Incidental Mutation 'R2270:Prkdc'
ID 242423
Institutional Source Beutler Lab
Gene Symbol Prkdc
Ensembl Gene ENSMUSG00000022672
Gene Name protein kinase, DNA activated, catalytic polypeptide
Synonyms slip, DNA-PK, XRCC7, DNAPDcs, DOXNPH, dxnph, DNA-PKcs
MMRRC Submission 040270-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.953) question?
Stock # R2270 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 15455730-15660099 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 15472681 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000023352 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023352]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000023352
SMART Domains Protein: ENSMUSP00000023352
Gene: ENSMUSG00000022672

DomainStartEndE-ValueType
low complexity region 125 138 N/A INTRINSIC
low complexity region 1253 1263 N/A INTRINSIC
low complexity region 1508 1522 N/A INTRINSIC
NUC194 1810 2206 2.37e-246 SMART
SCOP:d1gw5a_ 2210 2493 5e-3 SMART
low complexity region 2669 2681 N/A INTRINSIC
low complexity region 2841 2855 N/A INTRINSIC
Pfam:FAT 3024 3470 8.2e-75 PFAM
PI3Kc 3749 4068 3.67e-86 SMART
FATC 4096 4128 1.57e-9 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182134
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 94.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the catalytic subunit of the DNA-dependent protein kinase (DNA-PK). It functions with the Ku70/Ku80 heterodimer protein in DNA double strand break repair and recombination. The protein encoded is a member of the PI3/PI4-kinase family.[provided by RefSeq, Jul 2010]
PHENOTYPE: Mutations at this locus effect genome stability, radiation sensitivity and DNA repair. Nonsense (scid) and null homozygotes have severe combined immunodeficiency. A BALB/c variant allele reduces enzyme activity and predisposes to breast cancer. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim1 G A 19: 57,065,863 (GRCm39) R54W possibly damaging Het
Adam22 T C 5: 8,171,108 (GRCm39) E614G probably damaging Het
Ap4e1 T C 2: 126,889,083 (GRCm39) probably null Het
Arid3c T A 4: 41,724,744 (GRCm39) I364F probably damaging Het
Atp11b A G 3: 35,864,283 (GRCm39) probably null Het
Bmal2 T C 6: 146,723,612 (GRCm39) F314S probably damaging Het
Carnmt1 T C 19: 18,680,734 (GRCm39) L336P probably damaging Het
Cdh22 A T 2: 164,985,767 (GRCm39) probably null Het
Cdk5rap2 A C 4: 70,184,915 (GRCm39) S1178R probably benign Het
Chat T C 14: 32,176,538 (GRCm39) R79G probably damaging Het
Chek1 A G 9: 36,630,982 (GRCm39) L144P probably damaging Het
Cracr2a T A 6: 127,584,261 (GRCm39) F107I probably damaging Het
Crip2 A C 12: 113,108,486 (GRCm39) K62N probably damaging Het
Ddc T C 11: 11,785,764 (GRCm39) N308D probably damaging Het
Dnm3 A T 1: 162,305,358 (GRCm39) L12Q probably damaging Het
Eftud2 T C 11: 102,755,607 (GRCm39) N200S probably damaging Het
Fgfbp1 T A 5: 44,136,672 (GRCm39) M207L probably benign Het
Fry A G 5: 150,324,389 (GRCm39) I1151V probably null Het
Garem2 T G 5: 30,321,972 (GRCm39) L777R probably damaging Het
Garin5b T A 7: 4,761,186 (GRCm39) T509S probably benign Het
Gm10608 CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA 9: 118,989,784 (GRCm39) probably null Het
