Incidental Mutation 'R1396:Vps13c'
ID 162651
Institutional Source Beutler Lab
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
MMRRC Submission 039458-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1396 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 67840396-67995638 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 67955022 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 2974 (I2974V)
Ref Sequence ENSEMBL: ENSMUSP00000077040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077879]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000077879
AA Change: I2974V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: I2974V

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
Predicted Effect unknown
Transcript: ENSMUST00000213168
AA Change: I107V
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.4%
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921530L21Rik A G 14: 95,882,551 (GRCm38) N248S probably benign Het
4930486L24Rik G A 13: 60,853,243 (GRCm38) P160S probably benign Het
Adamts12 G T 15: 11,311,472 (GRCm38) D1272Y probably benign Het
Akr1c20 A T 13: 4,507,727 (GRCm38) V267D probably damaging Het
C1s1 A G 6: 124,531,051 (GRCm38) S660P probably damaging Het
Ccdc40 A G 11: 119,231,803 (GRCm38) T144A possibly damaging Het
Cdk20 T C 13: 64,437,403 (GRCm38) I167T probably damaging Het
Chd6 A G 2: 160,983,103 (GRCm38) L1212S probably damaging Het
Clock G C 5: 76,266,802 (GRCm38) D15E probably benign Het
Clstn2 A G 9: 97,461,393 (GRCm38) V667A probably benign Het
Cr2 A T 1: 195,169,253 (GRCm38) probably null Het
Cyp2e1 A G 7: 140,773,079 (GRCm38) D343G probably damaging Het
Dync1h1 G A 12: 110,636,509 (GRCm38) E2195K probably benign Het
Etf1 G A 18: 34,908,167 (GRCm38) T298I possibly damaging Het
Gm5431 T C 11: 48,895,434 (GRCm38) probably benign Het
Gss G A 2: 155,567,721 (GRCm38) T265I probably damaging Het
Heatr1 C T 13: 12,406,046 (GRCm38) S406L possibly damaging Het
Hgsnat C A 8: 25,957,335 (GRCm38) M310I possibly damaging Het
Inpp5b G A 4: 124,789,080 (GRCm38) R598H probably damaging Het
Ints2 G T 11: 86,249,248 (GRCm38) Q253K probably damaging Het
Kng1 A G 16: 23,078,980 (GRCm38) M377V probably benign Het
Krt72 C T 15: 101,786,005 (GRCm38) probably null Het
Lemd2 G C 17: 27,190,732 (GRCm38) R482G probably damaging Het
Lrpprc C T 17: 84,726,303 (GRCm38) D1049N possibly damaging Het
Lrrc49 A T 9: 60,680,527 (GRCm38) H117Q probably damaging Het
Mcm6 A T 1: 128,351,476 (GRCm38) F191Y probably damaging Het
Mecom T C 3: 29,979,800 (GRCm38) T252A possibly damaging Het
Mgat4e T C 1: 134,541,533 (GRCm38) T258A probably benign Het
Mpeg1 A G 19: 12,462,804 (GRCm38) N542S probably damaging Het
Nln C T 13: 104,061,753 (GRCm38) V184I probably benign Het
Nova1 A C 12: 46,816,893 (GRCm38) F91L unknown Het
Polk T C 13: 96,484,208 (GRCm38) I516V probably benign Het
Ppig C T 2: 69,749,018 (GRCm38) P357S unknown Het
Ptpro T A 6: 137,443,594 (GRCm38) V1007D probably damaging Het
Rasal2 A T 1: 157,164,666 (GRCm38) H552Q probably damaging Het
Rnf41 G A 10: 128,435,571 (GRCm38) E117K probably benign Het
Sbk3 A G 7: 4,967,453 (GRCm38) Y306H possibly damaging Het
Senp1 A G 15: 98,076,554 (GRCm38) S126P probably benign Het
