Incidental Mutation 'R7019:Prkdc'
ID 545534
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 045120-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.953) question?
Stock # R7019 (G1)
Quality Score 225.009
Status Validated
Chromosome 16
Chromosomal Location 15455730-15660099 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 15587830 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 2572 (I2572L)
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: I2572L

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000023352
Gene: ENSMUSG00000022672
AA Change: I2572L

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 100% (61/61)
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abat A T 16: 8,436,395 (GRCm39) K414* probably null Het
Aco1 T A 4: 40,186,376 (GRCm39) I596N probably damaging Het
Adgre1 A C 17: 57,717,945 (GRCm39) D319A probably damaging Het
Birc6 T C 17: 74,916,340 (GRCm39) V445A probably benign Het
Btd A C 14: 31,389,062 (GRCm39) Q261P probably damaging Het
Btd G T 14: 31,389,063 (GRCm39) Q261H possibly damaging Het
C7 T A 15: 5,075,164 (GRCm39) Y176F probably benign Het
Ccdc102a T C 8: 95,636,431 (GRCm39) S287G probably benign Het
Ccdc178 T A 18: 22,283,495 (GRCm39) T12S probably benign Het
Cnga4 G T 7: 105,055,036 (GRCm39) A104S probably benign Het
Col10a1 G T 10: 34,270,947 (GRCm39) L306F probably damaging Het
Cpne5 T C 17: 29,445,196 (GRCm39) D36G probably damaging Het
Csmd2 G A 4: 128,262,856 (GRCm39) D681N Het
Cspg4b C T 13: 113,488,284 (GRCm39) T102I probably benign Het
Cstl1 A G 2: 148,597,223 (GRCm39) M75V probably benign Het
Cyp26a1 T C 19: 37,687,260 (GRCm39) L149P probably damaging Het
D630045J12Rik T G 6: 38,171,570 (GRCm39) E866A probably benign Het
Dlec1 C T 9: 118,941,490 (GRCm39) P292L probably benign Het
Dpp3 T G 19: 4,966,817 (GRCm39) E402A possibly damaging Het
Egf T C 3: 129,511,713 (GRCm39) probably null Het
Epha5 T C 5: 84,564,321 (GRCm39) Q15R possibly damaging Het
Esyt3 A G 9: 99,197,338 (GRCm39) F831L probably benign Het
Fam50b G A 13: 34,931,084 (GRCm39) E187K possibly damaging Het
Fut7 A G 2: 25,315,792 (GRCm39) D350G probably benign Het
Gab1 C A 8: 81,511,446 (GRCm39) E466D probably damaging Het
Glrp1 A T 1: 88,430,890 (GRCm39) M160K unknown Het
Gngt1 T C 6: 3,994,088 (GRCm39) probably null Het
Gprc6a A T 10: 51,507,508 (GRCm39) V7E possibly damaging Het
Idh3b A T 2: 130,122,886 (GRCm39) V301D probably damaging Het
Ifi202b A C 1: 173,791,524 (GRCm39) C385G probably benign Het
Ilvbl T A 10: 78,414,920 (GRCm39) L261Q probably damaging Het
Irx6 T A 8: 93,405,362 (GRCm39) L410Q probably damaging Het
Ism2 T C 12: 87,346,437 (GRCm39) M15V unknown Het
Itih5 C A 2: 10,195,138 (GRCm39) R177S probably damaging Het
Klra3 C T 6: 130,304,087 (GRCm39) G202R probably damaging Het
Krt7 T C 15: 101,311,851 (GRCm39) V103A probably damaging Het
Lama3 T C 18: 12,661,475 (GRCm39) S2145P probably damaging Het
Mlph A G 1: 90,869,428 (GRCm39) R477G probably damaging Het
Mybpc1 T A 10: 88,379,581 (GRCm39) L653F probably damaging Het
Myrfl A G 10: 116,617,852 (GRCm39) probably null Het
Myrip T G 9: 120,251,573 (GRCm39) L232R probably damaging Het
Nrdc A T 4: 108,885,999 (GRCm39) H126L probably benign Het
Or4n5 A T 14: 50,133,124 (GRCm39) I45N probably damaging Het
Or5p50 G T 7: 107,422,365 (GRCm39) L104I probably benign Het
Or8c11 T A 9: 38,290,098 (GRCm39) L307Q possibly damaging Het
Pcdhb10 T A 18: 37,546,056 (GRCm39) N377K probably damaging Het
Pigt CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT 2: 164,341,589 (GRCm39) probably null Het
Ptpro C A 6: 137,357,476 (GRCm39) D322E probably benign Het
R3hcc1 A G 14: 69,941,574 (GRCm39) I332T probably damaging Het
Rab8a T C 8: 72,915,227 (GRCm39) F9L probably damaging Het
Ranbp3l A T 15: 9,057,241 (GRCm39) K165N probably damaging Het
Rock2 T A 12: 17,027,741 (GRCm39) C1353S probably damaging Het
Rsad2 T A 12: 26,506,418 (GRCm39) M1L possibly damaging Het
Tymp A T 15: 89,260,484 (GRCm39) probably null Het
Vmn1r104 A G 7: 20,268,491 (GRCm39) M244V probably benign Het
Vmn1r232 G A 17: 21,133,547 (GRCm39) T351M possibly damaging Het
Vmn2r50 A G 7: 9,784,172 (GRCm39) Y101H probably benign Het
Vmn2r57 A G 7: 41,078,089 (GRCm39) L123P probably damaging Het
Wdr17 T C 8: 55,134,488 (GRCm39) N331D probably damaging Het
Wdr47 C T 3: 108,521,671 (GRCm39) Q89* probably null Het
Zcchc4 A T 5: 52,941,375 (GRCm39) T57S 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
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
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'- CTAATTATTCGGAATTTCTGGAGCC -3'
(R):5'- AAAGTGAGTTGTCCAAGTGGC -3'

Sequencing Primer
(F):5'- TCGGAATTTCTGGAGCCATGAAAC -3'
(R):5'- TCCAAGTGGCGTCTGAGAG -3'
Posted On 2019-05-13