CPS1 (carbamoyl-phosphate synthase 1)
|
Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
1373 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Carbamoyl-phosphate synthase 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
CPS1 |
SynonymsGene synonyms aliases
|
CPSASE1, GATD6, PHN |
ChromosomeChromosome number
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2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q34 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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] |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs28940283 |
A>G |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, upstream transcript variant, genic upstream transcript variant |
rs41272669 |
C>T |
Likely-benign, uncertain-significance, conflicting-interpretations-of-pathogenicity |
Intron variant |
rs114819130 |
G>A |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, missense variant |
rs121912592 |
C>A,T |
Pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs121912593 |
C>T |
Pathogenic |
Non coding transcript variant, genic upstream transcript variant, stop gained, coding sequence variant |
rs121912594 |
A>C |
Benign, risk-factor |
Non coding transcript variant, coding sequence variant, missense variant |
rs121912595 |
G>A,C,T |
Uncertain-significance, pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs121912596 |
C>T |
Pathogenic |
Non coding transcript variant, stop gained, coding sequence variant |
rs138392504 |
G>A |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Non coding transcript variant, coding sequence variant, missense variant, genic upstream transcript variant |
rs138779023 |
T>C |
Benign, conflicting-interpretations-of-pathogenicity, benign-likely-benign |
Non coding transcript variant, coding sequence variant, synonymous variant, genic upstream transcript variant |
rs141373204 |
A>G |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Non coding transcript variant, coding sequence variant, missense variant |
rs192759073 |
C>T |
Likely-benign, uncertain-significance, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, non coding transcript variant, synonymous variant, genic upstream transcript variant |
rs200214298 |
G>A,T |
Pathogenic, likely-benign |
Non coding transcript variant, stop gained, missense variant, coding sequence variant, genic upstream transcript variant |
rs201716417 |
C>A,G,T |
Likely-pathogenic, pathogenic, uncertain-significance |
Coding sequence variant, non coding transcript variant, missense variant |
rs202107577 |
C>A,T |
Likely-benign, pathogenic-likely-pathogenic |
Coding sequence variant, non coding transcript variant, stop gained, synonymous variant |
rs369061090 |
T>A |
Pathogenic, uncertain-significance |
Coding sequence variant, non coding transcript variant, missense variant |
rs727502824 |
GTG>- |
Pathogenic |
Inframe deletion, non coding transcript variant, coding sequence variant |
rs755530984 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant, non coding transcript variant |
rs755882799 |
G>A,T |
Likely-pathogenic |
Splice acceptor variant |
rs756021170 |
G>A,T |
Likely-pathogenic |
Genic upstream transcript variant, coding sequence variant, missense variant, non coding transcript variant, stop gained |
rs757205958 |
G>A,C |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs758724746 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs759201450 |
C>T |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |
rs761225695 |
C>T |
Likely-pathogenic |
Coding sequence variant, stop gained, non coding transcript variant, genic upstream transcript variant |
rs764384490 |
G>- |
Pathogenic |
Frameshift variant, coding sequence variant, non coding transcript variant |
rs766584384 |
A>G |
Likely-pathogenic |
Splice acceptor variant |
rs767575696 |
T>C |
Likely-pathogenic |
Splice donor variant |
rs767694281 |
G>A,T |
Pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs772497399 |
G>A,C,T |
Likely-pathogenic, uncertain-significance |
Non coding transcript variant, coding sequence variant, missense variant |
rs778346264 |
T>- |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, stop gained, genic upstream transcript variant |
rs778766382 |
G>A |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs778958318 |
T>G |
Conflicting-interpretations-of-pathogenicity |
Missense variant, non coding transcript variant, coding sequence variant, genic upstream transcript variant |
rs781088670 |
C>- |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, stop gained |
rs961015305 |
C>A |
Likely-pathogenic |
Stop gained, non coding transcript variant, coding sequence variant |
rs1015051007 |
C>A,G,T |
Pathogenic |
Non coding transcript variant, missense variant, coding sequence variant |
rs1064794258 |
G>T |
Likely-pathogenic |
Genic upstream transcript variant, splice acceptor variant, upstream transcript variant |
rs1275489342 |
G>A,C |
Likely-pathogenic |
Intron variant |
rs1318756445 |
