Mutagenetix > Incidental Mutation

Incidental Mutation 'R0090:Ddx60'

20149

Institutional Source

Beutler Lab

Gene Symbol

Ddx60

Ensembl Gene

ENSMUSG00000037921

Gene Name

DEAD (Asp-Glu-Ala-Asp) box polypeptide 60

Synonyms

MMRRC Submission

038377-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.145) question?

Stock #

R0090 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

61928087-62038244 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 61942293 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 88 (D88G)

Ref Sequence

ENSEMBL: ENSMUSP00000122841 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000070631] [ENSMUST00000093485] [ENSMUST00000154398] [ENSMUST00000156980]

AlphaFold

E9PZQ1

Predicted Effect

probably damaging
Transcript: ENSMUST00000070631
AA Change: D88G

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

SMART Domains

Protein: ENSMUSP00000070741
Gene: ENSMUSG00000037921
AA Change: D88G

Domain	Start	End	E-Value	Type
low complexity region	99	110	N/A	INTRINSIC
low complexity region	364	376	N/A	INTRINSIC
DEXDc	758	949	1.05e-15	SMART
Blast:DEXDc	1007	1132	4e-24	BLAST
HELICc	1245	1328	4.35e-13	SMART
low complexity region	1362	1373	N/A	INTRINSIC
Blast:DEXDc	1503	1584	1e-20	BLAST

Predicted Effect

probably damaging
Transcript: ENSMUST00000093485
AA Change: D88G

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

SMART Domains

Protein: ENSMUSP00000091197
Gene: ENSMUSG00000037921
AA Change: D88G

Domain	Start	End	E-Value	Type
low complexity region	99	110	N/A	INTRINSIC
low complexity region	364	376	N/A	INTRINSIC
DEXDc	759	950	1.05e-15	SMART
Blast:DEXDc	1008	1133	4e-24	BLAST
HELICc	1246	1329	4.35e-13	SMART
low complexity region	1363	1374	N/A	INTRINSIC
Blast:DEXDc	1504	1585	1e-20	BLAST

Predicted Effect

probably damaging
Transcript: ENSMUST00000154398
AA Change: D88G

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

SMART Domains

Protein: ENSMUSP00000122841
Gene: ENSMUSG00000037921
AA Change: D88G

Domain	Start	End	E-Value	Type
low complexity region	99	110	N/A	INTRINSIC
low complexity region	364	376	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000156980

