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Aliases for CPS1 Gene

Aliases for CPS1 Gene

  • Carbamoyl-Phosphate Synthase 1 2 3 5
  • Carbamoyl-Phosphate Synthase 1, Mitochondrial 2 3
  • Carbamoyl-Phosphate Synthase (Ammonia) 2 3
  • EC 4 56
  • Carbamoyl-Phosphate Synthase [Ammonia], Mitochondrial 3
  • Carbamoyl-Phosphate Synthetase 1, Mitochondrial 2
  • Carbamoyl-Phosphate Synthetase I 4
  • Carbamoylphosphate Synthetase I 3
  • CPSase I 4
  • CPSASE1 3
  • PHN 3

External Ids for CPS1 Gene

Previous GeneCards Identifiers for CPS1 Gene

  • GC02P209696
  • GC02P210145
  • GC02P211385
  • GC02P211623
  • GC02P211246
  • GC02P211050
  • GC02P211129
  • GC02P211342
  • GC02P203189

Summaries for CPS1 Gene

Entrez Gene Summary for CPS1 Gene

  • The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.[provided by RefSeq, May 2010]

GeneCards Summary for CPS1 Gene

CPS1 (Carbamoyl-Phosphate Synthase 1) is a Protein Coding gene. Diseases associated with CPS1 include Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due To and Pulmonary Hypertension, Neonatal. Among its related pathways are CDK-mediated phosphorylation and removal of Cdc6 and Arginine biosynthesis. Gene Ontology (GO) annotations related to this gene include calcium ion binding and phospholipid binding. An important paralog of this gene is CAD.

UniProtKB/Swiss-Prot for CPS1 Gene

  • Involved in the urea cycle of ureotelic animals where the enzyme plays an important role in removing excess ammonia from the cell.

Additional gene information for CPS1 Gene

No data available for CIViC summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for CPS1 Gene

Genomics for CPS1 Gene

GeneHancer (GH) Regulatory Elements for CPS1 Gene

Promoters and enhancers for CPS1 Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH02I210475 Promoter/Enhancer 2.2 EPDnew Ensembl ENCODE dbSUPER 575.8 -0.8 -820 2.9 HDGF PKNOX1 ARID4B SIN3A DMAP1 ZNF2 ZNF48 YY1 SLC30A9 ZNF121 CPS1 LANCL1 GC02M210241
GH02I210556 Promoter/Enhancer 1.2 EPDnew dbSUPER 550.2 +78.9 78900 0.1 FOXA2 RXRA TAF1 MAX CEBPB REST RAD21 FOXA1 YY1 MAFF CPS1 GC02M210562
GH02I210593 Promoter 0.5 EPDnew 550.1 +115.7 115701 0.1 CPS1 GC02P210573 CPS1-IT1
GH02I210560 Enhancer 1 FANTOM5 ENCODE dbSUPER 30.2 +84.3 84263 3.5 JUND TAF1 CEBPA CEBPB HNF4A EP300 YY1 TCF7L2 CPS1 ACADL GC02M210562
GH02I210544 Enhancer 1.4 FANTOM5 ENCODE dbSUPER 19.4 +69.8 69805 6.4 FOXA2 MLX ARID4B DMAP1 BRCA1 ETS1 YY1 SLC30A9 ATF7 RXRA CPS1 ACADL GC02M210562
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data dump

GeneHancers around CPS1 on UCSC Golden Path with GeneCards custom track

Top Transcription factor binding sites by QIAGEN in the CPS1 gene promoter:

Genomic Locations for CPS1 Gene

Genomic Locations for CPS1 Gene
201,426 bases
Plus strand

Genomic View for CPS1 Gene

Genes around CPS1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
CPS1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for CPS1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for CPS1 Gene

Proteins for CPS1 Gene

  • Protein details for CPS1 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Carbamoyl-phosphate synthase [ammonia], mitochondrial
    Protein Accession:
    Secondary Accessions:
    • B7Z818
    • J3KQL0
    • O43774
    • Q53TL5
    • Q59HF8
    • Q7Z5I5

