Incidental Mutation 'R9189:Polq'
ID 697640
Institutional Source Beutler Lab
Gene Symbol Polq
Ensembl Gene ENSMUSG00000034206
Gene Name polymerase (DNA directed), theta
Synonyms A430110D14Rik
MMRRC Submission 068951-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.509) question?
Stock # R9189 (G1)
Quality Score 225.009
Status Not validated
Chromosome 16
Chromosomal Location 36832148-36915779 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 36865265 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 706 (Q706K)
Ref Sequence ENSEMBL: ENSMUSP00000059757 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054034] [ENSMUST00000071452] [ENSMUST00000182946] [ENSMUST00000183112]
AlphaFold Q8CGS6
Predicted Effect probably damaging
Transcript: ENSMUST00000054034
AA Change: Q706K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000059757
Gene: ENSMUSG00000034206
AA Change: Q706K

DomainStartEndE-ValueType
low complexity region 2 29 N/A INTRINSIC
low complexity region 38 55 N/A INTRINSIC
DEXDc 87 298 4.09e-18 SMART
HELICc 398 484 4.02e-17 SMART
Blast:DEXDc 485 550 2e-25 BLAST
low complexity region 609 626 N/A INTRINSIC
PDB:2ZJA|A 712 826 5e-9 PDB
low complexity region 845 852 N/A INTRINSIC
low complexity region 898 911 N/A INTRINSIC
low complexity region 1126 1149 N/A INTRINSIC
low complexity region 1813 1822 N/A INTRINSIC
POLAc 2265 2504 3.3e-101 SMART
low complexity region 2521 2531 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000071452
AA Change: Q427K

PolyPhen 2 Score 0.659 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000071396
Gene: ENSMUSG00000034206
AA Change: Q427K

DomainStartEndE-ValueType
low complexity region 2 29 N/A INTRINSIC
low complexity region 38 55 N/A INTRINSIC
Pfam:DEAD 92 216 5.9e-12 PFAM
low complexity region 330 347 N/A INTRINSIC
PDB:2ZJA|A 433 547 5e-9 PDB
low complexity region 566 573 N/A INTRINSIC
low complexity region 619 632 N/A INTRINSIC
low complexity region 847 870 N/A INTRINSIC
low complexity region 1534 1543 N/A INTRINSIC
POLAc 1986 2225 3.3e-101 SMART
low complexity region 2242 2252 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000182946
SMART Domains Protein: ENSMUSP00000138685
Gene: ENSMUSG00000034206

DomainStartEndE-ValueType
low complexity region 2 29 N/A INTRINSIC
low complexity region 38 55 N/A INTRINSIC
Pfam:DEAD 92 164 1.3e-9 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000183112
SMART Domains Protein: ENSMUSP00000138648
Gene: ENSMUSG00000034206

DomainStartEndE-ValueType
low complexity region 2 29 N/A INTRINSIC
low complexity region 38 55 N/A INTRINSIC
Pfam:DEAD 92 164 1.3e-9 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
Validation Efficiency
MGI Phenotype PHENOTYPE: Animals carrying a homozygous mutation at this locus display elevated levels of chromosomal damage. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acox1 T A 11: 116,065,231 (GRCm39) D608V probably damaging Het
Actg1 A T 11: 120,239,013 (GRCm39) C26S unknown Het
Ahnak T A 19: 8,988,247 (GRCm39) V3177E possibly damaging Het
Akap11 G A 14: 78,750,938 (GRCm39) T483I Het
Akr1cl A G 1: 65,063,830 (GRCm39) S120P probably benign Het
Ankle2 G A 5: 110,400,610 (GRCm39) V649M possibly damaging Het
Ankrd55 A T 13: 112,504,570 (GRCm39) I439F probably damaging Het
