Incidental Mutation 'R0685:Vps13a'
ID 61152
Institutional Source Beutler Lab
Gene Symbol Vps13a
Ensembl Gene ENSMUSG00000046230
Gene Name vacuolar protein sorting 13A
Synonyms 4930516E05Rik, 4930543C13Rik, D330038K10Rik
MMRRC Submission 038870-MU
Accession Numbers

Ncbi RefSeq: NM_173028.4; MGI:2444304

Essential gene? Non essential (E-score: 0.000) question?
Stock # R0685 (G1)
Quality Score 106
Status Validated
Chromosome 19
Chromosomal Location 16615366-16780933 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 16780741 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 10 (V10A)
Ref Sequence ENSEMBL: ENSMUSP00000068716 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068156] [ENSMUST00000224149]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000051080
Predicted Effect probably damaging
Transcript: ENSMUST00000068156
AA Change: V10A

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000068716
Gene: ENSMUSG00000046230
AA Change: V10A

DomainStartEndE-ValueType
Pfam:Chorein_N 3 117 5.4e-38 PFAM
Pfam:VPS13 139 371 3.7e-64 PFAM
low complexity region 553 563 N/A INTRINSIC
Pfam:VPS13_mid_rpt 567 791 1.4e-69 PFAM
Pfam:VPS13_mid_rpt 1138 1329 2e-10 PFAM
low complexity region 1367 1377 N/A INTRINSIC
Blast:INB 1575 1855 1e-149 BLAST
Pfam:SHR-BD 2200 2449 1.3e-35 PFAM
low complexity region 2510 2521 N/A INTRINSIC
low complexity region 2632 2648 N/A INTRINSIC
low complexity region 2719 2731 N/A INTRINSIC
Pfam:VPS13_C 2755 2935 8.9e-66 PFAM
Pfam:ATG_C 2938 3029 1.6e-16 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000224149
AA Change: V10A

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224428
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225764
Meta Mutation Damage Score 0.5676 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 95.6%
Validation Efficiency 98% (89/91)
MGI Phenotype Strain: 3531502
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene may control steps in the cycling of proteins through the trans-Golgi network to endosomes, lysosomes and the plasma membrane. Mutations in this gene cause the autosomal recessive disorder, chorea-acanthocytosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]
PHENOTYPE: Aging mice homozygous for a knock-out allele display motor dysfunction and abnormal social interaction, hematologic anomalies including acanthocytosis, selective atrophy of the striatum with significant apoptosis and gliosis, and reduced homovanillic acid levels in midbrain. [provided by MGI curators]
Allele List at MGI

All alleles(8) : Targeted(3) Gene trapped(5)

Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020N01Rik A G 10: 21,593,438 (GRCm38) D17G probably damaging Het
Abi3bp A G 16: 56,532,953 (GRCm38) T82A possibly damaging Het
Adgre4 A C 17: 55,792,035 (GRCm38) E180D probably benign Het
Ankrd28 G A 14: 31,743,450 (GRCm38) probably benign Het
