9	CCR4-NOT transcription complex subunit 8	CNOT8 CALIF POP2	0	1
Q9UIV1	CCR4-NOT transcription complex subunit 7	CNOT7 CAF1	0	1
Q96LI5	CCR4-NOT transcription complex subunit 6-like	CNOT6L CCR4B	1	2
Q9ULM6	CCR4-NOT transcription complex subunit 6	CNOT6 CCR4 CCR4a KIAA1194	0	1
O95628	CCR4-NOT transcription complex subunit 4	CNOT4 NOT4	12	8
O75175	CCR4-NOT transcription complex subunit 3	CNOT3 KIAA0691 LENG2 NOT3	2	2

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