Gpr143 T A X: 151,573,566 (GRCm39) V181E probably damaging Het
Gtf2f1 T C 17: 57,310,462 (GRCm39) I498V probably null Het
Ipo4 A G 14: 55,871,557 (GRCm39) L168P probably damaging Het
Ism1 T A 2: 139,599,293 (GRCm39) I415N probably damaging Het
Lipa T A 19: 34,488,290 (GRCm39) R119* probably null Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Mre11a A G 9: 14,726,470 (GRCm39) E411G probably benign Het
Mybpc1 C A 10: 88,387,269 (GRCm39) V106F probably benign Het
Myo5b G T 18: 74,866,996 (GRCm39) L1382F probably damaging Het
N4bp3 A T 11: 51,535,132 (GRCm39) N352K probably benign Het
Ncbp2 T C 16: 31,775,769 (GRCm39) Y138H probably damaging Het
Ncor2 A G 5: 125,115,019 (GRCm39) V515A probably benign Het
Ndufv1 C A 19: 4,058,347 (GRCm39) R359L probably benign Het
Nfix CAAAAA CAAAA 8: 85,442,876 (GRCm39) probably null Het
Olfm4 C A 14: 80,249,315 (GRCm39) T144K probably damaging Het
Or11g25 G T 14: 50,723,494 (GRCm39) C193F probably damaging Het
Or8b12i T A 9: 20,082,705 (GRCm39) H54L possibly damaging Het
Pes1 C A 11: 3,919,524 (GRCm39) L66I probably damaging Het
Phf12 G T 11: 77,875,001 (GRCm39) A76S possibly damaging Het
Plb1 G T 5: 32,450,586 (GRCm39) D376Y probably damaging Het
Prkg1 A G 19: 30,556,031 (GRCm39) V610A probably benign Het
Prrc2a T C 17: 35,368,512 (GRCm39) T2104A possibly damaging Het
Rab3gap2 T A 1: 185,015,739 (GRCm39) probably null Het
Ranbp2 T C 10: 58,291,749 (GRCm39) V252A probably benign Het
Rcn3 A G 7: 44,738,075 (GRCm39) S98P probably damaging Het
Rere T C 4: 150,561,837 (GRCm39) S248P unknown Het
Rnaseh2a T C 8: 85,692,048 (GRCm39) E75G probably benign Het
Slc15a1 A T 14: 121,717,406 (GRCm39) M292K probably damaging Het
Slc1a2 T G 2: 102,566,339 (GRCm39) L14R probably damaging Het
Slfn2 C T 11: 82,960,761 (GRCm39) R247C probably damaging Het
Ttn T C 2: 76,778,708 (GRCm39) I1218M probably damaging Het
Usp7 T C 16: 8,516,333 (GRCm39) S649G probably benign Het
Yme1l1 T C 2: 23,065,232 (GRCm39) I247T possibly damaging Het
Zc3h13 T C 14: 75,569,587 (GRCm39) M1478T probably benign Het
Zfp444 T C 7: 6,192,554 (GRCm39) C191R probably damaging Het
Zfp729b A T 13: 67,740,352 (GRCm39) C648S probably damaging Het
Znhit2 A G 19: 6,111,261 (GRCm39) E2G probably damaging Het
Zpbp A T 11: 11,368,272 (GRCm39) M133K probably benign Het
Other mutations in Prkdc
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00157:Prkdc APN 16 15,515,090 (GRCm39) missense probably damaging 1.00
IGL00225:Prkdc APN 16 15,627,508 (GRCm39) missense possibly damaging 0.64
IGL00481:Prkdc APN 16 15,608,330 (GRCm39) missense probably benign 0.41
IGL00488:Prkdc APN 16 15,593,711 (GRCm39) splice site probably null
IGL00489:Prkdc APN 16 15,617,790 (GRCm39) missense possibly damaging 0.51
IGL00579:Prkdc APN 16 15,482,103 (GRCm39) missense probably damaging 1.00
IGL00587:Prkdc APN 16 15,470,222 (GRCm39) splice site probably benign
IGL00666:Prkdc APN 16 15,554,699 (GRCm39) missense probably damaging 1.00
IGL00675:Prkdc APN 16 15,605,022 (GRCm39) missense probably benign 0.05
IGL00708:Prkdc APN 16 15,597,290 (GRCm39) missense probably damaging 0.97
IGL00725:Prkdc APN 16 15,634,503 (GRCm39) missense probably benign 0.10