Aoc3 A G 11: 101,336,447 (GRCm38) D382G possibly damaging Het
Apob C A 12: 8,010,742 (GRCm38) R3075S probably benign Het
Aqr A G 2: 114,140,977 (GRCm38) F459S probably damaging Het
Bcr T C 10: 75,131,643 (GRCm38) W570R probably damaging Het
Bloc1s5 C T 13: 38,603,919 (GRCm38) R163K probably benign Het
Bod1 A T 11: 31,669,267 (GRCm38) N101K possibly damaging Het
Bysl A T 17: 47,602,471 (GRCm38) S296T probably benign Het
Chl1 G A 6: 103,708,542 (GRCm38) probably null Het
Clstn1 G A 4: 149,646,855 (GRCm38) A885T probably benign Het
Cyp3a25 G T 5: 145,998,546 (GRCm38) P87T probably damaging Het
Dync1h1 T C 12: 110,657,192 (GRCm38) V3633A probably damaging Het
Elp4 C A 2: 105,792,277 (GRCm38) C241F possibly damaging Het
Fat4 T A 3: 39,001,178 (GRCm38) F4182Y probably benign Het
Gabbr2 G A 4: 46,787,521 (GRCm38) H381Y possibly damaging Het
Gm10577 G T 4: 101,020,318 (GRCm38) probably benign Het
Gm884 T C 11: 103,616,888 (GRCm38) probably benign Het
Gm9955 G T 18: 24,709,257 (GRCm38) probably benign Het
Gstm5 T A 3: 107,897,319 (GRCm38) I73N probably damaging Het
Gypa T A 8: 80,496,702 (GRCm38) probably benign Het
Hectd2 T A 19: 36,569,431 (GRCm38) V64D probably damaging Het
Igkv10-95 T A 6: 68,680,559 (GRCm38) Y20N probably benign Het
Il15 T C 8: 82,337,559 (GRCm38) probably benign Het
Iqca C A 1: 90,142,731 (GRCm38) G133V probably null Het
Kiz C A 2: 146,856,058 (GRCm38) probably benign Het
Lcmt2 C A 2: 121,139,240 (GRCm38) S234I probably benign Het
Lilra5 A G 7: 4,241,957 (GRCm38) probably benign Het
Lin37 T C 7: 30,555,874 (GRCm38) E187G probably damaging Het
Mcmdc2 T A 1: 9,911,814 (GRCm38) probably null Het
Mctp1 T C 13: 76,825,799 (GRCm38) probably null Het
Mdp1 C A 14: 55,659,269 (GRCm38) G112* probably null Het
Mmp15 T C 8: 95,372,134 (GRCm38) Y530H possibly damaging Het
Mtss1l T C 8: 110,727,397 (GRCm38) probably null Het
Muc5ac T C 7: 141,807,709 (GRCm38) S1586P probably benign Het
Nap1l5 A T 6: 58,906,772 (GRCm38) C66S possibly damaging Het
Ninl G T 2: 150,939,855 (GRCm38) Q1237K possibly damaging Het
Olfr1160 T C 2: 88,006,418 (GRCm38) E111G probably damaging Het
Olfr495 A T 7: 108,395,263 (GRCm38) T48S possibly damaging Het
Orc6 T G 8: 85,301,154 (GRCm38) S37R possibly damaging Het
Papss1 A C 3: 131,583,093 (GRCm38) N119H possibly damaging Het
Phf13 A T 4: 151,991,612 (GRCm38) F278I probably damaging Het
Pole2 C A 12: 69,211,413 (GRCm38) A239S probably damaging Het
Ppt2 T C 17: 34,626,572 (GRCm38) D75G probably damaging Het
Psd2 A G 18: 36,002,991 (GRCm38) D443G possibly damaging Het
Psen1 C A 12: 83,714,820 (GRCm38) S132* probably null Het
Psme4 A G 11: 30,878,415 (GRCm38) T1812A probably damaging Het
Rasgrf1 T C 9: 89,915,482 (GRCm38) probably benign Het
Reep3 A G 10: 67,021,739 (GRCm38) probably benign Het
Rexo4 A T 2: 26,958,574 (GRCm38) probably benign Het
Rnf6 A C 5: 146,211,658 (GRCm38) S183R probably damaging Het
