Incidental Mutation 'R2327:Vps13c'
ID 245711
Institutional Source Beutler Lab
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
MMRRC Submission 040318-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2327 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 67747678-67902920 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 67821102 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Threonine at position 1204 (N1204T)
Ref Sequence ENSEMBL: ENSMUSP00000077040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077879]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000077879
AA Change: N1204T

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: N1204T

DomainStartEndE-ValueType
Pfam:Chorein_N 3 117 1.3e-39 PFAM
low complexity region 151 165 N/A INTRINSIC
Pfam:VPS13 182 414 7.9e-70 PFAM
coiled coil region 422 443 N/A INTRINSIC
low complexity region 479 490 N/A INTRINSIC
Pfam:VPS13_mid_rpt 611 832 7.8e-71 PFAM
low complexity region 867 885 N/A INTRINSIC
low complexity region 1020 1036 N/A INTRINSIC
low complexity region 1112 1123 N/A INTRINSIC
Pfam:VPS13_mid_rpt 1172 1369 2.1e-14 PFAM
low complexity region 1552 1573 N/A INTRINSIC
Pfam:VPS13_mid_rpt 1685 1883 2.8e-13 PFAM
Blast:INB 2128 2403 2e-48 BLAST
Pfam:SHR-BD 2759 3013 9.9e-32 PFAM
Pfam:VPS13_C 3317 3495 5.7e-65 PFAM
Pfam:ATG_C 3498 3588 7.9e-12 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.2%
  • 20x: 94.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]
Allele List at MGI

All alleles(13) : Targeted, other(2) Gene trapped(11)

Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930578I06Rik A T 14: 64,208,569 (GRCm39) probably null Het
Agbl4 T G 4: 111,383,798 (GRCm39) S218A probably benign Het
Apol11b T C 15: 77,522,153 (GRCm39) E48G probably damaging Het
Atp4a T A 7: 30,419,666 (GRCm39) N676K probably benign Het
Capn5 T A 7: 97,775,574 (GRCm39) S456C probably benign Het
Ccar1 T C 10: 62,600,161 (GRCm39) Y590C probably damaging Het
Ccdc188 G T 16: 18,037,070 (GRCm39) G283W probably damaging Het
Cd69 A G 6: 129,248,351 (GRCm39) V45A probably damaging Het
Col3a1 G T 1: 45,377,771 (GRCm39) probably benign Het
Cyb561a3 A T 19: 10,564,166 (GRCm39) T169S probably benign Het
Cyp2c39 A T 19: 39,527,397 (GRCm39) I248L probably benign Het
Cyp2j13 T C 4: 95,947,344 (GRCm39) T236A possibly damaging Het
Efs A G 14: 55,154,961 (GRCm39) V426A probably benign Het
Eme2 A G 17: 25,113,157 (GRCm39) L136S probably damaging Het
Fastkd1 T A 2: 69,535,872 (GRCm39) K312* probably null Het
Fbxl12 A G 9: 20,553,530 (GRCm39) L19P probably damaging Het
Flg2 T A 3: 93,110,913 (GRCm39) Y980* probably null Het
Fscn2 T A 11: 120,257,527 (GRCm39) I296N probably damaging Het
Gabrg3 A G 7: 56,384,835 (GRCm39) V242A probably benign Het
Galk2 A G 2: 125,817,315 (GRCm39) H368R probably damaging Het
Gm12695 C T 4: 96,657,893 (GRCm39) S92N probably benign Het
Gpalpp1 A T 14: 76,336,031 (GRCm39) S196T probably benign Het