Meta Mutation Damage Score

0.4710

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.7%
20x: 91.4%

Validation Efficiency

99% (90/91)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal immunity to several viruses (IAV, EMCV, SINV) but increased susceptibility to VSV infection. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010315B03Rik	T	C	9: 124,295,159 (GRCm38)		probably benign	Het
4933427I04Rik	A	G	4: 123,860,982 (GRCm38)	T230A	possibly damaging	Het
9230110C19Rik	T	A	9: 8,027,183 (GRCm38)	N118I	probably benign	Het
Acsm1	T	C	7: 119,662,189 (GRCm38)		probably benign	Het
Acta1	T	C	8: 123,893,657 (GRCm38)	N14S	probably damaging	Het
Aff4	A	G	11: 53,392,782 (GRCm38)	T362A	probably benign	Het
Aggf1	A	G	13: 95,364,959 (GRCm38)	I305T	probably benign	Het
Ap4b1	A	G	3: 103,820,429 (GRCm38)	D325G	possibly damaging	Het
Ap4e1	C	T	2: 127,064,985 (GRCm38)	T1055I	possibly damaging	Het
Arhgef2	A	T	3: 88,639,348 (GRCm38)	Q496L	probably damaging	Het
Arhgef28	A	G	13: 98,075,110 (GRCm38)	F122L	probably damaging	Het
Baiap3	G	A	17: 25,250,070 (GRCm38)		probably benign	Het
Casp8ap2	T	A	4: 32,640,327 (GRCm38)	H460Q	probably damaging	Het
Casz1	A	G	4: 148,933,411 (GRCm38)	T386A	probably benign	Het
Cd53	A	T	3: 106,767,409 (GRCm38)	V114E	possibly damaging	Het
Celsr2	A	G	3: 108,393,327 (GRCm38)		probably benign	Het
Chaf1b	G	T	16: 93,887,124 (GRCm38)	A88S	possibly damaging	Het
Cldn10	A	T	14: 118,874,200 (GRCm38)	Y194F	probably damaging	Het
Clec2e	A	C	6: 129,095,218 (GRCm38)		probably null	Het
Cmpk2	A	T	12: 26,478,022 (GRCm38)	T413S	probably benign	Het
Col9a1	T	A	1: 24,223,562 (GRCm38)		probably null	Het
Dchs1	G	T	7: 105,755,932 (GRCm38)	Q2468K	probably benign	Het
Dnah8	A	G	17: 30,784,090 (GRCm38)	R3588G	probably benign	Het
Ect2	T	C	3: 27,115,476 (GRCm38)	T774A	probably benign	Het
Ect2	C	T	3: 27,138,502 (GRCm38)	E431K	probably null	Het
Ern1	A	G	11: 106,405,823 (GRCm38)	V767A	probably damaging	Het
Fbln1	A	C	15: 85,224,288 (GRCm38)	E75A	possibly damaging	Het
Fgf5	C	T	5: 98,261,987 (GRCm38)	R132*	probably null	Het
Folh1	T	C	7: 86,725,868 (GRCm38)		probably benign	Het
Gdf15	A	T	8: 70,629,684 (GRCm38)	H257Q	probably damaging	Het
Ghitm	T	C	14: 37,122,219 (GRCm38)	T322A	probably benign	Het
Gm13212	A	T	4: 145,622,625 (GRCm38)	K211*	probably null	Het
Gm5709	A	G	3: 59,618,771 (GRCm38)		noncoding transcript	Het
Hbb-y	C	T	7: 103,852,743 (GRCm38)		probably null	Het
Hmcn2	A	T	2: 31,426,198 (GRCm38)	D3771V	probably damaging	Het
Hspa12a	T	C	19: 58,799,509 (GRCm38)	D627G	probably benign	Het
Idh2	T	C	7: 80,097,914 (GRCm38)	E286G	probably damaging	Het
Idh3b	C	A	2: 130,280,979 (GRCm38)	A297S	probably benign	Het
Igsf3	A	G	3: 101,435,652 (GRCm38)	E535G	probably damaging	Het
Ilf3	T	A	9: 21,395,414 (GRCm38)	D314E	probably damaging	Het
Itgb8	A	G	12: 119,202,563 (GRCm38)	S78P	probably benign	Het
Itih5	G	A	2: 10,164,684 (GRCm38)	V31I	probably benign	Het