Scai A T 2: 39,103,737 (GRCm38) M297K probably damaging Het
Scn9a A T 2: 66,483,499 (GRCm38) S1947R probably benign Het
Sema6c T C 3: 95,172,710 (GRCm38) C772R possibly damaging Het
Skint7 T C 4: 111,980,345 (GRCm38) S107P possibly damaging Het
Slc24a3 A G 2: 145,606,795 (GRCm38) N420D probably benign Het
Smc1b T C 15: 85,070,820 (GRCm38) D1077G possibly damaging Het
Smg7 G A 1: 152,866,648 (GRCm38) P82L probably damaging Het
Sp3 A C 2: 72,970,998 (GRCm38) F268V probably damaging Het
Srms T C 2: 181,212,633 (GRCm38) D47G probably benign Het
Ss18 A C 18: 14,651,181 (GRCm38) M150R probably damaging Het
Taf5 G A 19: 47,074,854 (GRCm38) R281Q probably benign Het
Tars T C 15: 11,385,173 (GRCm38) K644R probably benign Het
Tctex1d1 T C 4: 103,002,538 (GRCm38) Y96H probably damaging Het
Tinag C A 9: 76,952,003 (GRCm38) W441L probably damaging Het
Tmtc1 T C 6: 148,411,240 (GRCm38) S244G probably benign Het
Tpr T C 1: 150,433,725 (GRCm38) V1670A possibly damaging Het
Trpv3 A G 11: 73,296,814 (GRCm38) probably benign Het
Uhrf1 G T 17: 56,310,742 (GRCm38) V155L probably damaging Het
Ush2a G A 1: 188,400,278 (GRCm38) C899Y probably damaging Het
Vmn2r115 G A 17: 23,359,275 (GRCm38) R574H probably benign Het
Vmn2r63 T C 7: 42,928,010 (GRCm38) D368G probably benign Het
Wbp11 A G 6: 136,814,638 (GRCm38) probably benign Het
Zcwpw1 A G 5: 137,799,592 (GRCm38) D145G probably benign Het
Zfp607a G A 7: 27,878,476 (GRCm38) V324I probably damaging Het
Zfp618 A G 4: 63,133,774 (GRCm38) I931V probably benign Het
Zfp821 T C 8: 109,724,542 (GRCm38) V389A possibly damaging Het
Zfp976 T A 7: 42,613,717 (GRCm38) H232L probably damaging Het
Other mutations in Vps13a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00465:Vps13a APN 19 16,752,175 (GRCm38) missense probably damaging 0.98
IGL00537:Vps13a APN 19 16,680,045 (GRCm38) missense probably benign 0.03
IGL00562:Vps13a APN 19 16,734,714 (GRCm38) critical splice donor site probably null
IGL00563:Vps13a APN 19 16,734,714 (GRCm38) critical splice donor site probably null
IGL00579:Vps13a APN 19 16,707,362 (GRCm38) missense probably benign 0.29
IGL00662:Vps13a APN 19 16,704,540 (GRCm38) missense probably damaging 0.96
IGL00667:Vps13a APN 19 16,759,676 (GRCm38) missense probably damaging 1.00
IGL01102:Vps13a APN 19 16,651,417 (GRCm38) critical splice donor site probably null
IGL01139:Vps13a APN 19 16,640,625 (GRCm38) missense probably damaging 0.99
IGL01142:Vps13a APN 19 16,687,115 (GRCm38) missense possibly damaging 0.86
IGL01361:Vps13a APN 19 16,743,007 (GRCm38) missense probably damaging 1.00
IGL01386:Vps13a APN 19 16,701,152 (GRCm38) missense possibly damaging 0.87
IGL01593:Vps13a APN 19 16,762,181 (GRCm38) missense probably damaging 0.98
IGL01700:Vps13a APN 19 16,744,857 (GRCm38) nonsense probably null
IGL01767:Vps13a APN 19 16,663,894 (GRCm38) missense probably damaging 1.00
