Incidental Mutation 'R5712:Vps13d'
ID 450934
Institutional Source Beutler Lab
Gene Symbol Vps13d
Ensembl Gene ENSMUSG00000020220
Gene Name vacuolar protein sorting 13D
Synonyms
MMRRC Submission 043334-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5712 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 144699192-144921575 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 144813743 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 3245 (S3245A)
Ref Sequence ENSEMBL: ENSMUSP00000020441 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020441] [ENSMUST00000036579] [ENSMUST00000130704]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000020441
AA Change: S3245A

PolyPhen 2 Score 0.068 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000020441
Gene: ENSMUSG00000020220
AA Change: S3245A

DomainStartEndE-ValueType
Pfam:Chorein_N 2 118 1.8e-37 PFAM
low complexity region 407 423 N/A INTRINSIC
low complexity region 534 555 N/A INTRINSIC
coiled coil region 665 685 N/A INTRINSIC
low complexity region 765 781 N/A INTRINSIC
low complexity region 1316 1329 N/A INTRINSIC
low complexity region 1590 1603 N/A INTRINSIC
Blast:IL1 1605 1726 2e-6 BLAST
low complexity region 1868 1883 N/A INTRINSIC
low complexity region 2128 2141 N/A INTRINSIC
UBA 2632 2669 3.73e-5 SMART
low complexity region 2674 2684 N/A INTRINSIC
low complexity region 2707 2718 N/A INTRINSIC
low complexity region 2866 2884 N/A INTRINSIC
low complexity region 2973 2983 N/A INTRINSIC
Pfam:DUF1162 3246 3530 1.1e-110 PFAM
low complexity region 3797 3810 N/A INTRINSIC
low complexity region 3913 3921 N/A INTRINSIC
low complexity region 4119 4132 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000036579
AA Change: S3276A
SMART Domains Protein: ENSMUSP00000043240
Gene: ENSMUSG00000020220
AA Change: S3276A

DomainStartEndE-ValueType
Pfam:Chorein_N 2 116 3.5e-35 PFAM
Pfam:VPS13 131 353 9.6e-57 PFAM
low complexity region 407 423 N/A INTRINSIC
low complexity region 534 555 N/A INTRINSIC
Pfam:VPS13_mid_rpt 608 896 4.3e-35 PFAM
low complexity region 1316 1329 N/A INTRINSIC
low complexity region 1590 1603 N/A INTRINSIC
Blast:IL1 1605 1726 2e-6 BLAST
low complexity region 1868 1883 N/A INTRINSIC
low complexity region 2128 2141 N/A INTRINSIC
UBA 2632 2669 3.73e-5 SMART
low complexity region 2674 2684 N/A INTRINSIC
low complexity region 2707 2718 N/A INTRINSIC
low complexity region 2891 2909 N/A INTRINSIC
low complexity region 2998 3008 N/A INTRINSIC
Pfam:SHR-BD 3271 3555 4.2e-86 PFAM
low complexity region 3822 3835 N/A INTRINSIC
low complexity region 3938 3946 N/A INTRINSIC
Pfam:VPS13_C 3978 4126 4.8e-24 PFAM
low complexity region 4144 4157 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000130704
AA Change: S161A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000118699
Gene: ENSMUSG00000020220
AA Change: S161A

DomainStartEndE-ValueType
Pfam:DUF1162 162 446 1.4e-111 PFAM
low complexity region 713 726 N/A INTRINSIC
low complexity region 829 837 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000185113
