Incidental Mutation 'R1932:Polq'
ID 215513
Institutional Source Beutler Lab
Gene Symbol Polq
Ensembl Gene ENSMUSG00000034206
Gene Name polymerase (DNA directed), theta
Synonyms A430110D14Rik
MMRRC Submission 039950-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.382) question?
Stock # R1932 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 37011786-37095417 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to A at 37062304 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Arginine to Glutamine at position 1610 (R1610Q)
Ref Sequence ENSEMBL: ENSMUSP00000059757 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054034] [ENSMUST00000071452] [ENSMUST00000182946] [ENSMUST00000183112]
AlphaFold Q8CGS6
Predicted Effect possibly damaging
Transcript: ENSMUST00000054034
AA Change: R1610Q

PolyPhen 2 Score 0.917 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000059757
Gene: ENSMUSG00000034206
AA Change: R1610Q

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: R1331Q

PolyPhen 2 Score 0.873 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000071396
Gene: ENSMUSG00000034206
AA Change: R1331Q

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 noncoding transcript
Transcript: ENSMUST00000182622
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: 97.5%
  • 3x: 97.0%
  • 10x: 95.6%
  • 20x: 93.3%
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: 92 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg4 T A 9: 44,279,394 (GRCm38) Q278H probably benign Het
Ace3 T C 11: 106,004,610 (GRCm38) probably null Het
Aco1 T C 4: 40,176,499 (GRCm38) V221A probably damaging Het
Adamts20 T A 15: 94,404,010 (GRCm38) H27L probably benign Het
Adamts8 A G 9: 30,956,512 (GRCm38) D544G probably benign Het
Angptl4 C A 17: 33,781,275 (GRCm38) E40* probably null Het
Arsi G A 18: 60,916,651 (GRCm38) G202E probably benign Het
Atf7ip2 T A 16: 10,241,703 (GRCm38) I369N possibly damaging Het
Atp6ap1l T A 13: 90,883,687 (GRCm38) Y292F probably damaging Het
Atp6v1b2 A T 8: 69,102,807 (GRCm38) K217* probably null Het
Bid C T 6: 120,897,255 (GRCm38) A110T possibly damaging Het
Blvra T A 2: 127,095,148 (GRCm38) W174R probably damaging Het
Catsperg1 C T 7: 29,198,143 (GRCm38) G239R probably damaging Het
Ccdc157 G T 11: 4,146,549 (GRCm38) A400D probably damaging Het
Chd2 G T 7: 73,454,445 (GRCm38) P1298T probably damaging Het
CK137956 G A 4: 127,946,858 (GRCm38) L352F possibly damaging Het
Col22a1 G A 15: 71,870,140 (GRCm38) P503S unknown Het
Cox15 C T 19: 43,746,785 (GRCm38) R181H probably benign Het
Crem C T 18: 3,299,284 (GRCm38) G47R probably benign Het
Crygs T A 16: 22,806,554 (GRCm38) T46S probably benign Het
Cts8 T A 13: 61,253,615 (GRCm38) H62L probably damaging Het
Cyp4a32 T A 4: 115,611,277 (GRCm38) F319I possibly damaging Het
Dchs1 T C 7: 105,765,902 (GRCm38) S692G probably damaging Het
Ddx23 G A 15: 98,650,718 (GRCm38) R370W possibly damaging Het
Defa29 A T 8: 21,326,849 (GRCm38) S43T probably damaging Het