IGL01782:Vps13a APN 19 16,754,337 (GRCm38) missense probably damaging 0.98
IGL01808:Vps13a APN 19 16,710,286 (GRCm38) missense probably damaging 1.00
IGL01812:Vps13a APN 19 16,715,060 (GRCm38) missense probably benign
IGL01829:Vps13a APN 19 16,619,443 (GRCm38) missense probably benign 0.01
IGL01893:Vps13a APN 19 16,663,775 (GRCm38) missense probably damaging 1.00
IGL02222:Vps13a APN 19 16,682,175 (GRCm38) missense probably benign 0.06
IGL02295:Vps13a APN 19 16,715,042 (GRCm38) splice site probably benign
IGL02465:Vps13a APN 19 16,710,941 (GRCm38) missense probably benign 0.11
IGL02492:Vps13a APN 19 16,647,637 (GRCm38) missense probably damaging 1.00
IGL02581:Vps13a APN 19 16,655,322 (GRCm38) missense probably benign 0.41
IGL02633:Vps13a APN 19 16,720,408 (GRCm38) missense possibly damaging 0.82
IGL02641:Vps13a APN 19 16,698,821 (GRCm38) missense probably benign 0.01
IGL02659:Vps13a APN 19 16,652,699 (GRCm38) missense probably damaging 1.00
IGL02827:Vps13a APN 19 16,641,634 (GRCm38) missense possibly damaging 0.91
IGL02943:Vps13a APN 19 16,663,886 (GRCm38) missense probably damaging 1.00
IGL03057:Vps13a APN 19 16,668,694 (GRCm38) missense probably damaging 1.00
IGL03077:Vps13a APN 19 16,710,882 (GRCm38) missense probably benign
IGL03184:Vps13a APN 19 16,654,370 (GRCm38) missense probably benign 0.00
eggs UTSW 19 16,701,165 (GRCm38) missense probably damaging 1.00
excambio UTSW 19 16,745,947 (GRCm38) splice site probably null
Faster UTSW 19 16,619,485 (GRCm38) missense probably damaging 1.00
Ham UTSW 19 16,677,969 (GRCm38) missense probably benign 0.08
interchange UTSW 19 16,668,690 (GRCm38) missense probably damaging 1.00
PIT4377001:Vps13a UTSW 19 16,740,901 (GRCm38) missense probably damaging 1.00
R0045:Vps13a UTSW 19 16,640,810 (GRCm38) nonsense probably null
R0045:Vps13a UTSW 19 16,640,810 (GRCm38) nonsense probably null
R0048:Vps13a UTSW 19 16,676,140 (GRCm38) missense probably damaging 1.00
R0062:Vps13a UTSW 19 16,668,690 (GRCm38) missense probably damaging 1.00
R0062:Vps13a UTSW 19 16,668,690 (GRCm38) missense probably damaging 1.00
R0107:Vps13a UTSW 19 16,691,824 (GRCm38) missense probably benign 0.03
R0135:Vps13a UTSW 19 16,780,765 (GRCm38) missense probably damaging 1.00
R0138:Vps13a UTSW 19 16,660,499 (GRCm38) missense possibly damaging 0.95
R0346:Vps13a UTSW 19 16,677,969 (GRCm38) missense probably benign 0.08
R0359:Vps13a UTSW 19 16,641,577 (GRCm38) missense probably damaging 0.99
R0530:Vps13a UTSW 19 16,655,206 (GRCm38) splice site probably benign
R0541:Vps13a UTSW 19 16,704,577 (GRCm38) missense probably benign 0.00
R0614:Vps13a UTSW 19 16,652,694 (GRCm38) missense probably damaging 1.00
R0801:Vps13a UTSW 19 16,686,656 (GRCm38) splice site probably benign
R0835:Vps13a UTSW 19 16,734,882 (GRCm38) splice site probably null
R0848:Vps13a UTSW 19 16,698,897 (GRCm38) missense probably damaging 1.00
R1114:Vps13a UTSW 19 16,750,151 (GRCm38) missense probably benign 0.41