Sfr1 A G 19: 47,733,690 (GRCm38) K182E probably benign Het
Slc25a4 C A 8: 46,209,288 (GRCm38) R111L probably damaging Het
Slc9c1 A T 16: 45,573,347 (GRCm38) Y551F probably benign Het
Stard4 A T 18: 33,206,210 (GRCm38) N80K probably damaging Het
Tbk1 G A 10: 121,571,916 (GRCm38) T104M probably damaging Het
Tedc2 T A 17: 24,216,317 (GRCm38) E366V probably damaging Het
Tedc2 C A 17: 24,216,318 (GRCm38) E366* probably null Het
Tmem102 A T 11: 69,804,370 (GRCm38) W259R probably damaging Het
Tnk1 A T 11: 69,853,136 (GRCm38) C466S probably benign Het
Tspoap1 A C 11: 87,766,120 (GRCm38) Q307P probably damaging Het
Ugt2b35 A G 5: 87,011,530 (GRCm38) N528D possibly damaging Het
Usp6nl A G 2: 6,426,998 (GRCm38) probably null Het
Vmn1r203 C T 13: 22,524,508 (GRCm38) T153M probably benign Het
Vmn1r89 T A 7: 13,220,011 (GRCm38) S157T probably damaging Het
Vmn2r103 A T 17: 19,792,968 (GRCm38) Y117F probably benign Het
Vmn2r116 A C 17: 23,386,141 (GRCm38) M143L probably benign Het
Vmn2r62 A T 7: 42,764,837 (GRCm38) D727E probably damaging Het
Wrn C T 8: 33,268,819 (GRCm38) G769D probably damaging Het
Zhx3 T A 2: 160,781,020 (GRCm38) H409L possibly damaging Het
Other mutations in Vps13c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Vps13c APN 9 67,945,999 (GRCm38) missense probably benign 0.20
IGL00336:Vps13c APN 9 67,945,942 (GRCm38) missense probably benign 0.01
IGL00418:Vps13c APN 9 67,876,262 (GRCm38) missense probably damaging 1.00
IGL00481:Vps13c APN 9 67,860,865 (GRCm38) missense probably damaging 1.00
IGL00491:Vps13c APN 9 67,893,136 (GRCm38) missense probably damaging 1.00
IGL00558:Vps13c APN 9 67,937,857 (GRCm38) missense possibly damaging 0.52
IGL00811:Vps13c APN 9 67,948,181 (GRCm38) missense probably damaging 0.99
IGL01011:Vps13c APN 9 67,926,955 (GRCm38) missense probably damaging 0.98
IGL01094:Vps13c APN 9 67,886,284 (GRCm38) missense probably damaging 1.00
IGL01330:Vps13c APN 9 67,964,108 (GRCm38) missense probably damaging 1.00
IGL01402:Vps13c APN 9 67,913,204 (GRCm38) critical splice acceptor site probably null
IGL01404:Vps13c APN 9 67,913,204 (GRCm38) critical splice acceptor site probably null
IGL01470:Vps13c APN 9 67,912,927 (GRCm38) splice site probably benign
IGL01615:Vps13c APN 9 67,955,781 (GRCm38) missense probably benign 0.01
IGL01694:Vps13c APN 9 67,895,349 (GRCm38) missense probably damaging 1.00
IGL01752:Vps13c APN 9 67,948,228 (GRCm38) missense probably damaging 1.00
IGL01810:Vps13c APN 9 67,955,780 (GRCm38) missense probably benign
IGL01954:Vps13c APN 9 67,969,298 (GRCm38) missense probably damaging 0.98
IGL01978:Vps13c APN 9 67,930,643 (GRCm38) missense probably benign 0.03
IGL01998:Vps13c APN 9 67,955,068 (GRCm38) splice site probably null
IGL02201:Vps13c APN 9 67,967,136 (GRCm38) missense probably damaging 1.00
IGL02205:Vps13c APN 9 67,883,454 (GRCm38) missense probably damaging 1.00
IGL02303:Vps13c APN 9 67,945,481 (GRCm38) splice site probably benign
IGL02322:Vps13c APN 9 67,937,901 (GRCm38) missense probably benign 0.02
IGL02456:Vps13c APN 9 67,952,976 (GRCm38) missense probably damaging 1.00
IGL02474:Vps13c APN 9 67,937,876 (GRCm38) missense probably benign 0.00