Dnajc14 A G 10: 128,816,792 (GRCm38) D573G probably damaging Het
Drd5 A G 5: 38,319,976 (GRCm38) Y104C probably benign Het
Efcab7 C T 4: 99,911,018 (GRCm38) P102L probably damaging Het
Efhc1 A G 1: 20,967,400 (GRCm38) Y267C probably damaging Het
Eif2ak4 T C 2: 118,448,486 (GRCm38) Y243H probably damaging Het
Gfm2 T A 13: 97,141,967 (GRCm38) I7N probably damaging Het
Gmds A G 13: 32,127,997 (GRCm38) F150L possibly damaging Het
Gp2 T C 7: 119,454,232 (GRCm38) T169A possibly damaging Het
Grb14 A G 2: 64,912,802 (GRCm38) F508L probably damaging Het
Hdac5 T A 11: 102,195,872 (GRCm38) probably benign Het
Heatr1 T A 13: 12,435,185 (GRCm38) M620K probably damaging Het
Herc3 A G 6: 58,876,793 (GRCm38) E608G probably damaging Het
Hoxb4 T C 11: 96,320,041 (GRCm38) Y156H probably damaging Het
Ifi205 T A 1: 174,028,414 (GRCm38) I17F possibly damaging Het
Il2rb A T 15: 78,491,777 (GRCm38) S25T possibly damaging Het
Kansl1 T C 11: 104,335,097 (GRCm38) T998A probably damaging Het
Kcna6 G T 6: 126,738,488 (GRCm38) H479Q probably benign Het
Kif2a T C 13: 106,978,091 (GRCm38) K350R probably benign Het
Lct G T 1: 128,294,161 (GRCm38) A1547E probably damaging Het
Lhx9 T A 1: 138,842,009 (GRCm38) probably benign Het
Lingo1 T A 9: 56,619,650 (GRCm38) I552F possibly damaging Het
Lrp4 G A 2: 91,497,355 (GRCm38) W1516* probably null Het
Lrp5 C T 19: 3,610,131 (GRCm38) V978I probably benign Het
Ltbp1 T A 17: 75,313,034 (GRCm38) D719E probably benign Het
Ltbp4 A G 7: 27,307,766 (GRCm38) probably null Het
Macf1 A G 4: 123,452,037 (GRCm38) I1326T probably damaging Het
Manba T C 3: 135,544,740 (GRCm38) F376S probably benign Het
Mink1 T C 11: 70,608,428 (GRCm38) probably null Het
Nfatc2ip C T 7: 126,384,992 (GRCm38) V410I probably damaging Het
Nlrp1b A T 11: 71,182,138 (GRCm38) I293N probably damaging Het
Olfr432 T C 1: 174,050,678 (GRCm38) Y102H probably damaging Het
Otol1 A C 3: 70,028,104 (GRCm38) E476D probably benign Het
Pcdhb4 C T 18: 37,309,541 (GRCm38) P635S probably benign Het
Pfkfb4 T A 9: 108,999,169 (GRCm38) F91I probably damaging Het
Polr3c A T 3: 96,719,298 (GRCm38) L270H probably damaging Het
Ppp1r15b C T 1: 133,131,625 (GRCm38) probably benign Het
Prkca T G 11: 108,192,149 (GRCm38) D90A probably benign Het
Sall3 T C 18: 80,969,753 (GRCm38) D1156G probably benign Het
Scn7a A T 2: 66,676,102 (GRCm38) L1481H probably damaging Het
Selenon A T 4: 134,544,618 (GRCm38) I292N probably damaging Het
Sema6d T A 2: 124,659,886 (GRCm38) probably null Het
Sgpp1 G T 12: 75,716,179 (GRCm38) Y409* probably null Het
Sh3pxd2a A G 19: 47,267,508 (GRCm38) S924P probably benign Het
Slc25a13 A G 6: 6,042,264 (GRCm38) V638A probably benign Het
Snhg11 T C 2: 158,376,826 (GRCm38) probably benign Het
Sorbs2 A G 8: 45,796,352 (GRCm38) Q800R probably benign Het
Srf C A 17: 46,549,986 (GRCm38) G401C probably damaging Het
Stradb A C 1: 58,991,105 (GRCm38) N173H probably benign Het
