Incidental Mutation 'R4720:Prkdc'
ID 354409
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 041958-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.953) question?
Stock # R4720 (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 15485579 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 469 (S469T)
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: S469T

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000023352
Gene: ENSMUSG00000022672
AA Change: S469T

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: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.0%
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: 91 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 A G 11: 110,018,248 (GRCm39) I1124T probably damaging Het
Acacb A G 5: 114,367,975 (GRCm39) T1658A possibly damaging Het
Acvrl1 C A 15: 101,033,654 (GRCm39) P112Q probably damaging Het
Ankar A T 1: 72,738,170 (GRCm39) I4K possibly damaging Het
Ankfn1 G C 11: 89,332,252 (GRCm39) D431E possibly damaging Het
Apobec4 T C 1: 152,632,425 (GRCm39) V151A possibly damaging Het
Atp10b A G 11: 43,093,949 (GRCm39) S498G probably benign Het
Azin1 A G 15: 38,493,744 (GRCm39) V293A probably benign Het
Ccdc88b T C 19: 6,835,083 (GRCm39) E46G probably damaging Het
Ccdc96 T C 5: 36,642,219 (GRCm39) probably benign Het
Ccnyl1 A G 1: 64,752,290 (GRCm39) D169G probably benign Het
Cdca3 T A 6: 124,809,127 (GRCm39) V89E probably damaging Het
Cdh19 A T 1: 110,823,111 (GRCm39) probably null Het
Chka G A 19: 3,936,375 (GRCm39) V238I probably damaging Het
Cntn3 T C 6: 102,218,983 (GRCm39) K546E possibly damaging Het
Crybg3 A G 16: 59,360,180 (GRCm39) V787A probably damaging Het
Dlgap3 T C 4: 127,089,508 (GRCm39) probably null Het
Dnah8 C T 17: 30,902,608 (GRCm39) L889F probably benign Het
Dnah9 T C 11: 65,967,184 (GRCm39) E1658G probably damaging Het
Dnajc11 A G 4: 152,052,996 (GRCm39) D102G probably damaging Het
Dync1i2 T G 2: 71,064,018 (GRCm39) S121A probably damaging Het
Ece1 G A 4: 137,684,486 (GRCm39) E591K probably damaging Het
Enthd1 G A 15: 80,444,510 (GRCm39) S15L probably damaging Het
Epb41l2 T A 10: 25,347,524 (GRCm39) H372Q probably damaging Het
Errfi1 T A 4: 150,951,204 (GRCm39) Y211N probably damaging Het
Fam193b G A 13: 55,691,250 (GRCm39) T208M probably benign Het
Flacc1 T C 1: 58,717,507 (GRCm39) I135V possibly damaging Het
Fmnl2 C T 2: 52,997,552 (GRCm39) T501M possibly damaging Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Gm4841 G T 18: 60,403,135 (GRCm39) D319E probably benign Het
Gucd1 A G 10: 75,345,494 (GRCm39) F187S probably damaging Het
Hcar2 GCGGATGCGCAC GC 5: 124,002,752 (GRCm39) probably null Het
Helz2 T C 2: 180,880,210 (GRCm39) D502G probably damaging Het
Hspa2 A G 12: 76,451,639 (GRCm39) E111G possibly damaging Het
Htr2a T A 14: 74,882,499 (GRCm39) S162T probably damaging Het
Ift80 A G 3: 68,869,623 (GRCm39) Y223H possibly damaging Het
Il1rl1 A G 1: 40,485,838 (GRCm39) K330E probably benign Het
Il23r A T 6: 67,400,645 (GRCm39) F562I probably damaging Het
Isx T C 8: 75,600,487 (GRCm39) probably null Het
Jcad G A 18: 4,674,055 (GRCm39) V606I probably benign Het
Kcnn2 A T 18: 45,816,187 (GRCm39) T333S possibly damaging Het
Kcnq5 C T 1: 21,473,274 (GRCm39) A630T probably damaging Het
