Mutagenetix > Incidental Mutation

Incidental Mutation 'R0440:Vps13c'

46695

Institutional Source

Beutler Lab

Gene Symbol

Vps13c

Ensembl Gene

ENSMUSG00000035284

Gene Name

vacuolar protein sorting 13C

Synonyms

C230055H22Rik

MMRRC Submission

038641-MU

Accession Numbers

Genbank: NM_177184; MGI: 2444207

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0440 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

67840396-67995638 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 67972861 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Serine at position 3442 (G3442S)

Ref Sequence

ENSEMBL: ENSMUSP00000077040 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077879]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000077879
AA Change: G3442S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: G3442S

Domain	Start	End	E-Value	Type
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: G575S

Predicted Effect

probably benign
Transcript: ENSMUST00000215524

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000216856

Meta Mutation Damage Score

0.4092

Coding Region Coverage

1x: 99.6%
3x: 98.8%
10x: 97.0%
20x: 94.1%

Validation Efficiency

99% (68/69)

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: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A4galt	G	A	15: 83,228,493 (GRCm38)	R30W	probably damaging	Het
Adam7	T	C	14: 68,510,856 (GRCm38)		probably null	Het
Agl	A	T	3: 116,758,806 (GRCm38)	L1158Q	probably damaging	Het
Akap9	T	C	5: 4,064,569 (GRCm38)	S66P	probably damaging	Het
Akr1c20	T	A	13: 4,487,208 (GRCm38)	D316V	probably benign	Het
App	C	A	16: 85,056,414 (GRCm38)	E259*	probably null	Het
Arhgef4	A	G	1: 34,745,448 (GRCm38)		probably null	Het
Armc9	G	A	1: 86,194,262 (GRCm38)		probably null	Het
Ass1	A	T	2: 31,514,819 (GRCm38)	N371Y	probably damaging	Het
Btaf1	C	T	19: 36,986,653 (GRCm38)	P875S	probably damaging	Het
Cc2d1b	T	A	4: 108,625,816 (GRCm38)		probably null	Het
Ccar1	C	T	10: 62,780,457 (GRCm38)	V165I	possibly damaging	Het
Ccdc106	A	T	7: 5,060,245 (GRCm38)	I250F	probably damaging	Het
Ccny	T	C	18: 9,332,917 (GRCm38)	I205V	probably benign	Het
Cfap52	T	A	11: 67,954,088 (GRCm38)	I52L	probably benign	Het
Chd8	T	A	14: 52,204,826 (GRCm38)	T2096S	possibly damaging	Het
Clstn3	G	A	6: 124,451,413 (GRCm38)	T423I	probably damaging	Het
Col13a1	T	C	10: 61,867,483 (GRCm38)	D440G	possibly damaging	Het
Dclk3	G	A	9: 111,469,163 (GRCm38)	V592M	probably damaging	Het
Ddx31	A	T	2: 28,857,132 (GRCm38)	I208F	probably damaging	Het
Dlat	A	T	9: 50,645,119 (GRCm38)		probably null	Het
Eml4	T	C	17: 83,446,058 (GRCm38)		probably null	Het
Enpp2	T	A	15: 54,847,237 (GRCm38)		probably benign	Het
Fryl	T	C	5: 73,086,972 (GRCm38)	S38G	possibly damaging	Het
Gcnt1	G	A	19: 17,330,316 (GRCm38)	T15I	probably benign	Het
Gm21834	T	C	17: 57,742,126 (GRCm38)	T32A	possibly damaging	Het
Golga2	A	G	2: 32,302,933 (GRCm38)	D394G	probably damaging	Het