Swap70 C T 7: 110,279,263 (GRCm38) A480V possibly damaging Het
Sycp2 A G 2: 178,381,957 (GRCm38) V422A probably damaging Het
Taf4 G A 2: 179,932,029 (GRCm38) T682M probably damaging Het
Tet3 T C 6: 83,404,379 (GRCm38) N269S possibly damaging Het
Thap12 A T 7: 98,716,838 (GRCm38) I738F possibly damaging Het
Tiam2 C T 17: 3,514,725 (GRCm38) R1413C possibly damaging Het
Tmem229a A T 6: 24,955,011 (GRCm38) F248Y probably damaging Het
Tmprss7 G A 16: 45,684,593 (GRCm38) Q145* probably null Het
Tnc A T 4: 63,993,025 (GRCm38) probably null Het
Tonsl A T 15: 76,624,597 (GRCm38) Y21N probably damaging Het
Tpr A G 1: 150,421,663 (GRCm38) D1009G probably benign Het
Trpm2 G A 10: 77,941,158 (GRCm38) A435V probably damaging Het
Ubr3 T A 2: 69,953,476 (GRCm38) probably null Het
Vcan T C 13: 89,705,534 (GRCm38) N436D possibly damaging Het
Vmn2r104 T A 17: 20,040,769 (GRCm38) Y464F probably damaging Het
Vmn2r44 T A 7: 8,367,982 (GRCm38) R688S probably benign Het
Wdr74 G T 19: 8,737,947 (GRCm38) V157L probably benign Het
Wnt7a T A 6: 91,394,548 (GRCm38) D144V probably benign Het
Zfp106 C T 2: 120,531,681 (GRCm38) A986T possibly damaging Het
Other mutations in Polq
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00336:Polq APN 16 37,065,247 (GRCm38) splice site probably benign
IGL00539:Polq APN 16 37,060,569 (GRCm38) missense probably damaging 0.98
IGL00960:Polq APN 16 37,060,512 (GRCm38) missense probably damaging 0.96
IGL01100:Polq APN 16 37,061,112 (GRCm38) missense probably benign
IGL01112:Polq APN 16 37,017,309 (GRCm38) missense probably damaging 1.00
IGL01138:Polq APN 16 37,045,869 (GRCm38) missense possibly damaging 0.94
IGL01432:Polq APN 16 37,071,822 (GRCm38) splice site probably benign
IGL01522:Polq APN 16 37,027,903 (GRCm38) missense probably damaging 1.00
IGL01565:Polq APN 16 37,013,113 (GRCm38) missense probably benign 0.00
IGL01592:Polq APN 16 37,034,850 (GRCm38) missense probably benign 0.01
IGL01690:Polq APN 16 37,062,838 (GRCm38) missense probably damaging 0.97
IGL01943:Polq APN 16 37,061,443 (GRCm38) missense possibly damaging 0.47
IGL02531:Polq APN 16 37,062,374 (GRCm38) missense possibly damaging 0.75
IGL02553:Polq APN 16 37,041,768 (GRCm38) missense probably damaging 1.00
IGL02623:Polq APN 16 37,060,375 (GRCm38) missense probably benign 0.04
IGL02692:Polq APN 16 37,060,627 (GRCm38) missense probably damaging 1.00
IGL02717:Polq APN 16 37,022,740 (GRCm38) missense probably damaging 1.00
IGL02937:Polq APN 16 37,013,109 (GRCm38) missense probably benign 0.14
IGL02959:Polq APN 16 37,086,566 (GRCm38) missense probably damaging 1.00
IGL03086:Polq APN 16 37,091,049 (GRCm38) missense probably benign 0.02
IGL03141:Polq APN 16 37,017,358 (GRCm38) splice site probably benign
IGL03302:Polq APN 16 37,071,772 (GRCm38) missense probably damaging 1.00
IGL03393:Polq APN 16 37,044,794 (GRCm38) missense probably damaging 1.00
R0013_Polq_667 UTSW 16 37,061,839 (GRCm38) missense possibly damaging 0.56