Asb8 A G 15: 98,040,635 (GRCm39) M9T possibly damaging Het
Ascc1 A T 10: 59,843,645 (GRCm39) Y69F probably benign Het
Atp9a A T 2: 168,518,060 (GRCm39) probably null Het
Cd8b1 T C 6: 71,306,752 (GRCm39) F160L probably benign Het
Cdh23 G A 10: 60,143,306 (GRCm39) A3005V possibly damaging Het
Cep250 A G 2: 155,818,350 (GRCm39) T842A probably benign Het
Cgnl1 T A 9: 71,630,847 (GRCm39) K552* probably null Het
Cntnap4 C T 8: 113,602,600 (GRCm39) T1227M possibly damaging Het
Cobll1 C A 2: 64,981,333 (GRCm39) V86F probably damaging Het
Dchs2 A G 3: 83,255,561 (GRCm39) N2419S probably damaging Het
Dhx30 A T 9: 109,914,494 (GRCm39) L1001* probably null Het
Diaph1 C T 18: 38,024,162 (GRCm39) V559M unknown Het
Dis3l A T 9: 64,217,731 (GRCm39) H783Q probably benign Het
Dock7 T G 4: 98,877,350 (GRCm39) T1063P unknown Het
Dsc1 T C 18: 20,232,214 (GRCm39) T265A possibly damaging Het
Eif2ak4 A T 2: 118,258,393 (GRCm39) Q581L probably damaging Het
Eprs1 A T 1: 185,106,334 (GRCm39) D183V possibly damaging Het
Fads2 G C 19: 10,069,183 (GRCm39) D80E probably benign Het
Fam167b G A 4: 129,470,875 (GRCm39) R158C probably damaging Het
Flnb T A 14: 7,892,976 (GRCm38) I682K possibly damaging Het
Garin4 G A 1: 190,894,900 (GRCm39) T581I possibly damaging Het
Gpatch2l C T 12: 86,291,152 (GRCm39) P112S probably benign Het
Gpn1 T A 5: 31,654,710 (GRCm39) H87Q unknown Het
Greb1l T C 18: 10,499,983 (GRCm39) V350A probably benign Het
Grm5 A T 7: 87,724,024 (GRCm39) K771N probably damaging Het
Gucy2c C T 6: 136,728,045 (GRCm39) S319N probably benign Het
H2bc8 A G 13: 23,755,761 (GRCm39) D52G probably damaging Het
Hcfc2 G T 10: 82,535,041 (GRCm39) A22S probably benign Het
Hnf4a A G 2: 163,393,497 (GRCm39) D39G probably benign Het
Il6st C T 13: 112,635,340 (GRCm39) T584M probably damaging Het
Irf3 T A 7: 44,650,246 (GRCm39) V254E possibly damaging Het
Iws1 G A 18: 32,213,213 (GRCm39) E214K possibly damaging Het
Kank4 T A 4: 98,668,289 (GRCm39) K53* probably null Het
Kcnj11 A T 7: 45,748,176 (GRCm39) F382L possibly damaging Het
Kcnq3 T C 15: 65,867,510 (GRCm39) Y711C probably damaging Het
Kctd3 A G 1: 188,704,636 (GRCm39) S712P possibly damaging Het
Krt20 A G 11: 99,323,087 (GRCm39) I245T possibly damaging Het
Larp1b T C 3: 40,925,039 (GRCm39) I219T probably damaging Het
Lman2l A G 1: 36,478,771 (GRCm39) F114L probably damaging Het
Loxl2 T A 14: 69,929,859 (GRCm39) Y746N possibly damaging Het
Lrrc43 T C 5: 123,646,109 (GRCm39) S628P probably benign Het
Mroh8 A C 2: 157,111,545 (GRCm39) D136E probably damaging Het
Nek8 T A 11: 78,063,342 (GRCm39) M141L probably benign Het
Nr2e1 C A 10: 42,454,268 (GRCm39) R22L probably damaging Het
Nr6a1 C T 2: 38,816,129 (GRCm39) probably null Het
Onecut2 A G 18: 64,473,890 (GRCm39) Y147C probably damaging Het
Or1ad1 T A 11: 50,876,166 (GRCm39) C213S probably damaging Het
Or1j1 T A 2: 36,702,214 (GRCm39) M297L possibly damaging Het
Or5d37 A G 2: 87,924,194 (GRCm39) F29L probably damaging Het
Or5d39 T C 2: 87,979,908 (GRCm39) M152V probably benign Het
Pcdhac2 T C 18: 37,277,316 (GRCm39) F99L probably benign Het
Pcdhga2 T G 18: 37,802,795 (GRCm39) V213G possibly damaging Het
Pgap1 A T 1: 54,519,908 (GRCm39) V909E probably benign Het