AA Change: S2096A
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein belonging to the vacuolar-protein-sorting-13 gene family. In yeast, vacuolar-protein-sorting-13 proteins are involved in trafficking of membrane proteins between the trans-Golgi network and the prevacuolar compartment. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode distinct isoforms. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit embryonic lethality at E7. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik A G 5: 144,981,563 (GRCm39) T133A probably benign Het
Adcy8 C T 15: 64,626,715 (GRCm39) E708K probably damaging Het
Alkbh1 A G 12: 87,475,883 (GRCm39) C300R probably benign Het
Arhgap11a T C 2: 113,675,646 (GRCm39) N52D probably benign Het
Ash1l T A 3: 88,959,297 (GRCm39) S2225T probably damaging Het
Aspn A T 13: 49,716,995 (GRCm39) Y257F probably damaging Het
Atp2b4 A C 1: 133,658,278 (GRCm39) V544G probably damaging Het
Bclaf1 T G 10: 20,209,277 (GRCm39) Y498D probably damaging Het
Cacna1d A G 14: 29,796,954 (GRCm39) I1520T probably damaging Het
Castor1 T C 11: 4,168,378 (GRCm39) L22P probably damaging Het
Cfap57 G T 4: 118,471,992 (GRCm39) P129Q probably damaging Het
Clcn3 A G 8: 61,390,332 (GRCm39) probably null Het
Epx A T 11: 87,765,679 (GRCm39) Y93* probably null Het
Erich6b T A 14: 75,896,340 (GRCm39) D75E possibly damaging Het
Exoc3l4 T A 12: 111,390,476 (GRCm39) Y350* probably null Het
Fam13a T A 6: 58,933,684 (GRCm39) D302V probably damaging Het
Fbxo17 G A 7: 28,436,897 (GRCm39) R284H probably damaging Het
Fga C T 3: 82,940,440 (GRCm39) T698I possibly damaging Het
Fsip2 T C 2: 82,839,192 (GRCm39) S6987P possibly damaging Het
Gbp9 T A 5: 105,242,421 (GRCm39) N106I possibly damaging Het
Gls T A 1: 52,235,911 (GRCm39) K401N probably damaging Het
Gpatch2l A G 12: 86,291,254 (GRCm39) K146E probably damaging Het
Gpr3 A G 4: 132,937,719 (GRCm39) S318P probably benign Het
Kbtbd7 T C 14: 79,666,205 (GRCm39) V679A possibly damaging Het
Kcnu1 T A 8: 26,409,678 (GRCm39) L127H probably damaging Het
Lck G T 4: 129,450,103 (GRCm39) H214Q probably benign Het
Lrch4 A C 5: 137,636,188 (GRCm39) S380R possibly damaging Het
Lrrk2 A T 15: 91,586,425 (GRCm39) K414* probably null Het
Maco1 A T 4: 134,555,369 (GRCm39) M368K probably benign Het
Med11 A G 11: 70,344,058 (GRCm39) E126G probably damaging Het
Mknk1 A G 4: 115,712,203 (GRCm39) probably null Het
Mst1 T C 9: 107,960,107 (GRCm39) C355R probably damaging Het
Mtcl2 T A 2: 156,872,841 (GRCm39) E890V probably damaging Het
Myl10 T C 5: 136,723,092 (GRCm39) F14L probably damaging Het
Nfrkb C T 9: 31,325,932 (GRCm39) T1125M probably benign Het
Nin T C 12: 70,089,543 (GRCm39) T1291A probably damaging Het
Pcnt T C 10: 76,265,105 (GRCm39) Q335R probably damaging Het
Phc2 A G 4: 128,638,888 (GRCm39) T83A probably damaging Het
Rdh19 T A 10: 127,692,756 (GRCm39) M141K probably benign Het
Rnf17 G A 14: 56,708,856 (GRCm39) V759I probably benign Het
Sirt7 A T 11: 120,511,677 (GRCm39) Y18* probably null Het