R4238_Polq_233 UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4280_polq_867 UTSW 16 37,082,057 (GRCm38) missense probably damaging 1.00
G1Funyon:Polq UTSW 16 37,061,819 (GRCm38) missense probably damaging 1.00
PIT4403001:Polq UTSW 16 37,060,587 (GRCm38) missense probably benign 0.00
R0013:Polq UTSW 16 37,061,839 (GRCm38) missense possibly damaging 0.56
R0082:Polq UTSW 16 37,017,257 (GRCm38) missense probably benign 0.01
R0212:Polq UTSW 16 37,066,854 (GRCm38) missense probably damaging 0.99
R0387:Polq UTSW 16 37,089,317 (GRCm38) missense probably damaging 1.00
R0387:Polq UTSW 16 37,029,430 (GRCm38) missense probably damaging 1.00
R0427:Polq UTSW 16 37,061,993 (GRCm38) nonsense probably null
R0454:Polq UTSW 16 37,034,890 (GRCm38) missense probably damaging 0.98
R0513:Polq UTSW 16 37,094,502 (GRCm38) missense probably damaging 1.00
R0622:Polq UTSW 16 37,060,993 (GRCm38) missense probably benign 0.02
R0848:Polq UTSW 16 37,062,130 (GRCm38) missense probably benign 0.08
R1142:Polq UTSW 16 37,013,217 (GRCm38) missense probably damaging 0.98
R1218:Polq UTSW 16 37,029,446 (GRCm38) missense possibly damaging 0.93
R1331:Polq UTSW 16 37,041,747 (GRCm38) missense probably damaging 1.00
R1398:Polq UTSW 16 37,062,495 (GRCm38) missense possibly damaging 0.87
R1424:Polq UTSW 16 37,086,528 (GRCm38) missense probably damaging 1.00
R1644:Polq UTSW 16 37,060,264 (GRCm38) missense probably damaging 0.96
R1777:Polq UTSW 16 37,060,224 (GRCm38) missense possibly damaging 0.94
R1820:Polq UTSW 16 37,029,418 (GRCm38) missense possibly damaging 0.48
R1854:Polq UTSW 16 37,062,109 (GRCm38) missense probably benign 0.01
R1880:Polq UTSW 16 37,086,592 (GRCm38) missense possibly damaging 0.90
R2008:Polq UTSW 16 37,062,482 (GRCm38) missense probably damaging 0.96
R2014:Polq UTSW 16 37,078,366 (GRCm38) missense probably damaging 1.00
R2026:Polq UTSW 16 37,062,745 (GRCm38) missense possibly damaging 0.93
R2178:Polq UTSW 16 37,062,829 (GRCm38) missense probably damaging 1.00
R2259:Polq UTSW 16 37,062,097 (GRCm38) missense probably benign 0.03
R2266:Polq UTSW 16 37,062,153 (GRCm38) missense possibly damaging 0.59
R2305:Polq UTSW 16 37,062,337 (GRCm38) missense probably damaging 0.99
R2370:Polq UTSW 16 37,073,939 (GRCm38) missense probably damaging 1.00
R2504:Polq UTSW 16 37,011,942 (GRCm38) missense unknown
R2517:Polq UTSW 16 37,089,325 (GRCm38) missense probably damaging 1.00
R2697:Polq UTSW 16 37,042,153 (GRCm38) missense probably damaging 1.00
R2858:Polq UTSW 16 37,062,753 (GRCm38) missense possibly damaging 0.88
R3436:Polq UTSW 16 37,062,337 (GRCm38) missense probably damaging 0.99
R3437:Polq UTSW 16 37,062,337 (GRCm38) missense probably damaging 0.99
R3699:Polq UTSW 16 37,042,156 (GRCm38) missense probably damaging 1.00
R3838:Polq UTSW 16 37,078,349 (GRCm38) missense probably damaging 1.00
R3875:Polq UTSW 16 37,074,027 (GRCm38) missense probably damaging 0.99
R4050:Polq UTSW 16 37,092,820 (GRCm38) critical splice acceptor site probably null
