Incidental Mutation 'R1793:Nav3'
ID 201957
Institutional Source Beutler Lab
Gene Symbol Nav3
Ensembl Gene ENSMUSG00000020181
Gene Name neuron navigator 3
Synonyms Pomfil1p, 9630020C08Rik, POMFIL1, steerin 3, 4732483H20Rik, unc53H3
MMRRC Submission 039823-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1793 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 109517120-110292065 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 109539233 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 2056 (T2056I)
Ref Sequence ENSEMBL: ENSMUSP00000032719 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032719]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000032719
AA Change: T2056I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000032719
Gene: ENSMUSG00000020181
AA Change: T2056I

DomainStartEndE-ValueType
CH 79 182 4.41e-12 SMART
low complexity region 184 194 N/A INTRINSIC
low complexity region 318 329 N/A INTRINSIC
low complexity region 353 363 N/A INTRINSIC
low complexity region 427 439 N/A INTRINSIC
low complexity region 522 536 N/A INTRINSIC
low complexity region 713 724 N/A INTRINSIC
low complexity region 807 818 N/A INTRINSIC
low complexity region 873 896 N/A INTRINSIC
low complexity region 904 916 N/A INTRINSIC
low complexity region 1077 1095 N/A INTRINSIC
low complexity region 1160 1173 N/A INTRINSIC
low complexity region 1207 1229 N/A INTRINSIC
low complexity region 1256 1266 N/A INTRINSIC
low complexity region 1274 1285 N/A INTRINSIC
low complexity region 1293 1312 N/A INTRINSIC
low complexity region 1327 1341 N/A INTRINSIC
low complexity region 1383 1397 N/A INTRINSIC
low complexity region 1462 1474 N/A INTRINSIC
low complexity region 1550 1563 N/A INTRINSIC
coiled coil region 1565 1656 N/A INTRINSIC
low complexity region 1675 1692 N/A INTRINSIC
low complexity region 1722 1733 N/A INTRINSIC
low complexity region 1756 1781 N/A INTRINSIC
low complexity region 1782 1795 N/A INTRINSIC
coiled coil region 1801 1842 N/A INTRINSIC
low complexity region 1848 1871 N/A INTRINSIC
AAA 2029 2184 4.94e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161582
SMART Domains Protein: ENSMUSP00000124591
Gene: ENSMUSG00000020181

DomainStartEndE-ValueType
low complexity region 84 95 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 181 193 N/A INTRINSIC
low complexity region 354 372 N/A INTRINSIC
low complexity region 437 450 N/A INTRINSIC
low complexity region 484 506 N/A INTRINSIC
low complexity region 533 543 N/A INTRINSIC
low complexity region 551 562 N/A INTRINSIC
low complexity region 570 589 N/A INTRINSIC
low complexity region 604 618 N/A INTRINSIC
low complexity region 660 674 N/A INTRINSIC
low complexity region 739 751 N/A INTRINSIC
low complexity region 827 840 N/A INTRINSIC
coiled coil region 842 933 N/A INTRINSIC
low complexity region 952 969 N/A INTRINSIC
low complexity region 992 1003 N/A INTRINSIC
low complexity region 1026 1051 N/A INTRINSIC
low complexity region 1052 1065 N/A INTRINSIC
coiled coil region 1071 1112 N/A INTRINSIC
low complexity region 1118 1141 N/A INTRINSIC