Gpld1 A T 13: 25,168,804 (GRCm39) M773L probably benign Het
Haus8 A G 8: 71,708,289 (GRCm39) probably null Het
Hirip3 A G 7: 126,462,038 (GRCm39) R19G probably damaging Het
Inpp4a A G 1: 37,405,247 (GRCm39) T92A probably damaging Het
Irgm2 A G 11: 58,111,218 (GRCm39) D303G probably damaging Het
Kpna2rt C A 17: 90,217,697 (GRCm39) R16S probably benign Het
Krtap5-2 T G 7: 141,728,748 (GRCm39) S311R unknown Het
Krtdap T A 7: 30,489,185 (GRCm39) probably null Het
Lce1g G T 3: 92,658,140 (GRCm39) S56Y unknown Het
Lrrn1 G A 6: 107,545,794 (GRCm39) V531I probably benign Het
Mctp2 T C 7: 71,861,358 (GRCm39) E429G probably damaging Het
Mrgpra2b T G 7: 47,113,793 (GRCm39) D287A probably damaging Het
Mterf3 T C 13: 67,076,258 (GRCm39) T150A probably damaging Het
Mtus2 A G 5: 148,014,725 (GRCm39) N506S probably benign Het
Myh15 G T 16: 48,963,313 (GRCm39) V1085L probably benign Het
Myo9a A G 9: 59,687,048 (GRCm39) N51S probably benign Het
Nlrc3 A T 16: 3,771,304 (GRCm39) L196Q probably damaging Het
Nlrp9c T A 7: 26,074,747 (GRCm39) N816I probably damaging Het
Nsun2 T C 13: 69,767,700 (GRCm39) V218A probably benign Het
Nt5dc1 T C 10: 34,189,673 (GRCm39) E339G possibly damaging Het
Or10ak14 C T 4: 118,611,331 (GRCm39) V135I probably benign Het
Or51b6b A G 7: 103,309,779 (GRCm39) V226A probably damaging Het
Or8j3c A T 2: 86,253,165 (GRCm39) L285* probably null Het
Pik3ap1 A G 19: 41,284,828 (GRCm39) I619T probably damaging Het
Plk1 A G 7: 121,759,118 (GRCm39) D118G probably benign Het
Ppat T C 5: 77,070,314 (GRCm39) D168G possibly damaging Het
Preb T C 5: 31,115,849 (GRCm39) E198G probably damaging Het
Psg21 T C 7: 18,386,378 (GRCm39) T203A possibly damaging Het
Rbm17 A G 2: 11,602,942 (GRCm39) V54A probably damaging Het
Rgma T A 7: 73,067,574 (GRCm39) D276E probably damaging Het
Ric8a T C 7: 140,439,471 (GRCm39) L77P probably damaging Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Scarf1 A C 11: 75,416,854 (GRCm39) E765D probably damaging Het
Scart1 A T 7: 139,803,890 (GRCm39) N363Y possibly damaging Het
Sec14l4 G A 11: 3,990,041 (GRCm39) M113I probably benign Het
Senp1 C T 15: 97,980,165 (GRCm39) C60Y probably damaging Het
Slc22a21 T A 11: 53,842,130 (GRCm39) K549N probably benign Het
Slc39a10 T C 1: 46,875,156 (GRCm39) S49G probably damaging Het
Spata13 T C 14: 60,947,004 (GRCm39) M684T probably damaging Het
Spns1 T C 7: 125,969,958 (GRCm39) T481A probably damaging Het
Stag1 A G 9: 100,668,666 (GRCm39) Y198C possibly damaging Het
Tgfbr1 T A 4: 47,402,833 (GRCm39) V210E probably damaging Het
Tnc C T 4: 63,893,475 (GRCm39) E1604K possibly damaging Het
Tspan31 T C 10: 126,904,365 (GRCm39) D143G probably benign Het
Tspan5 T A 3: 138,603,903 (GRCm39) Y131* probably null Het
Ttc21a A G 9: 119,795,189 (GRCm39) D1070G probably damaging Het
Vmn2r26 C T 6: 124,016,708 (GRCm39) P391S probably benign Het
Vmn2r72 A G 7: 85,387,464 (GRCm39) I700T probably damaging Het
Zfhx4 C T 3: 5,468,418 (GRCm39) P2859S probably benign Het