R4172:Polq UTSW 16 37,060,758 (GRCm38) missense probably benign 0.02
R4238:Polq UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4240:Polq UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4280:Polq UTSW 16 37,082,057 (GRCm38) missense probably damaging 1.00
R4296:Polq UTSW 16 37,061,301 (GRCm38) missense possibly damaging 0.94
R4360:Polq UTSW 16 37,060,339 (GRCm38) missense probably benign 0.00
R4373:Polq UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4375:Polq UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4376:Polq UTSW 16 37,013,181 (GRCm38) missense probably damaging 1.00
R4509:Polq UTSW 16 37,048,563 (GRCm38) missense probably damaging 1.00
R4510:Polq UTSW 16 37,048,563 (GRCm38) missense probably damaging 1.00
R4511:Polq UTSW 16 37,048,563 (GRCm38) missense probably damaging 1.00
R4543:Polq UTSW 16 37,060,785 (GRCm38) missense probably benign 0.43
R4633:Polq UTSW 16 37,048,542 (GRCm38) missense probably damaging 1.00
R4739:Polq UTSW 16 37,041,747 (GRCm38) missense probably damaging 1.00
R4834:Polq UTSW 16 37,027,814 (GRCm38) missense probably damaging 1.00
R4841:Polq UTSW 16 37,048,783 (GRCm38) critical splice donor site probably null
R4842:Polq UTSW 16 37,048,783 (GRCm38) critical splice donor site probably null
R4937:Polq UTSW 16 37,027,912 (GRCm38) missense probably benign 0.01
R4955:Polq UTSW 16 37,061,082 (GRCm38) missense probably benign 0.32
R4992:Polq UTSW 16 37,061,162 (GRCm38) missense possibly damaging 0.59
R5008:Polq UTSW 16 37,062,387 (GRCm38) missense probably benign
R5221:Polq UTSW 16 37,042,178 (GRCm38) missense probably damaging 0.98
R5254:Polq UTSW 16 37,089,319 (GRCm38) missense probably damaging 1.00
R5292:Polq UTSW 16 37,061,383 (GRCm38) missense probably damaging 1.00
R5375:Polq UTSW 16 37,082,784 (GRCm38) missense probably damaging 1.00
R5480:Polq UTSW 16 37,013,290 (GRCm38) splice site probably benign
R5552:Polq UTSW 16 37,094,510 (GRCm38) missense possibly damaging 0.93
R5591:Polq UTSW 16 37,011,885 (GRCm38) utr 5 prime probably benign
R5653:Polq UTSW 16 37,040,534 (GRCm38) missense probably damaging 1.00
R5708:Polq UTSW 16 37,061,018 (GRCm38) missense probably damaging 0.98
R5754:Polq UTSW 16 37,017,263 (GRCm38) missense probably benign
R5757:Polq UTSW 16 37,086,681 (GRCm38) missense probably benign 0.01
R5764:Polq UTSW 16 37,017,344 (GRCm38) missense probably damaging 0.97
R6019:Polq UTSW 16 37,061,764 (GRCm38) missense probably damaging 1.00
R6170:Polq UTSW 16 37,045,812 (GRCm38) missense possibly damaging 0.82
R6177:Polq UTSW 16 37,071,709 (GRCm38) missense probably damaging 0.98
R6307:Polq UTSW 16 37,017,356 (GRCm38) critical splice donor site probably null
R6499:Polq UTSW 16 37,060,827 (GRCm38) missense probably benign 0.03
R6520:Polq UTSW 16 37,060,377 (GRCm38) missense possibly damaging 0.88
R6598:Polq UTSW 16 37,061,631 (GRCm38) missense probably benign 0.39
R6694:Polq UTSW 16 37,015,173 (GRCm38) missense probably null 0.99