Slc27a5 T C 7: 12,732,010 (GRCm39) probably benign Het
Synpo2 T A 3: 122,914,859 (GRCm39) I56F probably damaging Het
Tdrd6 C A 17: 43,937,299 (GRCm39) G1250C probably damaging Het
Tmem190 G A 7: 4,787,288 (GRCm39) G164D probably damaging Het
Tmigd1 T C 11: 76,797,858 (GRCm39) Y67H probably damaging Het
Trim3 T A 7: 105,268,743 (GRCm39) E70D probably damaging Het
Uap1 A G 1: 169,994,414 (GRCm39) F21L possibly damaging Het
Vmn1r176 A T 7: 23,534,925 (GRCm39) V76D probably benign Het
Wnt7a T C 6: 91,343,186 (GRCm39) Y232C probably damaging Het
Zan A G 5: 137,398,360 (GRCm39) V4224A unknown Het
Other mutations in Vps13d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00163:Vps13d APN 4 144,895,110 (GRCm39) missense probably damaging 0.98
IGL00484:Vps13d APN 4 144,853,145 (GRCm39) missense probably benign 0.04
IGL00591:Vps13d APN 4 144,917,129 (GRCm39) missense possibly damaging 0.95
IGL00816:Vps13d APN 4 144,882,564 (GRCm39) missense probably benign 0.00
IGL00835:Vps13d APN 4 144,887,222 (GRCm39) missense probably damaging 0.97
IGL00847:Vps13d APN 4 144,811,978 (GRCm39) missense probably benign 0.26
IGL01084:Vps13d APN 4 144,881,525 (GRCm39) missense probably benign 0.00
IGL01116:Vps13d APN 4 144,699,320 (GRCm39) unclassified probably benign
IGL01150:Vps13d APN 4 144,875,845 (GRCm39) missense probably benign
IGL01329:Vps13d APN 4 144,882,776 (GRCm39) missense possibly damaging 0.69
IGL01338:Vps13d APN 4 144,814,892 (GRCm39) missense probably damaging 1.00
IGL01583:Vps13d APN 4 144,771,658 (GRCm39) missense probably damaging 1.00
IGL01598:Vps13d APN 4 144,743,471 (GRCm39) missense probably benign 0.21
IGL01620:Vps13d APN 4 144,821,437 (GRCm39) missense possibly damaging 0.70
IGL01636:Vps13d APN 4 144,801,618 (GRCm39) missense probably damaging 1.00
IGL01723:Vps13d APN 4 144,899,715 (GRCm39) missense possibly damaging 0.84
IGL01895:Vps13d APN 4 144,882,836 (GRCm39) missense possibly damaging 0.57
IGL01981:Vps13d APN 4 144,813,317 (GRCm39) missense probably damaging 0.99
IGL02192:Vps13d APN 4 144,875,428 (GRCm39) missense probably benign 0.02
IGL02197:Vps13d APN 4 144,854,879 (GRCm39) missense probably benign 0.01
IGL02209:Vps13d APN 4 144,882,671 (GRCm39) missense probably damaging 0.97
IGL02219:Vps13d APN 4 144,894,716 (GRCm39) missense probably benign 0.00
IGL02377:Vps13d APN 4 144,882,934 (GRCm39) missense probably damaging 1.00
IGL02404:Vps13d APN 4 144,875,305 (GRCm39) missense probably damaging 1.00
IGL02552:Vps13d APN 4 144,899,707 (GRCm39) missense possibly damaging 0.46
IGL02651:Vps13d APN 4 144,891,129 (GRCm39) missense probably benign 0.02
IGL02708:Vps13d APN 4 144,854,850 (GRCm39) missense probably benign 0.12
IGL02811:Vps13d APN 4 144,858,335 (GRCm39) missense possibly damaging 0.55
IGL02821:Vps13d APN 4 144,875,332 (GRCm39) missense probably damaging 0.98
IGL02838:Vps13d APN 4 144,801,595 (GRCm39) missense probably benign 0.31
IGL02968:Vps13d APN 4 144,849,068 (GRCm39) missense probably benign 0.32
IGL03176:Vps13d APN 4 144,801,533 (GRCm39) missense probably benign 0.16