Other mutations in Vps13c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Vps13c APN 9 67,853,281 (GRCm39) missense probably benign 0.20
IGL00336:Vps13c APN 9 67,853,224 (GRCm39) missense probably benign 0.01
IGL00418:Vps13c APN 9 67,783,544 (GRCm39) missense probably damaging 1.00
IGL00481:Vps13c APN 9 67,768,147 (GRCm39) missense probably damaging 1.00
IGL00491:Vps13c APN 9 67,800,418 (GRCm39) missense probably damaging 1.00
IGL00558:Vps13c APN 9 67,845,139 (GRCm39) missense possibly damaging 0.52
IGL00811:Vps13c APN 9 67,855,463 (GRCm39) missense probably damaging 0.99
IGL01011:Vps13c APN 9 67,834,237 (GRCm39) missense probably damaging 0.98
IGL01094:Vps13c APN 9 67,793,566 (GRCm39) missense probably damaging 1.00
IGL01330:Vps13c APN 9 67,871,390 (GRCm39) missense probably damaging 1.00
IGL01402:Vps13c APN 9 67,820,486 (GRCm39) critical splice acceptor site probably null
IGL01404:Vps13c APN 9 67,820,486 (GRCm39) critical splice acceptor site probably null
IGL01470:Vps13c APN 9 67,820,209 (GRCm39) splice site probably benign
IGL01615:Vps13c APN 9 67,863,063 (GRCm39) missense probably benign 0.01
IGL01694:Vps13c APN 9 67,802,631 (GRCm39) missense probably damaging 1.00
IGL01752:Vps13c APN 9 67,855,510 (GRCm39) missense probably damaging 1.00
IGL01810:Vps13c APN 9 67,863,062 (GRCm39) missense probably benign
IGL01954:Vps13c APN 9 67,876,580 (GRCm39) missense probably damaging 0.98
IGL01978:Vps13c APN 9 67,837,925 (GRCm39) missense probably benign 0.03
IGL01998:Vps13c APN 9 67,862,350 (GRCm39) splice site probably null
IGL02201:Vps13c APN 9 67,874,418 (GRCm39) missense probably damaging 1.00
IGL02205:Vps13c APN 9 67,790,736 (GRCm39) missense probably damaging 1.00
IGL02303:Vps13c APN 9 67,852,763 (GRCm39) splice site probably benign
IGL02322:Vps13c APN 9 67,845,183 (GRCm39) missense probably benign 0.02
IGL02456:Vps13c APN 9 67,860,258 (GRCm39) missense probably damaging 1.00
IGL02474:Vps13c APN 9 67,845,158 (GRCm39) missense probably benign 0.00
IGL02547:Vps13c APN 9 67,815,301 (GRCm39) missense possibly damaging 0.83
IGL02640:Vps13c APN 9 67,793,530 (GRCm39) splice site probably benign
IGL02673:Vps13c APN 9 67,785,380 (GRCm39) missense probably damaging 1.00
IGL02721:Vps13c APN 9 67,871,431 (GRCm39) splice site probably benign
IGL02834:Vps13c APN 9 67,845,137 (GRCm39) missense probably benign
IGL02838:Vps13c APN 9 67,883,133 (GRCm39) missense probably damaging 1.00
IGL03136:Vps13c APN 9 67,857,592 (GRCm39) missense probably damaging 1.00
IGL03137:Vps13c APN 9 67,797,662 (GRCm39) missense probably damaging 1.00
IGL03214:Vps13c APN 9 67,804,477 (GRCm39) missense probably null 0.81
IGL03240:Vps13c APN 9 67,862,329 (GRCm39) missense probably benign
IGL03303:Vps13c APN 9 67,841,786 (GRCm39) missense probably benign 0.27
IGL03336:Vps13c APN 9 67,858,924 (GRCm39) missense possibly damaging 0.76
IGL03366:Vps13c APN 9 67,853,308 (GRCm39) missense probably benign 0.00
