Incidental Mutation 'R9568:Ptgs2'
ID 721732
Institutional Source Beutler Lab
Gene Symbol Ptgs2
Ensembl Gene ENSMUSG00000032487
Gene Name prostaglandin-endoperoxide synthase 2
Synonyms prostaglandin G/H synthase, Pghs2, PGHS-2, cyclooxygenase-2, cyclooxygenase 2, COX2, Cox-2, Tis10, PHS-2
MMRRC Submission
Accession Numbers
Essential gene? Probably essential (E-score: 0.786) question?
Stock # R9568 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 149975851-149983978 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to T at 149976842 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000035065 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035065] [ENSMUST00000190784]
AlphaFold Q05769
PDB Structure CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2 [X-RAY DIFFRACTION]
CYCLOOXYGENASE-2 (PROSTAGLANDIN SYNTHASE-2) COMPLEXED WITH A SELECTIVE INHIBITOR, SC-558 [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF A MIXTURE OF ARACHIDONIC ACID AND PROSTAGLANDIN BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2: PROSTAGLANDIN STRUCTURE [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF DICLOFENAC BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2 [X-RAY DIFFRACTION]
X-ray crystal structure of arachidonic acid bound to the cyclooxygenase channel of cyclooxygenase-2 [X-RAY DIFFRACTION]
X-ray crystal structure of eicosapentaenoic acid bound to the cyclooxygenase channel of cyclooxygenase-2 [X-RAY DIFFRACTION]
X-ray crystal structure of docosahexaenoic acid bound to the cyclooxygenase channel of cyclooxygenase-2 [X-RAY DIFFRACTION]
X-ray crystal structure of arachidonic acid bound in the cyclooxygenase channel of L531F murine COX-2 [X-RAY DIFFRACTION]
Structure of compound 5c-S bound at the active site of COX-2 [X-RAY DIFFRACTION]
Structure of celecoxib bound at the COX-2 active site [X-RAY DIFFRACTION]
>> 23 additional structures at PDB <<
Predicted Effect probably null
Transcript: ENSMUST00000035065
SMART Domains Protein: ENSMUSP00000035065
Gene: ENSMUSG00000032487

DomainStartEndE-ValueType
EGF 20 55 2.64e1 SMART
low complexity region 182 198 N/A INTRINSIC
Pfam:An_peroxidase 206 562 7.3e-48 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000190784
SMART Domains Protein: ENSMUSP00000139904
Gene: ENSMUSG00000032487

DomainStartEndE-ValueType
Blast:EGF 1 23 2e-9 BLAST
SCOP:d1eqga2 1 26 5e-8 SMART
PDB:1CVU|B 1 62 1e-38 PDB
SCOP:d1cvua1 27 62 1e-20 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes an enzyme that is a member of the prostaglandin G/H synthase family. The encoded protein converts arachidonic acid to prostaglandin endoperoxide H2 which is a key enzymatic step in prostaglandin biosynthesis. This gene is the inducible prostaglandin G/H synthase family member that is upregulated during inflammation. Aberrant regulation of this gene is associated with cancer progression in several tissues and an increased risk of cardiovascular events. This gene is the target of many non-steroidal anti-inflammatory drugs. