Mutagenetix > Incidental Mutation

Incidental Mutation 'R7248:Vps13a'

563722

Institutional Source

Beutler Lab

Gene Symbol

Vps13a

Ensembl Gene

ENSMUSG00000046230

Gene Name

vacuolar protein sorting 13A

Synonyms

4930516E05Rik, 4930543C13Rik, D330038K10Rik

MMRRC Submission

045311-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7248 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

16615366-16780933 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 16678042 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Tyrosine at position 1874 (F1874Y)

Ref Sequence

ENSEMBL: ENSMUSP00000068716 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068156] [ENSMUST00000224149]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000068156
AA Change: F1874Y

PolyPhen 2 Score 0.252 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000068716
Gene: ENSMUSG00000046230
AA Change: F1874Y

Domain	Start	End	E-Value	Type
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 benign
Transcript: ENSMUST00000224149
AA Change: F1874Y

PolyPhen 2 Score 0.150 (Sensitivity: 0.92; Specificity: 0.87)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.4%

Validation Efficiency

97% (75/77)

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: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700006A11Rik	A	G	3: 124,414,310 (GRCm38)		probably null	Het
Aldh16a1	A	G	7: 45,145,594 (GRCm38)	Y484H	probably damaging	Het
Arhgap26	T	C	18: 39,306,854 (GRCm38)		probably null	Het
Atxn7l1	A	G	12: 33,367,195 (GRCm38)	T452A	probably benign	Het
Baz1a	C	T	12: 54,900,508 (GRCm38)	E1119K	probably damaging	Het
Btaf1	A	T	19: 36,945,314 (GRCm38)	E39D	possibly damaging	Het
Bud13	G	T	9: 46,283,115 (GRCm38)	E29*	probably null	Het
Ccdc150	C	T	1: 54,304,898 (GRCm38)	T530I	probably benign	Het
Chd6	G	A	2: 160,961,279 (GRCm38)	Q2160*	probably null	Het
Cluap1	T	A	16: 3,919,500 (GRCm38)	I172N	possibly damaging	Het
Cnot2	T	C	10: 116,498,373 (GRCm38)	N329S	probably benign	Het
Cog4	A	T	8: 110,882,202 (GRCm38)	T175S	unknown	Het
Coq7	C	A	7: 118,529,674 (GRCm38)	R46L	probably benign	Het
D630045J12Rik	A	T	6: 38,168,263 (GRCm38)	V1276E	probably damaging	Het
Dcaf15	A	G	8: 84,102,765 (GRCm38)	V116A	possibly damaging	Het
Ddr2	C	T	1: 169,994,629 (GRCm38)	V417I	probably benign	Het
Defa25	G	A	8: 21,085,200 (GRCm38)	C65Y	probably damaging	Het
Dhx38	T	C	8: 109,558,927 (GRCm38)	T425A	probably benign	Het
Diaph1	T	C	18: 37,889,776 (GRCm38)	T782A	probably benign	Het
Dnah7b	T	A	1: 46,142,085 (GRCm38)	M1044K	possibly damaging	Het
Dusp16	G	A	6: 134,718,977 (GRCm38)	T297M	probably benign	Het
Esyt2	A	G	12: 116,342,238 (GRCm38)	N363D	probably damaging	Het
Fasl	C	T	1: 161,788,191 (GRCm38)	C32Y	possibly damaging	Het
Flg	T	C	3: 93,281,734 (GRCm38)	V137A	probably benign	Het
Gm57858	T	A	3: 36,025,937 (GRCm38)	T224S	probably benign	Het
Gpr150	G	A	13: 76,056,007 (GRCm38)	A273V	probably benign	Het
Grk5	A	G	19: 60,890,607 (GRCm38)	T10A	probably benign	Het
Hivep2	A	G	10: 14,131,165 (GRCm38)	K1169R	possibly damaging	Het
Ido2	A	C	8: 24,540,641 (GRCm38)	Y224*	probably null	Het
Ido2	A	G	8: 24,548,823 (GRCm38)	I149T	probably damaging	Het
Iqca1l	C	T	5: 24,544,271 (GRCm38)	S743N	probably benign	Het