    Protein attributes for CPS1 Gene

    1500 amino acids
    Molecular mass:
    164939 Da
    Quaternary structure:
    • Can form homooligomers (monomers as predominant form and dimers).
    • Sequence=BAD92037.1; Type=Erroneous initiation; Note=Translation N-terminally shortened.; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for CPS1 Gene

    Alternative splice isoforms for CPS1 Gene


neXtProt entry for CPS1 Gene

Selected DME Specific Peptides for CPS1 Gene


Post-translational modifications for CPS1 Gene

  • Glutarylated. Glutarylation levels increase during fasting. Deglutarylated by SIRT5 at Lys-55, Lys-219, Lys-412, Lys-889, Lys-892, Lys-915, Lys-1360 and Lys-1486, leading to activation.
  • Succinylated at Lys-287 and Lys-1291. Desuccinylated at Lys-1291 by SIRT5, leading to activation (By similarity).
  • Undergoes proteolytic cleavage in the C-terminal region corresponding to the loss of approximately 12 AA residues from the C-terminus.
  • Glycosylation at posLast=537537, posLast=13311331, and posLast=13321332
  • Modification sites at PhosphoSitePlus

Domains & Families for CPS1 Gene

Gene Families for CPS1 Gene

Human Protein Atlas (HPA):
  • Disease related genes
  • Enzymes
  • FDA approved drug targets
  • Plasma proteins
  • Predicted intracellular proteins

Graphical View of Domain Structure for InterPro Entry



  • The type-1 glutamine amidotransferase domain is defective.
  • The type-1 glutamine amidotransferase domain is defective.
genes like me logo Genes that share domains with CPS1: view

Function for CPS1 Gene

Molecular function for CPS1 Gene

GENATLAS Biochemistry:
carbamoyl phosphate synthetase 1,mitochondrial,urea cycle
UniProtKB/Swiss-Prot BiophysicochemicalProperties:
Kinetic parameters: KM=0.47 mM for ATP {ECO:0000269 PubMed:23649895}; KM=4.0 mM for HCO(3)(-) {ECO:0000269 PubMed:23649895}; KM=1.00 mM for NH(4)(+) {ECO:0000269 PubMed:23649895}; Vmax=1.22 umol/min/mg enzyme for ATP {ECO:0000269 PubMed:23649895}; Vmax=1.23 umol/min/mg enzyme for HCO(3)(-) {ECO:0000269 PubMed:23649895}; Vmax=1.19 umol/min/mg enzyme for NH(4)(+) {ECO:0000269 PubMed:23649895};
UniProtKB/Swiss-Prot CatalyticActivity:
2 ATP + NH(3) + HCO(3)(-) = 2 ADP + phosphate + carbamoyl phosphate.
UniProtKB/Swiss-Prot EnzymeRegulation:
Requires N-acetyl-L-glutamate (NAG) as an allosteric activator. Activated by glycerol in the absence of NAG, whereas in the presence of NAG it is inhibited by increasing concentrations of glycerol.
UniProtKB/Swiss-Prot Function:
Involved in the urea cycle of ureotelic animals where the enzyme plays an important role in removing excess ammonia from the cell.

Enzyme Numbers (IUBMB) for CPS1 Gene

Phenotypes From GWAS Catalog for CPS1 Gene

Gene Ontology (GO) - Molecular Function for CPS1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000166 nucleotide binding IEA --
GO:0003824 catalytic activity IEA --
GO:0004087 carbamoyl-phosphate synthase (ammonia) activity IMP 8486760
GO:0004088 carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity IBA,IEA --
GO:0004175 endopeptidase activity IEA --
genes like me logo Genes that share ontologies with CPS1: view
genes like me logo Genes that share phenotypes with CPS1: view

Human Phenotype Ontology for CPS1 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for CPS1 Gene

MGI Knock Outs for CPS1:

miRNA for CPS1 Gene

miRTarBase miRNAs that target CPS1

Clone Products

No data available for Transcription Factor Targets and HOMER Transcription for CPS1 Gene

Localization for CPS1 Gene

Subcellular locations from UniProtKB/Swiss-Prot for CPS1 Gene

Mitochondrion. Nucleus, nucleolus.