IGL00818:Prkdc APN 16 15,577,618 (GRCm39) missense possibly damaging 0.92
IGL00917:Prkdc APN 16 15,557,428 (GRCm39) missense probably damaging 0.98
IGL00990:Prkdc APN 16 15,519,979 (GRCm39) missense probably benign 0.03
IGL01126:Prkdc APN 16 15,487,185 (GRCm39) missense probably benign 0.01
IGL01141:Prkdc APN 16 15,544,568 (GRCm39) missense probably damaging 0.99
IGL01306:Prkdc APN 16 15,485,595 (GRCm39) missense possibly damaging 0.67
IGL01326:Prkdc APN 16 15,647,556 (GRCm39) missense probably benign
IGL01335:Prkdc APN 16 15,634,760 (GRCm39) critical splice donor site probably null
IGL01419:Prkdc APN 16 15,653,030 (GRCm39) missense probably damaging 1.00
IGL01434:Prkdc APN 16 15,531,451 (GRCm39) missense probably benign 0.00
IGL01554:Prkdc APN 16 15,470,166 (GRCm39) missense probably benign 0.05
IGL01671:Prkdc APN 16 15,485,609 (GRCm39) missense possibly damaging 0.90
IGL01871:Prkdc APN 16 15,600,951 (GRCm39) missense probably benign 0.00
IGL01874:Prkdc APN 16 15,552,858 (GRCm39) missense possibly damaging 0.89
IGL01930:Prkdc APN 16 15,516,751 (GRCm39) missense probably damaging 1.00
IGL01984:Prkdc APN 16 15,526,643 (GRCm39) missense probably benign
IGL02121:Prkdc APN 16 15,535,048 (GRCm39) missense probably benign 0.18
IGL02152:Prkdc APN 16 15,487,149 (GRCm39) missense probably benign 0.15
IGL02172:Prkdc APN 16 15,627,623 (GRCm39) missense probably benign 0.10
IGL02336:Prkdc APN 16 15,603,843 (GRCm39) missense probably benign 0.01
IGL02336:Prkdc APN 16 15,603,842 (GRCm39) missense possibly damaging 0.47
IGL02393:Prkdc APN 16 15,634,622 (GRCm39) missense probably benign 0.42
IGL02406:Prkdc APN 16 15,488,399 (GRCm39) missense probably benign 0.00
IGL02500:Prkdc APN 16 15,532,146 (GRCm39) critical splice donor site probably null
IGL02568:Prkdc APN 16 15,544,406 (GRCm39) missense probably damaging 0.98
IGL02579:Prkdc APN 16 15,488,465 (GRCm39) missense possibly damaging 0.83
IGL02652:Prkdc APN 16 15,600,951 (GRCm39) missense probably benign 0.00
IGL02661:Prkdc APN 16 15,587,689 (GRCm39) missense possibly damaging 0.92
IGL02685:Prkdc APN 16 15,653,907 (GRCm39) missense possibly damaging 0.61
IGL02741:Prkdc APN 16 15,570,590 (GRCm39) splice site probably benign
IGL02803:Prkdc APN 16 15,651,530 (GRCm39) splice site probably benign
IGL02866:Prkdc APN 16 15,649,191 (GRCm39) missense probably damaging 1.00
IGL02882:Prkdc APN 16 15,469,383 (GRCm39) nonsense probably null
IGL02989:Prkdc APN 16 15,617,880 (GRCm39) missense possibly damaging 0.67
IGL03053:Prkdc APN 16 15,652,030 (GRCm39) missense probably benign 0.02
IGL03071:Prkdc APN 16 15,617,848 (GRCm39) missense probably benign 0.01
IGL03091:Prkdc APN 16 15,523,174 (GRCm39) splice site probably benign
IGL03100:Prkdc APN 16 15,531,499 (GRCm39) missense probably benign 0.08
IGL03128:Prkdc APN 16 15,518,608 (GRCm39) splice site probably benign
IGL03168:Prkdc APN 16 15,652,030 (GRCm39) missense probably benign 0.02
IGL03204:Prkdc APN 16 15,587,665 (GRCm39) missense probably benign 0.01
IGL03390:Prkdc APN 16 15,488,490 (GRCm39) nonsense probably null
anhimid UTSW 16 15,543,325 (GRCm39) critical splice donor site probably null