AAA 1299 1454 4.94e-7 SMART
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.4%
  • 20x: 92.9%
Validation Efficiency 100% (122/122)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 118 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930522L14Rik A T 5: 109,884,144 (GRCm39) H571Q probably damaging Het
Abcf2 T A 5: 24,773,774 (GRCm39) M372L probably benign Het
Acaca A C 11: 84,206,795 (GRCm39) T1552P probably damaging Het
Acaca A G 11: 84,229,219 (GRCm39) D1682G probably damaging Het
Acvr1b T C 15: 101,091,906 (GRCm39) V62A probably benign Het
Aimp1 C T 3: 132,379,825 (GRCm39) V97M probably benign Het
Aldh1l1 C T 6: 90,554,813 (GRCm39) T557I possibly damaging Het
Alpk1 T C 3: 127,471,447 (GRCm39) T1012A probably damaging Het
Amot G A X: 144,233,585 (GRCm39) probably benign Het
Arap1 T A 7: 101,037,829 (GRCm39) H477Q probably benign Het
Arhgap18 T A 10: 26,736,732 (GRCm39) probably benign Het
Arhgef10l C T 4: 140,242,684 (GRCm39) V862M probably damaging Het
Arl4d A G 11: 101,557,554 (GRCm39) I27V probably benign Het
Asb18 G A 1: 89,942,277 (GRCm39) P8L probably damaging Het
Ash1l A G 3: 88,977,616 (GRCm39) H2682R probably damaging Het
Aspm T A 1: 139,385,079 (GRCm39) V241E probably benign Het
Atf7ip G T 6: 136,586,217 (GRCm39) probably benign Het
AY358078 T G 14: 52,042,051 (GRCm39) M142R unknown Het
C3 T A 17: 57,526,592 (GRCm39) K796N possibly damaging Het
Ceacam16 T C 7: 19,590,041 (GRCm39) T301A probably damaging Het
Ceacam5 T G 7: 17,481,320 (GRCm39) Y356D probably benign Het
Cep192 C T 18: 67,984,838 (GRCm39) A1616V possibly damaging Het
Cfap91 T A 16: 38,141,781 (GRCm39) N384Y possibly damaging Het
Cherp A T 8: 73,216,994 (GRCm39) H645Q probably benign Het
CK137956 T C 4: 127,845,242 (GRCm39) D167G probably benign Het
Clcn1 T A 6: 42,275,860 (GRCm39) probably null Het
Cntn1 C T 15: 92,189,552 (GRCm39) T625I possibly damaging Het
Cpn2 T A 16: 30,078,142 (GRCm39) N520Y probably damaging Het
Crocc G A 4: 140,746,620 (GRCm39) R1762W probably damaging Het
Cts3 C A 13: 61,715,967 (GRCm39) V100F probably benign Het
Ddx56 A T 11: 6,216,934 (GRCm39) V87D probably damaging Het
Dnah9 C T 11: 66,010,420 (GRCm39) probably null Het
Dock1 T A 7: 134,700,456 (GRCm39) probably null Het
Dst T A 1: 34,191,552 (GRCm39) Y291* probably null Het
Eif4g3 T C 4: 137,898,442 (GRCm39) I1071T probably damaging Het
Fblim1 T C 4: 141,322,549 (GRCm39) Q78R probably damaging Het
Fcamr C T 1: 130,739,284 (GRCm39) P195S probably benign Het
Fcho1 G A 8: 72,161,666 (GRCm39) Q835* probably null Het
Frem3 A G 8: 81,339,741 (GRCm39) N678S probably benign Het
Frk G A 10: 34,483,878 (GRCm39) R413H probably benign Het
Gm10619 C A 7: 73,459,758 (GRCm39) noncoding transcript Het
Gm12185 G A 11: 48,806,583 (GRCm39) R203* probably null Het
Gm12886 A G 4: 121,280,174 (GRCm39) V34A probably benign Het
Gna12 A T 5: 140,746,707 (GRCm39) I246N probably damaging Het
Gpm6a T C 8: 55,507,867 (GRCm39) M201T probably benign Het
Gpsm2 T G 3: 108,608,225 (GRCm39) D220A probably benign Het
Grip2 C G 6: 91,760,623 (GRCm39) V325L probably benign Het
