Incidental Mutation 'R7127:Plscr4'
ID552398
Institutional Source Beutler Lab
Gene Symbol Plscr4
Ensembl Gene ENSMUSG00000032377
Gene Namephospholipid scramblase 4
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock #R7127 (G1)
Quality Score225.009
Status Not validated
Chromosome9
Chromosomal Location92457373-92492456 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) C to T at 92490778 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Stop codon at position 318 (R318*)
Ref Sequence ENSEMBL: ENSMUSP00000034941 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034941]
Predicted Effect probably null
Transcript: ENSMUST00000034941
AA Change: R318*
SMART Domains Protein: ENSMUSP00000034941
Gene: ENSMUSG00000032377
AA Change: R318*

DomainStartEndE-ValueType
low complexity region 38 51 N/A INTRINSIC
Pfam:Scramblase 96 318 7.5e-87 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810474O19Rik T C 6: 149,327,945 F830L possibly damaging Het
Abca15 C T 7: 120,332,602 T26I probably benign Het
Adam5 A T 8: 24,810,781 I244N probably damaging Het
Adam7 A G 14: 68,514,769 probably null Het
Aox4 T A 1: 58,228,874 N204K probably benign Het
Arl13b C T 16: 62,801,739 G397D probably damaging Het
AU041133 T C 10: 82,150,866 F118L probably benign Het
Brinp1 C T 4: 68,793,023 R316H probably benign Het
Cabcoco1 C T 10: 68,436,330 V268I probably benign Het
Car15 T C 16: 17,838,196 probably benign Het
Ccdc185 G T 1: 182,748,856 D89E possibly damaging Het
Cckar T A 5: 53,706,475 Y48F probably damaging Het
Cdyl T A 13: 35,856,668 S282T probably benign Het
Clca1 T C 3: 145,006,045 T730A probably damaging Het
Cracr2b T C 7: 141,465,782 S318P possibly damaging Het
Depdc1b T C 13: 108,323,928 F24S probably damaging Het
Duox2 C T 2: 122,291,949 G565D probably benign Het
Ehbp1 A T 11: 22,053,529 Y1073* probably null Het
Epg5 A T 18: 78,028,925 N2384I probably damaging Het
Fam171b A G 2: 83,879,766 D594G probably benign Het
Flad1 A G 3: 89,403,418 Y441H probably damaging Het
Fn1 T C 1: 71,597,544 T2150A probably benign Het
Fnta C A 8: 26,007,203 R206L probably damaging Het
Gadd45b A T 10: 80,931,165 M95L probably benign Het
Gbp8 A T 5: 105,017,712 H358Q probably benign Het
Glipr1l3 C A 10: 112,148,090 G157V probably damaging Het
Hoxc13 T C 15: 102,921,468 I94T possibly damaging Het
Hunk A G 16: 90,475,891 D361G probably damaging Het
Igkv3-4 T A 6: 70,672,171 Y51* probably null Het
Kif26a C T 12: 112,178,145 P1611L probably damaging Het
Lamb1 T C 12: 31,324,315 L1559P probably damaging Het
Lrrc8d T C 5: 105,812,963 V413A probably damaging Het
Med6 C T 12: 81,589,000 R86Q probably damaging Het
Myrf A T 19: 10,215,341 S605T probably benign Het
Olfr792 T A 10: 129,541,067 C177S probably damaging Het
Plk3 A T 4: 117,130,570 V429E probably benign Het
Plrg1 C T 3: 83,059,915 P131L probably damaging Het
Rab34 A T 11: 78,191,230 K152* probably null Het
Rasef A T 4: 73,744,132 S194T probably damaging Het
Rcc1 A G 4: 132,334,796 S269P probably damaging Het
Rsf1 CGGCGGCGG CGGCGGCGGGGGCGGCGG 7: 97,579,914 probably benign Het
Ryr2 C T 13: 11,655,713 V3466M probably damaging Het
Scin A G 12: 40,105,072 I174T possibly damaging Het
Serpinb8 A G 1: 107,597,470 M1V probably null Het
Smok3c A T 5: 138,064,709 I153F probably damaging Het
Spen G A 4: 141,476,108 S1736L possibly damaging Het
Sspo T A 6: 48,449,512 M155K probably benign Het
Stip1 C T 19: 7,021,810 G467S possibly damaging Het
Sun2 T C 15: 79,727,899 I528M probably benign Het
Syne1 G A 10: 5,243,180 A3956V probably damaging Het
Taok2 G T 7: 126,867,154 A831E possibly damaging Het
Tas2r126 T C 6: 42,434,805 F91L probably damaging Het
Tas2r140 A G 6: 133,054,959 S279P possibly damaging Het
Tiam1 A T 16: 89,860,260 L696H probably damaging Het
Trank1 T G 9: 111,365,796 S963A possibly damaging Het
Trf A G 9: 103,225,127 V184A probably benign Het
Ttll13 T A 7: 80,253,658 M231K possibly damaging Het
Tuba1a T G 15: 98,951,574 T41P probably benign Het
Zfhx4 A G 3: 5,413,044 Q3573R probably damaging Het
Zfp141 G A 7: 42,475,429 H540Y probably damaging Het
Other mutations in Plscr4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00763:Plscr4 APN 9 92484945 missense probably null 1.00
IGL02506:Plscr4 APN 9 92489991 missense possibly damaging 0.67
R0331:Plscr4 UTSW 9 92482642 missense probably damaging 1.00
R0360:Plscr4 UTSW 9 92488761 splice site probably benign
R0838:Plscr4 UTSW 9 92471760 splice site probably benign
R0898:Plscr4 UTSW 9 92484753 missense probably damaging 0.98
R1845:Plscr4 UTSW 9 92490046 missense probably damaging 1.00
R1895:Plscr4 UTSW 9 92483836 missense probably damaging 0.99
R1946:Plscr4 UTSW 9 92483836 missense probably damaging 0.99
R2127:Plscr4 UTSW 9 92488630 missense possibly damaging 0.82
R3427:Plscr4 UTSW 9 92488744 missense probably damaging 0.99
R4670:Plscr4 UTSW 9 92482867 critical splice donor site probably null
R4764:Plscr4 UTSW 9 92484780 missense probably damaging 0.99
R4958:Plscr4 UTSW 9 92484761 missense possibly damaging 0.95
R5126:Plscr4 UTSW 9 92488741 missense probably damaging 1.00
R5424:Plscr4 UTSW 9 92490022 missense possibly damaging 0.67
R6250:Plscr4 UTSW 9 92484828 missense possibly damaging 0.79
R6476:Plscr4 UTSW 9 92490766 missense probably benign 0.01
R6775:Plscr4 UTSW 9 92482805 missense probably benign
R6810:Plscr4 UTSW 9 92483836 missense probably damaging 0.99
R6982:Plscr4 UTSW 9 92482743 missense probably benign 0.00
R7190:Plscr4 UTSW 9 92488641 missense probably benign 0.11
Predicted Primers PCR Primer
(F):5'- CCTGAGCTTTTCCATCAGTTAATG -3'
(R):5'- AACCTAGTGCCTCAAGAAGC -3'

Sequencing Primer
(F):5'- TGCATTCTCACACATTAGCTGAAC -3'
(R):5'- TAGTGCCTCAAGAAGCTAAATACTC -3'
Posted On2019-05-15