Kcnj2	T	C	11: 111,073,027 (GRCm38)	V415A	probably benign	Het
Kin	A	G	2: 10,085,773 (GRCm38)	Q53R	possibly damaging	Het
Krt78	A	T	15: 101,947,837 (GRCm38)	M513K	probably benign	Het
Krtap4-8	A	T	11: 99,780,486 (GRCm38)		probably benign	Het
Ltbr	T	C	6: 125,309,449 (GRCm38)		probably benign	Het
Mgat4a	G	A	1: 37,490,333 (GRCm38)	T146I	probably damaging	Het
Mrps2	G	C	2: 28,468,256 (GRCm38)	W19C	probably damaging	Het
Mthfs	T	C	9: 89,211,291 (GRCm38)	S33P	probably damaging	Het
Myh6	T	C	14: 54,958,704 (GRCm38)	D546G	probably damaging	Het
Nanos3	C	T	8: 84,176,134 (GRCm38)	R133Q	probably damaging	Het
Ndst2	T	C	14: 20,727,267 (GRCm38)	T553A	probably damaging	Het
Nlrp12	T	C	7: 3,240,034 (GRCm38)	E616G	probably damaging	Het
Nrde2	T	C	12: 100,129,286 (GRCm38)		probably benign	Het
Nup210l	G	A	3: 90,211,779 (GRCm38)	V1832I	probably benign	Het
Olfr1283	A	T	2: 111,369,294 (GRCm38)	I221F	probably damaging	Het
Olfr376	G	A	11: 73,375,576 (GRCm38)	V276I	probably benign	Het
Pcm1	A	T	8: 41,256,041 (GRCm38)	E9D	probably damaging	Het
Pear1	A	T	3: 87,754,342 (GRCm38)	D541E	possibly damaging	Het
Peg10	A	G	6: 4,756,063 (GRCm38)		probably benign	Het
Prss1	G	A	6: 41,461,232 (GRCm38)	R31Q	probably benign	Het
Ptpn13	T	C	5: 103,569,503 (GRCm38)	V1837A	probably damaging	Het
Rasgrp3	A	G	17: 75,498,461 (GRCm38)	D149G	probably damaging	Het
Reg3d	A	T	6: 78,378,483 (GRCm38)	H8Q	possibly damaging	Het
Rhox4f	A	C	X: 37,607,469 (GRCm38)	V15G	probably benign	Het
Sacs	T	A	14: 61,205,440 (GRCm38)	L1645H	probably damaging	Het
Slc16a5	A	T	11: 115,464,925 (GRCm38)	S71C	probably damaging	Het
Slc9a3	A	G	13: 74,158,728 (GRCm38)	E324G	probably damaging	Het
Smgc	T	C	15: 91,859,762 (GRCm38)	V574A	possibly damaging	Het
Stac3	C	T	10: 127,503,930 (GRCm38)		probably benign	Het
Supv3l1	A	G	10: 62,429,706 (GRCm38)	L685P	probably benign	Het
Taar2	G	A	10: 23,941,495 (GRCm38)	R311H	probably benign	Het
Tas2r125	G	T	6: 132,910,398 (GRCm38)	A250S	probably benign	Het
Tdrd6	C	T	17: 43,628,241 (GRCm38)	V639I	probably benign	Het
Thap12	T	G	7: 98,715,893 (GRCm38)	W423G	probably damaging	Het
Tmem245	T	C	4: 56,899,410 (GRCm38)	I217V	probably benign	Het
Trip12	T	A	1: 84,732,136 (GRCm38)		probably benign	Het
Tshz3	T	C	7: 36,768,892 (GRCm38)	V102A	probably benign	Het
Ubap1	T	C	4: 41,379,826 (GRCm38)	S347P	probably damaging	Het
Usp10	C	T	8: 119,953,196 (GRCm38)	Q612*	probably null	Het
Vmn2r72	T	C	7: 85,754,876 (GRCm38)	I36V	probably benign	Het
Vps37a	T	C	8: 40,526,989 (GRCm38)	I63T	possibly damaging	Het
Whrn	C	A	4: 63,432,732 (GRCm38)	R9L	possibly damaging	Het
Xrcc1	T	C	7: 24,570,217 (GRCm38)	Y401H	probably damaging	Het
Ylpm1	GCCTAAGCAGCAACCTAAG	GCCTAAG	12: 85,029,040 (GRCm38)		probably benign	Het
Zfhx3	G	A	8: 108,950,057 (GRCm38)	D2580N	possibly damaging	Het
Zfhx4	A	G	3: 5,243,625 (GRCm38)	N637S	probably damaging	Het
Zyg11a	A	T	4: 108,201,347 (GRCm38)		probably benign	Het