Grk5 C A 19: 61,065,200 (GRCm39) A288D probably damaging Het
Herpud2 G A 9: 25,021,953 (GRCm39) A231V possibly damaging Het
Hmcn1 T C 1: 150,624,834 (GRCm39) S1024G probably benign Het
Hp1bp3 A G 4: 137,957,820 (GRCm39) D295G probably damaging Het
Igsf21 T C 4: 139,761,703 (GRCm39) H325R probably damaging Het
Ing2 T A 8: 48,122,364 (GRCm39) L61F probably damaging Het
Jak3 T C 8: 72,138,590 (GRCm39) probably benign Het
Kcnn3 T A 3: 89,516,712 (GRCm39) C374S probably benign Het
Klk1b22 A G 7: 43,765,775 (GRCm39) probably benign Het
Larp1 T C 11: 57,940,764 (GRCm39) M630T possibly damaging Het
Lhx5 T A 5: 120,572,725 (GRCm39) C115S probably damaging Het
Lmcd1 C A 6: 112,305,712 (GRCm39) T271K probably benign Het
Lpar1 G A 4: 58,486,798 (GRCm39) R158* probably null Het
Lyst T A 13: 13,821,668 (GRCm39) C1347* probably null Het
Map3k8 G A 18: 4,332,389 (GRCm39) Q441* probably null Het
Mboat1 T C 13: 30,403,633 (GRCm39) V144A probably damaging Het
Mcur1 C T 13: 43,713,491 (GRCm39) G38S unknown Het
Med13 T A 11: 86,220,177 (GRCm39) M276L probably benign Het
Mefv A G 16: 3,526,528 (GRCm39) S699P possibly damaging Het
Mfsd4a C A 1: 131,987,077 (GRCm39) A62S probably damaging Het
Mmp27 A G 9: 7,571,459 (GRCm39) M1V probably null Het
Myo1c C T 11: 75,548,415 (GRCm39) T58I probably damaging Het
Myom3 A T 4: 135,538,066 (GRCm39) D1316V probably benign Het
Naa25 T A 5: 121,555,478 (GRCm39) C235S possibly damaging Het
Naa25 C A 5: 121,558,656 (GRCm39) R333S probably damaging Het
Nol4 A G 18: 22,902,878 (GRCm39) Y378H probably damaging Het
Npat G A 9: 53,463,589 (GRCm39) R124Q probably damaging Het
Npr3 T A 15: 11,848,665 (GRCm39) E434V probably benign Het
Nptx2 A G 5: 144,485,130 (GRCm39) T208A probably benign Het
Obscn C T 11: 58,968,606 (GRCm39) V2798M probably damaging Het
Odad4 C A 11: 100,460,679 (GRCm39) probably null Het
Or10j7 A T 1: 173,011,976 (GRCm39) H8Q probably benign Het
Or52r1 A G 7: 102,537,250 (GRCm39) Y37H probably benign Het
Or5b122 C T 19: 13,562,779 (GRCm39) T37I probably benign Het
Padi1 G A 4: 140,541,967 (GRCm39) P652S probably damaging Het
Pcdh1 G T 18: 38,331,938 (GRCm39) P355Q probably damaging Het
Pck2 G A 14: 55,781,422 (GRCm39) R189H possibly damaging Het
Pcsk5 T A 19: 17,432,114 (GRCm39) K1500N possibly damaging Het
Phc3 A T 3: 31,002,865 (GRCm39) S218T probably damaging Het
Piezo2 T A 18: 63,239,355 (GRCm39) M510L possibly damaging Het
Polr1g T C 7: 19,091,904 (GRCm39) T68A possibly damaging Het
Ppp1r3a A T 6: 14,754,717 (GRCm39) Y177N probably damaging Het
Psme2b A T 11: 48,836,361 (GRCm39) D195E probably damaging Het
Ptprr T C 10: 116,088,827 (GRCm39) V463A probably damaging Het
Pwwp2b G A 7: 138,836,281 (GRCm39) R574Q probably damaging Het
Rap1gds1 T A 3: 138,756,314 (GRCm39) T14S possibly damaging Het
Rbm11 A T 16: 75,397,685 (GRCm39) K205M probably damaging Het
Rfx1 T A 8: 84,793,050 (GRCm39) probably benign Het
Rnasel C A 1: 153,630,169 (GRCm39) H228Q probably damaging Het
Sap130 T A 18: 31,831,640 (GRCm39) I710K probably benign Het
Slc27a4 C A 2: 29,695,733 (GRCm39) D89E probably benign Het