IGL02547:Vps13c APN 9 67,908,019 (GRCm38) missense possibly damaging 0.83
IGL02640:Vps13c APN 9 67,886,248 (GRCm38) splice site probably benign
IGL02673:Vps13c APN 9 67,878,098 (GRCm38) missense probably damaging 1.00
IGL02721:Vps13c APN 9 67,964,149 (GRCm38) splice site probably benign
IGL02834:Vps13c APN 9 67,937,855 (GRCm38) missense probably benign
IGL02838:Vps13c APN 9 67,975,851 (GRCm38) missense probably damaging 1.00
IGL03136:Vps13c APN 9 67,950,310 (GRCm38) missense probably damaging 1.00
IGL03137:Vps13c APN 9 67,890,380 (GRCm38) missense probably damaging 1.00
IGL03214:Vps13c APN 9 67,897,195 (GRCm38) missense probably null 0.81
IGL03240:Vps13c APN 9 67,955,047 (GRCm38) missense probably benign
IGL03303:Vps13c APN 9 67,934,504 (GRCm38) missense probably benign 0.27
IGL03336:Vps13c APN 9 67,951,642 (GRCm38) missense possibly damaging 0.76
IGL03366:Vps13c APN 9 67,946,026 (GRCm38) missense probably benign 0.00
Derivative UTSW 9 67,930,622 (GRCm38) missense possibly damaging 0.79
diversion UTSW 9 67,910,233 (GRCm38) missense possibly damaging 0.93
introversion UTSW 9 67,944,046 (GRCm38) missense probably damaging 0.98
Inversion UTSW 9 67,902,839 (GRCm38) critical splice acceptor site probably null
subversion UTSW 9 67,908,052 (GRCm38) missense probably damaging 1.00
Transversion UTSW 9 67,934,501 (GRCm38) missense probably damaging 0.98
3-1:Vps13c UTSW 9 67,936,373 (GRCm38) missense probably benign 0.00
IGL02991:Vps13c UTSW 9 67,913,877 (GRCm38) missense probably damaging 1.00
PIT4802001:Vps13c UTSW 9 67,937,786 (GRCm38) missense probably damaging 1.00
R0008:Vps13c UTSW 9 67,919,262 (GRCm38) missense probably benign
R0206:Vps13c UTSW 9 67,939,162 (GRCm38) splice site probably benign
R0288:Vps13c UTSW 9 67,927,366 (GRCm38) missense probably damaging 0.99
R0324:Vps13c UTSW 9 67,964,309 (GRCm38) missense possibly damaging 0.95
R0347:Vps13c UTSW 9 67,910,233 (GRCm38) missense possibly damaging 0.93
R0374:Vps13c UTSW 9 67,886,246 (GRCm38) splice site probably benign
R0388:Vps13c UTSW 9 67,922,915 (GRCm38) splice site probably benign
R0409:Vps13c UTSW 9 67,951,644 (GRCm38) missense probably benign 0.00
R0440:Vps13c UTSW 9 67,972,861 (GRCm38) missense probably damaging 1.00
R0513:Vps13c UTSW 9 67,930,735 (GRCm38) missense probably benign 0.02
R0520:Vps13c UTSW 9 67,945,851 (GRCm38) missense possibly damaging 0.88
R0569:Vps13c UTSW 9 67,973,719 (GRCm38) missense probably damaging 0.98
R0601:Vps13c UTSW 9 67,927,472 (GRCm38) missense probably benign 0.12
R0659:Vps13c UTSW 9 67,920,935 (GRCm38) missense probably benign 0.11
R0667:Vps13c UTSW 9 67,951,573 (GRCm38) nonsense probably null
R0670:Vps13c UTSW 9 67,925,857 (GRCm38) missense probably benign 0.35
R0698:Vps13c UTSW 9 67,889,723 (GRCm38) missense probably benign 0.45
R0729:Vps13c UTSW 9 67,961,649 (GRCm38) missense probably damaging 1.00
R0781:Vps13c UTSW 9 67,972,003 (GRCm38) missense probably damaging 1.00
R0811:Vps13c UTSW 9 67,934,476 (GRCm38) missense probably benign 0.06
R0812:Vps13c UTSW 9 67,934,476 (GRCm38) missense probably benign 0.06
R0839:Vps13c UTSW 9 67,898,738 (GRCm38) missense probably benign
R1373:Vps13c UTSW 9 67,927,511 (GRCm38) missense probably damaging 0.99