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous null mice exhibit increased perinatal mortality associated with frequent lack of closure and remodeling of the ductus arteriosus, background-sensitive kidney dysplasia with microcyst formation, and myocardial fibrosis. Mutant females show impaired fertility. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam6a T G 12: 113,508,020 (GRCm39) V131G possibly damaging Het
Agr3 G T 12: 35,998,349 (GRCm39) M149I probably benign Het
Alox12b T A 11: 69,054,836 (GRCm39) C280S possibly damaging Het
Amhr2 C A 15: 102,353,954 (GRCm39) Q16K probably benign Het
Ank1 A G 8: 23,609,381 (GRCm39) T1387A probably benign Het
B3gnt9 A C 8: 105,980,203 (GRCm39) F395C probably damaging Het
BC048562 A G 9: 108,322,905 (GRCm39) D80G probably damaging Het
Ccdc65 T A 15: 98,620,819 (GRCm39) M438K possibly damaging Het
Ccz1 T C 5: 143,938,251 (GRCm39) R240G probably damaging Het
Cish A T 9: 107,177,593 (GRCm39) S90C probably benign Het
Col5a2 A T 1: 45,430,998 (GRCm39) S881T possibly damaging Het
Col6a6 G A 9: 105,657,926 (GRCm39) T762I possibly damaging Het
Cpa1 A G 6: 30,640,060 (GRCm39) K49E probably benign Het
Cpb1 T C 3: 20,320,697 (GRCm39) probably null Het
Csmd3 A G 15: 48,150,942 (GRCm39) S483P probably damaging Het
Cul9 G A 17: 46,831,044 (GRCm39) T1643I possibly damaging Het
Dock2 T C 11: 34,599,638 (GRCm39) K314E possibly damaging Het
Elp1 G T 4: 56,786,711 (GRCm39) P411T probably damaging Het
Fam186b T G 15: 99,176,571 (GRCm39) K773T probably damaging Het
Fancl T A 11: 26,418,672 (GRCm39) V259E probably benign Het
Fat4 T G 3: 38,946,156 (GRCm39) I1683S probably damaging Het
Fcamr T A 1: 130,732,356 (GRCm39) H114Q probably damaging Het
Fndc11 T C 2: 180,864,046 (GRCm39) F284L probably damaging Het
Galns A G 8: 123,311,649 (GRCm39) probably null Het
Gch1 A G 14: 47,426,637 (GRCm39) S30P probably benign Het
Gcnt3 A G 9: 69,942,346 (GRCm39) I74T probably benign Het
Gfral A T 9: 76,104,383 (GRCm39) C210S probably damaging Het
Gm26566 G A 4: 88,640,247 (GRCm39) A13T unknown Het
Gm9936 A T 5: 114,995,166 (GRCm39) D150E unknown Het
Gsn C A 2: 35,174,003 (GRCm39) D75E probably benign Het
Ighd2-7 T C 12: 113,420,344 (GRCm39) T5A possibly damaging Het
Itsn1 G T 16: 91,649,782 (GRCm39) R152L probably benign Het
Klhl3 A T 13: 58,157,126 (GRCm39) L620Q probably damaging Het
Larp7-ps G T 4: 92,079,915 (GRCm39) Y24* probably null Het
Lpl G A 8: 69,340,235 (GRCm39) V77M probably benign Het
Lrfn3 A T 7: 30,058,916 (GRCm39) H436Q probably benign Het
Lrp1b A G 2: 40,569,227 (GRCm39) C3965R Het
Lrrc2 G A 9: 110,799,228 (GRCm39) probably null Het
Manea C A 4: 26,340,468 (GRCm39) D165Y probably damaging Het
Myom1 A T 17: 71,394,476 (GRCm39) Q992L probably damaging Het
Naip5 T C 13: 100,359,821 (GRCm39) T472A probably benign Het
Naip5 T A 13: 100,356,338 (GRCm39) E1092D probably benign Het
Nyap1 C T 5: 137,733,394 (GRCm39) W546* probably null Het