IGL03352:Vps13d APN 4 144,894,072 (GRCm39) missense possibly damaging 0.49
IGL03374:Vps13d APN 4 144,835,145 (GRCm39) missense possibly damaging 0.70
IGL03375:Vps13d APN 4 144,818,517 (GRCm39) missense probably damaging 1.00
IGL03383:Vps13d APN 4 144,894,889 (GRCm39) critical splice acceptor site probably null
IGL03411:Vps13d APN 4 144,875,894 (GRCm39) missense probably damaging 1.00
broken UTSW 4 144,813,305 (GRCm39) missense
demotion UTSW 4 144,865,183 (GRCm39) missense
BB008:Vps13d UTSW 4 144,822,854 (GRCm39) nonsense probably null
BB018:Vps13d UTSW 4 144,822,854 (GRCm39) nonsense probably null
PIT4283001:Vps13d UTSW 4 144,835,158 (GRCm39) missense
PIT4434001:Vps13d UTSW 4 144,881,817 (GRCm39) missense
R0069:Vps13d UTSW 4 144,789,133 (GRCm39) missense probably benign 0.09
R0069:Vps13d UTSW 4 144,789,133 (GRCm39) missense probably benign 0.09
R0076:Vps13d UTSW 4 144,891,264 (GRCm39) splice site probably benign
R0211:Vps13d UTSW 4 144,841,348 (GRCm39) missense probably benign 0.08
R0219:Vps13d UTSW 4 144,832,479 (GRCm39) missense probably benign 0.01
R0284:Vps13d UTSW 4 144,871,372 (GRCm39) missense probably benign 0.01
R0345:Vps13d UTSW 4 144,844,195 (GRCm39) missense possibly damaging 0.81
R0400:Vps13d UTSW 4 144,792,397 (GRCm39) missense probably benign 0.00
R0417:Vps13d UTSW 4 144,703,130 (GRCm39) missense probably benign 0.19
R0538:Vps13d UTSW 4 144,771,665 (GRCm39) missense probably damaging 1.00
R0560:Vps13d UTSW 4 144,780,760 (GRCm39) missense probably damaging 1.00
R0627:Vps13d UTSW 4 144,813,754 (GRCm39) missense probably damaging 1.00
R0707:Vps13d UTSW 4 144,882,502 (GRCm39) missense probably damaging 1.00
R0782:Vps13d UTSW 4 144,853,195 (GRCm39) splice site probably benign
R0925:Vps13d UTSW 4 144,883,121 (GRCm39) missense probably damaging 1.00
R0993:Vps13d UTSW 4 144,844,262 (GRCm39) nonsense probably null
R1135:Vps13d UTSW 4 144,882,159 (GRCm39) missense probably benign 0.01
R1165:Vps13d UTSW 4 144,853,041 (GRCm39) missense probably benign
R1263:Vps13d UTSW 4 144,896,918 (GRCm39) missense probably benign 0.01
R1397:Vps13d UTSW 4 144,867,904 (GRCm39) missense probably damaging 1.00
R1398:Vps13d UTSW 4 144,826,553 (GRCm39) missense probably null
R1521:Vps13d UTSW 4 144,832,431 (GRCm39) missense probably benign 0.00
R1522:Vps13d UTSW 4 144,824,742 (GRCm39) splice site probably null
R1725:Vps13d UTSW 4 144,869,830 (GRCm39) missense possibly damaging 0.90
R1759:Vps13d UTSW 4 144,882,427 (GRCm39) missense probably benign
R1826:Vps13d UTSW 4 144,881,573 (GRCm39) missense probably damaging 0.96
R1900:Vps13d UTSW 4 144,853,176 (GRCm39) missense probably benign 0.23
R1943:Vps13d UTSW 4 144,882,427 (GRCm39) missense probably benign
R1955:Vps13d UTSW 4 144,882,713 (GRCm39) missense probably damaging 1.00
R2008:Vps13d UTSW 4 144,881,813 (GRCm39) missense probably benign 0.00
R2013:Vps13d UTSW 4 144,835,078 (GRCm39) missense probably damaging 0.99
R2014:Vps13d UTSW 4 144,835,078 (GRCm39) missense probably damaging 0.99