Spata31d1b T C 13: 59,863,779 (GRCm39) V309A probably benign Het
Syt7 T G 19: 10,421,354 (GRCm39) Y420D probably damaging Het
Tanc2 A G 11: 105,515,859 (GRCm39) probably null Het
Tbc1d10b A G 7: 126,802,930 (GRCm39) S333P possibly damaging Het
Tenm2 G A 11: 35,914,209 (GRCm39) P2442S probably damaging Het
Tenm3 C T 8: 49,127,579 (GRCm39) C33Y probably damaging Het
Timmdc1 A G 16: 38,319,419 (GRCm39) L245P possibly damaging Het
Tlr5 T C 1: 182,800,012 (GRCm39) F5L probably benign Het
Ttll4 T A 1: 74,726,999 (GRCm39) F784L possibly damaging Het
Tulp4 A G 17: 6,189,387 (GRCm39) T70A possibly damaging Het
Txndc17 T A 11: 72,099,571 (GRCm39) N81K probably benign Het
Ubr3 C T 2: 69,830,895 (GRCm39) probably benign Het
Uri1 A C 7: 37,681,116 (GRCm39) V96G probably damaging Het
Uspl1 T A 5: 149,150,246 (GRCm39) I482N probably damaging Het
Vmn1r229 A G 17: 21,034,974 (GRCm39) N73S possibly damaging Het
Vwa7 G T 17: 35,243,388 (GRCm39) G689* probably null Het
Zfp114 T A 7: 23,877,164 (GRCm39) probably null Het
Zfp618 A G 4: 63,051,474 (GRCm39) S659G probably damaging Het
Zfp872 A G 9: 22,111,349 (GRCm39) K275R probably damaging Het
Zzef1 C T 11: 72,777,535 (GRCm39) P1789S probably damaging Het
Other mutations in Nav3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00095:Nav3 APN 10 109,677,594 (GRCm39) missense probably damaging 0.99
IGL00425:Nav3 APN 10 109,539,368 (GRCm39) missense probably benign 0.13
IGL00465:Nav3 APN 10 109,688,607 (GRCm39) missense probably damaging 0.99
IGL00531:Nav3 APN 10 109,539,171 (GRCm39) missense probably null 0.99
IGL00575:Nav3 APN 10 109,600,626 (GRCm39) missense probably damaging 0.98
IGL00770:Nav3 APN 10 109,652,124 (GRCm39) missense probably damaging 1.00
IGL00774:Nav3 APN 10 109,652,124 (GRCm39) missense probably damaging 1.00
IGL00858:Nav3 APN 10 109,578,493 (GRCm39) missense probably damaging 0.98
IGL00935:Nav3 APN 10 109,541,527 (GRCm39) missense probably benign
IGL01638:Nav3 APN 10 109,688,724 (GRCm39) missense probably damaging 1.00
IGL01662:Nav3 APN 10 109,605,119 (GRCm39) missense possibly damaging 0.56
IGL01670:Nav3 APN 10 109,550,102 (GRCm39) missense possibly damaging 0.92
IGL01885:Nav3 APN 10 109,578,521 (GRCm39) nonsense probably null
IGL01979:Nav3 APN 10 109,540,790 (GRCm39) missense probably benign 0.01
IGL02121:Nav3 APN 10 109,594,897 (GRCm39) missense probably damaging 0.99
IGL02210:Nav3 APN 10 109,602,851 (GRCm39) missense probably benign
IGL02523:Nav3 APN 10 109,605,157 (GRCm39) missense probably damaging 1.00
IGL02573:Nav3 APN 10 109,702,835 (GRCm39) missense probably benign 0.23
IGL02633:Nav3 APN 10 109,527,997 (GRCm39) missense probably benign 0.09
IGL02810:Nav3 APN 10 109,652,135 (GRCm39) missense probably damaging 1.00
IGL02964:Nav3 APN 10 109,572,814 (GRCm39) missense probably damaging 0.99
IGL03015:Nav3 APN 10 109,554,158 (GRCm39) missense probably damaging 0.98
IGL03288:Nav3 APN 10 109,594,878 (GRCm39) missense probably damaging 1.00
IGL03310:Nav3 APN 10 109,660,433 (GRCm39) critical splice donor site probably null