Derivative UTSW 9 67,837,904 (GRCm39) missense possibly damaging 0.79
diversion UTSW 9 67,817,515 (GRCm39) missense possibly damaging 0.93
introversion UTSW 9 67,851,328 (GRCm39) missense probably damaging 0.98
Inversion UTSW 9 67,810,121 (GRCm39) critical splice acceptor site probably null
subversion UTSW 9 67,815,334 (GRCm39) missense probably damaging 1.00
Transversion UTSW 9 67,841,783 (GRCm39) missense probably damaging 0.98
3-1:Vps13c UTSW 9 67,843,655 (GRCm39) missense probably benign 0.00
IGL02991:Vps13c UTSW 9 67,821,159 (GRCm39) missense probably damaging 1.00
PIT4802001:Vps13c UTSW 9 67,845,068 (GRCm39) missense probably damaging 1.00
R0008:Vps13c UTSW 9 67,826,544 (GRCm39) missense probably benign
R0206:Vps13c UTSW 9 67,846,444 (GRCm39) splice site probably benign
R0288:Vps13c UTSW 9 67,834,648 (GRCm39) missense probably damaging 0.99
R0324:Vps13c UTSW 9 67,871,591 (GRCm39) missense possibly damaging 0.95
R0347:Vps13c UTSW 9 67,817,515 (GRCm39) missense possibly damaging 0.93
R0374:Vps13c UTSW 9 67,793,528 (GRCm39) splice site probably benign
R0388:Vps13c UTSW 9 67,830,197 (GRCm39) splice site probably benign
R0409:Vps13c UTSW 9 67,858,926 (GRCm39) missense probably benign 0.00
R0440:Vps13c UTSW 9 67,880,143 (GRCm39) missense probably damaging 1.00
R0513:Vps13c UTSW 9 67,838,017 (GRCm39) missense probably benign 0.02
R0520:Vps13c UTSW 9 67,853,133 (GRCm39) missense possibly damaging 0.88
R0569:Vps13c UTSW 9 67,881,001 (GRCm39) missense probably damaging 0.98
R0601:Vps13c UTSW 9 67,834,754 (GRCm39) missense probably benign 0.12
R0659:Vps13c UTSW 9 67,828,217 (GRCm39) missense probably benign 0.11
R0667:Vps13c UTSW 9 67,858,855 (GRCm39) nonsense probably null
R0670:Vps13c UTSW 9 67,833,139 (GRCm39) missense probably benign 0.35
R0698:Vps13c UTSW 9 67,797,005 (GRCm39) missense probably benign 0.45
R0729:Vps13c UTSW 9 67,868,931 (GRCm39) missense probably damaging 1.00
R0781:Vps13c UTSW 9 67,879,285 (GRCm39) missense probably damaging 1.00
R0811:Vps13c UTSW 9 67,841,758 (GRCm39) missense probably benign 0.06
R0812:Vps13c UTSW 9 67,841,758 (GRCm39) missense probably benign 0.06
R0839:Vps13c UTSW 9 67,806,020 (GRCm39) missense probably benign
R1373:Vps13c UTSW 9 67,834,793 (GRCm39) missense probably damaging 0.99
R1396:Vps13c UTSW 9 67,862,304 (GRCm39) missense probably benign 0.00
R1499:Vps13c UTSW 9 67,864,787 (GRCm39) missense probably benign 0.00
R1556:Vps13c UTSW 9 67,837,993 (GRCm39) missense probably damaging 0.98
R1560:Vps13c UTSW 9 67,843,745 (GRCm39) critical splice donor site probably null
R1584:Vps13c UTSW 9 67,800,394 (GRCm39) missense possibly damaging 0.74
R1654:Vps13c UTSW 9 67,858,969 (GRCm39) missense probably damaging 1.00
R1674:Vps13c UTSW 9 67,760,985 (GRCm39) nonsense probably null
R1676:Vps13c UTSW 9 67,834,244 (GRCm39) missense probably benign 0.20
R1695:Vps13c UTSW 9 67,879,357 (GRCm39) nonsense probably null
R1710:Vps13c UTSW 9 67,818,811 (GRCm39) missense probably benign 0.00