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for CPS1 gene
Compartment Confidence
mitochondrion 5
nucleus 5
cytosol 3
endoplasmic reticulum 2

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for CPS1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus IEA --
GO:0005730 nucleolus IEA,IDA --
GO:0005737 cytoplasm IEA --
GO:0005739 mitochondrion IEA --
GO:0005743 mitochondrial inner membrane IEA --
genes like me logo Genes that share ontologies with CPS1: view

Pathways & Interactions for CPS1 Gene

genes like me logo Genes that share pathways with CPS1: view

Gene Ontology (GO) - Biological Process for CPS1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000050 urea cycle TAS --
GO:0001889 liver development IEA --
GO:0006207 de novo pyrimidine nucleobase biosynthetic process IEA --
GO:0006508 proteolysis IEA --
GO:0006526 arginine biosynthetic process IBA --
genes like me logo Genes that share ontologies with CPS1: view

No data available for SIGNOR curated interactions for CPS1 Gene

Drugs & Compounds for CPS1 Gene

(18) Drugs for CPS1 Gene - From: DrugBank, PharmGKB, HMDB, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Carglumic acid Approved Pharma Target, allosteric modulator 0
Valproic Acid Approved, Investigational Pharma HDAC1 inhibitor, Histone deacetylase (HDAC)inhibitors 333
Ammonia Approved Pharma 0
Carbon dioxide Approved, Investigational, Vet_approved Pharma 0
Phosphoric acid Approved Pharma 0

(8) Additional Compounds for CPS1 Gene - From: HMDB and Novoseek

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
Carbamoyl phosphate
  • Carbamic acid monoanhydride with phosphorate
  • Carbamic acid monoanhydride with phosphoric acid
  • Carbamoyl-P
  • Carbamoyl-phosphate
  • Carbamoylphosphate
  • Adenosindiphosphorsaeure
  • Adenosine 5'-pyrophosphate
  • Adenosine diphosphate
  • Adenosine pyrophosphate
  • Adenosine-5'-diphosphate
Full agonist, Agonist 58-64-0
  • NFB Orthophosphate
  • O-Phosphoric acid
  • Ortho-phosphate
  • Orthophosphate (PO43-)
  • Orthophosphate(3-)
genes like me logo Genes that share compounds with CPS1: view

Transcripts for CPS1 Gene

Unigene Clusters for CPS1 Gene

Carbamoyl-phosphate synthase 1, mitochondrial:
Representative Sequences:

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for CPS1 Gene

No ASD Table

Relevant External Links for CPS1 Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for CPS1 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for CPS1 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for CPS1 Gene

This gene is overexpressed in Liver (x45.4).

Protein differential expression in normal tissues from HIPED for CPS1 Gene

This gene is overexpressed in Liver (34.1), Liver, secretome (18.0), and Fetal Liver (12.6).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for CPS1 Gene

Protein tissue co-expression partners for CPS1 Gene

NURSA nuclear receptor signaling pathways regulating expression of CPS1 Gene:


SOURCE GeneReport for Unigene cluster for CPS1 Gene:


mRNA Expression by UniProt/SwissProt for CPS1 Gene:

Tissue specificity: Primarily in the liver and small intestine.

Evidence on tissue expression from TISSUES for CPS1 Gene

  • Liver(4.9)
  • Nervous system(4.5)
  • Intestine(4.4)
  • Eye(2)
  • Gall bladder(2)

Phenotype-based relationships between genes and organs from Gene ORGANizer for CPS1 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
  • cardiovascular
  • digestive
  • nervous
  • respiratory
  • skeletal muscle
  • urinary
Head and neck:
  • brain
  • head
  • esophagus
  • lung
  • kidney
  • liver
  • stomach
  • blood
genes like me logo Genes that share expression patterns with CPS1: view

Orthologs for CPS1 Gene

This gene was present in the common ancestor of eukaryotes.