Other mutations in Ddx60

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00340:Ddx60	APN	8	61,958,646 (GRCm38)	missense	probably damaging	1.00
IGL00915:Ddx60	APN	8	61,987,431 (GRCm38)	missense	possibly damaging	0.79
IGL00931:Ddx60	APN	8	61,969,583 (GRCm38)	missense	probably benign	0.18
IGL01023:Ddx60	APN	8	61,942,514 (GRCm38)	missense	probably damaging	0.99
IGL01313:Ddx60	APN	8	61,982,526 (GRCm38)	missense	probably damaging	1.00
IGL01615:Ddx60	APN	8	61,963,740 (GRCm38)	missense	probably null	0.81
IGL01733:Ddx60	APN	8	61,983,865 (GRCm38)	missense	probably damaging	0.99
IGL01779:Ddx60	APN	8	62,017,823 (GRCm38)	missense	possibly damaging	0.94
IGL01900:Ddx60	APN	8	62,000,709 (GRCm38)	splice site	probably benign
IGL02110:Ddx60	APN	8	62,017,247 (GRCm38)	critical splice donor site	probably null
IGL02302:Ddx60	APN	8	61,975,832 (GRCm38)	missense	possibly damaging	0.85
IGL02468:Ddx60	APN	8	61,958,642 (GRCm38)	missense	probably damaging	1.00
IGL02569:Ddx60	APN	8	62,024,951 (GRCm38)	missense	possibly damaging	0.93
IGL02622:Ddx60	APN	8	61,942,436 (GRCm38)	splice site	probably null
IGL02657:Ddx60	APN	8	61,984,115 (GRCm38)	missense	probably benign	0.01
IGL02677:Ddx60	APN	8	61,988,132 (GRCm38)	missense	probably damaging	1.00
IGL02701:Ddx60	APN	8	61,979,341 (GRCm38)	missense	probably damaging	0.96
IGL02806:Ddx60	APN	8	61,956,122 (GRCm38)	missense	probably benign	0.00
IGL03137:Ddx60	APN	8	61,988,083 (GRCm38)	missense	possibly damaging	0.61
IGL03295:Ddx60	APN	8	61,956,121 (GRCm38)	missense	possibly damaging	0.82
IGL03387:Ddx60	APN	8	62,012,449 (GRCm38)	missense	probably damaging	1.00
IGL03411:Ddx60	APN	8	61,977,882 (GRCm38)	critical splice acceptor site	probably null
Scatter	UTSW	8	62,021,314 (GRCm38)	missense	possibly damaging	0.80
shotgun	UTSW	8	62,037,067 (GRCm38)	missense	probably benign	0.28
splay	UTSW	8	62,021,309 (GRCm38)	missense	possibly damaging	0.80
G1Funyon:Ddx60	UTSW	8	62,000,597 (GRCm38)	missense	probably benign	0.01
PIT4504001:Ddx60	UTSW	8	61,958,113 (GRCm38)	missense	probably benign
PIT4677001:Ddx60	UTSW	8	61,972,254 (GRCm38)	missense	possibly damaging	0.87
R0266:Ddx60	UTSW	8	62,033,493 (GRCm38)	missense	possibly damaging	0.92
R0325:Ddx60	UTSW	8	61,983,855 (GRCm38)	missense	probably benign	0.00
R0367:Ddx60	UTSW	8	62,017,749 (GRCm38)	missense	possibly damaging	0.78
R0403:Ddx60	UTSW	8	61,994,541 (GRCm38)	splice site	probably benign
R0479:Ddx60	UTSW	8	61,969,657 (GRCm38)	missense	probably damaging	1.00
R0561:Ddx60	UTSW	8	62,017,794 (GRCm38)	missense	possibly damaging	0.93
R0844:Ddx60	UTSW	8	61,987,361 (GRCm38)	missense	probably benign	0.27
R1119:Ddx60	UTSW	8	61,942,544 (GRCm38)	missense	probably damaging	1.00
R1428:Ddx60	UTSW	8	61,958,159 (GRCm38)	splice site	probably benign
R1778:Ddx60	UTSW	8	61,974,176 (GRCm38)	missense	possibly damaging	0.85
R1840:Ddx60	UTSW	8	61,969,553 (GRCm38)	missense	probably damaging	0.99
R1964:Ddx60	UTSW	8	61,948,869 (GRCm38)	missense	probably benign	0.10
R1970:Ddx60	UTSW	8	61,972,206 (GRCm38)	missense	possibly damaging	0.93