R1769:Vps13c UTSW 9 67,873,003 (GRCm39) missense probably benign 0.00
R1775:Vps13c UTSW 9 67,788,729 (GRCm39) missense probably damaging 1.00
R1795:Vps13c UTSW 9 67,801,267 (GRCm39) nonsense probably null
R1799:Vps13c UTSW 9 67,851,399 (GRCm39) missense probably damaging 0.98
R1835:Vps13c UTSW 9 67,900,295 (GRCm39) missense probably benign 0.08
R1848:Vps13c UTSW 9 67,843,622 (GRCm39) missense probably benign
R1903:Vps13c UTSW 9 67,801,334 (GRCm39) missense probably damaging 1.00
R1944:Vps13c UTSW 9 67,793,558 (GRCm39) missense probably damaging 1.00
R1945:Vps13c UTSW 9 67,793,558 (GRCm39) missense probably damaging 1.00
R1951:Vps13c UTSW 9 67,881,041 (GRCm39) critical splice donor site probably null
R1993:Vps13c UTSW 9 67,883,138 (GRCm39) missense probably damaging 1.00
R2023:Vps13c UTSW 9 67,843,567 (GRCm39) splice site probably benign
R2059:Vps13c UTSW 9 67,768,115 (GRCm39) missense probably damaging 1.00
R2086:Vps13c UTSW 9 67,857,571 (GRCm39) missense probably benign 0.29
R2120:Vps13c UTSW 9 67,826,616 (GRCm39) missense possibly damaging 0.92
R2249:Vps13c UTSW 9 67,895,335 (GRCm39) critical splice donor site probably null
R2257:Vps13c UTSW 9 67,860,228 (GRCm39) missense possibly damaging 0.87
R2258:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2259:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2260:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2265:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2266:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2269:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2278:Vps13c UTSW 9 67,846,354 (GRCm39) missense probably benign
R2306:Vps13c UTSW 9 67,895,275 (GRCm39) missense probably damaging 0.99
R2349:Vps13c UTSW 9 67,864,808 (GRCm39) missense possibly damaging 0.89
R2483:Vps13c UTSW 9 67,883,189 (GRCm39) critical splice donor site probably null
R3031:Vps13c UTSW 9 67,831,052 (GRCm39) missense probably benign 0.00
R3623:Vps13c UTSW 9 67,883,189 (GRCm39) critical splice donor site probably null
R3870:Vps13c UTSW 9 67,792,008 (GRCm39) missense probably benign 0.00
R4173:Vps13c UTSW 9 67,843,595 (GRCm39) missense probably benign 0.00
R4445:Vps13c UTSW 9 67,889,777 (GRCm39) splice site probably null
R4491:Vps13c UTSW 9 67,817,475 (GRCm39) missense probably benign
R4505:Vps13c UTSW 9 67,846,316 (GRCm39) missense probably benign 0.02
R4574:Vps13c UTSW 9 67,858,965 (GRCm39) missense probably damaging 1.00
R4691:Vps13c UTSW 9 67,860,217 (GRCm39) missense possibly damaging 0.95
R4766:Vps13c UTSW 9 67,785,506 (GRCm39) splice site probably null
R4771:Vps13c UTSW 9 67,836,821 (GRCm39) missense probably benign
R4801:Vps13c UTSW 9 67,871,564 (GRCm39) missense probably damaging 1.00
R4802:Vps13c UTSW 9 67,871,564 (GRCm39) missense probably damaging 1.00
R4962:Vps13c UTSW 9 67,781,173 (GRCm39) missense probably damaging 1.00
R4995:Vps13c UTSW 9 67,826,603 (GRCm39) missense probably benign 0.00