Kif2c T C 4: 117,028,946 (GRCm39) M188V probably benign Het
Kntc1 T C 5: 123,903,086 (GRCm39) V321A possibly damaging Het
Krtap4-8 A T 11: 99,671,271 (GRCm39) probably benign Het
Lcor G C 19: 41,574,334 (GRCm39) A1030P probably benign Het
Lgals3bp A C 11: 118,289,295 (GRCm39) L52R probably damaging Het
Lipk C A 19: 33,999,099 (GRCm39) H126Q probably damaging Het
Lpgat1 T C 1: 191,495,779 (GRCm39) Y323H probably damaging Het
Lrp2 T G 2: 69,311,517 (GRCm39) N2654H probably damaging Het
Lsm14b C T 2: 179,669,774 (GRCm39) Q6* probably null Het
Lysmd3 C T 13: 81,817,584 (GRCm39) A187V possibly damaging Het
Map2k5 A G 9: 63,201,001 (GRCm39) S211P probably damaging Het
Mlph A T 1: 90,869,419 (GRCm39) I474F probably damaging Het
Mpped2 T C 2: 106,614,091 (GRCm39) S142P probably damaging Het
Nemf A C 12: 69,371,062 (GRCm39) M678R probably benign Het
Nfe2l1 A T 11: 96,718,515 (GRCm39) Y7N probably damaging Het
Nfkbie T G 17: 45,867,232 (GRCm39) D122E probably benign Het
Noc3l C A 19: 38,778,066 (GRCm39) A783S probably benign Het
Nol8 T C 13: 49,816,229 (GRCm39) V761A probably damaging Het
Nvl A G 1: 180,929,152 (GRCm39) L743P probably damaging Het
Or1j1 T A 2: 36,702,484 (GRCm39) I207F probably benign Het
Plcb1 A G 2: 135,093,667 (GRCm39) K160R possibly damaging Het
Plekhg3 G T 12: 76,625,096 (GRCm39) G1313C possibly damaging Het
Plekhh1 GTCAAA G 12: 79,122,194 (GRCm39) probably null Het
Popdc3 G A 10: 45,191,002 (GRCm39) V38I probably benign Het
Prdx3 A T 19: 60,858,551 (GRCm39) V114D possibly damaging Het
Rbm22 G A 18: 60,697,463 (GRCm39) R56H probably damaging Het
Reln A T 5: 22,491,894 (GRCm39) F113I possibly damaging Het
Rims1 A G 1: 22,497,731 (GRCm39) Y808H probably damaging Het
Rsbn1 C A 3: 103,836,336 (GRCm39) T458N possibly damaging Het
Serpina3b A G 12: 104,096,889 (GRCm39) S57G possibly damaging Het
Skor2 G T 18: 76,948,878 (GRCm39) probably null Het
Slc22a4 A T 11: 53,879,719 (GRCm39) Y447N probably damaging Het
Slco1a7 C A 6: 141,668,948 (GRCm39) A495S probably damaging Het
Stx19 G T 16: 62,642,682 (GRCm39) R166L probably damaging Het
Svep1 T C 4: 58,205,869 (GRCm39) T170A possibly damaging Het
Sycp2 T G 2: 178,016,225 (GRCm39) S746R probably benign Het
Tchh G T 3: 93,355,189 (GRCm39) R1543L unknown Het
Tjp2 T C 19: 24,078,169 (GRCm39) D908G probably damaging Het
Ttc8 C A 12: 98,946,068 (GRCm39) A452E possibly damaging Het
Unc5a T A 13: 55,151,696 (GRCm39) W709R probably null Het
Unc80 T A 1: 66,549,951 (GRCm39) S736R possibly damaging Het
Vmn2r100 C A 17: 19,742,788 (GRCm39) H387Q probably benign Het
Vmn2r39 C T 7: 9,026,469 (GRCm39) probably null Het
Vmn2r88 T A 14: 51,650,702 (GRCm39) D138E probably benign Het
Vwce T C 19: 10,625,831 (GRCm39) F448L possibly damaging Het
Wdr75 C T 1: 45,861,645 (GRCm39) S695F probably benign Het
Zfand4 T C 6: 116,265,122 (GRCm39) probably null Het
Zfp511 T A 7: 139,617,424 (GRCm39) probably null Het
Zfyve9 T C 4: 108,501,565 (GRCm39) K584E 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
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
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'- CACTCAGTTTGATTTTGGCAGC -3'
(R):5'- AGTAGGTACCACTGACTCCAAAG -3'

Sequencing Primer
(F):5'- TTGGCAGCTACAATAGTTAGATAGG -3'
(R):5'- GAATTAGGGAACCAGATTTTC -3'
Posted On 2015-10-21