R1205:Vps13a UTSW 19 16,640,541 (GRCm38) missense probably damaging 1.00
R1365:Vps13a UTSW 19 16,619,446 (GRCm38) missense probably damaging 1.00
R1445:Vps13a UTSW 19 16,701,238 (GRCm38) nonsense probably null
R1451:Vps13a UTSW 19 16,710,864 (GRCm38) missense probably benign 0.01
R1479:Vps13a UTSW 19 16,750,114 (GRCm38) splice site probably benign
R1533:Vps13a UTSW 19 16,701,130 (GRCm38) nonsense probably null
R1600:Vps13a UTSW 19 16,666,272 (GRCm38) missense probably benign 0.01
R1870:Vps13a UTSW 19 16,759,952 (GRCm38) missense probably damaging 1.00
R1871:Vps13a UTSW 19 16,664,664 (GRCm38) missense probably benign 0.01
R1959:Vps13a UTSW 19 16,677,938 (GRCm38) missense possibly damaging 0.49
R1960:Vps13a UTSW 19 16,725,631 (GRCm38) missense probably damaging 1.00
R1993:Vps13a UTSW 19 16,722,458 (GRCm38) missense probably benign 0.07
R2257:Vps13a UTSW 19 16,682,174 (GRCm38) missense possibly damaging 0.85
R2276:Vps13a UTSW 19 16,710,426 (GRCm38) missense possibly damaging 0.47
R2326:Vps13a UTSW 19 16,743,057 (GRCm38) missense possibly damaging 0.71
R2338:Vps13a UTSW 19 16,720,453 (GRCm38) missense probably damaging 1.00
R2359:Vps13a UTSW 19 16,652,679 (GRCm38) splice site probably benign
R2421:Vps13a UTSW 19 16,759,671 (GRCm38) missense probably benign
R2847:Vps13a UTSW 19 16,703,599 (GRCm38) missense probably damaging 0.98
R3081:Vps13a UTSW 19 16,664,737 (GRCm38) missense probably benign 0.02
R3522:Vps13a UTSW 19 16,766,493 (GRCm38) splice site probably benign
R3613:Vps13a UTSW 19 16,685,402 (GRCm38) missense probably damaging 1.00
R3797:Vps13a UTSW 19 16,745,947 (GRCm38) splice site probably null
R3874:Vps13a UTSW 19 16,744,953 (GRCm38) missense probably benign 0.01
R4032:Vps13a UTSW 19 16,616,899 (GRCm38) missense probably damaging 1.00
R4111:Vps13a UTSW 19 16,640,628 (GRCm38) missense probably damaging 1.00
R4383:Vps13a UTSW 19 16,701,165 (GRCm38) missense probably damaging 1.00
R4504:Vps13a UTSW 19 16,695,502 (GRCm38) missense possibly damaging 0.93
R4578:Vps13a UTSW 19 16,682,110 (GRCm38) missense probably damaging 0.98
R4587:Vps13a UTSW 19 16,640,039 (GRCm38) missense probably damaging 1.00
R4588:Vps13a UTSW 19 16,640,039 (GRCm38) missense probably damaging 1.00
R4605:Vps13a UTSW 19 16,640,039 (GRCm38) missense probably damaging 1.00
R4714:Vps13a UTSW 19 16,749,856 (GRCm38) missense probably benign 0.01
R4756:Vps13a UTSW 19 16,655,216 (GRCm38) missense probably benign 0.01
R4831:Vps13a UTSW 19 16,677,992 (GRCm38) missense probably benign 0.04
R5068:Vps13a UTSW 19 16,746,058 (GRCm38) missense probably benign 0.01
R5070:Vps13a UTSW 19 16,654,484 (GRCm38) missense probably benign
R5082:Vps13a UTSW 19 16,744,893 (GRCm38) missense probably damaging 1.00
R5182:Vps13a UTSW 19 16,695,499 (GRCm38) missense possibly damaging 0.81
R5189:Vps13a UTSW 19 16,685,315 (GRCm38) missense probably damaging 1.00