Gtf3c4	G	T	2: 28,840,169 (GRCm38)		probably null	Het
Igkv4-69	A	G	6: 69,284,269 (GRCm38)		probably benign	Het
Inpp5j	T	C	11: 3,501,150 (GRCm38)	R500G	possibly damaging	Het
Kif5b	A	T	18: 6,226,980 (GRCm38)		probably benign	Het
Klhl36	A	G	8: 119,876,551 (GRCm38)	E515G	probably damaging	Het
Lifr	C	T	15: 7,157,191 (GRCm38)	R59*	probably null	Het
Lrif1	A	T	3: 106,734,398 (GRCm38)	Q10L	possibly damaging	Het
Lrp8	A	G	4: 107,869,098 (GRCm38)	E908G	probably damaging	Het
Lrrc23	A	T	6: 124,770,704 (GRCm38)	D307E	probably benign	Het
Mpv17l	T	C	16: 13,944,719 (GRCm38)	F27L	probably damaging	Het
Mta3	C	T	17: 83,766,587 (GRCm38)	A76V	probably damaging	Het
Muc5ac	T	A	7: 141,792,034 (GRCm38)	Y202*	probably null	Het
Naprt	A	G	15: 75,891,069 (GRCm38)		probably benign	Het
Npr2	T	A	4: 43,650,315 (GRCm38)	V960D	probably damaging	Het
Oca2	A	T	7: 56,423,352 (GRCm38)	Y765F	probably benign	Het
Olfr715	A	T	7: 107,128,732 (GRCm38)	H220Q	probably benign	Het
Plxna2	T	A	1: 194,644,404 (GRCm38)	Y215*	probably null	Het
Prdm16	G	A	4: 154,476,627 (GRCm38)		probably benign	Het
Ptn	A	G	6: 36,744,497 (GRCm38)	S3P	probably benign	Het
Pus10	T	C	11: 23,673,331 (GRCm38)		probably benign	Het
Rad21	A	T	15: 51,968,358 (GRCm38)	D442E	probably benign	Het
Rmdn2	A	G	17: 79,667,955 (GRCm38)	H291R	probably damaging	Het
Rp1	A	G	1: 4,345,640 (GRCm38)	S1750P	probably damaging	Het
Samd4b	A	T	7: 28,408,160 (GRCm38)	I228N	probably benign	Het
Sdr9c7	G	T	10: 127,898,953 (GRCm38)		probably benign	Het
Slc13a2	T	C	11: 78,403,175 (GRCm38)	N254D	probably benign	Het
Slc16a8	T	A	15: 79,252,607 (GRCm38)	I132F	probably damaging	Het
Slc18b1	T	A	10: 23,819,078 (GRCm38)	Y274N	probably benign	Het
Slc45a2	A	T	15: 11,000,817 (GRCm38)	M1L	probably benign	Het
Smc1b	A	G	15: 85,112,673 (GRCm38)		probably benign	Het
Stab2	T	C	10: 86,949,928 (GRCm38)	S617G	probably benign	Het
Stk10	A	G	11: 32,604,190 (GRCm38)	M626V	probably damaging	Het
Synpo2l	T	G	14: 20,661,398 (GRCm38)	I385L	possibly damaging	Het
Tmprss11d	T	C	5: 86,338,812 (GRCm38)	Y73C	probably damaging	Het
Ttc21b	A	G	2: 66,236,382 (GRCm38)	V309A	probably benign	Het
Tubgcp6	A	G	15: 89,103,065 (GRCm38)	I1235T	probably benign	Het
Usp8	A	G	2: 126,725,390 (GRCm38)	I110V	probably benign	Het
Wdr59	GGGTGGTG	GGGTG	8: 111,480,540 (GRCm38)		probably benign	Het
Zfp207	T	A	11: 80,395,507 (GRCm38)		probably benign	Het
Zfp748	A	C	13: 67,553,025 (GRCm38)		probably null	Het

Other mutations in Vps13c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH 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
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
R1396:Vps13c	UTSW	9	67,955,022 (GRCm38)	missense	probably benign	0.00
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'- AGTCCAGAGGCCCAAAGTCATAAGG -3'
(R):5'- AGTCACTGTTGCAGTCACACCC -3'

Sequencing Primer
(F):5'- TAGCCAGTGATTGACACCTG -3'
(R):5'- GTCACACCCAGTTGAAATGATG -3'

Posted On

2013-06-11