anhinga UTSW 16 15,526,796 (GRCm39) critical splice donor site probably null
Bushtit UTSW 16 15,570,628 (GRCm39) missense probably damaging 0.97
clover UTSW 16 15,520,020 (GRCm39) splice site probably benign
crackle UTSW 16 15,603,914 (GRCm39) critical splice donor site probably null
Daffy UTSW 16 15,647,561 (GRCm39) missense possibly damaging 0.86
darter UTSW 16 15,591,477 (GRCm39) missense possibly damaging 0.93
Elmer_fudd UTSW 16 15,625,922 (GRCm39) missense probably benign 0.01
envenomation UTSW 16 15,653,091 (GRCm39) nonsense probably null
hobgoblin UTSW 16 15,633,850 (GRCm39) missense probably damaging 1.00
Incubus UTSW 16 15,490,191 (GRCm39) missense probably damaging 1.00
liming UTSW 16 15,570,693 (GRCm39) nonsense probably null
newt UTSW 16 15,545,590 (GRCm39) missense probably benign 0.04
ornithorhynchus UTSW 16 15,634,523 (GRCm39) critical splice donor site probably null
primitive UTSW 16 15,653,022 (GRCm39) frame shift probably null
roadrunner UTSW 16 15,651,751 (GRCm39) missense probably damaging 1.00
Schreier UTSW 16 15,488,392 (GRCm39) missense probably benign 0.00
screamer UTSW 16 15,649,146 (GRCm39) nonsense probably null
Screamer10 UTSW 16 15,585,889 (GRCm39) missense probably damaging 0.98
screamer2 UTSW 16 15,470,416 (GRCm39) critical splice donor site probably null
screamer3 UTSW 16 15,558,196 (GRCm39) critical splice donor site probably null
screamer4 UTSW 16 15,600,943 (GRCm39) missense probably benign 0.00
screamer5 UTSW 16 15,505,268 (GRCm39) missense probably benign
screamer6 UTSW 16 15,577,469 (GRCm39) missense probably damaging 1.00
screamer7 UTSW 16 15,472,681 (GRCm39) splice site probably null
Screamer8 UTSW 16 15,537,297 (GRCm39) missense probably benign 0.00
Screamer9 UTSW 16 15,552,786 (GRCm39) missense probably benign 0.01
Tweetie UTSW 16 15,535,665 (GRCm39) missense probably damaging 1.00
updock UTSW 16 15,612,958 (GRCm39) missense probably benign
ANU23:Prkdc UTSW 16 15,485,595 (GRCm39) missense possibly damaging 0.67
R0008:Prkdc UTSW 16 15,526,565 (GRCm39) splice site probably benign
R0018:Prkdc UTSW 16 15,544,406 (GRCm39) missense probably benign 0.03
R0018:Prkdc UTSW 16 15,544,406 (GRCm39) missense probably benign 0.03
R0069:Prkdc UTSW 16 15,544,368 (GRCm39) missense probably benign 0.03
R0125:Prkdc UTSW 16 15,516,871 (GRCm39) missense probably damaging 0.98
R0131:Prkdc UTSW 16 15,531,517 (GRCm39) missense probably benign 0.09
R0131:Prkdc UTSW 16 15,531,517 (GRCm39) missense probably benign 0.09
R0132:Prkdc UTSW 16 15,531,517 (GRCm39) missense probably benign 0.09
R0137:Prkdc UTSW 16 15,558,196 (GRCm39) critical splice donor site probably null
R0334:Prkdc UTSW 16 15,554,663 (GRCm39) missense probably benign 0.00
R0373:Prkdc UTSW 16 15,609,791 (GRCm39) missense probably damaging 1.00
R0485:Prkdc UTSW 16 15,651,604 (GRCm39) missense probably damaging 0.97
R0511:Prkdc UTSW 16 15,649,146 (GRCm39) nonsense probably null
R0538:Prkdc UTSW 16 15,651,652 (GRCm39) missense probably damaging 1.00
R0595:Prkdc UTSW 16 15,625,952 (GRCm39) missense probably damaging 1.00
R0607:Prkdc UTSW 16 15,589,921 (GRCm39) missense probably damaging 0.98
R0616:Prkdc UTSW 16 15,508,271 (GRCm39) missense probably damaging 1.00