R6788:Polq UTSW 16 37,077,148 (GRCm38) missense probably damaging 1.00
R7104:Polq UTSW 16 37,089,353 (GRCm38) nonsense probably null
R7159:Polq UTSW 16 37,062,853 (GRCm38) missense possibly damaging 0.87
R7222:Polq UTSW 16 37,086,633 (GRCm38) nonsense probably null
R7340:Polq UTSW 16 37,060,926 (GRCm38) missense probably benign 0.00
R7361:Polq UTSW 16 37,060,428 (GRCm38) missense probably benign 0.00
R7384:Polq UTSW 16 37,029,418 (GRCm38) missense probably damaging 1.00
R7509:Polq UTSW 16 37,060,344 (GRCm38) missense probably benign 0.00
R7509:Polq UTSW 16 37,060,343 (GRCm38) missense probably benign
R7575:Polq UTSW 16 37,091,134 (GRCm38) missense probably benign 0.00
R7785:Polq UTSW 16 37,027,877 (GRCm38) missense probably damaging 1.00
R7787:Polq UTSW 16 37,017,309 (GRCm38) missense probably damaging 1.00
R7891:Polq UTSW 16 37,027,882 (GRCm38) missense probably damaging 1.00
R7898:Polq UTSW 16 37,044,883 (GRCm38) missense probably damaging 0.98
R7917:Polq UTSW 16 37,065,288 (GRCm38) missense probably benign 0.08
R7940:Polq UTSW 16 37,060,642 (GRCm38) missense probably benign 0.27
R8028:Polq UTSW 16 37,061,316 (GRCm38) missense possibly damaging 0.82
R8114:Polq UTSW 16 37,042,215 (GRCm38) missense possibly damaging 0.94
R8144:Polq UTSW 16 37,029,484 (GRCm38) missense probably benign 0.01
R8288:Polq UTSW 16 37,027,910 (GRCm38) missense probably damaging 1.00
R8301:Polq UTSW 16 37,061,819 (GRCm38) missense probably damaging 1.00
R8341:Polq UTSW 16 37,071,771 (GRCm38) missense possibly damaging 0.96
R8348:Polq UTSW 16 37,017,197 (GRCm38) critical splice acceptor site probably null
R8448:Polq UTSW 16 37,017,197 (GRCm38) critical splice acceptor site probably null
R8815:Polq UTSW 16 37,033,531 (GRCm38) missense probably damaging 1.00
R8843:Polq UTSW 16 37,011,918 (GRCm38) missense unknown
R8878:Polq UTSW 16 37,040,507 (GRCm38) missense probably benign 0.02
R9016:Polq UTSW 16 37,022,797 (GRCm38) missense probably damaging 1.00
R9189:Polq UTSW 16 37,044,903 (GRCm38) missense probably damaging 1.00
R9209:Polq UTSW 16 37,048,649 (GRCm38) missense possibly damaging 0.94
R9352:Polq UTSW 16 37,041,890 (GRCm38) missense probably damaging 0.98
R9398:Polq UTSW 16 37,061,032 (GRCm38) missense probably benign 0.02
R9403:Polq UTSW 16 37,061,853 (GRCm38) missense probably benign 0.00
R9489:Polq UTSW 16 37,022,811 (GRCm38) missense probably benign 0.00
R9605:Polq UTSW 16 37,022,811 (GRCm38) missense probably benign 0.00
R9664:Polq UTSW 16 37,027,814 (GRCm38) missense probably damaging 0.98
R9801:Polq UTSW 16 37,092,828 (GRCm38) missense probably damaging 1.00
X0060:Polq UTSW 16 37,017,237 (GRCm38) nonsense probably null
Z1176:Polq UTSW 16 37,042,257 (GRCm38) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- CAGTGATTCTGCAGTGCTGG -3'
(R):5'- ACTTTCTTTACGAGGCAAGGG -3'

Sequencing Primer
(F):5'- CTGGGTAATGAGTGTCCCCAAG -3'
(R):5'- ACTTTCTTTACGAGGCAAGGGAGATG -3'
Posted On 2014-07-14