R5283:Vps13a UTSW 19 16,677,970 (GRCm38) missense probably damaging 0.96
R5294:Vps13a UTSW 19 16,641,667 (GRCm38) missense probably damaging 1.00
R5304:Vps13a UTSW 19 16,710,387 (GRCm38) missense possibly damaging 0.78
R5554:Vps13a UTSW 19 16,722,411 (GRCm38) missense probably damaging 1.00
R5592:Vps13a UTSW 19 16,725,571 (GRCm38) missense probably damaging 1.00
R5611:Vps13a UTSW 19 16,725,572 (GRCm38) missense probably damaging 1.00
R5665:Vps13a UTSW 19 16,668,690 (GRCm38) missense probably damaging 1.00
R5671:Vps13a UTSW 19 16,715,100 (GRCm38) missense probably benign 0.03
R5684:Vps13a UTSW 19 16,699,045 (GRCm38) missense probably benign 0.00
R5767:Vps13a UTSW 19 16,664,564 (GRCm38) missense probably damaging 1.00
R5810:Vps13a UTSW 19 16,666,324 (GRCm38) missense probably benign 0.00
R5866:Vps13a UTSW 19 16,680,023 (GRCm38) missense probably benign 0.04
R5886:Vps13a UTSW 19 16,664,562 (GRCm38) missense probably benign 0.01
R5933:Vps13a UTSW 19 16,660,530 (GRCm38) missense probably benign 0.34
R5965:Vps13a UTSW 19 16,619,028 (GRCm38) splice site probably null
R6259:Vps13a UTSW 19 16,687,170 (GRCm38) nonsense probably null
R6346:Vps13a UTSW 19 16,682,214 (GRCm38) missense possibly damaging 0.94
R6459:Vps13a UTSW 19 16,664,018 (GRCm38) missense possibly damaging 0.56
R6485:Vps13a UTSW 19 16,680,050 (GRCm38) missense probably damaging 0.99
R6520:Vps13a UTSW 19 16,725,579 (GRCm38) missense probably damaging 1.00
R6644:Vps13a UTSW 19 16,744,919 (GRCm38) missense possibly damaging 0.90
R6932:Vps13a UTSW 19 16,678,075 (GRCm38) missense probably benign 0.01
R6934:Vps13a UTSW 19 16,676,194 (GRCm38) missense probably damaging 1.00
R6951:Vps13a UTSW 19 16,723,740 (GRCm38) missense probably benign 0.00
R7027:Vps13a UTSW 19 16,664,664 (GRCm38) missense probably benign 0.01
R7126:Vps13a UTSW 19 16,710,879 (GRCm38) missense probably benign
R7206:Vps13a UTSW 19 16,754,298 (GRCm38) missense probably damaging 1.00
R7248:Vps13a UTSW 19 16,678,042 (GRCm38) missense probably benign 0.25
R7252:Vps13a UTSW 19 16,661,064 (GRCm38) missense probably benign 0.00
R7255:Vps13a UTSW 19 16,654,339 (GRCm38) critical splice donor site probably null
R7382:Vps13a UTSW 19 16,619,485 (GRCm38) missense probably damaging 1.00
R7422:Vps13a UTSW 19 16,750,173 (GRCm38) missense probably damaging 1.00
R7425:Vps13a UTSW 19 16,723,702 (GRCm38) missense probably benign 0.13
R7523:Vps13a UTSW 19 16,703,789 (GRCm38) missense probably benign
R7586:Vps13a UTSW 19 16,647,598 (GRCm38) missense probably benign 0.08
R7587:Vps13a UTSW 19 16,703,789 (GRCm38) missense probably benign 0.00
R7593:Vps13a UTSW 19 16,725,663 (GRCm38) missense probably damaging 1.00
R7637:Vps13a UTSW 19 16,750,149 (GRCm38) missense probably benign 0.02
R7763:Vps13a UTSW 19 16,746,000 (GRCm38) missense possibly damaging 0.95
R7813:Vps13a UTSW 19 16,651,456 (GRCm38) missense possibly damaging 0.81