Orthologs for CPS1 Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia CPS1 33 34
  • 99.42 (n)
(Monodelphis domestica)
Mammalia CPS1 34
  • 93 (a)
(Canis familiaris)
Mammalia CPS1 33 34
  • 92.91 (n)
(Bos Taurus)
Mammalia CPS1 33 34
  • 92.37 (n)
(Rattus norvegicus)
Mammalia Cps1 33
  • 89.36 (n)
(Mus musculus)
Mammalia Cps1 33 16 34
  • 89.24 (n)
(Ornithorhynchus anatinus)
Mammalia CPS1 34
  • 80 (a)
(Gallus gallus)
Aves CPS1 33 34
  • 76.59 (n)
(Anolis carolinensis)
Reptilia CPS1 34
  • 79 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia cps1 33
  • 73.75 (n)
Str.8825 33
African clawed frog
(Xenopus laevis)
Amphibia Xl.24543 33
(Danio rerio)
Actinopterygii cps1 33 34
  • 69.41 (n)
rainbow trout
(Oncorhynchus mykiss)
Actinopterygii Omy.11701 33
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes URA2 34
  • 34 (a)
thale cress
(Arabidopsis thaliana)
eudicotyledons CARB 33
  • 49.03 (n)
(Oryza sativa)
Liliopsida Os01g0570700 33
  • 45.19 (n)
Species where no ortholog for CPS1 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • fruit fly (Drosophila melanogaster)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)
  • worm (Caenorhabditis elegans)

Evolution for CPS1 Gene

Gene Tree for CPS1 (if available)
Gene Tree for CPS1 (if available)

Paralogs for CPS1 Gene

Paralogs for CPS1 Gene

(1) SIMAP similar genes for CPS1 Gene using alignment to 10 proteins:

genes like me logo Genes that share paralogs with CPS1: view

Variants for CPS1 Gene

Sequence variations from dbSNP and Humsavar for CPS1 Gene

SNP ID Clin Chr 02 pos Variation AA Info Type
rs1015051007 phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] 210,612,273(+) C/T coding_sequence_variant, missense_variant
rs1047883 conflicting-interpretations-of-pathogenicity, benign, likely-benign, not specified, Congenital hyperammonemia, type I 210,591,913(+) A/G/T coding_sequence_variant, genic_upstream_transcript_variant, missense_variant, upstream_transcript_variant
rs1047891 conflicting-interpretations-of-pathogenicity, benign, not specified, Congenital hyperammonemia, type I 210,675,783(+) C/A coding_sequence_variant, missense_variant
rs1048119191 phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] 210,602,271(+) G/C coding_sequence_variant, missense_variant
rs1053661397 uncertain-significance, Congenital hyperammonemia, type I 210,679,102(+) A/G 3_prime_UTR_variant

Structural Variations from Database of Genomic Variants (DGV) for CPS1 Gene

Variant ID Type Subtype PubMed ID
esv2674073 CNV deletion 23128226
esv3594156 CNV loss 21293372
esv3594159 CNV loss 21293372
nsv477718 CNV novel sequence insertion 20440878
nsv821631 CNV loss 15273396

Variation tolerance for CPS1 Gene

Residual Variation Intolerance Score: 7.54% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 17.82; 98.35% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for CPS1 Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for CPS1 Gene

