Incidental Mutation 'R0711:Psg25'
ID 62734
Institutional Source Beutler Lab
Gene Symbol Psg25
Ensembl Gene ENSMUSG00000070798
Gene Name pregnancy-specific beta-1-glycoprotein 25
Synonyms cea13
MMRRC Submission 038894-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R0711 (G1)
Quality Score 116
Status Validated
Chromosome 7
Chromosomal Location 18253627-18266191 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 18263485 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 113 (Q113*)
Ref Sequence ENSEMBL: ENSMUSP00000092389 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094795]
AlphaFold Q497W1
Predicted Effect probably null
Transcript: ENSMUST00000094795
AA Change: Q113*
SMART Domains Protein: ENSMUSP00000092389
Gene: ENSMUSG00000070798
AA Change: Q113*

DomainStartEndE-ValueType
IG 40 141 2.15e-3 SMART
IG 160 261 1.55e0 SMART
IG 280 381 3.59e-5 SMART
IGc2 397 461 1.02e-9 SMART
Meta Mutation Damage Score 0.9653 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.4%
  • 20x: 91.4%
Validation Efficiency 100% (91/91)
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik T A 3: 137,773,986 (GRCm39) D1058E probably damaging Het
4933405L10Rik A T 8: 106,435,563 (GRCm39) probably null Het
Adamtsl3 T A 7: 82,114,907 (GRCm39) probably benign Het
Afdn C T 17: 14,072,698 (GRCm39) P874S probably damaging Het
Ankrd6 G A 4: 32,815,326 (GRCm39) A391V probably damaging Het
Arhgef28 T G 13: 98,067,762 (GRCm39) T1388P probably damaging Het
Asxl3 G T 18: 22,657,508 (GRCm39) M1839I probably benign Het
BC005537 T C 13: 24,989,923 (GRCm39) F129L probably damaging Het
Celf2 A G 2: 6,726,226 (GRCm39) probably null Het
Chid1 C T 7: 141,076,590 (GRCm39) V325I probably benign Het
Cnn3 T A 3: 121,243,633 (GRCm39) D31E probably benign Het
Col12a1 G A 9: 79,559,317 (GRCm39) P1857L probably damaging Het
Cpeb1 T A 7: 81,001,618 (GRCm39) R430W probably benign Het
Daw1 T C 1: 83,169,059 (GRCm39) probably benign Het
Dcaf13 A G 15: 39,001,484 (GRCm39) Y264C probably damaging Het
Dnah6 T C 6: 73,064,585 (GRCm39) I2666V probably damaging Het
Dnai2 A C 11: 114,645,158 (GRCm39) D531A probably benign Het
Dock10 A T 1: 80,501,692 (GRCm39) F1833I probably damaging Het
Efhd2 C T 4: 141,587,183 (GRCm39) A200T probably damaging Het
Epb41l5 T A 1: 119,551,641 (GRCm39) probably benign Het
Ermp1 A G 19: 29,608,788 (GRCm39) Y164H possibly damaging Het
Gkn2 T C 6: 87,350,401 (GRCm39) probably benign Het
Golgb1 A T 16: 36,739,152 (GRCm39) Q2497L probably damaging Het
Gzme A T 14: 56,355,196 (GRCm39) M245K probably damaging Het
Iars2 A T 1: 185,054,585 (GRCm39) probably benign Het
Icosl T A 10: 77,909,775 (GRCm39) V240D probably damaging Het
Igsf3 T C 3: 101,334,709 (GRCm39) M262T probably benign Het
Ing3 G T 6: 21,971,236 (GRCm39) E336* probably null Het
Kat2a A T 11: 100,597,297 (GRCm39) V625E probably damaging Het
Ksr1 A G 11: 78,929,073 (GRCm39) probably benign Het
Lypd8 A T 11: 58,277,583 (GRCm39) M122L probably benign Het
Mdfi A T 17: 48,143,855 (GRCm39) probably benign Het
Med13 A G 11: 86,192,179 (GRCm39) probably benign Het
Msh6 C T 17: 88,294,112 (GRCm39) R956C probably damaging Het
Myo15b A G 11: 115,774,664 (GRCm39) E670G probably damaging Het
Myo1d A G 11: 80,375,158 (GRCm39) L972P probably damaging Het
Or4s2b A G 2: 88,509,018 (GRCm39) D266G probably damaging Het
Or51ai2 G A 7: 103,587,024 (GRCm39) A146T probably benign Het
Or7g12 T A 9: 18,899,447 (GRCm39) N54K probably benign Het
Pde8b C G 13: 95,244,325 (GRCm39) S143T possibly damaging Het
Pias4 G T 10: 80,993,364 (GRCm39) probably benign Het
Prkca A G 11: 107,872,480 (GRCm39) Y427H probably benign Het
Rab3gap2 T A 1: 184,982,123 (GRCm39) S392T probably damaging Het
Scrib A G 15: 75,938,756 (GRCm39) probably benign Het
Sdk2 A G 11: 113,793,970 (GRCm39) probably benign Het
Serpinb1c T A 13: 33,070,266 (GRCm39) probably benign Het
Serpinb9f T A 13: 33,511,904 (GRCm39) W136R probably damaging Het
Skic3 C T 13: 76,331,010 (GRCm39) P1480L probably damaging Het
Skint10 C A 4: 112,573,102 (GRCm39) probably benign Het
