GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2326 - 2350** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
27344	proprotein convertase subtilisin/kexin type 1 inhibitor	PCSK1N
5122	proprotein convertase subtilisin/kexin type 1	PCSK1
5096	propionyl-CoA carboxylase subunit beta	PCCB	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia anxiety disorder cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy generalized anxiety disorder granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis schizophrenia severe congenital neutropenia sick sinus syndrome thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
5095	propionyl-CoA carboxylase subunit alpha	PCCA	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia nicotine dependence obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis refractive error severe congenital neutropenia sick sinus syndrome stomach cancer stomach carcinoma thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
5443	proopiomelanocortin	POMC
150696	prominin 2	PROM2
8842	prominin 1	PROM1
5547	prolylcarboxypeptidase	PRCP
54681	prolyl 4-hydroxylase, transmembrane	P4HTM
5034	prolyl 4-hydroxylase subunit beta	P4HB
283208	prolyl 4-hydroxylase subunit alpha 3	P4HA3
8974	prolyl 4-hydroxylase subunit alpha 2	P4HA2
5033	prolyl 4-hydroxylase subunit alpha 1	P4HA1
10609	prolyl 3-hydroxylase family member 4 (inactive)	P3H4
10536	prolyl 3-hydroxylase 3	P3H3
55214	prolyl 3-hydroxylase 2	P3H2
64175	prolyl 3-hydroxylase 1	P3H1
9050	proline-serine-threonine phosphatase interacting protein 2	PSTPIP2
9051	proline-serine-threonine phosphatase interacting protein 1	PSTPIP1
27043	proline, glutamate and leucine rich protein 1	PELP1
401399	proline rich transmembrane protein 4	PRRT4
285368	proline rich transmembrane protein 3	PRRT3
5555	proline rich protein HaeIII subfamily 2	PRH2
5554	proline rich protein HaeIII subfamily 1	PRH1
653247	proline rich protein BstNI subfamily 2	PRB2

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