Incidental Mutation 'R1826:Vps13d'
ID 206761
Institutional Source Beutler Lab
Gene Symbol Vps13d
Ensembl Gene ENSMUSG00000020220
Gene Name vacuolar protein sorting 13D
Synonyms
MMRRC Submission 039853-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1826 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 144699192-144921575 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 144881573 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 1334 (M1334K)
Ref Sequence ENSEMBL: ENSMUSP00000020441 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020441] [ENSMUST00000036579]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000020441
AA Change: M1334K

PolyPhen 2 Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000020441
Gene: ENSMUSG00000020220
AA Change: M1334K

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: M1340K
SMART Domains Protein: ENSMUSP00000043240
Gene: ENSMUSG00000020220
AA Change: M1340K

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 unknown
Transcript: ENSMUST00000185113
AA Change: M161K
Meta Mutation Damage Score 0.1963 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.8%
  • 10x: 95.1%
  • 20x: 92.0%
Validation Efficiency 95% (116/122)
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: 112 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 T C 19: 43,810,453 (GRCm39) S917P probably benign Het
Acsbg1 C T 9: 54,529,840 (GRCm39) V256M possibly damaging Het
Adam34 T A 8: 44,104,379 (GRCm39) D422V probably damaging Het
Adam6a T A 12: 113,509,742 (GRCm39) V705E possibly damaging Het
Adamts12 C A 15: 11,071,606 (GRCm39) P50Q probably benign Het
Arfgap3 C T 15: 83,187,303 (GRCm39) probably null Het
Aspg T A 12: 112,089,852 (GRCm39) D463E probably damaging Het
Atad2b G A 12: 5,024,094 (GRCm39) S73N probably benign Het
Atp11a T C 8: 12,896,154 (GRCm39) L788P probably damaging Het
B3gnt8 T C 7: 25,328,188 (GRCm39) F206S probably damaging Het
Baz2b T C 2: 59,799,077 (GRCm39) E349G probably benign Het
Bmp2k A T 5: 97,209,261 (GRCm39) probably benign Het
Camta2 A G 11: 70,574,134 (GRCm39) F128L probably damaging Het
Ccdc88a A T 11: 29,439,637 (GRCm39) Q30L possibly damaging Het
Cdh1 T C 8: 107,392,898 (GRCm39) M794T probably benign Het
Cdh5 A G 8: 104,857,723 (GRCm39) N383S possibly damaging Het
Cep85l T C 10: 53,224,908 (GRCm39) D227G possibly damaging Het
Clec4e A G 6: 123,260,591 (GRCm39) S156P probably damaging Het
Col10a1 G T 10: 34,270,645 (GRCm39) G206C probably damaging Het
Col4a2 T C 8: 11,363,509 (GRCm39) probably null Het
Copg2 A G 6: 30,789,777 (GRCm39) M517T probably benign Het
Cyp2f2 T A 7: 26,831,987 (GRCm39) L414Q probably damaging Het
Dact1 G A 12: 71,365,118 (GRCm39) G596D probably damaging Het
Dcaf13 T C 15: 38,982,294 (GRCm39) C87R probably damaging Het
Dchs1 T G 7: 105,406,834 (GRCm39) T2224P probably damaging Het
Dnah12 A G 14: 26,432,174 (GRCm39) M429V probably benign Het
Dppa2 G A 16: 48,137,711 (GRCm39) R231H probably damaging Het
Elavl4 T C 4: 110,108,489 (GRCm39) D78G probably damaging Het
Enthd1 T C 15: 80,358,482 (GRCm39) E346G probably damaging Het
Exoc3l A T 8: 106,020,250 (GRCm39) I225N probably damaging Het
Fasn C T 11: 120,699,325 (GRCm39) probably benign Het
Fbxl7 G A 15: 26,552,851 (GRCm39) R139C possibly damaging Het
Fbxw15 C A 9: 109,388,782 (GRCm39) probably null Het
Flnc A G 6: 29,455,184 (GRCm39) T1971A probably damaging Het
Fnip1 T G 11: 54,356,990 (GRCm39) V33G probably damaging Het
Foxn2 A G 17: 88,794,233 (GRCm39) E390G possibly damaging Het
Fry C T 5: 150,360,174 (GRCm39) S1940L possibly damaging Het
Fzd3 A T 14: 65,490,555 (GRCm39) D9E probably benign Het
Gabrd T C 4: 155,470,943 (GRCm39) Y255C probably damaging Het
Garem1 A T 18: 21,262,509 (GRCm39) F768L probably benign Het
Gas2 T A 7: 51,593,421 (GRCm39) L167Q probably damaging Het
Gm16391 A G 17: 76,591,418 (GRCm39) noncoding transcript Het
Gm1979 A T 5: 26,206,240 (GRCm39) N113K probably damaging Het
Gpr83 G T 9: 14,779,629 (GRCm39) C269F possibly damaging Het
Hdac4 T A 1: 91,912,421 (GRCm39) N352Y probably damaging Het
Hdac9 A G 12: 34,479,491 (GRCm39) probably benign Het
Hhipl2 G A 1: 183,217,253 (GRCm39) S673N probably benign Het
Iffo2 T A 4: 139,341,376 (GRCm39) S417T probably benign Het
