Incidental Mutation 'R1579:Prkdc'
ID 171322
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 039616-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.953) question?
Stock # R1579 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 15455730-15660099 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 15493192 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 700 (Y700N)
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: Y700N

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000023352
Gene: ENSMUSG00000022672
AA Change: Y700N

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
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.0%
  • 20x: 91.8%
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: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700037C18Rik T C 16: 3,724,039 (GRCm39) R162G probably benign Het
Adamtsl4 T A 3: 95,592,807 (GRCm39) probably benign Het
Adgrv1 A T 13: 81,711,898 (GRCm39) L306H probably damaging Het
Aknad1 T A 3: 108,659,452 (GRCm39) Y155* probably null Het
Aldh6a1 C T 12: 84,488,622 (GRCm39) R88H possibly damaging Het
Apc2 G C 10: 80,147,179 (GRCm39) K715N probably damaging Het
Arhgap45 G A 10: 79,864,811 (GRCm39) V798M probably damaging Het
Calcrl T C 2: 84,163,881 (GRCm39) T437A probably benign Het
Cdan1 A G 2: 120,561,220 (GRCm39) F183L probably damaging Het
Chmp7 C T 14: 69,956,899 (GRCm39) M336I probably benign Het
Cntnap4 A G 8: 113,608,462 (GRCm39) E1294G possibly damaging Het
Crybg3 C A 16: 59,350,561 (GRCm39) G2607V probably damaging Het
Dhx29 G T 13: 113,072,132 (GRCm39) probably null Het
Dmrtb1 T A 4: 107,541,322 (GRCm39) H13L probably damaging Het
Echdc2 A G 4: 108,031,006 (GRCm39) M162V probably benign Het
Entpd8 A G 2: 24,974,986 (GRCm39) D439G possibly damaging Het
Fastkd2 C G 1: 63,785,046 (GRCm39) H477Q probably null Het
Fbrs A G 7: 127,084,529 (GRCm39) E517G probably damaging Het
Gchfr A G 2: 119,002,502 (GRCm39) T71A possibly damaging Het
Hecw1 A T 13: 14,552,492 (GRCm39) C35S probably damaging Het
Izumo1r C T 9: 14,813,098 (GRCm39) R58H probably benign Het
Kif13a T C 13: 46,906,332 (GRCm39) E537G possibly damaging Het
Kif13b G A 14: 65,019,790 (GRCm39) probably null Het
Kremen1 CGGG CGGGGGG 11: 5,151,791 (GRCm39) probably benign Het
Lnpk A T 2: 74,378,340 (GRCm39) D140E probably damaging Het
Ltbp1 A G 17: 75,559,362 (GRCm39) M284V probably benign Het
Me3 A T 7: 89,495,050 (GRCm39) T323S possibly damaging Het
Mtus1 A G 8: 41,535,895 (GRCm39) V607A probably damaging Het
Myh14 A T 7: 44,305,118 (GRCm39) probably null Het
Myo1h T A 5: 114,485,496 (GRCm39) C545* probably null Het
Nbn T A 4: 15,964,289 (GRCm39) D121E probably damaging Het
Nox4 A G 7: 87,019,231 (GRCm39) Y408C probably damaging Het
Nup214 C T 2: 31,924,478 (GRCm39) S1669F probably damaging Het
Or10q1b A G 19: 13,682,566 (GRCm39) D125G probably damaging Het
Or52d3 T A 7: 104,229,268 (GRCm39) Y138* probably null Het
Or5w20 G A 2: 87,727,286 (GRCm39) A248T probably benign Het
Osbpl5 T C 7: 143,262,939 (GRCm39) T150A possibly damaging Het
Pgap3 C A 11: 98,280,879 (GRCm39) M265I probably benign Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Pkd2l2 A T 18: 34,560,446 (GRCm39) N351I possibly damaging Het
Pzp A G 6: 128,500,931 (GRCm39) probably null Het
Rfwd3 C T 8: 112,014,874 (GRCm39) R326Q probably damaging Het
Rptor A T 11: 119,786,827 (GRCm39) Q1264L probably benign Het
Scnn1a T C 6: 125,299,103 (GRCm39) F61S probably damaging Het
Tenm2 C A 11: 35,997,610 (GRCm39) W825C probably damaging Het
Tex264 A T 9: 106,559,116 (GRCm39) I70N possibly damaging Het
Tns2 G T 15: 102,019,645 (GRCm39) D504Y probably damaging Het
Trappc14 T C 5: 138,260,128 (GRCm39) I338V probably benign Het
Trpc2 T A 7: 101,733,447 (GRCm39) F132Y probably damaging Het
Trpm4 A G 7: 44,958,021 (GRCm39) F816S probably damaging Het
Uqcc1 G A 2: 155,763,641 (GRCm39) Q5* probably null Het
Usp36 G T 11: 118,175,771 (GRCm39) T130N probably damaging Het
Vav1 A G 17: 57,604,252 (GRCm39) M165V probably benign Het
Vmn1r64 A T 7: 5,886,803 (GRCm39) F247I probably damaging Het
Vmn2r26 G C 6: 124,016,706 (GRCm39) R390P probably benign Het
Vmn2r57 G T 7: 41,049,548 (GRCm39) H734N probably benign Het
Wfdc16 G T 2: 164,477,843 (GRCm39) H69N possibly damaging Het
Zfp316 C T 5: 143,239,317 (GRCm39) E901K probably damaging Het
Zfp334 T C 2: 165,223,719 (GRCm39) E108G probably damaging Het
Zfp407 T C 18: 84,227,763 (GRCm39) S1949G probably benign Het
Zfp408 A G 2: 91,476,473 (GRCm39) L227P probably benign Het
Zfp560 T C 9: 20,259,287 (GRCm39) H525R possibly damaging Het
Zfp609 G A 9: 65,611,754 (GRCm39) A403V possibly 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
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
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'- TCCTCCAAACTAGACTATGGCAACATGA -3'
(R):5'- GCAGGGTGCAACCCACCAAT -3'

Sequencing Primer
(F):5'- CTAGACTATGGCAACATGAAAAGG -3'
(R):5'- tgagaaggcagaggcaaac -3'
Posted On 2014-04-13