Olfml3 T G 3: 103,644,282 (GRCm39) Y129S possibly damaging Het
Or4d5 A T 9: 40,011,864 (GRCm39) D307E probably benign Het
Or5h19 C A 16: 58,856,213 (GRCm39) V296F probably damaging Het
Or6z5 A G 7: 6,477,334 (GRCm39) E75G probably damaging Het
Or9k2b T A 10: 130,015,814 (GRCm39) I312F probably benign Het
P2rx6 A C 16: 17,385,300 (GRCm39) probably null Het
Plxnb2 A T 15: 89,045,160 (GRCm39) Y1095* probably null Het
Pmepa1 G A 2: 173,069,794 (GRCm39) R216C probably damaging Het
Prodh A G 16: 17,902,619 (GRCm39) probably benign Het
Ptch1 A G 13: 63,689,987 (GRCm39) Y389H probably damaging Het
Rbm14 A G 19: 4,861,464 (GRCm39) Y25H probably damaging Het
Rfc2 T C 5: 134,622,112 (GRCm39) L197P probably damaging Het
Rnf19b G T 4: 128,967,397 (GRCm39) W313L probably damaging Het
Sh3rf1 G T 8: 61,825,585 (GRCm39) A527S probably benign Het
Slc12a1 A G 2: 125,032,218 (GRCm39) Y623C probably damaging Het
Slc25a54 T A 3: 109,005,932 (GRCm39) W147R probably damaging Het
Slc4a1 A G 11: 102,247,680 (GRCm39) L401P probably damaging Het
Slc4a7 A G 14: 14,796,073 (GRCm38) probably null Het
Stab2 A G 10: 86,699,420 (GRCm39) Y1933H probably damaging Het
Supt5 A T 7: 28,014,688 (GRCm39) V1037E probably damaging Het
Sv2b A T 7: 74,775,428 (GRCm39) H466Q probably benign Het
Tmco5 G A 2: 116,710,730 (GRCm39) E17K probably damaging Het
Tmem69 G A 4: 116,411,972 (GRCm39) S12F probably damaging Het
Trp53 C A 11: 69,478,392 (GRCm39) Y100* probably null Het
Trpm7 A T 2: 126,664,510 (GRCm39) H956Q probably benign Het
Tsnaxip1 G A 8: 106,569,135 (GRCm39) R495H probably benign Het
Vmn1r237 A T 17: 21,534,777 (GRCm39) I167F probably benign Het
Vmn1r70 A G 7: 10,368,292 (GRCm39) D260G probably benign Het
Zbtb38 G A 9: 96,570,944 (GRCm39) H47Y probably damaging Het
Zfp184 G T 13: 22,142,897 (GRCm39) C201F probably benign Het
Zfp384 T A 6: 125,001,796 (GRCm39) I147N possibly damaging Het
Other mutations in Ptgs2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00903:Ptgs2 APN 1 149,980,175 (GRCm39) missense probably damaging 1.00
IGL01626:Ptgs2 APN 1 149,979,478 (GRCm39) missense probably damaging 1.00
IGL01758:Ptgs2 APN 1 149,977,740 (GRCm39) critical splice acceptor site probably null
IGL02168:Ptgs2 APN 1 149,979,430 (GRCm39) splice site probably null
IGL02309:Ptgs2 APN 1 149,981,307 (GRCm39) missense probably damaging 1.00
IGL02363:Ptgs2 APN 1 149,981,460 (GRCm39) splice site probably null
IGL02574:Ptgs2 APN 1 149,978,526 (GRCm39) nonsense probably null
IGL03156:Ptgs2 APN 1 149,981,228 (GRCm39) missense probably damaging 1.00
R0436:Ptgs2 UTSW 1 149,980,028 (GRCm39) unclassified probably benign
R0629:Ptgs2 UTSW 1 149,976,788 (GRCm39) missense probably benign
R0631:Ptgs2 UTSW 1 149,980,288 (GRCm39) missense probably benign 0.30
R0811:Ptgs2 UTSW 1 149,977,105 (GRCm39) missense probably benign 0.03
R0812:Ptgs2 UTSW 1 149,977,105 (GRCm39) missense probably benign 0.03
R0980:Ptgs2 UTSW 1 149,980,061 (GRCm39) missense probably damaging 1.00