R1499:Vps13c UTSW 9 67,957,505 (GRCm38) missense probably benign 0.00
R1556:Vps13c UTSW 9 67,930,711 (GRCm38) missense probably damaging 0.98
R1560:Vps13c UTSW 9 67,936,463 (GRCm38) critical splice donor site probably null
R1584:Vps13c UTSW 9 67,893,112 (GRCm38) missense possibly damaging 0.74
R1654:Vps13c UTSW 9 67,951,687 (GRCm38) missense probably damaging 1.00
R1674:Vps13c UTSW 9 67,853,703 (GRCm38) nonsense probably null
R1676:Vps13c UTSW 9 67,926,962 (GRCm38) missense probably benign 0.20
R1695:Vps13c UTSW 9 67,972,075 (GRCm38) nonsense probably null
R1710:Vps13c UTSW 9 67,911,529 (GRCm38) missense probably benign 0.00
R1769:Vps13c UTSW 9 67,965,721 (GRCm38) missense probably benign 0.00
R1775:Vps13c UTSW 9 67,881,447 (GRCm38) missense probably damaging 1.00
R1795:Vps13c UTSW 9 67,893,985 (GRCm38) nonsense probably null
R1799:Vps13c UTSW 9 67,944,117 (GRCm38) missense probably damaging 0.98
R1835:Vps13c UTSW 9 67,993,013 (GRCm38) missense probably benign 0.08
R1848:Vps13c UTSW 9 67,936,340 (GRCm38) missense probably benign
R1903:Vps13c UTSW 9 67,894,052 (GRCm38) missense probably damaging 1.00
R1944:Vps13c UTSW 9 67,886,276 (GRCm38) missense probably damaging 1.00
R1945:Vps13c UTSW 9 67,886,276 (GRCm38) missense probably damaging 1.00
R1951:Vps13c UTSW 9 67,973,759 (GRCm38) critical splice donor site probably null
R1993:Vps13c UTSW 9 67,975,856 (GRCm38) missense probably damaging 1.00
R2023:Vps13c UTSW 9 67,936,285 (GRCm38) splice site probably benign
R2059:Vps13c UTSW 9 67,860,833 (GRCm38) missense probably damaging 1.00
R2086:Vps13c UTSW 9 67,950,289 (GRCm38) missense probably benign 0.29
R2120:Vps13c UTSW 9 67,919,334 (GRCm38) missense possibly damaging 0.92
R2249:Vps13c UTSW 9 67,988,053 (GRCm38) critical splice donor site probably null
R2257:Vps13c UTSW 9 67,952,946 (GRCm38) missense possibly damaging 0.87
R2258:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2259:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2260:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2265:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2266:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2269:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2278:Vps13c UTSW 9 67,939,072 (GRCm38) missense probably benign
R2306:Vps13c UTSW 9 67,987,993 (GRCm38) missense probably damaging 0.99
R2327:Vps13c UTSW 9 67,913,820 (GRCm38) missense probably damaging 0.98
R2349:Vps13c UTSW 9 67,957,526 (GRCm38) missense possibly damaging 0.89
R2483:Vps13c UTSW 9 67,975,907 (GRCm38) critical splice donor site probably null
R3031:Vps13c UTSW 9 67,923,770 (GRCm38) missense probably benign 0.00
R3623:Vps13c UTSW 9 67,975,907 (GRCm38) critical splice donor site probably null
R3870:Vps13c UTSW 9 67,884,726 (GRCm38) missense probably benign 0.00
R4173:Vps13c UTSW 9 67,936,313 (GRCm38) missense probably benign 0.00
R4445:Vps13c UTSW 9 67,982,495 (GRCm38) splice site probably null
R4491:Vps13c UTSW 9 67,910,193 (GRCm38) missense probably benign
R4505:Vps13c UTSW 9 67,939,034 (GRCm38) missense probably benign 0.02
R4574:Vps13c UTSW 9 67,951,683 (GRCm38) missense probably damaging 1.00
R4691:Vps13c UTSW 9 67,952,935 (GRCm38) missense possibly damaging 0.95