PIT4377001:Nav3 UTSW 10 109,552,466 (GRCm39) missense probably damaging 0.99
R0010:Nav3 UTSW 10 109,659,087 (GRCm39) splice site probably benign
R0043:Nav3 UTSW 10 109,603,379 (GRCm39) missense possibly damaging 0.95
R0053:Nav3 UTSW 10 109,602,778 (GRCm39) splice site probably benign
R0053:Nav3 UTSW 10 109,602,778 (GRCm39) splice site probably benign
R0077:Nav3 UTSW 10 109,552,503 (GRCm39) missense possibly damaging 0.87
R0219:Nav3 UTSW 10 109,702,791 (GRCm39) critical splice donor site probably null
R0310:Nav3 UTSW 10 109,602,989 (GRCm39) missense possibly damaging 0.82
R0380:Nav3 UTSW 10 109,594,740 (GRCm39) splice site probably benign
R0403:Nav3 UTSW 10 109,602,964 (GRCm39) missense probably damaging 0.98
R0480:Nav3 UTSW 10 109,689,161 (GRCm39) missense probably damaging 1.00
R0626:Nav3 UTSW 10 109,659,325 (GRCm39) missense probably damaging 1.00
R0637:Nav3 UTSW 10 109,606,058 (GRCm39) missense probably benign 0.25
R0847:Nav3 UTSW 10 109,739,718 (GRCm39) missense possibly damaging 0.94
R0988:Nav3 UTSW 10 109,552,389 (GRCm39) missense probably damaging 1.00
R1272:Nav3 UTSW 10 109,572,860 (GRCm39) missense probably damaging 0.98
R1295:Nav3 UTSW 10 109,527,963 (GRCm39) missense probably damaging 1.00
R1405:Nav3 UTSW 10 109,606,194 (GRCm39) splice site probably benign
R1406:Nav3 UTSW 10 109,719,495 (GRCm39) missense possibly damaging 0.64
R1406:Nav3 UTSW 10 109,719,495 (GRCm39) missense possibly damaging 0.64
R1420:Nav3 UTSW 10 109,659,115 (GRCm39) missense probably benign 0.02
R1449:Nav3 UTSW 10 109,689,372 (GRCm39) missense probably benign 0.13
R1458:Nav3 UTSW 10 109,555,905 (GRCm39) missense probably damaging 1.00
R1469:Nav3 UTSW 10 109,596,369 (GRCm39) missense probably damaging 1.00
R1469:Nav3 UTSW 10 109,596,369 (GRCm39) missense probably damaging 1.00
R1472:Nav3 UTSW 10 109,563,802 (GRCm39) missense probably damaging 0.99
R1537:Nav3 UTSW 10 109,702,846 (GRCm39) missense probably damaging 1.00
R1539:Nav3 UTSW 10 109,603,031 (GRCm39) missense probably damaging 0.99
R1581:Nav3 UTSW 10 109,659,289 (GRCm39) missense probably damaging 1.00
R1586:Nav3 UTSW 10 109,689,115 (GRCm39) missense probably damaging 1.00
R1654:Nav3 UTSW 10 109,688,984 (GRCm39) missense possibly damaging 0.85
R1725:Nav3 UTSW 10 109,659,451 (GRCm39) missense probably damaging 1.00
R1742:Nav3 UTSW 10 109,605,074 (GRCm39) missense probably benign
R1830:Nav3 UTSW 10 109,659,184 (GRCm39) missense probably damaging 1.00
R1834:Nav3 UTSW 10 109,555,883 (GRCm39) missense probably damaging 0.99
R1881:Nav3 UTSW 10 109,688,420 (GRCm39) missense probably damaging 0.96
R1922:Nav3 UTSW 10 109,541,467 (GRCm39) missense probably benign 0.43
R1944:Nav3 UTSW 10 109,552,391 (GRCm39) missense probably damaging 0.99
R1981:Nav3 UTSW 10 109,554,951 (GRCm39) splice site probably benign
R1985:Nav3 UTSW 10 109,606,045 (GRCm39) splice site probably benign
R1996:Nav3 UTSW 10 109,689,262 (GRCm39) missense probably damaging 1.00
R2051:Nav3 UTSW 10 109,660,536 (GRCm39) missense probably damaging 0.99
R2062:Nav3 UTSW 10 109,555,882 (GRCm39) missense probably damaging 1.00