R2038:Vps13d UTSW 4 144,907,685 (GRCm39) critical splice donor site probably null
R2108:Vps13d UTSW 4 144,801,617 (GRCm39) missense probably damaging 0.99
R2130:Vps13d UTSW 4 144,882,671 (GRCm39) missense probably benign 0.17
R2134:Vps13d UTSW 4 144,874,909 (GRCm39) missense probably benign 0.00
R2168:Vps13d UTSW 4 144,813,893 (GRCm39) splice site probably benign
R2220:Vps13d UTSW 4 144,904,890 (GRCm39) missense probably damaging 1.00
R2240:Vps13d UTSW 4 144,837,465 (GRCm39) missense possibly damaging 0.70
R2332:Vps13d UTSW 4 144,875,256 (GRCm39) missense probably benign
R2357:Vps13d UTSW 4 144,801,547 (GRCm39) frame shift probably null
R2365:Vps13d UTSW 4 144,813,894 (GRCm39) splice site probably benign
R2571:Vps13d UTSW 4 144,875,706 (GRCm39) missense probably benign 0.20
R3149:Vps13d UTSW 4 144,853,147 (GRCm39) missense possibly damaging 0.70
R3150:Vps13d UTSW 4 144,813,360 (GRCm39) missense probably damaging 0.98
R3547:Vps13d UTSW 4 144,801,545 (GRCm39) missense probably damaging 0.99
R3716:Vps13d UTSW 4 144,802,296 (GRCm39) missense probably damaging 1.00
R3718:Vps13d UTSW 4 144,802,296 (GRCm39) missense probably damaging 1.00
R3725:Vps13d UTSW 4 144,842,218 (GRCm39) splice site probably benign
R3794:Vps13d UTSW 4 144,812,007 (GRCm39) splice site probably benign
R3875:Vps13d UTSW 4 144,917,114 (GRCm39) missense probably damaging 1.00
R3948:Vps13d UTSW 4 144,867,910 (GRCm39) missense probably damaging 1.00
R3953:Vps13d UTSW 4 144,875,450 (GRCm39) missense probably damaging 1.00
R4021:Vps13d UTSW 4 144,801,631 (GRCm39) missense possibly damaging 0.90
R4323:Vps13d UTSW 4 144,879,348 (GRCm39) missense probably benign 0.28
R4346:Vps13d UTSW 4 144,799,099 (GRCm39) intron probably benign
R4509:Vps13d UTSW 4 144,789,172 (GRCm39) missense probably damaging 1.00
R4613:Vps13d UTSW 4 144,858,225 (GRCm39) missense possibly damaging 0.95
R4657:Vps13d UTSW 4 144,801,412 (GRCm39) missense probably damaging 1.00
R4680:Vps13d UTSW 4 144,835,080 (GRCm39) missense possibly damaging 0.94
R4688:Vps13d UTSW 4 144,904,782 (GRCm39) missense probably benign
R4797:Vps13d UTSW 4 144,780,725 (GRCm39) missense probably damaging 1.00
R4798:Vps13d UTSW 4 144,904,626 (GRCm39) missense probably damaging 0.98
R4817:Vps13d UTSW 4 144,795,735 (GRCm39) missense probably damaging 1.00
R4839:Vps13d UTSW 4 144,812,000 (GRCm39) missense possibly damaging 0.95
R4860:Vps13d UTSW 4 144,813,731 (GRCm39) missense probably benign
R4860:Vps13d UTSW 4 144,813,731 (GRCm39) missense probably benign
R4869:Vps13d UTSW 4 144,854,612 (GRCm39) missense probably damaging 1.00
R4904:Vps13d UTSW 4 144,882,015 (GRCm39) missense probably damaging 1.00
R4912:Vps13d UTSW 4 144,882,427 (GRCm39) missense probably benign
R4916:Vps13d UTSW 4 144,709,963 (GRCm39) missense probably damaging 1.00
R4976:Vps13d UTSW 4 144,832,468 (GRCm39) missense possibly damaging 0.82
R5029:Vps13d UTSW 4 144,882,852 (GRCm39) missense probably benign 0.02
R5049:Vps13d UTSW 4 144,813,336 (GRCm39) missense probably damaging 1.00