Slc25a13 T C 6: 6,117,128 (GRCm39) T196A probably damaging Het
Slc26a5 T C 5: 22,052,230 (GRCm39) H33R probably damaging Het
Slc27a6 T C 18: 58,731,829 (GRCm39) probably benign Het
Slitrk6 A T 14: 110,987,251 (GRCm39) Y819N probably damaging Het
Spata46 C T 1: 170,139,603 (GRCm39) Q201* probably null Het
Sptbn1 A T 11: 30,064,739 (GRCm39) V1920E probably damaging Het
Taf6l A G 19: 8,755,881 (GRCm39) F256L probably benign Het
Tmco3 T A 8: 13,342,039 (GRCm39) N104K probably damaging Het
Tmem200c A G 17: 69,149,249 (GRCm39) T611A probably damaging Het
Tmem202 T G 9: 59,432,655 (GRCm39) Y24S probably damaging Het
Tpp1 A G 7: 105,398,626 (GRCm39) L230P probably damaging Het
Trim56 C T 5: 137,141,846 (GRCm39) E557K probably benign Het
Trrap C T 5: 144,790,309 (GRCm39) L3590F probably damaging Het
Tulp4 A G 17: 6,189,387 (GRCm39) T70A possibly damaging Het
Vcp G C 4: 42,986,201 (GRCm39) A297G probably benign Het
Vwf T A 6: 125,603,234 (GRCm39) H861Q probably benign Het
Wdr64 T C 1: 175,599,751 (GRCm39) I536T probably benign Het
Zfp850 T C 7: 27,689,698 (GRCm39) N170S probably benign Het
Zfp87 G A 13: 74,524,544 (GRCm39) probably benign Het
Other mutations in Psg25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:Psg25 APN 7 18,260,106 (GRCm39) splice site probably benign
IGL00508:Psg25 APN 7 18,263,656 (GRCm39) missense probably benign
IGL01154:Psg25 APN 7 18,258,624 (GRCm39) missense probably benign 0.01
IGL01388:Psg25 APN 7 18,263,590 (GRCm39) missense possibly damaging 0.87
IGL02222:Psg25 APN 7 18,263,652 (GRCm39) missense probably damaging 1.00
IGL02261:Psg25 APN 7 18,255,268 (GRCm39) missense probably benign 0.09
IGL02309:Psg25 APN 7 18,260,349 (GRCm39) missense probably damaging 0.98
IGL02803:Psg25 APN 7 18,260,212 (GRCm39) missense possibly damaging 0.47
IGL03334:Psg25 APN 7 18,263,699 (GRCm39) missense probably benign 0.01
R1458:Psg25 UTSW 7 18,263,512 (GRCm39) missense probably damaging 1.00
R1598:Psg25 UTSW 7 18,265,928 (GRCm39) nonsense probably null
R2064:Psg25 UTSW 7 18,255,178 (GRCm39) missense probably damaging 0.96
R2066:Psg25 UTSW 7 18,263,487 (GRCm39) missense probably damaging 1.00
R4485:Psg25 UTSW 7 18,260,203 (GRCm39) missense probably damaging 1.00
R4499:Psg25 UTSW 7 18,258,816 (GRCm39) missense possibly damaging 0.89
R4514:Psg25 UTSW 7 18,263,533 (GRCm39) nonsense probably null
R4547:Psg25 UTSW 7 18,258,629 (GRCm39) missense probably damaging 1.00
R4604:Psg25 UTSW 7 18,263,728 (GRCm39) missense probably benign 0.05
R4886:Psg25 UTSW 7 18,258,838 (GRCm39) missense probably benign 0.00
R5121:Psg25 UTSW 7 18,260,461 (GRCm39) missense possibly damaging 0.68
R5208:Psg25 UTSW 7 18,260,460 (GRCm39) missense probably benign 0.00
R5267:Psg25 UTSW 7 18,258,711 (GRCm39) missense possibly damaging 0.78
R5376:Psg25 UTSW 7 18,260,460 (GRCm39) missense probably benign 0.00
R5425:Psg25 UTSW 7 18,258,709 (GRCm39) nonsense probably null
R5749:Psg25 UTSW 7 18,258,776 (GRCm39) missense probably damaging 1.00
R6050:Psg25 UTSW 7 18,260,403 (GRCm39) missense probably benign 0.37
R6862:Psg25 UTSW 7 18,255,323 (GRCm39) missense probably benign 0.03
R6962:Psg25 UTSW 7 18,263,679 (GRCm39) missense probably damaging 1.00
R7238:Psg25 UTSW 7 18,266,127 (GRCm39) start gained probably benign
R7782:Psg25 UTSW 7 18,255,227 (GRCm39) missense probably benign 0.15
R7812:Psg25 UTSW 7 18,255,093 (GRCm39) missense possibly damaging 0.71
R8155:Psg25 UTSW 7 18,260,445 (GRCm39) missense probably benign 0.00
R8775:Psg25 UTSW 7 18,255,153 (GRCm39) missense probably damaging 1.00
R8775-TAIL:Psg25 UTSW 7 18,255,153 (GRCm39) missense probably damaging 1.00
R8865:Psg25 UTSW 7 18,263,519 (GRCm39) missense possibly damaging 0.71
R9013:Psg25 UTSW 7 18,258,690 (GRCm39) missense probably benign 0.02
R9755:Psg25 UTSW 7 18,260,460 (GRCm39) missense probably benign 0.00
Z1088:Psg25 UTSW 7 18,263,516 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGTCCTGCACTAAATGTTCAAGCCC -3'
(R):5'- CCACTGCCAGAGTCATCATCCATTC -3'

Sequencing Primer
(F):5'- TGTTCAAGCCCCAACATGGAG -3'
(R):5'- CCACTCCAAGTGGTTGAAGG -3'
Posted On 2013-07-30