Incidental Mutation 'R0334:Prkdc'
ID 26175
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 038543-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.953) question?
Stock # R0334 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location 15455730-15660099 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 15554663 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 2128 (D2128G)
Ref Sequence ENSEMBL: ENSMUSP00000023352 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023352]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000023352
AA Change: D2128G

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000023352
Gene: ENSMUSG00000022672
AA Change: D2128G

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
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.6%
Validation Efficiency 99% (68/69)
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: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aggf1 T C 13: 95,508,105 (GRCm39) N87S probably benign Het
Ap2b1 T C 11: 83,258,700 (GRCm39) probably benign Het
Arfgef3 A G 10: 18,468,029 (GRCm39) Y1724H probably damaging Het
Arhgef10l G A 4: 140,311,237 (GRCm39) Q243* probably null Het
Atp8a2 A T 14: 59,928,961 (GRCm39) F1031Y probably damaging Het
Bmp8b A G 4: 123,008,553 (GRCm39) probably null Het
Brinp2 G T 1: 158,123,155 (GRCm39) T37K probably benign Het
Bsph1 T A 7: 13,184,864 (GRCm39) L9* probably null Het
C6 T G 15: 4,784,849 (GRCm39) N238K probably benign Het
Cbs T C 17: 31,838,130 (GRCm39) D373G probably damaging Het
Clec4a3 T C 6: 122,946,329 (GRCm39) F191S possibly damaging Het
Cpz A G 5: 35,661,025 (GRCm39) V530A probably damaging Het
Ctsc G T 7: 87,927,550 (GRCm39) S47I possibly damaging Het
Cyp7b1 T G 3: 18,157,960 (GRCm39) Y53S probably damaging Het
Dach1 C T 14: 98,406,184 (GRCm39) G188R probably damaging Het
Defb4 T C 8: 19,251,220 (GRCm39) I29T probably benign Het
Disc1 A T 8: 125,987,836 (GRCm39) probably null Het
Dnah2 A G 11: 69,327,662 (GRCm39) M3429T probably damaging Het
Dnah7a A T 1: 53,472,213 (GRCm39) I3518N possibly damaging Het
Dnah8 A T 17: 31,090,325 (GRCm39) H4609L probably damaging Het
Evi5 C A 5: 107,968,401 (GRCm39) C182F probably damaging Het
Fam149b G A 14: 20,413,492 (GRCm39) R237H probably damaging Het
Fut8 T A 12: 77,440,536 (GRCm39) D174E possibly damaging Het
Ghr T C 15: 3,370,580 (GRCm39) probably benign Het
Gm10801 G C 2: 98,494,352 (GRCm39) R143T possibly damaging Het
Gpr176 T C 2: 118,110,189 (GRCm39) S357G probably benign Het
Grwd1 A T 7: 45,476,601 (GRCm39) probably null Het
H2-T24 A G 17: 36,325,772 (GRCm39) V273A possibly damaging Het
Hdac4 A C 1: 91,883,760 (GRCm39) probably benign Het
Herc3 A G 6: 58,895,802 (GRCm39) T1017A probably damaging Het
Hsd11b1 T C 1: 192,924,476 (GRCm39) probably benign Het
Igsf23 T C 7: 19,675,678 (GRCm39) S143G probably benign Het
Kbtbd12 T A 6: 88,594,888 (GRCm39) Y314F probably damaging Het
Kcnmb2 A G 3: 32,252,508 (GRCm39) probably null Het
Kdm5b A G 1: 134,532,260 (GRCm39) I479M probably damaging Het
Kidins220 A G 12: 25,058,068 (GRCm39) T600A probably damaging Het
Mrgprb2 A C 7: 48,202,077 (GRCm39) I216S probably damaging Het
Muc21 A G 17: 35,933,614 (GRCm39) probably benign Het
Myo1g A G 11: 6,461,084 (GRCm39) probably benign Het
Nrxn3 T C 12: 89,780,412 (GRCm39) probably null Het
Or2ag2 A G 7: 106,485,622 (GRCm39) V134A probably benign Het
Or8b54 A T 9: 38,686,535 (GRCm39) probably null Het
Or8g26 A G 9: 39,095,980 (GRCm39) I169V probably benign Het
Pdia5 A T 16: 35,284,760 (GRCm39) S66T possibly damaging Het
Plec T C 15: 76,062,206 (GRCm39) E2604G probably damaging Het
Plekha6 G T 1: 133,209,918 (GRCm39) A654S probably benign Het
Pnpla2 G A 7: 141,039,433 (GRCm39) probably null Het
Pramel19 T C 4: 101,798,781 (GRCm39) F251L probably benign Het
Prb1c T A 6: 132,341,021 (GRCm39) Q17L unknown Het
Rabggta A T 14: 55,958,268 (GRCm39) L131Q probably damaging Het
Rbks A T 5: 31,781,863 (GRCm39) Y312* probably null Het
Rnf139 A G 15: 58,771,322 (GRCm39) Y449C probably damaging Het
Sanbr A G 11: 23,567,129 (GRCm39) probably benign Het
Sbno1 A G 5: 124,524,931 (GRCm39) V1058A possibly damaging Het
Sema3a A T 5: 13,607,268 (GRCm39) N321I probably damaging Het
Slit3 T A 11: 35,469,928 (GRCm39) V310E probably damaging Het
Slitrk5 T C 14: 111,918,256 (GRCm39) S627P probably benign Het
Stat2 T A 10: 128,113,736 (GRCm39) F172I probably damaging Het
Tchh C A 3: 93,352,923 (GRCm39) R788S unknown Het
Tnks T A 8: 35,320,413 (GRCm39) K753* probably null Het
Trank1 T A 9: 111,194,421 (GRCm39) V815D probably benign Het
Trank1 T A 9: 111,222,008 (GRCm39) I2915N probably damaging Het
Trpc6 T C 9: 8,610,344 (GRCm39) S271P probably damaging Het
Trpm5 T C 7: 142,640,613 (GRCm39) Q213R probably benign Het
Ulk3 C T 9: 57,501,510 (GRCm39) probably benign Het
Usp31 T C 7: 121,258,185 (GRCm39) D694G probably damaging Het
Wnt3a A G 11: 59,147,144 (GRCm39) S181P probably damaging Het
Yipf3 T C 17: 46,559,238 (GRCm39) F22S possibly damaging Het
Zbtb40 A T 4: 136,713,867 (GRCm39) H1094Q probably damaging 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
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
R2270:Prkdc UTSW 16 15,472,681 (GRCm39) splice site probably null
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'- TGAAAGCTGTCGCTAGGCACAC -3'
(R):5'- CAAAAGCCTGTTGCCCCTGAAAG -3'

Sequencing Primer
(F):5'- GCTAGGCACACAGATTTTCG -3'
(R):5'- tgaaagaaactttcagaacatgacc -3'
Posted On 2013-04-16