Pik3r4 A T 9: 105,547,038 (GRCm39) T939S probably benign Het
Pip4k2c T C 10: 127,035,246 (GRCm39) D374G possibly damaging Het
Plxdc1 A T 11: 97,844,788 (GRCm39) D252E probably benign Het
Pm20d1 A C 1: 131,730,115 (GRCm39) D218A probably damaging Het
Pram1 A T 17: 33,860,131 (GRCm39) I233F probably benign Het
Prr27 C A 5: 87,990,994 (GRCm39) P202Q probably benign Het
Prss41 A T 17: 24,061,361 (GRCm39) H143Q probably damaging Het
Ptpn21 A G 12: 98,655,261 (GRCm39) Y569H probably damaging Het
Rad17 T C 13: 100,773,564 (GRCm39) K142E probably damaging Het
Rcan3 T C 4: 135,152,607 (GRCm39) E38G probably benign Het
Rgl3 C A 9: 21,885,356 (GRCm39) R658L possibly damaging Het
Rnf125 T A 18: 21,116,240 (GRCm39) *141K probably null Het
Ros1 G T 10: 52,019,502 (GRCm39) N711K probably damaging Het
Rsph10b T A 5: 143,896,504 (GRCm39) Y421N probably benign Het
Ryr1 C T 7: 28,776,471 (GRCm39) V2222I probably damaging Het
Samsn1 C T 16: 75,656,449 (GRCm39) C333Y probably damaging Het
Slc9a2 G A 1: 40,794,944 (GRCm39) E502K probably benign Het
Stard9 A T 2: 120,533,500 (GRCm39) E3252D possibly damaging Het
Syne1 C A 10: 5,123,008 (GRCm39) R309S probably damaging Het
Syne1 T C 10: 5,172,289 (GRCm39) I5051V probably benign Het
Syngap1 A G 17: 27,183,948 (GRCm39) S1241G probably damaging Het
Tbpl2 T C 2: 23,966,030 (GRCm39) K321R probably damaging Het
Tnrc18 C T 5: 142,717,107 (GRCm39) G2449E probably damaging Het
Trim25 A G 11: 88,901,731 (GRCm39) D342G probably benign Het
Tssk4 T A 14: 55,887,904 (GRCm39) H33Q probably benign Het
Ttc3 G A 16: 94,268,831 (GRCm39) G1971D possibly damaging Het
Tufm C T 7: 126,088,849 (GRCm39) Q347* probably null Het
Ubxn10 G A 4: 138,448,133 (GRCm39) S181F possibly damaging Het
Ushbp1 T C 8: 71,841,539 (GRCm39) E430G probably benign Het
Vmn1r33 T C 6: 66,588,716 (GRCm39) I279M possibly damaging Het
Vmn2r115 T C 17: 23,564,784 (GRCm39) F224L probably damaging Het
Vmn2r23 A T 6: 123,681,323 (GRCm39) H77L probably benign Het
Vps13a T C 19: 16,663,961 (GRCm39) I1481V probably benign Het
Vps35 T C 8: 86,007,898 (GRCm39) N294S possibly damaging Het
Washc3 A T 10: 88,051,916 (GRCm39) T102S probably benign Het
Zfp27 T A 7: 29,595,359 (GRCm39) E202V possibly damaging Het
Zfp58 T C 13: 67,640,035 (GRCm39) H152R possibly damaging Het
Zfr2 T C 10: 81,080,496 (GRCm39) V390A probably damaging Het
Other mutations in Polq
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00336:Polq APN 16 36,885,609 (GRCm39) splice site probably benign
IGL00539:Polq APN 16 36,880,931 (GRCm39) missense probably damaging 0.98
IGL00960:Polq APN 16 36,880,874 (GRCm39) missense probably damaging 0.96
IGL01100:Polq APN 16 36,881,474 (GRCm39) missense probably benign
IGL01112:Polq APN 16 36,837,671 (GRCm39) missense probably damaging 1.00
IGL01138:Polq APN 16 36,866,231 (GRCm39) missense possibly damaging 0.94
IGL01432:Polq APN 16 36,892,184 (GRCm39) splice site probably benign
IGL01522:Polq APN 16 36,848,265 (GRCm39) missense probably damaging 1.00
IGL01565:Polq APN 16 36,833,475 (GRCm39) missense probably benign 0.00
IGL01592:Polq APN 16 36,855,212 (GRCm39) missense probably benign 0.01
IGL01690:Polq APN 16 36,883,200 (GRCm39) missense probably damaging 0.97
IGL01943:Polq APN 16 36,881,805 (GRCm39) missense possibly damaging 0.47