R5077:Vps13d UTSW 4 144,814,811 (GRCm39) missense probably damaging 0.98
R5119:Vps13d UTSW 4 144,832,468 (GRCm39) missense possibly damaging 0.82
R5227:Vps13d UTSW 4 144,907,777 (GRCm39) splice site probably null
R5291:Vps13d UTSW 4 144,789,139 (GRCm39) missense probably damaging 0.99
R5344:Vps13d UTSW 4 144,904,904 (GRCm39) missense probably damaging 0.98
R5348:Vps13d UTSW 4 144,792,459 (GRCm39) missense probably damaging 0.99
R5478:Vps13d UTSW 4 144,894,120 (GRCm39) missense probably damaging 0.99
R5632:Vps13d UTSW 4 144,801,452 (GRCm39) missense probably damaging 0.99
R5642:Vps13d UTSW 4 144,896,872 (GRCm39) missense possibly damaging 0.66
R5747:Vps13d UTSW 4 144,894,853 (GRCm39) missense probably benign 0.00
R5752:Vps13d UTSW 4 144,875,540 (GRCm39) missense probably benign 0.06
R5804:Vps13d UTSW 4 144,826,640 (GRCm39) missense probably benign 0.03
R5917:Vps13d UTSW 4 144,826,580 (GRCm39) missense probably damaging 0.96
R5932:Vps13d UTSW 4 144,771,611 (GRCm39) missense possibly damaging 0.71
R5940:Vps13d UTSW 4 144,801,545 (GRCm39) missense probably benign 0.09
R5978:Vps13d UTSW 4 144,849,181 (GRCm39) missense probably benign
R6031:Vps13d UTSW 4 144,895,079 (GRCm39) missense probably benign 0.01
R6031:Vps13d UTSW 4 144,895,079 (GRCm39) missense probably benign 0.01
R6143:Vps13d UTSW 4 144,875,135 (GRCm39) missense possibly damaging 0.95
R6174:Vps13d UTSW 4 144,701,763 (GRCm39) nonsense probably null
R6191:Vps13d UTSW 4 144,875,918 (GRCm39) missense probably damaging 1.00
R6198:Vps13d UTSW 4 144,875,560 (GRCm39) missense probably benign 0.28
R6374:Vps13d UTSW 4 144,849,251 (GRCm39) missense probably damaging 1.00
R6379:Vps13d UTSW 4 144,814,828 (GRCm39) missense probably benign
R6388:Vps13d UTSW 4 144,882,144 (GRCm39) missense probably benign 0.06
R6418:Vps13d UTSW 4 144,818,850 (GRCm39) missense probably damaging 0.98
R6466:Vps13d UTSW 4 144,784,065 (GRCm39) missense possibly damaging 0.47
R6602:Vps13d UTSW 4 144,830,234 (GRCm39) intron probably benign
R6604:Vps13d UTSW 4 144,907,694 (GRCm39) missense probably damaging 1.00
R7051:Vps13d UTSW 4 144,889,914 (GRCm39) missense probably benign 0.00
R7052:Vps13d UTSW 4 144,889,914 (GRCm39) missense probably benign 0.00
R7103:Vps13d UTSW 4 144,842,062 (GRCm39) missense
R7231:Vps13d UTSW 4 144,784,032 (GRCm39) missense
R7246:Vps13d UTSW 4 144,882,620 (GRCm39) missense
R7339:Vps13d UTSW 4 144,847,938 (GRCm39) missense
R7409:Vps13d UTSW 4 144,867,824 (GRCm39) missense
R7419:Vps13d UTSW 4 144,842,073 (GRCm39) missense
R7424:Vps13d UTSW 4 144,875,317 (GRCm39) missense
R7439:Vps13d UTSW 4 144,832,426 (GRCm39) missense
R7440:Vps13d UTSW 4 144,854,981 (GRCm39) missense
R7528:Vps13d UTSW 4 144,818,492 (GRCm39) missense
R7547:Vps13d UTSW 4 144,784,108 (GRCm39) missense
R7558:Vps13d UTSW 4 144,881,150 (GRCm39) missense
R7699:Vps13d UTSW 4 144,811,975 (GRCm39) missense
R7729:Vps13d UTSW 4 144,801,622 (GRCm39) missense
R7789:Vps13d UTSW 4 144,826,635 (GRCm39) missense
R7813:Vps13d UTSW 4 144,904,633 (GRCm39) nonsense probably null