Itgb5 G T 16: 33,685,930 (GRCm39) R90L possibly damaging Het
Jade1 T G 3: 41,567,648 (GRCm39) L572W probably damaging Het
Kcnh1 T A 1: 192,095,376 (GRCm39) M478K possibly damaging Het
Kcnma1 C A 14: 23,380,997 (GRCm39) D903Y probably damaging Het
Kcnq4 T A 4: 120,561,701 (GRCm39) H456L probably benign Het
Kif9 C A 9: 110,346,701 (GRCm39) T613K probably benign Het
Krt36 T G 11: 99,993,856 (GRCm39) probably benign Het
Kyat3 A T 3: 142,428,940 (GRCm39) D89V possibly damaging Het
Lnpep A T 17: 17,783,098 (GRCm39) F568I probably damaging Het
Lpl T C 8: 69,354,943 (GRCm39) F444L possibly damaging Het
Lrp1 A T 10: 127,389,576 (GRCm39) V3153E probably damaging Het
Lrrn1 A T 6: 107,544,529 (GRCm39) N109I probably benign Het
Ltn1 A G 16: 87,212,504 (GRCm39) Y686H probably damaging Het
Mcoln2 A C 3: 145,881,227 (GRCm39) D166A possibly damaging Het
Ms4a6b A T 19: 11,501,298 (GRCm39) I103F probably damaging Het
Mtmr10 T G 7: 63,987,214 (GRCm39) S585A probably benign Het
Mx1 T C 16: 97,256,837 (GRCm39) N114S possibly damaging Het
Mysm1 A T 4: 94,858,923 (GRCm39) N75K probably benign Het
Nkx1-1 A G 5: 33,591,277 (GRCm39) V15A unknown Het
Nlrp1a G A 11: 71,013,573 (GRCm39) T559I possibly damaging Het
Nlrp1a T A 11: 70,998,806 (GRCm39) probably benign Het
Oas1f A G 5: 120,993,652 (GRCm39) K288R probably benign Het
Or10q1 T A 19: 13,726,711 (GRCm39) D80E probably benign Het
Or55b3 A G 7: 102,126,720 (GRCm39) L119P probably damaging Het
Or9e1 T A 11: 58,732,257 (GRCm39) C106S probably benign Het
Pcdhb2 T A 18: 37,429,038 (GRCm39) V337D probably damaging Het
Pcdhb5 C T 18: 37,454,522 (GRCm39) R301* probably null Het
Phf12 T C 11: 77,915,780 (GRCm39) probably benign Het
Pik3c2a C T 7: 115,967,352 (GRCm39) D862N probably benign Het
Pkhd1l1 T A 15: 44,366,741 (GRCm39) L740I possibly damaging Het
Ppp1r9a A T 6: 5,111,060 (GRCm39) probably benign Het
Prg4 T C 1: 150,327,760 (GRCm39) D820G probably benign Het
Prmt9 C T 8: 78,282,303 (GRCm39) Q67* probably null Het
Prob1 T C 18: 35,786,628 (GRCm39) E542G possibly damaging Het
Pttg1 A G 11: 43,311,193 (GRCm39) V188A probably damaging Het
Rassf1 T A 9: 107,435,392 (GRCm39) L260H probably damaging Het
Rbm5 T A 9: 107,619,613 (GRCm39) Q766L probably damaging Het
Rbms3 T A 9: 116,651,936 (GRCm39) Y137F probably damaging Het
Rccd1 T C 7: 79,969,966 (GRCm39) probably benign Het
Rnf182 G A 13: 43,822,010 (GRCm39) W187* probably null Het
S100a11 A T 3: 93,433,428 (GRCm39) I91F probably benign Het
Setd4 T A 16: 93,388,187 (GRCm39) K100* probably null Het
Simc1 T A 13: 54,672,452 (GRCm39) C267S probably benign Het
Slc16a1 G T 3: 104,558,255 (GRCm39) A91S probably benign Het
Slc36a1 A G 11: 55,111,279 (GRCm39) N133S probably benign Het
Ssxb16 T A X: 8,746,944 (GRCm39) Y133* probably null Het
Svil C T 18: 5,063,383 (GRCm39) P885S probably benign Het
Svop A T 5: 114,198,117 (GRCm39) probably null Het
Taar7d T C 10: 23,903,474 (GRCm39) Y119H probably damaging Het
Tasor2 T A 13: 3,631,759 (GRCm39) N914I probably damaging Het
Tgfb3 T C 12: 86,108,818 (GRCm39) T304A probably benign Het
Tmem94 C A 11: 115,684,039 (GRCm39) C786* probably null Het
Tnfrsf4 T A 4: 156,100,736 (GRCm39) probably null Het
Tns1 C A 1: 73,992,793 (GRCm39) M1I probably null Het
Trappc13 C T 13: 104,306,327 (GRCm39) probably null Het
Trim72 T C 7: 127,607,016 (GRCm39) F182L possibly damaging Het
Ttc6 T C 12: 57,707,033 (GRCm39) S647P probably benign Het
Tulp1 A G 17: 28,575,341 (GRCm39) L400P possibly damaging Het
Vegfc C T 8: 54,634,347 (GRCm39) T342M possibly damaging Het
Vit T A 17: 78,842,105 (GRCm39) V15E probably benign Het
Zfp280d T C 9: 72,206,062 (GRCm39) V23A probably damaging Het
Zfp608 A G 18: 55,031,648 (GRCm39) I764T probably benign Het
Zfp94 T C 7: 24,008,540 (GRCm39) Y33C probably damaging Het
Zfyve26 T A 12: 79,315,823 (GRCm39) I1218F probably damaging 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
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
R5712:Vps13d UTSW 4 144,813,743 (GRCm39) missense probably benign 0.07
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'- ATTTGCCCCAAGTGTCCCAC -3'
(R):5'- GAGTTTCACCTTTGCTGAGAAATC -3'

Sequencing Primer
(F):5'- GTGTCCCACCAACAGCTCAG -3'
(R):5'- CCTTTGCTGAGAAATCAAAACAGG -3'
Posted On 2014-06-23