Incidental Mutation 'R7195:Vps13c'
ID 559865
Institutional Source Beutler Lab
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
MMRRC Submission 045336-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7195 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 67747678-67902920 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 67853107 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Aspartic acid at position 2400 (G2400D)
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: G2400D

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: G2400D

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: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.8%
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: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930438A08Rik T C 11: 58,179,242 (GRCm39) probably null Het
Abca2 A G 2: 25,332,088 (GRCm39) D1400G probably benign Het
Actl11 A T 9: 107,806,069 (GRCm39) K131* probably null Het
Adam39 A T 8: 41,277,812 (GRCm39) R68* probably null Het
Akap7 A T 10: 25,147,405 (GRCm39) N108K probably damaging Het
Arhgef10l C A 4: 140,338,721 (GRCm39) A14S probably benign Het
Ccdc141 T G 2: 76,879,927 (GRCm39) N632T probably benign Het
Ccm2 T C 11: 6,546,302 (GRCm39) S435P probably damaging Het
Cd36 A G 5: 18,019,187 (GRCm39) L178P probably damaging Het
Cd7 T C 11: 120,929,075 (GRCm39) I59V probably benign Het
Cds2 T A 2: 132,135,204 (GRCm39) S32T probably benign Het
Cep19 A G 16: 31,925,904 (GRCm39) D104G probably damaging Het
Col1a2 C T 6: 4,510,753 (GRCm39) P68S unknown Het
Col20a1 A G 2: 180,649,024 (GRCm39) H1011R probably damaging Het
Cspg4b A T 13: 113,504,463 (GRCm39) D1864V Het
D7Ertd443e A G 7: 133,896,851 (GRCm39) V513A probably damaging Het
Egfr C T 11: 16,818,162 (GRCm39) P228L probably damaging Het
Fam243 C T 16: 92,118,037 (GRCm39) V84M probably damaging Het
Fam78b A G 1: 166,906,131 (GRCm39) R97G probably damaging Het
Flt1 C T 5: 147,540,386 (GRCm39) V768M probably damaging Het
Gdap1l1 A T 2: 163,288,050 (GRCm39) N96Y probably damaging Het
Gm7168 T A 17: 14,169,622 (GRCm39) Y330N probably benign Het
Hnrnpul1 T C 7: 25,424,203 (GRCm39) N683S unknown Het
Ice2 C T 9: 69,335,782 (GRCm39) P922S possibly damaging Het
Iglv2 A G 16: 19,079,260 (GRCm39) V81A not run Het
Irs1 A G 1: 82,265,177 (GRCm39) I1013T probably benign Het
Itih4 T C 14: 30,621,432 (GRCm39) S832P probably damaging Het
Klhl1 A T 14: 96,517,513 (GRCm39) Y388N probably benign Het
Lrrc37a G A 11: 103,348,601 (GRCm39) S2698L unknown Het
Map4k4 T C 1: 40,058,829 (GRCm39) Y1008H possibly damaging Het
Mdn1 G T 4: 32,701,823 (GRCm39) G1519W probably damaging Het
Mga T A 2: 119,747,809 (GRCm39) D653E probably damaging Het
Npas1 T C 7: 16,208,733 (GRCm39) E48G probably damaging Het
Nup188 G A 2: 30,231,842 (GRCm39) probably null Het
Or1p1b G T 11: 74,130,394 (GRCm39) M1I probably null Het
Or3a4 T A 11: 73,945,223 (GRCm39) M121L probably damaging Het
Or4c110 G A 2: 88,832,075 (GRCm39) L186F Het
Or51a39 A G 7: 102,362,873 (GRCm39) V249A possibly damaging Het
Or55b4 A T 7: 102,133,574 (GRCm39) V251D probably damaging Het
Or7h8 A G 9: 20,123,840 (GRCm39) N65S probably damaging Het
Oxct1 T C 15: 4,158,383 (GRCm39) V439A probably damaging Het
Pcdhb22 G T 18: 37,652,341 (GRCm39) G13W probably damaging Het
Pex11g A G 8: 3,509,237 (GRCm39) V230A probably benign Het
Pop1 C T 15: 34,510,525 (GRCm39) S439L probably damaging Het
Ptpn9 T A 9: 56,929,533 (GRCm39) H83Q probably benign Het
Qrfp C T 2: 31,698,704 (GRCm39) R76H probably benign Het
Slc30a3 A G 5: 31,246,139 (GRCm39) V197A probably benign Het
Slc8a3 T C 12: 81,361,047 (GRCm39) N591D possibly damaging Het
Sp4 G T 12: 118,263,807 (GRCm39) Q80K possibly damaging Het
Spock1 C T 13: 58,055,316 (GRCm39) G29D possibly damaging Het
Sprr1a G T 3: 92,391,674 (GRCm39) P109Q probably damaging Het
Suz12 T A 11: 79,904,309 (GRCm39) F239L probably damaging Het
Tbx3 A G 5: 119,813,648 (GRCm39) Y248C probably damaging Het
Trabd2b T C 4: 114,266,637 (GRCm39) L217P probably damaging Het
Ubxn11 A C 4: 133,853,726 (GRCm39) I398L possibly damaging Het
Vmn1r173 T A 7: 23,401,884 (GRCm39) S40T probably damaging Het
Vmn2r2 T C 3: 64,023,900 (GRCm39) S894G probably benign Het
Vmn2r65 A G 7: 84,592,347 (GRCm39) probably null Het
Vps8 T C 16: 21,275,032 (GRCm39) Y197H probably damaging Het
Wdr91 T C 6: 34,866,209 (GRCm39) N486D possibly damaging Het
Wwp1 A G 4: 19,627,908 (GRCm39) I695T possibly damaging Het
Zc3hc1 T C 6: 30,382,547 (GRCm39) D133G probably benign Het
Zcchc14 T C 8: 122,335,200 (GRCm39) I307V unknown Het
Zfp933 G A 4: 147,910,636 (GRCm39) T320I 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
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
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'- TTCTTCAGGAGCTACGATGAATATC -3'
(R):5'- TAGTCCAGCTCCAAGTGCTG -3'

Sequencing Primer
(F):5'- CCAAAAGCTGTCTTAATGTTTTCAGC -3'
(R):5'- AGCTCCAAGTGCTGACCAG -3'
Posted On 2019-06-26