R7834:Vps13d UTSW 4 144,835,143 (GRCm39) missense
R7840:Vps13d UTSW 4 144,830,246 (GRCm39) missense
R7880:Vps13d UTSW 4 144,907,684 (GRCm39) critical splice donor site probably null
R7912:Vps13d UTSW 4 144,899,697 (GRCm39) missense
R7915:Vps13d UTSW 4 144,813,389 (GRCm39) missense
R7931:Vps13d UTSW 4 144,822,854 (GRCm39) nonsense probably null
R8021:Vps13d UTSW 4 144,875,245 (GRCm39) missense
R8048:Vps13d UTSW 4 144,882,137 (GRCm39) missense
R8057:Vps13d UTSW 4 144,701,753 (GRCm39) missense
R8063:Vps13d UTSW 4 144,841,327 (GRCm39) missense
R8131:Vps13d UTSW 4 144,882,707 (GRCm39) missense
R8190:Vps13d UTSW 4 144,879,321 (GRCm39) missense
R8226:Vps13d UTSW 4 144,875,860 (GRCm39) missense
R8241:Vps13d UTSW 4 144,875,047 (GRCm39) missense
R8254:Vps13d UTSW 4 144,709,882 (GRCm39) splice site probably benign
R8305:Vps13d UTSW 4 144,818,858 (GRCm39) missense
R8415:Vps13d UTSW 4 144,818,549 (GRCm39) missense
R8460:Vps13d UTSW 4 144,897,009 (GRCm39) intron probably benign
R8487:Vps13d UTSW 4 144,881,817 (GRCm39) missense probably benign 0.11
R8543:Vps13d UTSW 4 144,743,353 (GRCm39) nonsense probably null
R8679:Vps13d UTSW 4 144,811,977 (GRCm39) missense
R8716:Vps13d UTSW 4 144,802,348 (GRCm39) missense
R8749:Vps13d UTSW 4 144,865,183 (GRCm39) missense
R8772:Vps13d UTSW 4 144,801,602 (GRCm39) missense
R8788:Vps13d UTSW 4 144,813,305 (GRCm39) missense
R8789:Vps13d UTSW 4 144,795,743 (GRCm39) missense
R8836:Vps13d UTSW 4 144,882,648 (GRCm39) missense
R8874:Vps13d UTSW 4 144,881,772 (GRCm39) missense
R8918:Vps13d UTSW 4 144,772,873 (GRCm39) missense
R9129:Vps13d UTSW 4 144,898,249 (GRCm39) missense
R9220:Vps13d UTSW 4 144,783,058 (GRCm39) missense
R9233:Vps13d UTSW 4 144,879,344 (GRCm39) missense
R9234:Vps13d UTSW 4 144,875,792 (GRCm39) missense
R9256:Vps13d UTSW 4 144,882,374 (GRCm39) missense
R9350:Vps13d UTSW 4 144,882,333 (GRCm39) missense
R9398:Vps13d UTSW 4 144,896,956 (GRCm39) nonsense probably null
R9415:Vps13d UTSW 4 144,796,527 (GRCm39) missense
R9438:Vps13d UTSW 4 144,858,314 (GRCm39) missense
R9469:Vps13d UTSW 4 144,780,691 (GRCm39) missense
R9487:Vps13d UTSW 4 144,807,869 (GRCm39) critical splice donor site probably null
R9524:Vps13d UTSW 4 144,822,814 (GRCm39) missense
R9616:Vps13d UTSW 4 144,824,701 (GRCm39) missense
R9655:Vps13d UTSW 4 144,813,305 (GRCm39) missense
R9709:Vps13d UTSW 4 144,875,915 (GRCm39) missense
R9767:Vps13d UTSW 4 144,879,306 (GRCm39) missense
R9773:Vps13d UTSW 4 144,818,619 (GRCm39) missense
R9779:Vps13d UTSW 4 144,798,972 (GRCm39) missense
R9796:Vps13d UTSW 4 144,854,505 (GRCm39) critical splice donor site probably null
X0021:Vps13d UTSW 4 144,881,595 (GRCm39) missense probably damaging 0.99
Z1176:Vps13d UTSW 4 144,833,637 (GRCm39) missense
Z1177:Vps13d UTSW 4 144,904,866 (GRCm39) missense
Z1177:Vps13d UTSW 4 144,881,478 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- GCCCAACCCACTGTTTGAAG -3'
(R):5'- TCCAGAAAAGGCAATGTCTTGTAC -3'

Sequencing Primer
(F):5'- CCTAATGAGCAGCTTGACAATGGTC -3'
(R):5'- TACCTTTAGGGGTGTCACTGGAAAAC -3'
Posted On 2017-01-03