R7815:Vps13a UTSW 19 16,725,572 (GRCm38) missense probably damaging 1.00
R7861:Vps13a UTSW 19 16,655,304 (GRCm38) missense probably damaging 1.00
R7909:Vps13a UTSW 19 16,720,430 (GRCm38) nonsense probably null
R7939:Vps13a UTSW 19 16,740,791 (GRCm38) missense possibly damaging 0.94
R8108:Vps13a UTSW 19 16,640,787 (GRCm38) missense probably damaging 1.00
R8123:Vps13a UTSW 19 16,647,702 (GRCm38) missense probably benign 0.01
R8134:Vps13a UTSW 19 16,654,354 (GRCm38) missense possibly damaging 0.71
R8168:Vps13a UTSW 19 16,749,548 (GRCm38) missense probably benign 0.09
R8272:Vps13a UTSW 19 16,749,845 (GRCm38) critical splice donor site probably null
R8293:Vps13a UTSW 19 16,668,605 (GRCm38) missense possibly damaging 0.81
R8303:Vps13a UTSW 19 16,616,906 (GRCm38) missense probably benign 0.00
R8383:Vps13a UTSW 19 16,723,705 (GRCm38) missense possibly damaging 0.83
R8386:Vps13a UTSW 19 16,701,119 (GRCm38) critical splice donor site probably null
R8433:Vps13a UTSW 19 16,741,236 (GRCm38) missense possibly damaging 0.56
R8436:Vps13a UTSW 19 16,740,793 (GRCm38) missense probably benign 0.10
R8450:Vps13a UTSW 19 16,654,507 (GRCm38) splice site probably null
R8476:Vps13a UTSW 19 16,722,457 (GRCm38) missense possibly damaging 0.60
R8501:Vps13a UTSW 19 16,682,120 (GRCm38) missense probably benign 0.39
R8552:Vps13a UTSW 19 16,754,320 (GRCm38) missense probably damaging 0.99
R8680:Vps13a UTSW 19 16,645,906 (GRCm38) missense possibly damaging 0.84
R8784:Vps13a UTSW 19 16,664,789 (GRCm38) missense probably damaging 1.00
R8871:Vps13a UTSW 19 16,663,822 (GRCm38) missense probably damaging 1.00
R8945:Vps13a UTSW 19 16,664,750 (GRCm38) missense probably damaging 1.00
R8948:Vps13a UTSW 19 16,745,976 (GRCm38) missense probably damaging 0.99
R8950:Vps13a UTSW 19 16,745,976 (GRCm38) missense probably damaging 0.99
R8960:Vps13a UTSW 19 16,705,883 (GRCm38) missense possibly damaging 0.67
R9189:Vps13a UTSW 19 16,686,597 (GRCm38) missense probably benign
R9366:Vps13a UTSW 19 16,695,530 (GRCm38) missense probably damaging 1.00
R9505:Vps13a UTSW 19 16,742,544 (GRCm38) missense possibly damaging 0.94
R9601:Vps13a UTSW 19 16,645,973 (GRCm38) missense possibly damaging 0.84
R9735:Vps13a UTSW 19 16,723,747 (GRCm38) missense probably damaging 1.00
R9776:Vps13a UTSW 19 16,759,594 (GRCm38) missense probably benign
R9796:Vps13a UTSW 19 16,654,464 (GRCm38) missense probably benign 0.01
X0061:Vps13a UTSW 19 16,645,868 (GRCm38) missense probably benign 0.40
X0066:Vps13a UTSW 19 16,742,553 (GRCm38) missense probably benign 0.33
Z1177:Vps13a UTSW 19 16,699,113 (GRCm38) critical splice acceptor site probably null
Z31818:Vps13a UTSW 19 16,780,754 (GRCm38) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- CGCCCCGCTTTACATAACTTGAAGG -3'
(R):5'- GGCGTTCCTGTCGGTTATCATCAC -3'

Sequencing Primer
(F):5'- CTTTACATAACTTGAAGGGCGAGG -3'
(R):5'- TCCTAGAGAAAGTTCGCTGC -3'
Posted On 2013-07-30