IGL02531:Polq APN 16 36,882,736 (GRCm39) missense possibly damaging 0.75
IGL02553:Polq APN 16 36,862,130 (GRCm39) missense probably damaging 1.00
IGL02623:Polq APN 16 36,880,737 (GRCm39) missense probably benign 0.04
IGL02692:Polq APN 16 36,880,989 (GRCm39) missense probably damaging 1.00
IGL02717:Polq APN 16 36,843,102 (GRCm39) missense probably damaging 1.00
IGL02937:Polq APN 16 36,833,471 (GRCm39) missense probably benign 0.14
IGL02959:Polq APN 16 36,906,928 (GRCm39) missense probably damaging 1.00
IGL03086:Polq APN 16 36,911,411 (GRCm39) missense probably benign 0.02
IGL03141:Polq APN 16 36,837,720 (GRCm39) splice site probably benign
IGL03302:Polq APN 16 36,892,134 (GRCm39) missense probably damaging 1.00
IGL03393:Polq APN 16 36,865,156 (GRCm39) missense probably damaging 1.00
R0013_Polq_667 UTSW 16 36,882,201 (GRCm39) missense possibly damaging 0.56
R4238_Polq_233 UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4280_polq_867 UTSW 16 36,902,419 (GRCm39) missense probably damaging 1.00
G1Funyon:Polq UTSW 16 36,882,181 (GRCm39) missense probably damaging 1.00
PIT4403001:Polq UTSW 16 36,880,949 (GRCm39) missense probably benign 0.00
R0013:Polq UTSW 16 36,882,201 (GRCm39) missense possibly damaging 0.56
R0082:Polq UTSW 16 36,837,619 (GRCm39) missense probably benign 0.01
R0212:Polq UTSW 16 36,887,216 (GRCm39) missense probably damaging 0.99
R0387:Polq UTSW 16 36,909,679 (GRCm39) missense probably damaging 1.00
R0387:Polq UTSW 16 36,849,792 (GRCm39) missense probably damaging 1.00
R0427:Polq UTSW 16 36,882,355 (GRCm39) nonsense probably null
R0454:Polq UTSW 16 36,855,252 (GRCm39) missense probably damaging 0.98
R0513:Polq UTSW 16 36,914,864 (GRCm39) missense probably damaging 1.00
R0622:Polq UTSW 16 36,881,355 (GRCm39) missense probably benign 0.02
R0848:Polq UTSW 16 36,882,492 (GRCm39) missense probably benign 0.08
R1142:Polq UTSW 16 36,833,579 (GRCm39) missense probably damaging 0.98
R1218:Polq UTSW 16 36,849,808 (GRCm39) missense possibly damaging 0.93
R1331:Polq UTSW 16 36,862,109 (GRCm39) missense probably damaging 1.00
R1398:Polq UTSW 16 36,882,857 (GRCm39) missense possibly damaging 0.87
R1424:Polq UTSW 16 36,906,890 (GRCm39) missense probably damaging 1.00
R1644:Polq UTSW 16 36,880,626 (GRCm39) missense probably damaging 0.96
R1777:Polq UTSW 16 36,880,586 (GRCm39) missense possibly damaging 0.94
R1820:Polq UTSW 16 36,849,780 (GRCm39) missense possibly damaging 0.48
R1854:Polq UTSW 16 36,882,471 (GRCm39) missense probably benign 0.01
R1880:Polq UTSW 16 36,906,954 (GRCm39) missense possibly damaging 0.90
R1932:Polq UTSW 16 36,882,666 (GRCm39) missense possibly damaging 0.92
R2008:Polq UTSW 16 36,882,844 (GRCm39) missense probably damaging 0.96
R2014:Polq UTSW 16 36,898,728 (GRCm39) missense probably damaging 1.00
R2026:Polq UTSW 16 36,883,107 (GRCm39) missense possibly damaging 0.93
R2178:Polq UTSW 16 36,883,191 (GRCm39) missense probably damaging 1.00
R2259:Polq UTSW 16 36,882,459 (GRCm39) missense probably benign 0.03
R2266:Polq UTSW 16 36,882,515 (GRCm39) missense possibly damaging 0.59
R2305:Polq UTSW 16 36,882,699 (GRCm39) missense probably damaging 0.99
R2370:Polq UTSW 16 36,894,301 (GRCm39) missense probably damaging 1.00