R0630:Prkdc UTSW 16 15,628,665 (GRCm39) missense probably damaging 1.00
R0694:Prkdc UTSW 16 15,586,501 (GRCm39) missense probably damaging 1.00
R0702:Prkdc UTSW 16 15,603,835 (GRCm39) missense possibly damaging 0.95
R0965:Prkdc UTSW 16 15,647,580 (GRCm39) missense probably benign
R1027:Prkdc UTSW 16 15,468,576 (GRCm39) missense possibly damaging 0.80
R1029:Prkdc UTSW 16 15,472,613 (GRCm39) splice site probably benign
R1033:Prkdc UTSW 16 15,585,815 (GRCm39) missense probably damaging 1.00
R1067:Prkdc UTSW 16 15,570,646 (GRCm39) missense probably damaging 0.99
R1116:Prkdc UTSW 16 15,600,943 (GRCm39) missense probably benign 0.00
R1187:Prkdc UTSW 16 15,577,610 (GRCm39) missense probably damaging 0.98
R1226:Prkdc UTSW 16 15,491,861 (GRCm39) missense possibly damaging 0.80
R1279:Prkdc UTSW 16 15,508,146 (GRCm39) missense probably damaging 1.00
R1304:Prkdc UTSW 16 15,577,587 (GRCm39) missense probably damaging 0.99
R1314:Prkdc UTSW 16 15,482,091 (GRCm39) missense possibly damaging 0.68
R1351:Prkdc UTSW 16 15,485,564 (GRCm39) missense possibly damaging 0.62
R1509:Prkdc UTSW 16 15,549,430 (GRCm39) missense probably damaging 1.00
R1512:Prkdc UTSW 16 15,505,268 (GRCm39) missense probably benign
R1531:Prkdc UTSW 16 15,589,970 (GRCm39) missense probably benign 0.01
R1579:Prkdc UTSW 16 15,493,192 (GRCm39) missense probably benign 0.00
R1669:Prkdc UTSW 16 15,551,922 (GRCm39) missense probably damaging 1.00
R1682:Prkdc UTSW 16 15,494,853 (GRCm39) missense probably benign 0.19
R1713:Prkdc UTSW 16 15,612,958 (GRCm39) missense probably benign
R1762:Prkdc UTSW 16 15,455,825 (GRCm39) missense probably benign
R1789:Prkdc UTSW 16 15,557,388 (GRCm39) missense probably damaging 1.00
R1822:Prkdc UTSW 16 15,577,469 (GRCm39) missense probably damaging 1.00
R1848:Prkdc UTSW 16 15,625,922 (GRCm39) missense probably benign 0.01
R1887:Prkdc UTSW 16 15,647,499 (GRCm39) missense probably benign 0.00
R1891:Prkdc UTSW 16 15,543,300 (GRCm39) missense probably benign 0.02
R1921:Prkdc UTSW 16 15,532,079 (GRCm39) missense possibly damaging 0.80
R1922:Prkdc UTSW 16 15,532,130 (GRCm39) missense probably benign 0.00
R1929:Prkdc UTSW 16 15,472,681 (GRCm39) splice site probably null
R1939:Prkdc UTSW 16 15,653,777 (GRCm39) missense possibly damaging 0.95
R2021:Prkdc UTSW 16 15,494,873 (GRCm39) missense probably benign 0.00
R2033:Prkdc UTSW 16 15,505,216 (GRCm39) splice site probably benign
R2056:Prkdc UTSW 16 15,545,469 (GRCm39) missense probably benign 0.03
R2057:Prkdc UTSW 16 15,545,469 (GRCm39) missense probably benign 0.03
R2058:Prkdc UTSW 16 15,545,469 (GRCm39) missense probably benign 0.03
R2082:Prkdc UTSW 16 15,533,827 (GRCm39) missense probably damaging 1.00
R2109:Prkdc UTSW 16 15,505,254 (GRCm39) missense probably benign 0.01
R2124:Prkdc UTSW 16 15,537,297 (GRCm39) missense probably benign 0.00
R2164:Prkdc UTSW 16 15,523,071 (GRCm39) missense probably damaging 1.00
R2174:Prkdc UTSW 16 15,552,786 (GRCm39) missense probably benign 0.01
R2191:Prkdc UTSW 16 15,516,688 (GRCm39) missense probably damaging 1.00
R2271:Prkdc UTSW 16 15,472,681 (GRCm39) splice site probably null
R2272:Prkdc UTSW 16 15,472,681 (GRCm39) splice site probably null