R1340:Ptgs2 UTSW 1 149,981,228 (GRCm39) missense probably damaging 1.00
R1626:Ptgs2 UTSW 1 149,979,619 (GRCm39) critical splice acceptor site probably null
R1666:Ptgs2 UTSW 1 149,977,021 (GRCm39) missense probably damaging 1.00
R1742:Ptgs2 UTSW 1 149,980,150 (GRCm39) missense probably damaging 1.00
R1926:Ptgs2 UTSW 1 149,975,979 (GRCm39) missense possibly damaging 0.48
R2148:Ptgs2 UTSW 1 149,981,465 (GRCm39) missense probably benign
R2361:Ptgs2 UTSW 1 149,979,726 (GRCm39) missense probably benign 0.00
R2927:Ptgs2 UTSW 1 149,977,011 (GRCm39) missense possibly damaging 0.95
R3966:Ptgs2 UTSW 1 149,981,226 (GRCm39) missense probably damaging 0.99
R4291:Ptgs2 UTSW 1 149,976,002 (GRCm39) missense probably benign
R4580:Ptgs2 UTSW 1 149,979,845 (GRCm39) missense possibly damaging 0.78
R4668:Ptgs2 UTSW 1 149,976,835 (GRCm39) missense probably benign 0.32
R4751:Ptgs2 UTSW 1 149,979,771 (GRCm39) missense probably damaging 1.00
R4777:Ptgs2 UTSW 1 149,981,138 (GRCm39) missense probably benign 0.03
R5264:Ptgs2 UTSW 1 149,978,481 (GRCm39) missense possibly damaging 0.62
R5570:Ptgs2 UTSW 1 149,979,859 (GRCm39) missense
R5587:Ptgs2 UTSW 1 149,981,306 (GRCm39) missense probably damaging 1.00
R5761:Ptgs2 UTSW 1 149,981,279 (GRCm39) missense probably benign 0.18
R5850:Ptgs2 UTSW 1 149,981,127 (GRCm39) missense probably benign 0.03
R6137:Ptgs2 UTSW 1 149,976,744 (GRCm39) missense probably benign 0.08
R6513:Ptgs2 UTSW 1 149,975,879 (GRCm39) unclassified probably benign
R6553:Ptgs2 UTSW 1 149,979,738 (GRCm39) missense possibly damaging 0.93
R6585:Ptgs2 UTSW 1 149,979,738 (GRCm39) missense possibly damaging 0.93
R6593:Ptgs2 UTSW 1 149,976,784 (GRCm39) missense possibly damaging 0.63
R6772:Ptgs2 UTSW 1 149,977,829 (GRCm39) missense probably damaging 1.00
R6850:Ptgs2 UTSW 1 149,981,291 (GRCm39) missense probably damaging 1.00
R7205:Ptgs2 UTSW 1 149,978,512 (GRCm39) missense probably benign 0.01
R7320:Ptgs2 UTSW 1 149,978,446 (GRCm39) missense probably damaging 1.00
R7567:Ptgs2 UTSW 1 149,978,448 (GRCm39) missense probably damaging 0.99
R7751:Ptgs2 UTSW 1 149,980,258 (GRCm39) missense probably benign 0.14
R7863:Ptgs2 UTSW 1 149,977,090 (GRCm39) missense probably damaging 1.00
R8100:Ptgs2 UTSW 1 149,978,472 (GRCm39) missense probably damaging 1.00
R8117:Ptgs2 UTSW 1 149,979,785 (GRCm39) missense probably damaging 1.00
R8128:Ptgs2 UTSW 1 149,977,099 (GRCm39) missense probably damaging 0.99
R8906:Ptgs2 UTSW 1 149,979,859 (GRCm39) missense
R8964:Ptgs2 UTSW 1 149,980,798 (GRCm39) missense probably damaging 1.00
R9184:Ptgs2 UTSW 1 149,980,175 (GRCm39) missense probably damaging 1.00
R9563:Ptgs2 UTSW 1 149,981,419 (GRCm39) missense probably benign
R9615:Ptgs2 UTSW 1 149,980,802 (GRCm39) missense probably damaging 1.00
Z1176:Ptgs2 UTSW 1 149,981,472 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CATTGTAAAGTTGACCCATAGTGACAG -3'
(R):5'- GGTCAGGATGTAGTGCACTG -3'

Sequencing Primer
(F):5'- TGACCCATAGTGACAGAATTAAATCC -3'
(R):5'- CAGGATGTAGTGCACTGTGTTTG -3'
Posted On 2022-08-09