R2504:Polq UTSW 16 36,832,304 (GRCm39) missense unknown
R2517:Polq UTSW 16 36,909,687 (GRCm39) missense probably damaging 1.00
R2697:Polq UTSW 16 36,862,515 (GRCm39) missense probably damaging 1.00
R2858:Polq UTSW 16 36,883,115 (GRCm39) missense possibly damaging 0.88
R3436:Polq UTSW 16 36,882,699 (GRCm39) missense probably damaging 0.99
R3437:Polq UTSW 16 36,882,699 (GRCm39) missense probably damaging 0.99
R3699:Polq UTSW 16 36,862,518 (GRCm39) missense probably damaging 1.00
R3838:Polq UTSW 16 36,898,711 (GRCm39) missense probably damaging 1.00
R3875:Polq UTSW 16 36,894,389 (GRCm39) missense probably damaging 0.99
R4050:Polq UTSW 16 36,913,182 (GRCm39) critical splice acceptor site probably null
R4172:Polq UTSW 16 36,881,120 (GRCm39) missense probably benign 0.02
R4238:Polq UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4240:Polq UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4280:Polq UTSW 16 36,902,419 (GRCm39) missense probably damaging 1.00
R4296:Polq UTSW 16 36,881,663 (GRCm39) missense possibly damaging 0.94
R4360:Polq UTSW 16 36,880,701 (GRCm39) missense probably benign 0.00
R4373:Polq UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4375:Polq UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4376:Polq UTSW 16 36,833,543 (GRCm39) missense probably damaging 1.00
R4509:Polq UTSW 16 36,868,925 (GRCm39) missense probably damaging 1.00
R4510:Polq UTSW 16 36,868,925 (GRCm39) missense probably damaging 1.00
R4511:Polq UTSW 16 36,868,925 (GRCm39) missense probably damaging 1.00
R4543:Polq UTSW 16 36,881,147 (GRCm39) missense probably benign 0.43
R4633:Polq UTSW 16 36,868,904 (GRCm39) missense probably damaging 1.00
R4739:Polq UTSW 16 36,862,109 (GRCm39) missense probably damaging 1.00
R4834:Polq UTSW 16 36,848,176 (GRCm39) missense probably damaging 1.00
R4841:Polq UTSW 16 36,869,145 (GRCm39) critical splice donor site probably null
R4842:Polq UTSW 16 36,869,145 (GRCm39) critical splice donor site probably null
R4937:Polq UTSW 16 36,848,274 (GRCm39) missense probably benign 0.01
R4955:Polq UTSW 16 36,881,444 (GRCm39) missense probably benign 0.32
R4992:Polq UTSW 16 36,881,524 (GRCm39) missense possibly damaging 0.59
R5008:Polq UTSW 16 36,882,749 (GRCm39) missense probably benign
R5221:Polq UTSW 16 36,862,540 (GRCm39) missense probably damaging 0.98
R5254:Polq UTSW 16 36,909,681 (GRCm39) missense probably damaging 1.00
R5292:Polq UTSW 16 36,881,745 (GRCm39) missense probably damaging 1.00
R5375:Polq UTSW 16 36,903,146 (GRCm39) missense probably damaging 1.00
R5480:Polq UTSW 16 36,833,652 (GRCm39) splice site probably benign
R5552:Polq UTSW 16 36,914,872 (GRCm39) missense possibly damaging 0.93
R5591:Polq UTSW 16 36,832,247 (GRCm39) utr 5 prime probably benign
R5653:Polq UTSW 16 36,860,896 (GRCm39) missense probably damaging 1.00
R5708:Polq UTSW 16 36,881,380 (GRCm39) missense probably damaging 0.98
R5754:Polq UTSW 16 36,837,625 (GRCm39) missense probably benign
R5757:Polq UTSW 16 36,907,043 (GRCm39) missense probably benign 0.01
R5764:Polq UTSW 16 36,837,706 (GRCm39) missense probably damaging 0.97
R6019:Polq UTSW 16 36,882,126 (GRCm39) missense probably damaging 1.00
R6170:Polq UTSW 16 36,866,174 (GRCm39) missense possibly damaging 0.82