R2356:Prkdc UTSW 16 15,502,068 (GRCm39) missense probably benign
R2852:Prkdc UTSW 16 15,470,416 (GRCm39) critical splice donor site probably null
R3115:Prkdc UTSW 16 15,482,222 (GRCm39) missense probably benign 0.01
R3116:Prkdc UTSW 16 15,482,222 (GRCm39) missense probably benign 0.01
R3499:Prkdc UTSW 16 15,585,889 (GRCm39) missense probably damaging 0.98
R3687:Prkdc UTSW 16 15,617,831 (GRCm39) missense probably benign
R3834:Prkdc UTSW 16 15,609,810 (GRCm39) missense probably damaging 1.00
R3835:Prkdc UTSW 16 15,609,810 (GRCm39) missense probably damaging 1.00
R3961:Prkdc UTSW 16 15,647,475 (GRCm39) splice site probably null
R4151:Prkdc UTSW 16 15,634,637 (GRCm39) missense probably benign
R4233:Prkdc UTSW 16 15,653,783 (GRCm39) missense probably benign 0.11
R4281:Prkdc UTSW 16 15,623,963 (GRCm39) splice site probably null
R4296:Prkdc UTSW 16 15,555,769 (GRCm39) missense probably damaging 0.99
R4344:Prkdc UTSW 16 15,585,886 (GRCm39) missense probably damaging 0.98
R4424:Prkdc UTSW 16 15,653,946 (GRCm39) missense probably damaging 1.00
R4424:Prkdc UTSW 16 15,591,603 (GRCm39) missense probably damaging 0.98
R4497:Prkdc UTSW 16 15,518,517 (GRCm39) missense probably benign 0.43
R4549:Prkdc UTSW 16 15,554,734 (GRCm39) missense possibly damaging 0.89
R4594:Prkdc UTSW 16 15,585,830 (GRCm39) missense possibly damaging 0.64
R4603:Prkdc UTSW 16 15,628,688 (GRCm39) missense probably damaging 0.98
R4615:Prkdc UTSW 16 15,480,938 (GRCm39) missense probably damaging 0.99
R4648:Prkdc UTSW 16 15,634,638 (GRCm39) missense probably benign 0.05
R4662:Prkdc UTSW 16 15,551,916 (GRCm39) missense probably damaging 1.00
R4680:Prkdc UTSW 16 15,589,894 (GRCm39) missense probably benign 0.00
R4700:Prkdc UTSW 16 15,519,976 (GRCm39) missense probably damaging 1.00
R4716:Prkdc UTSW 16 15,628,701 (GRCm39) missense probably benign 0.32
R4720:Prkdc UTSW 16 15,485,579 (GRCm39) missense probably benign
R4785:Prkdc UTSW 16 15,466,840 (GRCm39) missense probably benign 0.21
R4822:Prkdc UTSW 16 15,468,576 (GRCm39) missense possibly damaging 0.80
R4829:Prkdc UTSW 16 15,519,939 (GRCm39) missense possibly damaging 0.80
R4981:Prkdc UTSW 16 15,496,173 (GRCm39) missense probably damaging 1.00
R4989:Prkdc UTSW 16 15,491,861 (GRCm39) missense possibly damaging 0.80
R5059:Prkdc UTSW 16 15,655,882 (GRCm39) missense probably damaging 1.00
R5074:Prkdc UTSW 16 15,589,912 (GRCm39) missense probably damaging 1.00
R5115:Prkdc UTSW 16 15,608,444 (GRCm39) missense probably benign
R5151:Prkdc UTSW 16 15,533,899 (GRCm39) missense probably damaging 1.00
R5165:Prkdc UTSW 16 15,496,136 (GRCm39) missense probably damaging 1.00
R5215:Prkdc UTSW 16 15,589,985 (GRCm39) missense possibly damaging 0.64
R5270:Prkdc UTSW 16 15,552,819 (GRCm39) missense probably damaging 1.00
R5278:Prkdc UTSW 16 15,532,838 (GRCm39) missense probably damaging 1.00
R5351:Prkdc UTSW 16 15,649,176 (GRCm39) missense probably benign 0.03
R5416:Prkdc UTSW 16 15,623,814 (GRCm39) missense probably damaging 1.00
R5418:Prkdc UTSW 16 15,612,961 (GRCm39) missense probably benign 0.20
R5437:Prkdc UTSW 16 15,587,739 (GRCm39) missense possibly damaging 0.46
R5452:Prkdc UTSW 16 15,586,501 (GRCm39) missense possibly damaging 0.96