R5010:Vps13c UTSW 9 67,823,661 (GRCm39) missense probably benign 0.19
R5183:Vps13c UTSW 9 67,815,334 (GRCm39) missense probably damaging 1.00
R5226:Vps13c UTSW 9 67,852,835 (GRCm39) missense probably benign 0.17
R5297:Vps13c UTSW 9 67,785,413 (GRCm39) missense probably damaging 1.00
R5456:Vps13c UTSW 9 67,834,729 (GRCm39) missense possibly damaging 0.53
R5494:Vps13c UTSW 9 67,855,428 (GRCm39) missense probably benign 0.00
R5521:Vps13c UTSW 9 67,858,721 (GRCm39) missense probably benign 0.08
R5524:Vps13c UTSW 9 67,864,838 (GRCm39) missense probably damaging 1.00
R5685:Vps13c UTSW 9 67,870,455 (GRCm39) missense possibly damaging 0.64
R5731:Vps13c UTSW 9 67,802,661 (GRCm39) missense probably damaging 1.00
R5812:Vps13c UTSW 9 67,889,777 (GRCm39) splice site probably benign
R5867:Vps13c UTSW 9 67,889,904 (GRCm39) splice site probably null
R5893:Vps13c UTSW 9 67,810,121 (GRCm39) critical splice acceptor site probably null
R5902:Vps13c UTSW 9 67,841,729 (GRCm39) missense probably benign 0.00
R5957:Vps13c UTSW 9 67,862,253 (GRCm39) missense probably damaging 1.00
R6076:Vps13c UTSW 9 67,818,884 (GRCm39) missense probably damaging 1.00
R6187:Vps13c UTSW 9 67,822,939 (GRCm39) missense probably damaging 1.00
R6268:Vps13c UTSW 9 67,858,731 (GRCm39) missense probably benign 0.10
R6547:Vps13c UTSW 9 67,880,647 (GRCm39) missense probably damaging 1.00
R6716:Vps13c UTSW 9 67,858,749 (GRCm39) missense probably benign 0.00
R6837:Vps13c UTSW 9 67,817,504 (GRCm39) missense probably benign
R6919:Vps13c UTSW 9 67,834,734 (GRCm39) missense probably damaging 0.97
R7039:Vps13c UTSW 9 67,845,045 (GRCm39) missense probably damaging 1.00
R7058:Vps13c UTSW 9 67,831,110 (GRCm39) missense probably benign 0.39
R7082:Vps13c UTSW 9 67,790,735 (GRCm39) missense probably damaging 1.00
R7195:Vps13c UTSW 9 67,853,107 (GRCm39) missense possibly damaging 0.95
R7244:Vps13c UTSW 9 67,797,086 (GRCm39) missense probably benign 0.00
R7300:Vps13c UTSW 9 67,847,826 (GRCm39) missense probably benign 0.20
R7314:Vps13c UTSW 9 67,850,622 (GRCm39) splice site probably null
R7352:Vps13c UTSW 9 67,747,728 (GRCm39) missense possibly damaging 0.94
R7368:Vps13c UTSW 9 67,821,355 (GRCm39) missense probably benign 0.23
R7411:Vps13c UTSW 9 67,879,283 (GRCm39) missense probably damaging 0.98
R7497:Vps13c UTSW 9 67,747,761 (GRCm39) missense probably damaging 1.00
R7516:Vps13c UTSW 9 67,862,289 (GRCm39) missense possibly damaging 0.89
R7638:Vps13c UTSW 9 67,852,791 (GRCm39) missense probably damaging 1.00
R7732:Vps13c UTSW 9 67,847,798 (GRCm39) missense probably damaging 0.97
R7748:Vps13c UTSW 9 67,870,371 (GRCm39) missense probably benign 0.03
R7779:Vps13c UTSW 9 67,788,704 (GRCm39) missense probably damaging 1.00
R7788:Vps13c UTSW 9 67,847,765 (GRCm39) missense probably benign 0.01
R7894:Vps13c UTSW 9 67,834,265 (GRCm39) missense probably damaging 0.99
R8163:Vps13c UTSW 9 67,857,720 (GRCm39) missense probably benign 0.08
R8165:Vps13c UTSW 9 67,766,072 (GRCm39) missense probably benign 0.00