Kctd2	A	G	11: 115,422,019 (GRCm38)	T126A	possibly damaging	Het
Khdc4	T	C	3: 88,693,579 (GRCm38)	S228P	probably damaging	Het
Kif1a	T	C	1: 93,041,583 (GRCm38)	D1090G	probably benign	Het
Klrb1a	A	T	6: 128,609,734 (GRCm38)	H222Q	possibly damaging	Het
Kndc1	A	C	7: 139,920,783 (GRCm38)	H688P	probably damaging	Het
Lrriq1	C	A	10: 103,223,750 (GRCm38)	V141F	possibly damaging	Het
Malrd1	A	G	2: 16,101,911 (GRCm38)	I1845V	unknown	Het
Mob3c	G	A	4: 115,831,684 (GRCm38)	R138H	probably benign	Het
Mre11a	T	A	9: 14,811,913 (GRCm38)	D394E	possibly damaging	Het
Myh7b	A	T	2: 155,622,186 (GRCm38)	I536F	probably damaging	Het
Nacad	T	A	11: 6,598,589 (GRCm38)	K1382*	probably null	Het
Ncor1	T	C	11: 62,384,772 (GRCm38)	K128R	possibly damaging	Het
Or10am5	T	C	7: 6,514,521 (GRCm38)	N303D	probably damaging	Het
Ostn	T	A	16: 27,346,969 (GRCm38)		probably null	Het
Pacs1	G	A	19: 5,138,975 (GRCm38)	T793I	probably damaging	Het
Pcdhb2	T	C	18: 37,296,494 (GRCm38)	S507P	probably damaging	Het
Pde2a	A	G	7: 101,503,390 (GRCm38)	K393E	possibly damaging	Het
Pfkl	T	A	10: 77,989,589 (GRCm38)	N656Y	probably damaging	Het
Phf20	T	A	2: 156,293,411 (GRCm38)		probably null	Het
Plekha6	G	T	1: 133,275,848 (GRCm38)	E550*	probably null	Het
Plxna4	A	T	6: 32,162,160 (GRCm38)	V1691E	probably damaging	Het
Rag1	A	T	2: 101,641,778 (GRCm38)	H1006Q	probably damaging	Het
Rfx4	C	T	10: 84,905,055 (GRCm38)	P679L	probably benign	Het
Ripor2	A	G	13: 24,694,145 (GRCm38)	H301R	probably damaging	Het
Rrp12	A	T	19: 41,883,438 (GRCm38)	I469N	possibly damaging	Het
Serpinb6b	A	G	13: 32,977,576 (GRCm38)	T211A	probably benign	Het
Sf1	A	T	19: 6,376,353 (GRCm38)	H547L	unknown	Het
Slc29a1	T	C	17: 45,592,182 (GRCm38)	D9G	probably damaging	Het
Sptan1	T	A	2: 30,002,299 (GRCm38)	M1075K	probably benign	Het
Syngap1	A	G	17: 26,957,767 (GRCm38)	D474G	probably damaging	Het
Syt16	C	T	12: 74,266,709 (GRCm38)	R470C	probably damaging	Het
Timeless	A	G	10: 128,252,001 (GRCm38)	T1148A	probably benign	Het
Tmem116	A	T	5: 121,463,836 (GRCm38)		probably null	Het
Tmem158	A	T	9: 123,260,325 (GRCm38)	I74N	probably damaging	Het
Traf5	T	A	1: 192,059,017 (GRCm38)	D174V	probably benign	Het
Trim65	A	T	11: 116,127,708 (GRCm38)	I247N	probably benign	Het
Tsfm	A	T	10: 127,011,631 (GRCm38)	V197E	probably benign	Het
Utrn	A	G	10: 12,728,818 (GRCm38)	C539R	possibly damaging	Het
Wdr6	A	G	9: 108,576,039 (GRCm38)	M215T	possibly damaging	Het
Wdr75	T	A	1: 45,817,400 (GRCm38)	W528R	probably damaging	Het
Zc3h7b	A	G	15: 81,771,787 (GRCm38)	D112G	possibly damaging	Het
Zc3hav1	C	T	6: 38,353,976 (GRCm38)	D83N	probably benign	Het
Zfp369	T	A	13: 65,296,117 (GRCm38)	V358E	probably damaging	Het
Zfp946	T	A	17: 22,453,508 (GRCm38)	C29*	probably null	Het
Zng1	A	G	19: 24,921,141 (GRCm38)	S318P	probably damaging	Het

Other mutations in Vps13a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH 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
R0685:Vps13a	UTSW	19	16,780,741 (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
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'- TTTACAAAGCCCCAGGAAGG -3'
(R):5'- TATCCAAATGTGGCCTTGTGATG -3'

Sequencing Primer
(F):5'- GCCCCAGGAAGGAAAATATCTC -3'
(R):5'- ACTATGCTCATATCCTTGCC -3'

Posted On

2019-06-26