R2139:Nav3 UTSW 10 109,688,996 (GRCm39) missense probably benign 0.22
R2248:Nav3 UTSW 10 109,532,088 (GRCm39) missense probably damaging 1.00
R2420:Nav3 UTSW 10 109,699,674 (GRCm39) missense probably damaging 0.98
R2444:Nav3 UTSW 10 109,600,776 (GRCm39) missense probably benign 0.09
R3026:Nav3 UTSW 10 109,660,465 (GRCm39) missense probably damaging 0.99
R3052:Nav3 UTSW 10 109,739,613 (GRCm39) missense probably damaging 0.99
R3441:Nav3 UTSW 10 109,540,789 (GRCm39) missense probably benign 0.01
R3845:Nav3 UTSW 10 109,689,237 (GRCm39) missense possibly damaging 0.82
R3929:Nav3 UTSW 10 109,520,064 (GRCm39) missense probably damaging 1.00
R3932:Nav3 UTSW 10 109,529,896 (GRCm39) missense probably damaging 0.99
R4056:Nav3 UTSW 10 109,716,394 (GRCm39) critical splice donor site probably null
R4057:Nav3 UTSW 10 109,716,394 (GRCm39) critical splice donor site probably null
R4120:Nav3 UTSW 10 109,739,605 (GRCm39) critical splice donor site probably null
R4244:Nav3 UTSW 10 109,605,157 (GRCm39) missense probably damaging 1.00
R4361:Nav3 UTSW 10 109,688,847 (GRCm39) missense probably damaging 1.00
R4512:Nav3 UTSW 10 109,529,943 (GRCm39) missense possibly damaging 0.89
R4514:Nav3 UTSW 10 109,529,943 (GRCm39) missense possibly damaging 0.89
R4700:Nav3 UTSW 10 109,600,796 (GRCm39) missense probably benign 0.10
R4815:Nav3 UTSW 10 109,659,413 (GRCm39) missense probably benign
R4981:Nav3 UTSW 10 109,716,553 (GRCm39) missense probably benign
R5042:Nav3 UTSW 10 109,605,129 (GRCm39) missense probably benign 0.27
R5251:Nav3 UTSW 10 109,689,114 (GRCm39) missense probably damaging 0.99
R5252:Nav3 UTSW 10 109,550,152 (GRCm39) small deletion probably benign
R5273:Nav3 UTSW 10 109,528,899 (GRCm39) critical splice donor site probably null
R5288:Nav3 UTSW 10 109,688,966 (GRCm39) missense probably benign 0.10
R5407:Nav3 UTSW 10 109,702,796 (GRCm39) missense probably benign 0.28
R5533:Nav3 UTSW 10 109,719,539 (GRCm39) missense possibly damaging 0.61
R5561:Nav3 UTSW 10 109,552,413 (GRCm39) missense probably damaging 1.00
R5577:Nav3 UTSW 10 109,605,264 (GRCm39) missense probably damaging 1.00
R5656:Nav3 UTSW 10 109,600,494 (GRCm39) missense probably damaging 0.96
R5872:Nav3 UTSW 10 109,600,648 (GRCm39) missense probably damaging 1.00
R6023:Nav3 UTSW 10 109,659,376 (GRCm39) missense possibly damaging 0.95
R6061:Nav3 UTSW 10 109,702,845 (GRCm39) nonsense probably null
R6189:Nav3 UTSW 10 109,555,880 (GRCm39) missense probably damaging 0.98
R6214:Nav3 UTSW 10 109,688,426 (GRCm39) missense probably damaging 1.00
R6215:Nav3 UTSW 10 109,688,426 (GRCm39) missense probably damaging 1.00
R6264:Nav3 UTSW 10 109,524,694 (GRCm39) missense probably damaging 0.97
R6500:Nav3 UTSW 10 109,600,617 (GRCm39) missense probably damaging 1.00
R6524:Nav3 UTSW 10 109,555,891 (GRCm39) missense probably damaging 0.99
R6868:Nav3 UTSW 10 109,529,027 (GRCm39) missense possibly damaging 0.49
R7079:Nav3 UTSW 10 109,603,153 (GRCm39) missense probably benign 0.16
R7099:Nav3 UTSW 10 109,539,195 (GRCm39) missense probably benign 0.11
R7139:Nav3 UTSW 10 109,689,338 (GRCm39) missense probably benign 0.44
