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Pathways

PathWhiz ID Pathway Meta Data

PW176159

Pw176159 View Pathway
metabolic

Umbralisib Predicted Metabolism Pathway new

Homo sapiens
Metabolites of Umbralisib are predicted with biotransformer.

PW145957

Pw145957 View Pathway
drug action

Umeclidinium Drug Metabolism Action Pathway

Homo sapiens

PW121986

Pw121986 View Pathway
disease

UMP Synthase Deficiency (Orotic Aciduria)

Rattus norvegicus
Orotic aciduria, also known as UMP synthase deficiency, is an autosomal recessive disorder of pyrimidine metabolism caused by a defective uridine monophosphate synthetase (UMPS). UMPS is a multifunctional protein which carries out the functions of both orotate phosphoribosyltransferase (OPRT) and orotidine 5'-phosphate decarboxylase (ODC). UMPS catalyzes the conversion of orotic acid into uridine monophosphate (UMP) which is a nucleotide incorporated into ribonucleic acid (RNA). This disease is characterized by a very large accumulation of orotic acid in the urine, occasionally causing urinary obstruction. Symptoms of the disease include megaloblastic anemia as well as retarded growth and development.

PW121761

Pw121761 View Pathway
disease

UMP Synthase Deficiency (Orotic Aciduria)

Mus musculus
Orotic aciduria, also known as UMP synthase deficiency, is an autosomal recessive disorder of pyrimidine metabolism caused by a defective uridine monophosphate synthetase (UMPS). UMPS is a multifunctional protein which carries out the functions of both orotate phosphoribosyltransferase (OPRT) and orotidine 5'-phosphate decarboxylase (ODC). UMPS catalyzes the conversion of orotic acid into uridine monophosphate (UMP) which is a nucleotide incorporated into ribonucleic acid (RNA). This disease is characterized by a very large accumulation of orotic acid in the urine, occasionally causing urinary obstruction. Symptoms of the disease include megaloblastic anemia as well as retarded growth and development.

PW000188

Pw000188 View Pathway
disease

UMP Synthase Deficiency (Orotic Aciduria)

Homo sapiens
Orotic aciduria, also known as UMP synthase deficiency, is an autosomal recessive disorder of pyrimidine metabolism caused by a defective uridine monophosphate synthetase (UMPS). UMPS is a multifunctional protein which carries out the functions of both orotate phosphoribosyltransferase (OPRT) and orotidine 5'-phosphate decarboxylase (ODC). UMPS catalyzes the conversion of orotic acid into uridine monophosphate (UMP) which is a nucleotide incorporated into ribonucleic acid (RNA). This disease is characterized by a very large accumulation of orotic acid in the urine, occasionally causing urinary obstruction. Symptoms of the disease include megaloblastic anemia as well as retarded growth and development.

PW127284

Pw127284 View Pathway
disease

UMP Synthase Deficiency (Orotic Aciduria)

Homo sapiens
Orotic aciduria, also known as UMP synthase deficiency, is an autosomal recessive disorder of pyrimidine metabolism caused by a defective uridine monophosphate synthetase (UMPS). UMPS is a multifunctional protein which carries out the functions of both orotate phosphoribosyltransferase (OPRT) and orotidine 5'-phosphate decarboxylase (ODC). UMPS catalyzes the conversion of orotic acid into uridine monophosphate (UMP) which is a nucleotide incorporated into ribonucleic acid (RNA). This disease is characterized by a very large accumulation of orotic acid in the urine, occasionally causing urinary obstruction. Symptoms of the disease include megaloblastic anemia as well as retarded growth and development.

PW132278

Pw132278 View Pathway
metabolic

Undecoylium chloride iodine complex Drug Metabolism

Homo sapiens
Undecoylium chloride iodine complex is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. Undecoylium chloride iodine complex passes through the liver and is then excreted from the body mainly through the kidney.

PW146123

Pw146123 View Pathway
drug action

Undecoylium chloride iodine complex Drug Metabolism Action Pathway

Homo sapiens

PW146241

Pw146241 View Pathway
drug action

Undecylenic acid Drug Metabolism Action Pathway

Homo sapiens

PW123869

Pw123869 View Pathway
metabolic

Unico ajajaj

Homo sapiens