R4766:Vps13c UTSW 9 67,878,224 (GRCm38) splice site probably null
R4771:Vps13c UTSW 9 67,929,539 (GRCm38) missense probably benign
R4801:Vps13c UTSW 9 67,964,282 (GRCm38) missense probably damaging 1.00
R4802:Vps13c UTSW 9 67,964,282 (GRCm38) missense probably damaging 1.00
R4962:Vps13c UTSW 9 67,873,891 (GRCm38) missense probably damaging 1.00
R4995:Vps13c UTSW 9 67,919,321 (GRCm38) missense probably benign 0.00
R5010:Vps13c UTSW 9 67,916,379 (GRCm38) missense probably benign 0.19
R5183:Vps13c UTSW 9 67,908,052 (GRCm38) missense probably damaging 1.00
R5226:Vps13c UTSW 9 67,945,553 (GRCm38) missense probably benign 0.17
R5297:Vps13c UTSW 9 67,878,131 (GRCm38) missense probably damaging 1.00
R5456:Vps13c UTSW 9 67,927,447 (GRCm38) missense possibly damaging 0.53
R5494:Vps13c UTSW 9 67,948,146 (GRCm38) missense probably benign 0.00
R5521:Vps13c UTSW 9 67,951,439 (GRCm38) missense probably benign 0.08
R5524:Vps13c UTSW 9 67,957,556 (GRCm38) missense probably damaging 1.00
R5685:Vps13c UTSW 9 67,963,173 (GRCm38) missense possibly damaging 0.64
R5731:Vps13c UTSW 9 67,895,379 (GRCm38) missense probably damaging 1.00
R5812:Vps13c UTSW 9 67,982,495 (GRCm38) splice site probably benign
R5867:Vps13c UTSW 9 67,982,622 (GRCm38) splice site probably null
R5893:Vps13c UTSW 9 67,902,839 (GRCm38) critical splice acceptor site probably null
R5902:Vps13c UTSW 9 67,934,447 (GRCm38) missense probably benign 0.00
R5957:Vps13c UTSW 9 67,954,971 (GRCm38) missense probably damaging 1.00
R6076:Vps13c UTSW 9 67,911,602 (GRCm38) missense probably damaging 1.00
R6187:Vps13c UTSW 9 67,915,657 (GRCm38) missense probably damaging 1.00
R6268:Vps13c UTSW 9 67,951,449 (GRCm38) missense probably benign 0.10
R6547:Vps13c UTSW 9 67,973,365 (GRCm38) missense probably damaging 1.00
R6716:Vps13c UTSW 9 67,951,467 (GRCm38) missense probably benign 0.00
R6837:Vps13c UTSW 9 67,910,222 (GRCm38) missense probably benign
R6919:Vps13c UTSW 9 67,927,452 (GRCm38) missense probably damaging 0.97
R7039:Vps13c UTSW 9 67,937,763 (GRCm38) missense probably damaging 1.00
R7058:Vps13c UTSW 9 67,923,828 (GRCm38) missense probably benign 0.39
R7082:Vps13c UTSW 9 67,883,453 (GRCm38) missense probably damaging 1.00
R7195:Vps13c UTSW 9 67,945,825 (GRCm38) missense possibly damaging 0.95
R7244:Vps13c UTSW 9 67,889,804 (GRCm38) missense probably benign 0.00
R7300:Vps13c UTSW 9 67,940,544 (GRCm38) missense probably benign 0.20
R7314:Vps13c UTSW 9 67,943,340 (GRCm38) splice site probably null
R7352:Vps13c UTSW 9 67,840,446 (GRCm38) missense possibly damaging 0.94
R7368:Vps13c UTSW 9 67,914,073 (GRCm38) missense probably benign 0.23
R7411:Vps13c UTSW 9 67,972,001 (GRCm38) missense probably damaging 0.98
R7497:Vps13c UTSW 9 67,840,479 (GRCm38) missense probably damaging 1.00
R7516:Vps13c UTSW 9 67,955,007 (GRCm38) missense possibly damaging 0.89
R7638:Vps13c UTSW 9 67,945,509 (GRCm38) missense probably damaging 1.00
R7732:Vps13c UTSW 9 67,940,516 (GRCm38) missense probably damaging 0.97
R7748:Vps13c UTSW 9 67,963,089 (GRCm38) missense probably benign 0.03
R7779:Vps13c UTSW 9 67,881,422 (GRCm38) missense probably damaging 1.00
R7788:Vps13c UTSW 9 67,940,483 (GRCm38) missense probably benign 0.01
