GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6401 - 6425** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
56111	protocadherin gamma subfamily A, 4	PCDHGA4
56110	protocadherin gamma subfamily A, 5	PCDHGA5
56109	protocadherin gamma subfamily A, 6	PCDHGA6
56108	protocadherin gamma subfamily A, 7	PCDHGA7
9708	protocadherin gamma subfamily A, 8	PCDHGA8
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
51585	PCF11 cleavage and polyadenylation factor subunit	PCF11
7703	polycomb group ring finger 2	PCGF2
5105	phosphoenolpyruvate carboxykinase 1	PCK1 PEPCK-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 Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 biliary atresia cancer celiac disease cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congestive heart failure cryptococcosis cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma epilepsy gestational diabetes hepatic coma hepatic encephalopathy hepatocellular carcinoma hyperglycemia hypoglycemia lactic acidosis large intestine cancer leprosy lipoatrophic diabetes mellitus lipodystrophy liver cancer liver carcinoma maturity-onset diabetes of the young metabolic dysfunction-associated steatohepatitis multiple sclerosis obesity optic atrophy placental insufficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency schizophrenia steatotic liver disease type 2 diabetes mellitus visual epilepsy
5106	phosphoenolpyruvate carboxykinase 2, mitochondrial	PCK2 PEPCK PEPCK2	abdominal obesity-metabolic syndrome 1 bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma hepatitis C hepatocellular carcinoma hyperglycemia hypoglycemia kwashiorkor liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus melanoma nutrition disease obesity osteosarcoma prostate cancer prostate carcinoma protein-energy malnutrition pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer skin melanoma steatotic liver disease type 2 diabetes mellitus viral infectious disease
9768	PCNA clamp associated factor	PCLAF
27445	piccolo presynaptic cytomatrix protein	PCLO
5108	pericentriolar material 1	PCM1
5110	protein-L-isoaspartate (D-aspartate) O-methyltransferase	PCMT1
5111	proliferating cell nuclear antigen	PCNA	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia

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