R5518:Prkdc UTSW 16 15,496,172 (GRCm39) missense probably damaging 1.00
R5538:Prkdc UTSW 16 15,469,333 (GRCm39) missense probably damaging 1.00
R5589:Prkdc UTSW 16 15,524,655 (GRCm39) missense probably benign 0.02
R5618:Prkdc UTSW 16 15,627,476 (GRCm39) missense probably damaging 1.00
R5640:Prkdc UTSW 16 15,647,633 (GRCm39) missense possibly damaging 0.86
R5661:Prkdc UTSW 16 15,628,634 (GRCm39) missense possibly damaging 0.81
R5771:Prkdc UTSW 16 15,482,097 (GRCm39) missense probably damaging 1.00
R5772:Prkdc UTSW 16 15,597,252 (GRCm39) missense possibly damaging 0.49
R5783:Prkdc UTSW 16 15,535,665 (GRCm39) missense probably damaging 1.00
R5792:Prkdc UTSW 16 15,634,616 (GRCm39) missense probably damaging 1.00
R5797:Prkdc UTSW 16 15,555,698 (GRCm39) nonsense probably null
R5826:Prkdc UTSW 16 15,551,962 (GRCm39) missense probably benign
R5883:Prkdc UTSW 16 15,533,778 (GRCm39) missense probably benign
R5895:Prkdc UTSW 16 15,570,693 (GRCm39) nonsense probably null
R5998:Prkdc UTSW 16 15,601,021 (GRCm39) missense probably damaging 1.00
R6000:Prkdc UTSW 16 15,647,561 (GRCm39) missense possibly damaging 0.86
R6120:Prkdc UTSW 16 15,557,335 (GRCm39) missense probably benign 0.00
R6145:Prkdc UTSW 16 15,589,937 (GRCm39) missense probably damaging 1.00
R6209:Prkdc UTSW 16 15,608,456 (GRCm39) missense probably damaging 1.00
R6293:Prkdc UTSW 16 15,605,019 (GRCm39) missense probably benign 0.00
R6321:Prkdc UTSW 16 15,532,783 (GRCm39) missense probably benign
R6376:Prkdc UTSW 16 15,587,749 (GRCm39) missense probably benign 0.06
R6387:Prkdc UTSW 16 15,516,679 (GRCm39) missense probably benign 0.01
R6406:Prkdc UTSW 16 15,535,665 (GRCm39) missense probably damaging 1.00
R6469:Prkdc UTSW 16 15,612,939 (GRCm39) missense probably benign 0.10
R6486:Prkdc UTSW 16 15,570,628 (GRCm39) missense probably damaging 0.97
R6665:Prkdc UTSW 16 15,603,914 (GRCm39) critical splice donor site probably null
R6703:Prkdc UTSW 16 15,488,392 (GRCm39) missense probably benign 0.00
R6774:Prkdc UTSW 16 15,543,325 (GRCm39) critical splice donor site probably null
R6854:Prkdc UTSW 16 15,469,402 (GRCm39) missense probably damaging 1.00
R6878:Prkdc UTSW 16 15,594,936 (GRCm39) missense probably benign 0.31
R6882:Prkdc UTSW 16 15,626,020 (GRCm39) missense probably benign 0.33
R6882:Prkdc UTSW 16 15,601,127 (GRCm39) critical splice donor site probably null
R6949:Prkdc UTSW 16 15,617,853 (GRCm39) missense probably benign
R6950:Prkdc UTSW 16 15,633,850 (GRCm39) missense probably damaging 1.00
R7019:Prkdc UTSW 16 15,587,830 (GRCm39) missense probably benign 0.00
R7064:Prkdc UTSW 16 15,608,317 (GRCm39) missense probably benign 0.00
R7097:Prkdc UTSW 16 15,507,207 (GRCm39) missense probably damaging 1.00
R7201:Prkdc UTSW 16 15,516,667 (GRCm39) missense probably benign 0.12
R7235:Prkdc UTSW 16 15,532,127 (GRCm39) missense probably benign
R7283:Prkdc UTSW 16 15,535,628 (GRCm39) missense probably benign 0.00
R7401:Prkdc UTSW 16 15,466,602 (GRCm39) missense probably damaging 1.00
R7525:Prkdc UTSW 16 15,490,191 (GRCm39) missense probably damaging 1.00
R7647:Prkdc UTSW 16 15,555,807 (GRCm39) missense probably damaging 1.00
R7679:Prkdc UTSW 16 15,649,183 (GRCm39) missense probably damaging 1.00