R8202:Vps13c UTSW 9 67,851,328 (GRCm39) missense probably damaging 0.98
R8235:Vps13c UTSW 9 67,863,063 (GRCm39) missense probably benign 0.01
R8235:Vps13c UTSW 9 67,834,678 (GRCm39) missense probably damaging 1.00
R8253:Vps13c UTSW 9 67,850,770 (GRCm39) nonsense probably null
R8261:Vps13c UTSW 9 67,862,262 (GRCm39) missense probably damaging 1.00
R8348:Vps13c UTSW 9 67,786,385 (GRCm39) missense possibly damaging 0.79
R8547:Vps13c UTSW 9 67,852,848 (GRCm39) missense probably damaging 1.00
R8734:Vps13c UTSW 9 67,880,685 (GRCm39) missense probably damaging 1.00
R8806:Vps13c UTSW 9 67,853,110 (GRCm39) missense probably damaging 1.00
R8807:Vps13c UTSW 9 67,766,122 (GRCm39) missense probably damaging 0.99
R8813:Vps13c UTSW 9 67,778,566 (GRCm39) missense probably damaging 1.00
R8883:Vps13c UTSW 9 67,855,479 (GRCm39) missense probably benign 0.10
R8885:Vps13c UTSW 9 67,850,736 (GRCm39) missense probably benign
R8899:Vps13c UTSW 9 67,841,783 (GRCm39) missense probably damaging 0.98
R8970:Vps13c UTSW 9 67,852,803 (GRCm39) missense probably benign 0.11
R9007:Vps13c UTSW 9 67,845,006 (GRCm39) missense probably benign 0.00
R9026:Vps13c UTSW 9 67,861,863 (GRCm39) missense probably damaging 1.00
R9029:Vps13c UTSW 9 67,855,429 (GRCm39) missense probably damaging 0.98
R9057:Vps13c UTSW 9 67,828,209 (GRCm39) missense probably benign 0.00
R9105:Vps13c UTSW 9 67,778,081 (GRCm39) intron probably benign
R9130:Vps13c UTSW 9 67,836,805 (GRCm39) missense probably damaging 1.00
R9286:Vps13c UTSW 9 67,880,203 (GRCm39) missense probably benign 0.00
R9338:Vps13c UTSW 9 67,858,977 (GRCm39) missense probably damaging 1.00
R9432:Vps13c UTSW 9 67,830,137 (GRCm39) missense probably benign 0.02
R9460:Vps13c UTSW 9 67,837,904 (GRCm39) missense possibly damaging 0.79
R9464:Vps13c UTSW 9 67,858,674 (GRCm39) missense probably damaging 1.00
R9561:Vps13c UTSW 9 67,872,794 (GRCm39) missense probably damaging 1.00
R9609:Vps13c UTSW 9 67,841,831 (GRCm39) missense probably damaging 1.00
R9622:Vps13c UTSW 9 67,856,715 (GRCm39) missense probably damaging 1.00
R9665:Vps13c UTSW 9 67,863,025 (GRCm39) nonsense probably null
R9731:Vps13c UTSW 9 67,826,526 (GRCm39) missense probably benign
R9763:Vps13c UTSW 9 67,818,860 (GRCm39) missense probably benign 0.00
R9774:Vps13c UTSW 9 67,791,873 (GRCm39) missense possibly damaging 0.85
R9798:Vps13c UTSW 9 67,826,646 (GRCm39) missense probably damaging 1.00
U24488:Vps13c UTSW 9 67,813,198 (GRCm39) missense probably benign 0.13
X0021:Vps13c UTSW 9 67,845,063 (GRCm39) missense probably damaging 0.99
X0058:Vps13c UTSW 9 67,834,701 (GRCm39) missense probably damaging 1.00
X0065:Vps13c UTSW 9 67,781,145 (GRCm39) missense probably damaging 1.00
Z1088:Vps13c UTSW 9 67,821,257 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCAAAGCTGGGCAGTGACTG -3'
(R):5'- AGACACCAGACTGAACCGATTG -3'

Sequencing Primer
(F):5'- CAGTGACTGAGGATGGCC -3'
(R):5'- AGACTGAACCGATTGTGAACTC -3'
Posted On 2014-10-30