CPS1 Chromosome 2

Carbamoyl-phosphate synthase 1
413 variants 413 Health Risk

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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
RS1034733261 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS112199960 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS114819130 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS1202306773 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS121912595 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS1221447754 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS1245845692 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS1354079241 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS138392504 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS138424013 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS138718997 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS1392559810 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS1392934477 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS140475976 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS140578009 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS141178702 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS141373204 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS141481633 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS141562755 Health Risk Conflicting classifications of pathogenicity Pulmonary hypertension, neonatal, susceptibility to
RS142369181 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS142468138 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS142693704 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS142916171 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS143913650 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS144230667 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS1458915316 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS146064786 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS146968493 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS1472190012 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS148584272 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS148708735 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS149518280 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS149570645 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS150012540 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS150314086 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS150463750 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS150485422 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS150601728 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, CPS1-related disorder
RS150966847 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
RS1574632659 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS182678639 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS199878637 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS200465544 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS200569046 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS200616712 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS201058019 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS201246466 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Intellectual disability
RS201340295 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Inborn genetic diseases
RS201710257 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Congenital hyperammonemia
RS201955205 Health Risk Conflicting classifications of pathogenicity Congenital hyperammonemia, type I, Pulmonary hypertension
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