GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7901 - 7925** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
56107	protocadherin gamma subfamily A, 9	PCDHGA9
56104	protocadherin gamma subfamily B, 1	PCDHGB1
56103	protocadherin gamma subfamily B, 2	PCDHGB2
56102	protocadherin gamma subfamily B, 3	PCDHGB3
8641	protocadherin gamma subfamily B, 4	PCDHGB4
56101	protocadherin gamma subfamily B, 5	PCDHGB5
56100	protocadherin gamma subfamily B, 6	PCDHGB6
56099	protocadherin gamma subfamily B, 7	PCDHGB7
5098	protocadherin gamma subfamily C, 3	PCDHGC3
56098	protocadherin gamma subfamily C, 4	PCDHGC4
56097	protocadherin gamma subfamily C, 5	PCDHGC5
65217	protocadherin related 15	PCDH15
283659	protogenin	PRTG
55248	proton activated chloride channel 1	PACC1
58497	prune exopolyphosphatase 1	PRUNE1 DRES-17 H-PRUNE HTCD37
79834	pseudopodium enriched atypical kinase 1	PEAK1
150962	pseudouridine synthase 10	PUS10
83480	pseudouridine synthase 3	PUS3
54517	pseudouridine synthase 7	PUS7
9698	pumilio RNA binding family member 1	PUM1
23369	pumilio RNA binding family member 2	PUM2
9933	pumilio RNA binding family member 3	PUM3
4860	purine nucleoside phosphorylase	PNP PUNP	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 Chagas disease Evans' syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lesch-Nyhan syndrome MELAS syndrome MHC class II deficiency Nezelof syndrome Omenn syndrome Pick's disease Reye syndrome Richter's syndrome T cell deficiency acute lymphoblastic leukemia adenosine deaminase deficiency adult lymphoma agammaglobulinemia agnosia alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma carotid artery disease central nervous system disease central nervous system lymphoma central nervous system vasculitis central retinal vein occlusion cerebral degeneration cerebral malaria cerebral palsy childhood acute lymphocytic leukemia childhood lymphoma chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer combined T cell and B cell immunodeficiency coronary artery disease critical illness polyneuropathy cutaneous leishmaniasis cyclic hematopoiesis developmental coordination disorder diabetic cataract diabetic retinopathy disease of metabolism embryoma esophageal cancer esophageal carcinoma fetal erythroblastosis gangliosidosis giant cell glioblastoma glioblastoma granulomatous angiitis head and neck squamous cell carcinoma hematologic cancer hepatocellular carcinoma herpes simplex high grade glioma hyperuricemia immune system disease inflammatory and toxic neuropathy intellectual disability large intestine cancer learning disability liver cancer locked-in syndrome lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia macrocytic anemia malaria maxillary sinus squamous cell carcinoma melanoma meningoencephalitis molybdenum cofactor deficiency type A monoclonal gammopathy of uncertain significance nervous system disease neuroblastoma neurodegenerative disease neuropathy obsolete T lymphocyte deficiency obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma periodontal disease periodontitis peripheral T-cell lymphoma peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pneumonia polyneuropathy primary immunodeficiency disease prostate cancer prostate carcinoma purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder quadriplegia reflex sympathetic dystrophy retinal vein occlusion sarcomatoid carcinoma severe combined immunodeficiency sinusitis skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy substance abuse substance-related disorder systemic lupus erythematosus thyroid gland medullary carcinoma trypanosomiasis tuberculosis urinary bladder cancer urinary tract obstruction vascular disease
5023	purinergic receptor P2X 1	P2RX1
22953	purinergic receptor P2X 2	P2RX2

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