R2101:Ddx60	UTSW	8	61,940,645 (GRCm38)	missense	probably damaging	1.00
R2174:Ddx60	UTSW	8	62,017,200 (GRCm38)	missense	probably benign	0.01
R2174:Ddx60	UTSW	8	61,956,141 (GRCm38)	missense	probably damaging	1.00
R2198:Ddx60	UTSW	8	61,958,063 (GRCm38)	missense	possibly damaging	0.79
R2332:Ddx60	UTSW	8	62,037,091 (GRCm38)	missense	probably benign	0.08
R2338:Ddx60	UTSW	8	62,012,436 (GRCm38)	missense	possibly damaging	0.91
R2379:Ddx60	UTSW	8	62,037,088 (GRCm38)	missense	probably damaging	1.00
R4010:Ddx60	UTSW	8	61,956,144 (GRCm38)	missense	probably benign	0.25
R4010:Ddx60	UTSW	8	61,954,535 (GRCm38)	missense	possibly damaging	0.65
R4133:Ddx60	UTSW	8	61,972,220 (GRCm38)	missense	probably damaging	0.99
R4282:Ddx60	UTSW	8	61,994,393 (GRCm38)	missense	probably damaging	0.99
R4382:Ddx60	UTSW	8	61,948,978 (GRCm38)	splice site	probably null
R4561:Ddx60	UTSW	8	61,942,461 (GRCm38)	missense	probably damaging	0.96
R4572:Ddx60	UTSW	8	61,987,421 (GRCm38)	missense	probably damaging	1.00
R4581:Ddx60	UTSW	8	62,023,261 (GRCm38)	missense	possibly damaging	0.90
R4635:Ddx60	UTSW	8	62,037,067 (GRCm38)	missense	probably benign	0.28
R4698:Ddx60	UTSW	8	62,012,424 (GRCm38)	missense	probably benign	0.01
R4807:Ddx60	UTSW	8	61,979,338 (GRCm38)	missense	probably damaging	1.00
R4858:Ddx60	UTSW	8	62,021,314 (GRCm38)	missense	possibly damaging	0.80
R4964:Ddx60	UTSW	8	61,979,338 (GRCm38)	missense	probably damaging	1.00
R5120:Ddx60	UTSW	8	61,945,906 (GRCm38)	missense	probably benign	0.01
R5187:Ddx60	UTSW	8	61,974,188 (GRCm38)	missense	probably damaging	1.00
R5222:Ddx60	UTSW	8	61,984,158 (GRCm38)	missense	probably damaging	0.99
R5400:Ddx60	UTSW	8	62,010,002 (GRCm38)	missense	possibly damaging	0.65
R5500:Ddx60	UTSW	8	61,950,451 (GRCm38)	missense	probably benign	0.28
R5514:Ddx60	UTSW	8	61,958,057 (GRCm38)	missense	probably damaging	1.00
R5668:Ddx60	UTSW	8	62,000,578 (GRCm38)	missense	probably benign	0.38
R5742:Ddx60	UTSW	8	61,948,921 (GRCm38)	missense	probably benign
R5772:Ddx60	UTSW	8	61,948,897 (GRCm38)	missense	probably damaging	1.00
R5810:Ddx60	UTSW	8	62,012,388 (GRCm38)	nonsense	probably null
R5815:Ddx60	UTSW	8	61,963,722 (GRCm38)	missense	probably damaging	0.98
R5820:Ddx60	UTSW	8	61,956,121 (GRCm38)	missense	possibly damaging	0.82
R5866:Ddx60	UTSW	8	61,940,740 (GRCm38)	missense	probably damaging	1.00
R5881:Ddx60	UTSW	8	62,037,070 (GRCm38)	missense	probably damaging	1.00
R5977:Ddx60	UTSW	8	62,021,410 (GRCm38)	critical splice donor site	probably null
R6048:Ddx60	UTSW	8	62,000,582 (GRCm38)	missense	probably benign	0.01
R6061:Ddx60	UTSW	8	62,023,241 (GRCm38)	missense	probably null	0.01
R6153:Ddx60	UTSW	8	61,945,940 (GRCm38)	missense	possibly damaging	0.47
R6287:Ddx60	UTSW	8	61,950,578 (GRCm38)	missense	probably damaging	1.00
R6415:Ddx60	UTSW	8	61,983,905 (GRCm38)	missense	probably benign	0.00
R6416:Ddx60	UTSW	8	61,998,681 (GRCm38)	missense	probably benign
R6416:Ddx60	UTSW	8	61,977,950 (GRCm38)	missense	probably benign	0.00