Disorders for CPS1 Gene

MalaCards: The human disease database

(12) MalaCards diseases for CPS1 Gene - From: HGMD, OMIM, ClinVar, GTR, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
  • carbamoyl phosphate synthetase i deficiency
pulmonary hypertension, neonatal
  • pulmonary hypertension, neonatal, susceptibility to
ornithine transcarbamylase deficiency, hyperammonemia due to
  • ornithine carbamoyltransferase deficiency
urea cycle disorder
  • disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia
pulmonary hypertension
  • primary pulmonary hypertension
- elite association - COSMIC cancer census association via MalaCards
Search CPS1 in MalaCards View complete list of genes associated with diseases


  • Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300]: An autosomal recessive disorder of the urea cycle causing hyperammonemia. It can present as a devastating metabolic disease dominated by severe hyperammonemia in neonates or as a more insidious late-onset condition, generally manifesting as life-threatening hyperammonemic crises under catabolic situations. Clinical features include protein intolerance, intermittent ataxia, seizures, lethargy, developmental delay and mental retardation. {ECO:0000269 PubMed:11388595, ECO:0000269 PubMed:11474210, ECO:0000269 PubMed:12655559, ECO:0000269 PubMed:12955727, ECO:0000269 PubMed:15164414, ECO:0000269 PubMed:15617192, ECO:0000269 PubMed:16737834, ECO:0000269 PubMed:17310273, ECO:0000269 PubMed:20578160, ECO:0000269 PubMed:21120950, ECO:0000269 PubMed:22173106, ECO:0000269 PubMed:23649895, ECO:0000269 PubMed:24813853, ECO:0000269 PubMed:26440671, ECO:0000269 PubMed:9711878}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Pulmonary hypertension, neonatal (PHN) [MIM:615371]: A disease characterized by elevated pulmonary artery pressure. Pulmonary hypertension in the neonate is associated with multiple underlying problems such as respiratory distress syndrome, meconium aspiration syndrome, congenital diaphragmatic hernia, bronchopulmonary dysplasia, sepsis, or congenital heart disease. {ECO:0000269 PubMed:11407344}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. CPS1 variants influence the availability of precursors for nitric oxide (NO) synthesis and play a role in clinical situations where endogenous NO production is critically important, such as neonatal pulmonary hypertension, increased pulmonary artery pressure following surgical repair of congenital heart defects or hepatovenocclusive disease following bone marrow transplantation. Infants with neonatal pulmonary hypertension homozygous for Thr-1406 have lower L-arginine concentrations than neonates homozygous for Asn-1406 (PubMed:11407344). {ECO:0000269 PubMed:11407344}.

Genatlas disease for CPS1 Gene

neonatal distress and hyperammonemia

Additional Disease Information for CPS1

Genetic Association Database
Human Genome Epidemiology Navigator
Tumor Gene Database
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
genes like me logo Genes that share disorders with CPS1: view

Publications for CPS1 Gene

  1. The T1405N carbamoyl phosphate synthetase polymorphism does not affect plasma arginine concentrations in preterm infants. (PMID: 20520828) Moonen RM … Villamor E (PloS one 2010) 3 4 22 44 58
  2. Structural insight on the control of urea synthesis: identification of the binding site for N-acetyl-L-glutamate, the essential allosteric activator of mitochondrial carbamoyl phosphate synthetase. (PMID: 19754428) Pekkala S … Cervera J (The Biochemical journal 2009) 3 4 22 58
  3. Genetic variation in the mitochondrial enzyme carbamyl-phosphate synthetase I predisposes children to increased pulmonary artery pressure following surgical repair of congenital heart defects: a validated genetic association study. (PMID: 17188582) Canter JA … Barr FE (Mitochondrion 2007) 3 22 44 58
  4. Carbamoyl phosphate synthetase polymorphisms as a risk factor for necrotizing enterocolitis. (PMID: 17597649) Moonen RM … Villamor E (Pediatric research 2007) 3 22 44 58
  5. Relationship between carbamoyl-phosphate synthetase genotype and systemic vascular function. (PMID: 14718356) Summar ML … Brown NJ (Hypertension (Dallas, Tex. : 1979) 2004) 3 22 44 58

Products for CPS1 Gene

Sources for CPS1 Gene

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