R7238:Nav3 UTSW 10 109,689,185 (GRCm39) missense possibly damaging 0.75
R7338:Nav3 UTSW 10 109,605,073 (GRCm39) missense probably benign 0.04
R7343:Nav3 UTSW 10 109,739,619 (GRCm39) missense probably damaging 0.98
R7383:Nav3 UTSW 10 109,552,532 (GRCm39) missense probably damaging 0.98
R7391:Nav3 UTSW 10 109,539,317 (GRCm39) missense probably benign 0.07
R7399:Nav3 UTSW 10 109,688,795 (GRCm39) missense possibly damaging 0.74
R7457:Nav3 UTSW 10 109,532,189 (GRCm39) nonsense probably null
R7462:Nav3 UTSW 10 109,659,439 (GRCm39) missense probably damaging 1.00
R7542:Nav3 UTSW 10 109,659,394 (GRCm39) missense possibly damaging 0.89
R7659:Nav3 UTSW 10 109,602,851 (GRCm39) missense probably benign 0.09
R7749:Nav3 UTSW 10 109,539,213 (GRCm39) missense probably damaging 0.99
R7794:Nav3 UTSW 10 109,524,717 (GRCm39) missense probably benign 0.08
R7876:Nav3 UTSW 10 109,689,359 (GRCm39) missense probably benign 0.26
R8048:Nav3 UTSW 10 109,600,779 (GRCm39) missense probably benign 0.13
R8104:Nav3 UTSW 10 109,594,828 (GRCm39) missense probably damaging 0.99
R8125:Nav3 UTSW 10 109,688,520 (GRCm39) missense probably damaging 0.99
R8275:Nav3 UTSW 10 109,527,984 (GRCm39) missense noncoding transcript
R8325:Nav3 UTSW 10 109,541,464 (GRCm39) missense probably benign 0.24
R8336:Nav3 UTSW 10 109,603,430 (GRCm39) missense probably damaging 0.99
R8523:Nav3 UTSW 10 109,659,138 (GRCm39) missense probably damaging 1.00
R8529:Nav3 UTSW 10 109,689,192 (GRCm39) missense probably benign 0.09
R8745:Nav3 UTSW 10 109,659,311 (GRCm39) missense probably benign 0.08
R8752:Nav3 UTSW 10 109,596,165 (GRCm39) intron probably benign
R8794:Nav3 UTSW 10 109,605,032 (GRCm39) nonsense probably null
R8816:Nav3 UTSW 10 109,699,721 (GRCm39) missense possibly damaging 0.69
R9029:Nav3 UTSW 10 109,699,613 (GRCm39) missense possibly damaging 0.68
R9117:Nav3 UTSW 10 109,520,100 (GRCm39) missense probably benign 0.41
R9126:Nav3 UTSW 10 109,541,524 (GRCm39) missense probably benign
R9258:Nav3 UTSW 10 109,550,243 (GRCm39) missense probably damaging 0.99
R9347:Nav3 UTSW 10 109,738,955 (GRCm39) missense probably damaging 0.98
R9353:Nav3 UTSW 10 109,554,065 (GRCm39) missense probably damaging 0.99
R9366:Nav3 UTSW 10 109,659,364 (GRCm39) missense probably damaging 0.99
R9384:Nav3 UTSW 10 109,554,158 (GRCm39) missense probably damaging 0.98
R9428:Nav3 UTSW 10 109,605,176 (GRCm39) missense probably benign
R9454:Nav3 UTSW 10 109,835,864 (GRCm39) missense probably benign 0.01
R9516:Nav3 UTSW 10 109,520,015 (GRCm39) missense probably damaging 1.00
R9521:Nav3 UTSW 10 109,835,845 (GRCm39) missense possibly damaging 0.95
R9622:Nav3 UTSW 10 109,603,103 (GRCm39) missense probably benign
R9689:Nav3 UTSW 10 109,605,034 (GRCm39) missense probably damaging 1.00
R9796:Nav3 UTSW 10 109,527,969 (GRCm39) missense probably damaging 0.99
X0012:Nav3 UTSW 10 109,527,958 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTGACTGTTTGTAAAAGCAGCC -3'
(R):5'- TTCCTTCAGGGGTAGAAGAAAATAG -3'

Sequencing Primer
(F):5'- TGTAAAAGCAGCCTTTGTATGC -3'
(R):5'- TTCAGGGGTAGAAGAAAATAGTTTGG -3'
Posted On 2014-06-23