R6177:Polq UTSW 16 36,892,071 (GRCm39) missense probably damaging 0.98
R6307:Polq UTSW 16 36,837,718 (GRCm39) critical splice donor site probably null
R6499:Polq UTSW 16 36,881,189 (GRCm39) missense probably benign 0.03
R6520:Polq UTSW 16 36,880,739 (GRCm39) missense possibly damaging 0.88
R6598:Polq UTSW 16 36,881,993 (GRCm39) missense probably benign 0.39
R6694:Polq UTSW 16 36,835,535 (GRCm39) missense probably null 0.99
R6788:Polq UTSW 16 36,897,510 (GRCm39) missense probably damaging 1.00
R7104:Polq UTSW 16 36,909,715 (GRCm39) nonsense probably null
R7159:Polq UTSW 16 36,883,215 (GRCm39) missense possibly damaging 0.87
R7222:Polq UTSW 16 36,906,995 (GRCm39) nonsense probably null
R7340:Polq UTSW 16 36,881,288 (GRCm39) missense probably benign 0.00
R7361:Polq UTSW 16 36,880,790 (GRCm39) missense probably benign 0.00
R7384:Polq UTSW 16 36,849,780 (GRCm39) missense probably damaging 1.00
R7509:Polq UTSW 16 36,880,706 (GRCm39) missense probably benign 0.00
R7509:Polq UTSW 16 36,880,705 (GRCm39) missense probably benign
R7575:Polq UTSW 16 36,911,496 (GRCm39) missense probably benign 0.00
R7785:Polq UTSW 16 36,848,239 (GRCm39) missense probably damaging 1.00
R7787:Polq UTSW 16 36,837,671 (GRCm39) missense probably damaging 1.00
R7891:Polq UTSW 16 36,848,244 (GRCm39) missense probably damaging 1.00
R7898:Polq UTSW 16 36,865,245 (GRCm39) missense probably damaging 0.98
R7917:Polq UTSW 16 36,885,650 (GRCm39) missense probably benign 0.08
R7940:Polq UTSW 16 36,881,004 (GRCm39) missense probably benign 0.27
R8028:Polq UTSW 16 36,881,678 (GRCm39) missense possibly damaging 0.82
R8114:Polq UTSW 16 36,862,577 (GRCm39) missense possibly damaging 0.94
R8144:Polq UTSW 16 36,849,846 (GRCm39) missense probably benign 0.01
R8288:Polq UTSW 16 36,848,272 (GRCm39) missense probably damaging 1.00
R8301:Polq UTSW 16 36,882,181 (GRCm39) missense probably damaging 1.00
R8341:Polq UTSW 16 36,892,133 (GRCm39) missense possibly damaging 0.96
R8348:Polq UTSW 16 36,837,559 (GRCm39) critical splice acceptor site probably null
R8448:Polq UTSW 16 36,837,559 (GRCm39) critical splice acceptor site probably null
R8815:Polq UTSW 16 36,853,893 (GRCm39) missense probably damaging 1.00
R8843:Polq UTSW 16 36,832,280 (GRCm39) missense unknown
R8878:Polq UTSW 16 36,860,869 (GRCm39) missense probably benign 0.02
R9016:Polq UTSW 16 36,843,159 (GRCm39) missense probably damaging 1.00
R9209:Polq UTSW 16 36,869,011 (GRCm39) missense possibly damaging 0.94
R9352:Polq UTSW 16 36,862,252 (GRCm39) missense probably damaging 0.98
R9398:Polq UTSW 16 36,881,394 (GRCm39) missense probably benign 0.02
R9403:Polq UTSW 16 36,882,215 (GRCm39) missense probably benign 0.00
R9489:Polq UTSW 16 36,843,173 (GRCm39) missense probably benign 0.00
R9605:Polq UTSW 16 36,843,173 (GRCm39) missense probably benign 0.00
R9664:Polq UTSW 16 36,848,176 (GRCm39) missense probably damaging 0.98
R9801:Polq UTSW 16 36,913,190 (GRCm39) missense probably damaging 1.00
X0060:Polq UTSW 16 36,837,599 (GRCm39) nonsense probably null
Z1176:Polq UTSW 16 36,862,619 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- CTGCCTTTGTTCTGTCAATGAG -3'
(R):5'- TGACTTTCAAGGTCTGTAGGC -3'

Sequencing Primer
(F):5'- TGCTAAGGCTTGAACCCATG -3'
(R):5'- TCAAGGTCTGTAGGCATAATGACTGC -3'
Posted On 2022-02-07