GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3051 - 3075** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
6860	synaptotagmin 4	SYT4
6862	T-box transcription factor T	TBXT
6865	tachykinin receptor 2	TACR2
6868	ADAM metallopeptidase domain 17	ADAM17
6869	tachykinin receptor 1	TACR1
6870	tachykinin receptor 3	TACR3
6873	TATA-box binding protein associated factor 2	TAF2
6874	TATA-box binding protein associated factor 4	TAF4
6875	TATA-box binding protein associated factor 4b	TAF4B
6876	transgelin	TAGLN
6877	TATA-box binding protein associated factor 5	TAF5
6878	TATA-box binding protein associated factor 6	TAF6
6879	TATA-box binding protein associated factor 7	TAF7
6880	TATA-box binding protein associated factor 9	TAF9
6883	TATA-box binding protein associated factor 12	TAF12
6885	mitogen-activated protein kinase kinase kinase 7	MAP3K7
6888	transaldolase 1	TALDO1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease carbohydrate metabolic disorder childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
6890	transporter 1, ATP binding cassette subfamily B member	TAP1
6892	TAP binding protein	TAPBP
6895	TARBP2 subunit of RISC loading complex	TARBP2
6897	threonyl-tRNA synthetase 1	TARS1
6900	contactin 2	CNTN2 TAG-1 TAX1	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 familial adult myoclonic epilepsy 5 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 disease 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
6904	tubulin folding cofactor D	TBCD
6905	tubulin folding cofactor E	TBCE
6906	serpin family A member 7	SERPINA7

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