Incidental Mutation 'R2265:Vps13c'
ID 244083
Institutional Source Beutler Lab
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
MMRRC Submission 040265-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2265 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 67747678-67902920 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 67828229 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 1461 (V1461A)
Ref Sequence ENSEMBL: ENSMUSP00000077040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077879]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000077879
AA Change: V1461A

PolyPhen 2 Score 0.820 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: V1461A

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
Meta Mutation Damage Score 0.1528 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 94.9%
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: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830018L16Rik T C 1: 12,042,328 (GRCm39) probably null Het
Aadac T A 3: 59,944,737 (GRCm39) D136E probably damaging Het
Abca16 A G 7: 120,030,383 (GRCm39) D165G probably benign Het
Adam24 T A 8: 41,133,110 (GRCm39) S193T possibly damaging Het
Adra2b T C 2: 127,205,791 (GRCm39) S103P probably damaging Het
Agrn C T 4: 156,263,675 (GRCm39) G173R probably damaging Het
Alg11 T A 8: 22,555,630 (GRCm39) V255E probably benign Het
Aox1 C A 1: 58,120,679 (GRCm39) D857E probably damaging Het
Apob T C 12: 8,065,475 (GRCm39) F4115S possibly damaging Het
Bdkrb2 A G 12: 105,558,484 (GRCm39) T242A probably benign Het
Cdca7 T C 2: 72,312,834 (GRCm39) L190P probably benign Het
Cenpe A G 3: 134,967,397 (GRCm39) T2180A probably benign Het
Cep41 T A 6: 30,660,915 (GRCm39) I126F possibly damaging Het
Col16a1 C A 4: 129,946,711 (GRCm39) H111Q probably benign Het
Cops3 T C 11: 59,718,716 (GRCm39) T193A probably benign Het
Dbr1 G A 9: 99,461,463 (GRCm39) V153M probably damaging Het
Ddx4 A G 13: 112,757,810 (GRCm39) Y290H probably benign Het
Dgkb T A 12: 38,240,107 (GRCm39) S461R possibly damaging Het
Dipk2b A G X: 18,289,926 (GRCm39) S179P possibly damaging Het
Dnajc28 T C 16: 91,413,200 (GRCm39) N372S probably benign Het
Dner CGCTGCTGCTGCTGCTGCTGCTGCTGC CGCTGCTGCTGCTGCTGCTGCTGC 1: 84,563,270 (GRCm39) probably benign Het
Dock3 C A 9: 106,818,525 (GRCm39) V1190F probably damaging Het
Exosc1 A G 19: 41,919,857 (GRCm39) S54P probably damaging Het
Fbxw22 C T 9: 109,213,062 (GRCm39) R295K probably benign Het
Foxo1 T C 3: 52,253,333 (GRCm39) S499P probably benign Het
Heatr5a T C 12: 51,940,528 (GRCm39) D1444G possibly damaging Het
Hspa2 T G 12: 76,452,962 (GRCm39) I552S probably benign Het
Imp4 T A 1: 34,482,928 (GRCm39) I173N probably damaging Het
Itgal A G 7: 126,905,873 (GRCm39) I352V possibly damaging Het
Kcnh6 G A 11: 105,924,643 (GRCm39) R816Q probably benign Het
Kcnh8 GAGACCAACGAGCAGCTGATGCTTCAGA GAGA 17: 53,032,934 (GRCm39) 74 probably benign Het
Kcnip3 G T 2: 127,306,981 (GRCm39) A173D probably benign Het
Kir3dl1 A G X: 135,425,784 (GRCm39) R53G probably benign Het
Klhl31 A G 9: 77,557,440 (GRCm39) D52G possibly damaging Het
Klk1b21 T C 7: 43,753,863 (GRCm39) I49T possibly damaging Het
Lama2 T A 10: 26,868,932 (GRCm39) I2838F probably damaging Het
Lilrb4a T A 10: 51,367,633 (GRCm39) Y58* probably null Het
Lsmem1 GTACATACATACATACATACATACATACA GTACATACATACATACATACATACATACATACA 12: 40,235,260 (GRCm39) probably null Het
Mpdz A G 4: 81,301,628 (GRCm39) S266P probably damaging Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Mroh7 T C 4: 106,578,124 (GRCm39) N185D probably benign Het
Mybphl A G 3: 108,272,317 (GRCm39) E2G probably damaging Het
Mycbp2 T C 14: 103,500,185 (GRCm39) D937G probably benign Het
Myo18b A G 5: 112,930,539 (GRCm39) M1799T probably damaging Het
Nr4a2 T A 2: 57,002,018 (GRCm39) D145V possibly damaging Het
Ntmt1 C A 2: 30,710,472 (GRCm39) N58K probably benign Het
Or10ak16 A T 4: 118,751,071 (GRCm39) R264W probably damaging Het
Or2m12 A G 16: 19,105,305 (GRCm39) Y63H probably damaging Het
Or4f54 A G 2: 111,123,524 (GRCm39) T304A probably benign Het
Or51f1d G A 7: 102,701,344 (GRCm39) V280I probably benign Het
Or52n20 T C 7: 104,320,067 (GRCm39) F53L probably benign Het
Or8k28 T C 2: 86,286,558 (GRCm39) Y19C possibly damaging Het
Ovch2 A T 7: 107,383,782 (GRCm39) M521K probably damaging Het
P2ry13 T C 3: 59,117,449 (GRCm39) M110V probably damaging Het
P2ry14 T C 3: 59,022,992 (GRCm39) N165S probably damaging Het
Pcdhb19 A T 18: 37,630,736 (GRCm39) H177L probably damaging Het
Phf8 T C X: 150,355,597 (GRCm39) L520S possibly damaging Het
Pjvk T G 2: 76,487,797 (GRCm39) S230A possibly damaging Het
Plch2 T C 4: 155,077,461 (GRCm39) E423G probably benign Het
Rad9b T C 5: 122,489,405 (GRCm39) Y41C probably damaging Het
Ranbp3l A T 15: 9,057,194 (GRCm39) I286F probably damaging Het
Rtel1 T A 2: 180,996,161 (GRCm39) V739D probably damaging Het
Slc35a3 T C 3: 116,467,285 (GRCm39) K325E possibly damaging Het
Spag17 C A 3: 99,969,182 (GRCm39) probably null Het
Spg11 A T 2: 121,938,788 (GRCm39) C389S possibly damaging Het
Srsf4 T C 4: 131,624,993 (GRCm39) V130A probably damaging Het
Taar8b T C 10: 23,967,270 (GRCm39) N308S probably damaging Het
Tas2r117 T A 6: 132,780,188 (GRCm39) C109S probably benign Het
Tlr5 T A 1: 182,802,600 (GRCm39) S635T possibly damaging Het
Ttc21a G T 9: 119,788,074 (GRCm39) C833F possibly damaging Het
Vash2 T C 1: 190,682,410 (GRCm39) N347D probably damaging Het
Vcp G A 4: 42,980,833 (GRCm39) A759V possibly damaging Het
Vmn2r18 T C 5: 151,510,127 (GRCm39) E82G probably damaging Het
Zfp616 T C 11: 73,976,289 (GRCm39) Y853H possibly damaging 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
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
R2327:Vps13c UTSW 9 67,821,102 (GRCm39) missense probably damaging 0.98
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'- ACAGTGGTGGTATCTCAAATGC -3'
(R):5'- TCACCAACACACTGTATATGTAAGG -3'

Sequencing Primer
(F):5'- TGGAACTCACTTTGTAGACCACG -3'
(R):5'- CTGTATATGTAAGGAATAGACACAGC -3'
Posted On 2014-10-16