CPS1 Chromosome 2

Carbamoyl-phosphate synthase 1
413 variants 413 Health Risk

Upload your DNA to see your personal genotypes for variants in CPS1.

What This Gene Does
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]
Gene Info
Gene Group
Glutamine amidotransferase class 1 domain containing
Locus Type
gene with protein product
Location
2q34
Ensembl
ENSG00000021826
Associated Conditions (11)
Congenital hyperammonemia
type I
Inborn genetic diseases
CPS1-related disorder
Pulmonary hypertension
neonatal
susceptibility to
Intellectual disability
Uterine corpus endometrial carcinoma
Lung cancer
Hereditary breast ovarian cancer syndrome
Key Variants
RS1034733261
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Inborn genetic diseases
Health Risk
RS112199960
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Congenital hyperammonemia
Health Risk
RS114819130
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Inborn genetic diseases
Health Risk
RS1202306773
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Pulmonary hypertension
Health Risk
RS121912595
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Congenital hyperammonemia
Health Risk
RS1221447754
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Inborn genetic diseases
Health Risk
RS1245845692
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Pulmonary hypertension
Health Risk
RS1354079241
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Congenital hyperammonemia
Health Risk
RS138392504
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, CPS1-related disorder
Health Risk
RS138424013
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Pulmonary hypertension
Health Risk
RS138718997
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Congenital hyperammonemia
Health Risk
RS1392559810
Conflicting classifications of pathogenicity
Congenital hyperammonemia, type I, Congenital hyperammonemia
Health Risk
All Variants (413)
RSID Category Clinical Significance Conditions
RS202117044 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS2106116333 Health Risk Conflicting classifications of pathogenicity Pulmonary hypertension, neonatal, susceptibility to
RS368785491 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS368890059 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS368909569 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS369030433 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS369682093 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS372217508 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS373056604 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS373841124 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS374335271 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS375785288 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS376699772 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS529836556 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS534835336 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS548763994 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS554763314 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS555151297 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS561995236 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS563304664 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS576303662 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS587780323 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS746628905 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS746685859 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS749825961 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS750006303 Health Risk Conflicting classifications of pathogenicity CPS1-related disorder, Congenital hyperammonemia, type I
RS752339705 Health Risk Conflicting classifications of pathogenicity Pulmonary hypertension, neonatal, susceptibility to
RS753665308 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS754433289 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS755530984 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS757451824 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS760714614 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS760851899 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Congenital hyperammonemia, type I
RS760895692 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS761921978 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS764456030 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS765106604 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS765712117 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS767905306 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS769593170 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS770552464 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS772497399 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS773539595 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS775865903 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS778117194 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS778764720 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Congenital hyperammonemia, type I
RS778766382 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS778958318 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS79627159 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS866921933 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Congenital hyperammonemia, type I
« Prev 1 2 3 4 5 ... 9 Next »
Sign Up to Analyze Your DNA Log In