R7894:Vps13c UTSW 9 67,926,983 (GRCm38) missense probably damaging 0.99
R8163:Vps13c UTSW 9 67,950,438 (GRCm38) missense probably benign 0.08
R8165:Vps13c UTSW 9 67,858,790 (GRCm38) missense probably benign 0.00
R8202:Vps13c UTSW 9 67,944,046 (GRCm38) missense probably damaging 0.98
R8235:Vps13c UTSW 9 67,955,781 (GRCm38) missense probably benign 0.01
R8235:Vps13c UTSW 9 67,927,396 (GRCm38) missense probably damaging 1.00
R8253:Vps13c UTSW 9 67,943,488 (GRCm38) nonsense probably null
R8261:Vps13c UTSW 9 67,954,980 (GRCm38) missense probably damaging 1.00
R8348:Vps13c UTSW 9 67,879,103 (GRCm38) missense possibly damaging 0.79
R8547:Vps13c UTSW 9 67,945,566 (GRCm38) missense probably damaging 1.00
R8734:Vps13c UTSW 9 67,973,403 (GRCm38) missense probably damaging 1.00
R8806:Vps13c UTSW 9 67,945,828 (GRCm38) missense probably damaging 1.00
R8807:Vps13c UTSW 9 67,858,840 (GRCm38) missense probably damaging 0.99
R8813:Vps13c UTSW 9 67,871,284 (GRCm38) missense probably damaging 1.00
R8883:Vps13c UTSW 9 67,948,197 (GRCm38) missense probably benign 0.10
R8885:Vps13c UTSW 9 67,943,454 (GRCm38) missense probably benign
R8899:Vps13c UTSW 9 67,934,501 (GRCm38) missense probably damaging 0.98
R8970:Vps13c UTSW 9 67,945,521 (GRCm38) missense probably benign 0.11
R9007:Vps13c UTSW 9 67,937,724 (GRCm38) missense probably benign 0.00
R9026:Vps13c UTSW 9 67,954,581 (GRCm38) missense probably damaging 1.00
R9029:Vps13c UTSW 9 67,948,147 (GRCm38) missense probably damaging 0.98
R9057:Vps13c UTSW 9 67,920,927 (GRCm38) missense probably benign 0.00
R9105:Vps13c UTSW 9 67,870,799 (GRCm38) intron probably benign
R9130:Vps13c UTSW 9 67,929,523 (GRCm38) missense probably damaging 1.00
R9286:Vps13c UTSW 9 67,972,921 (GRCm38) missense probably benign 0.00
R9338:Vps13c UTSW 9 67,951,695 (GRCm38) missense probably damaging 1.00
R9432:Vps13c UTSW 9 67,922,855 (GRCm38) missense probably benign 0.02
R9460:Vps13c UTSW 9 67,930,622 (GRCm38) missense possibly damaging 0.79
R9464:Vps13c UTSW 9 67,951,392 (GRCm38) missense probably damaging 1.00
R9561:Vps13c UTSW 9 67,965,512 (GRCm38) missense probably damaging 1.00
R9609:Vps13c UTSW 9 67,934,549 (GRCm38) missense probably damaging 1.00
R9622:Vps13c UTSW 9 67,949,433 (GRCm38) missense probably damaging 1.00
R9665:Vps13c UTSW 9 67,955,743 (GRCm38) nonsense probably null
R9731:Vps13c UTSW 9 67,919,244 (GRCm38) missense probably benign
R9763:Vps13c UTSW 9 67,911,578 (GRCm38) missense probably benign 0.00
R9774:Vps13c UTSW 9 67,884,591 (GRCm38) missense possibly damaging 0.85
R9798:Vps13c UTSW 9 67,919,364 (GRCm38) missense probably damaging 1.00
U24488:Vps13c UTSW 9 67,905,916 (GRCm38) missense probably benign 0.13
X0021:Vps13c UTSW 9 67,937,781 (GRCm38) missense probably damaging 0.99
X0058:Vps13c UTSW 9 67,927,419 (GRCm38) missense probably damaging 1.00
X0065:Vps13c UTSW 9 67,873,863 (GRCm38) missense probably damaging 1.00
Z1088:Vps13c UTSW 9 67,913,975 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAGCCAGAGCCAGTGAGAACTTTAG -3'
(R):5'- ACACGCATTTACAGGAACGGGG -3'

Sequencing Primer
(F):5'- GTGTTTGTAAAGCTGATTGAACGTG -3'
(R):5'- agcatctctttgtcccagttc -3'
Posted On 2014-03-17