R6660:Ddx60	UTSW	8	61,956,239 (GRCm38)	missense	probably benign	0.00
R6694:Ddx60	UTSW	8	62,037,070 (GRCm38)	missense	probably damaging	1.00
R6715:Ddx60	UTSW	8	61,983,890 (GRCm38)	missense	probably benign	0.03
R6720:Ddx60	UTSW	8	62,000,689 (GRCm38)	missense	probably benign	0.10
R6937:Ddx60	UTSW	8	62,037,069 (GRCm38)	missense	probably damaging	1.00
R7153:Ddx60	UTSW	8	61,988,108 (GRCm38)	missense	possibly damaging	0.71
R7274:Ddx60	UTSW	8	61,940,108 (GRCm38)	critical splice donor site	probably null
R7409:Ddx60	UTSW	8	61,958,578 (GRCm38)	missense	probably benign	0.24
R7464:Ddx60	UTSW	8	61,940,674 (GRCm38)	missense	possibly damaging	0.82
R7670:Ddx60	UTSW	8	61,975,792 (GRCm38)	missense	probably damaging	1.00
R7904:Ddx60	UTSW	8	61,977,890 (GRCm38)	missense	possibly damaging	0.81
R7992:Ddx60	UTSW	8	61,954,535 (GRCm38)	missense	probably benign	0.03
R8124:Ddx60	UTSW	8	61,983,911 (GRCm38)	missense	probably benign
R8125:Ddx60	UTSW	8	61,983,911 (GRCm38)	missense	probably benign
R8126:Ddx60	UTSW	8	61,983,911 (GRCm38)	missense	probably benign
R8155:Ddx60	UTSW	8	62,017,171 (GRCm38)	missense	possibly damaging	0.61
R8174:Ddx60	UTSW	8	62,017,250 (GRCm38)	splice site	probably null
R8192:Ddx60	UTSW	8	61,977,968 (GRCm38)	missense	probably damaging	1.00
R8271:Ddx60	UTSW	8	61,940,108 (GRCm38)	critical splice donor site	probably null
R8301:Ddx60	UTSW	8	62,000,597 (GRCm38)	missense	probably benign	0.01
R8304:Ddx60	UTSW	8	61,998,769 (GRCm38)	missense	possibly damaging	0.67
R8319:Ddx60	UTSW	8	61,942,635 (GRCm38)	critical splice donor site	probably null
R8374:Ddx60	UTSW	8	61,974,171 (GRCm38)	missense	probably benign	0.01
R8401:Ddx60	UTSW	8	61,956,243 (GRCm38)	missense	possibly damaging	0.57
R8487:Ddx60	UTSW	8	61,974,150 (GRCm38)	missense	probably damaging	1.00
R8804:Ddx60	UTSW	8	61,958,606 (GRCm38)	missense	probably benign	0.27
R8826:Ddx60	UTSW	8	61,945,956 (GRCm38)	missense	probably benign	0.02
R8829:Ddx60	UTSW	8	61,940,661 (GRCm38)	missense	probably damaging	1.00
R8881:Ddx60	UTSW	8	62,021,309 (GRCm38)	missense	possibly damaging	0.80
R8884:Ddx60	UTSW	8	61,994,519 (GRCm38)	missense	possibly damaging	0.86
R8990:Ddx60	UTSW	8	61,974,134 (GRCm38)	nonsense	probably null
R9122:Ddx60	UTSW	8	61,989,864 (GRCm38)	missense	probably benign	0.16
R9225:Ddx60	UTSW	8	62,017,841 (GRCm38)	missense	probably benign	0.36
R9278:Ddx60	UTSW	8	61,977,978 (GRCm38)	missense	possibly damaging	0.83
R9293:Ddx60	UTSW	8	62,009,960 (GRCm38)	missense	possibly damaging	0.89
R9405:Ddx60	UTSW	8	61,972,214 (GRCm38)	missense	probably benign	0.03
R9766:Ddx60	UTSW	8	62,012,278 (GRCm38)	missense	probably damaging	1.00
X0003:Ddx60	UTSW	8	62,033,417 (GRCm38)	missense	possibly damaging	0.88
X0019:Ddx60	UTSW	8	61,963,692 (GRCm38)	missense	probably benign	0.01
Z1177:Ddx60	UTSW	8	62,000,588 (GRCm38)	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- CATTTGTGAAACAGCACCAGTGCC -3'
(R):5'- ACCTCCTTGAAGAACATCTGCATTCC -3'

Sequencing Primer
(F):5'- GCACCAGTGCCAATTTACTGAC -3'
(R):5'- TGTCTGTCCTGAGAAGAGCAC -3'

Posted On

2013-04-11