R7803:Prkdc UTSW 16 15,623,960 (GRCm39) missense probably null 0.05
R7858:Prkdc UTSW 16 15,507,141 (GRCm39) missense probably benign 0.11
R7872:Prkdc UTSW 16 15,532,870 (GRCm39) missense probably benign 0.05
R7896:Prkdc UTSW 16 15,526,767 (GRCm39) missense probably damaging 0.97
R8032:Prkdc UTSW 16 15,597,315 (GRCm39) missense probably benign 0.00
R8055:Prkdc UTSW 16 15,634,749 (GRCm39) missense probably benign 0.09
R8153:Prkdc UTSW 16 15,482,108 (GRCm39) missense probably damaging 1.00
R8281:Prkdc UTSW 16 15,523,117 (GRCm39) missense probably damaging 1.00
R8302:Prkdc UTSW 16 15,653,946 (GRCm39) missense probably damaging 1.00
R8322:Prkdc UTSW 16 15,532,005 (GRCm39) splice site probably benign
R8401:Prkdc UTSW 16 15,591,477 (GRCm39) missense possibly damaging 0.93
R8440:Prkdc UTSW 16 15,653,022 (GRCm39) frame shift probably null
R8458:Prkdc UTSW 16 15,608,540 (GRCm39) critical splice donor site probably null
R8472:Prkdc UTSW 16 15,469,400 (GRCm39) missense probably damaging 1.00
R8478:Prkdc UTSW 16 15,466,788 (GRCm39) missense probably benign 0.00
R8515:Prkdc UTSW 16 15,482,232 (GRCm39) missense probably damaging 1.00
R8546:Prkdc UTSW 16 15,480,899 (GRCm39) missense probably damaging 1.00
R8678:Prkdc UTSW 16 15,526,796 (GRCm39) critical splice donor site probably null
R8739:Prkdc UTSW 16 15,626,068 (GRCm39) missense probably benign 0.01
R8749:Prkdc UTSW 16 15,601,029 (GRCm39) missense possibly damaging 0.85
R8836:Prkdc UTSW 16 15,545,523 (GRCm39) missense probably damaging 1.00
R8904:Prkdc UTSW 16 15,545,590 (GRCm39) missense probably benign 0.04
R8952:Prkdc UTSW 16 15,491,624 (GRCm39) intron probably benign
R8971:Prkdc UTSW 16 15,493,229 (GRCm39) missense probably null 0.99
R8974:Prkdc UTSW 16 15,617,726 (GRCm39) splice site probably null
R9052:Prkdc UTSW 16 15,508,160 (GRCm39) missense probably benign 0.05
R9069:Prkdc UTSW 16 15,653,091 (GRCm39) nonsense probably null
R9200:Prkdc UTSW 16 15,523,153 (GRCm39) missense probably damaging 1.00
R9235:Prkdc UTSW 16 15,651,751 (GRCm39) missense probably damaging 1.00
R9278:Prkdc UTSW 16 15,634,523 (GRCm39) critical splice donor site probably null
R9309:Prkdc UTSW 16 15,526,792 (GRCm39) nonsense probably null
R9386:Prkdc UTSW 16 15,496,136 (GRCm39) missense probably damaging 0.99
R9452:Prkdc UTSW 16 15,485,465 (GRCm39) missense possibly damaging 0.90
R9500:Prkdc UTSW 16 15,657,079 (GRCm39) missense possibly damaging 0.76
R9608:Prkdc UTSW 16 15,548,335 (GRCm39) missense probably damaging 1.00
R9608:Prkdc UTSW 16 15,548,334 (GRCm39) missense possibly damaging 0.96
R9636:Prkdc UTSW 16 15,548,341 (GRCm39) missense probably benign 0.19
R9656:Prkdc UTSW 16 15,617,818 (GRCm39) missense probably benign 0.00
R9674:Prkdc UTSW 16 15,533,819 (GRCm39) missense probably damaging 0.98
R9760:Prkdc UTSW 16 15,657,044 (GRCm39) nonsense probably null
X0023:Prkdc UTSW 16 15,558,142 (GRCm39) missense probably benign
Z1176:Prkdc UTSW 16 15,505,286 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- AAAGCTGACACTTGCAAGTATCTG -3'
(R):5'- CATCCCAGTAAGACTTTATGTGC -3'

Sequencing Primer
(F):5'- ACACTTGCAAGTATCTGATAAATAGC -3'
(R):5'- CCAGTAAGACTTTATGTGCTTCAATC -3'
Posted On 2014-10-16