AT>- |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, frameshift variant, non coding transcript variant |
rs1326644714 |
C>- |
Pathogenic, likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs1341782266 |
->T |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs1374322297 |
T>C |
Conflicting-interpretations-of-pathogenicity |
Splice donor variant |
rs1375304341 |
CTACAATGGTCAG>- |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, coding sequence variant |
rs1392934477 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, missense variant |
rs1414143303 |
C>T |
Pathogenic |
Non coding transcript variant, stop gained, coding sequence variant |
rs1553507155 |
G>T |
Likely-pathogenic |
Coding sequence variant, missense variant, initiator codon variant, genic upstream transcript variant, non coding transcript variant |
rs1553507167 |
A>T |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, stop gained, coding sequence variant |
rs1553507183 |
G>A |
Likely-pathogenic |
Splice donor variant, genic upstream transcript variant |
rs1553509010 |
->AAGTGGTT |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, frameshift variant |
rs1553509023 |
G>T |
Likely-pathogenic |
Splice donor variant, genic upstream transcript variant |
rs1553509303 |
A>- |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, frameshift variant |
rs1553509924 |
GA>- |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, frameshift variant |
rs1553510520 |
G>C |
Likely-pathogenic |
Splice donor variant, genic upstream transcript variant |
rs1553510944 |
G>- |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, frameshift variant |
rs1553511326 |
G>A |
Likely-pathogenic |
Splice donor variant, upstream transcript variant, genic upstream transcript variant |
rs1553511789 |
->T |
Likely-pathogenic |
Non coding transcript variant, stop gained, coding sequence variant |
rs1553512225 |
->C |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, coding sequence variant |
rs1553512642 |
G>A |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs1553513387 |
G>T |
Likely-pathogenic |
Splice acceptor variant |
rs1553513429 |
G>C |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs1553513433 |
G>A |
Likely-pathogenic |
Splice donor variant |
rs1553513864 |
A>G |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs1553516660 |
G>A |
Likely-pathogenic |
Splice donor variant |
rs1553517122 |
A>- |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, coding sequence variant |
rs1553517224 |
C>- |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, coding sequence variant |
rs1553517670 |
->GG |
Likely-pathogenic |
Splice donor variant, non coding transcript variant, coding sequence variant |
rs1553518389 |
G>A |
Pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs1553518395 |
T>A |
Likely-pathogenic |
Splice donor variant |
rs1553518719 |
A>T |
Likely-pathogenic |
Splice acceptor variant |
rs1553518720 |
G>C |
Likely-pathogenic |
Splice acceptor variant |
rs1553518726 |
C>- |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, coding sequence variant |
rs1559129372 |
G>C |
Pathogenic |
Splice donor variant |
rs1574543988 |
T>C |
Likely-pathogenic |
Genic upstream transcript variant, splice donor variant |
rs1574548003 |
T>C |
Likely-pathogenic |
Genic upstream transcript variant, splice donor variant |
rs1574566578 |
G>- |
Pathogenic |
Coding sequence variant, non coding transcript variant, frameshift variant |
rs1574567901 |
C>G |
Pathogenic |
Coding sequence variant, non coding transcript variant, stop gained |
rs1574577755 |
T>C |
Likely-pathogenic |
Splice donor variant |
rs1574632659 |
A>C |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs1574646079 |
G>C |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
P31327 |
Protein name |
Carbamoyl-phosphate synthase [ammonia], mitochondrial (EC 6.3.4.16) (Carbamoyl-phosphate synthetase I) (CPSase I) |
Protein function |
Involved in the urea cycle of ureotelic animals where the enzyme plays an important role in removing excess ammonia from the cell. |
PDB |
2YVQ
,
4UTR
,
4UTV
,
4UTX
,
4UTZ
,
4UU7
,
4UU8
,
4UUA
,
4UUB
,
5DOT
,
5DOU
,
5OJO
,
6UEL
,
6W2J
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00988 |
CPSase_sm_chain |
45 → 183 |
Carbamoyl-phosphate synthase small chain, CPSase domain |
Domain |
PF00117 |
GATase |
221 → 397 |
Glutamine amidotransferase class-I |
Domain |
PF02786 |
CPSase_L_D2 |
546 → 750 |
Carbamoyl-phosphate synthase L chain, ATP binding domain |
Domain |
PF02787 |
CPSase_L_D3 |
841 → 920 |
Carbamoyl-phosphate synthetase large chain, oligomerisation domain |
Domain |
PF02786 |
CPSase_L_D2 |
1088 → 1291 |
Carbamoyl-phosphate synthase L chain, ATP binding domain |
Domain |
PF02142 |
MGS |
1373 → 1465 |
MGS-like domain |
Domain |
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Sequence |
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Sequence length |
1500 |
Interactions |
View interactions |
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