Mutagenetix > Incidental Mutation

Incidental Mutation 'R1929:Fry'

215165

Institutional Source

Beutler Lab

Gene Symbol

Fry

Ensembl Gene

ENSMUSG00000056602

Gene Name

FRY microtubule binding protein

Synonyms

9330186A19Rik, cg003

MMRRC Submission

039947-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.585) question?

Stock #

R1929 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

150118645-150497753 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 150400924 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 1151 (I1151V)

Ref Sequence

ENSEMBL: ENSMUSP00000084454 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087204]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000087204
AA Change: I1151V

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000084454
Gene: ENSMUSG00000056602
AA Change: I1151V

Domain	Start	End	E-Value	Type
Pfam:MOR2-PAG1_N	165	697	5.3e-170	PFAM
low complexity region	1014	1040	N/A	INTRINSIC
Pfam:MOR2-PAG1_mid	1188	1380	1.2e-15	PFAM
Pfam:MOR2-PAG1_mid	1398	1534	1.5e-5	PFAM
Pfam:MOR2-PAG1_mid	1632	1704	1.8e-7	PFAM
Pfam:MOR2-PAG1_mid	1772	1906	4.9e-10	PFAM
low complexity region	1936	1956	N/A	INTRINSIC
low complexity region	1962	1980	N/A	INTRINSIC
Pfam:MOR2-PAG1_C	2050	2303	1.9e-74	PFAM
low complexity region	2369	2385	N/A	INTRINSIC
low complexity region	2463	2482	N/A	INTRINSIC
low complexity region	2525	2534	N/A	INTRINSIC
low complexity region	2836	2852	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200964

Meta Mutation Damage Score

0.1468

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.4%

Validation Efficiency

98% (107/109)

Allele List at MGI

Other mutations in this stock

Total: 103 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adcy10	A	T	1: 165,510,297 (GRCm38)	E160V	probably damaging	Het
Amdhd2	T	C	17: 24,157,886 (GRCm38)		probably null	Het
Angel1	A	C	12: 86,702,319 (GRCm38)	L656V	probably damaging	Het
Ankrd12	G	A	17: 65,986,686 (GRCm38)	S584L	possibly damaging	Het
Apbb2	T	A	5: 66,307,615 (GRCm38)	N679Y	probably benign	Het
Arid3c	T	A	4: 41,724,744 (GRCm38)	I364F	probably damaging	Het
Bcan	T	A	3: 87,993,094 (GRCm38)	S611C	probably damaging	Het
Bnip3	T	G	7: 138,894,630 (GRCm38)		silent	Het
Btc	T	C	5: 91,362,401 (GRCm38)	Y111C	probably damaging	Het
Carnmt1	T	C	19: 18,703,370 (GRCm38)	L336P	probably damaging	Het
Ccdc83	C	T	7: 90,224,077 (GRCm38)	V357I	probably damaging	Het
Cd2bp2	T	C	7: 127,193,878 (GRCm38)	D324G	probably benign	Het
Cdc20b	A	G	13: 113,071,917 (GRCm38)	T216A	probably benign	Het
Cdk17	T	C	10: 93,228,678 (GRCm38)	Y270H	probably damaging	Het
Cenpv	T	C	11: 62,525,233 (GRCm38)	E230G	probably benign	Het
Chst11	T	C	10: 83,191,170 (GRCm38)	Y144H	probably damaging	Het
Cracr2a	T	A	6: 127,607,298 (GRCm38)	F107I	probably damaging	Het
Cyfip1	G	T	7: 55,899,957 (GRCm38)	R624L	probably null	Het
Cyp27b1	T	A	10: 127,048,312 (GRCm38)	V11D	probably damaging	Het
Ddc	T	C	11: 11,835,764 (GRCm38)	N308D	probably damaging	Het
Des	T	G	1: 75,363,493 (GRCm38)	M348R	probably damaging	Het
Dis3l	T	A	9: 64,330,883 (GRCm38)	D109V	probably damaging	Het
Dnah3	T	A	7: 119,975,129 (GRCm38)	I2136F	probably benign	Het
Dnah9	T	C	11: 65,976,398 (GRCm38)	S2785G	probably benign	Het
Dop1a	T	G	9: 86,494,418 (GRCm38)	V235G	probably damaging	Het
Dtx3l	A	T	16: 35,933,689 (GRCm38)	D182E	possibly damaging	Het
Efcab6	A	G	15: 83,892,962 (GRCm38)		probably benign	Het
Elac2	T	A	11: 64,979,189 (GRCm38)	S27T	probably benign	Het
Emsy	T	G	7: 98,626,623 (GRCm38)	K352N	probably damaging	Het
Erbb4	T	C	1: 68,198,888 (GRCm38)	N814S	probably damaging	Het
Fgd6	T	C	10: 94,045,006 (GRCm38)	V574A	probably benign	Het
Filip1	T	C	9: 79,819,930 (GRCm38)	E469G	probably damaging	Het
Fmo1	A	T	1: 162,833,855 (GRCm38)	D286E	probably damaging	Het
Fmo4	A	T	1: 162,799,047 (GRCm38)	I310N	possibly damaging	Het
Focad	A	G	4: 88,342,212 (GRCm38)	N902D	unknown	Het
Focad	A	G	4: 88,397,179 (GRCm38)	S1525G	probably benign	Het
Fras1	T	C	5: 96,667,437 (GRCm38)	W1338R	probably benign	Het
Garin5b	T	A	7: 4,758,187 (GRCm38)	T509S	probably benign	Het
Gm10076	T	G	14: 105,681,870 (GRCm38)		noncoding transcript	Het
Gm5698	T	G	1: 30,977,961 (GRCm38)	D3A	probably damaging	Het
Gngt2	C	T	11: 95,845,146 (GRCm38)		probably benign	Het
Gsdma	T	C	11: 98,671,367 (GRCm38)		probably null	Het
Gtf2h3	A	T	5: 124,602,199 (GRCm38)		probably benign	Het
Hkdc1	T	C	10: 62,417,898 (GRCm38)	T35A	probably benign	Het
Irs1	T	C	1: 82,288,459 (GRCm38)	S679G	probably benign	Het
Itpr1	T	A	6: 108,493,755 (GRCm38)	C2214S	probably damaging	Het
Kcnh8	GAGACCAACGAGCAGCTGATGCTTCAGA	GAGA	17: 52,725,906 (GRCm38)	74	probably benign	Het
Kcnk16	A	G	14: 20,265,279 (GRCm38)	V72A	probably damaging	Het
Lipa	T	A	19: 34,510,890 (GRCm38)	R119*	probably null	Het
Matr3	T	A	18: 35,588,325 (GRCm38)		probably benign	Het
Med13l	T	G	5: 118,728,833 (GRCm38)	F651V	probably benign	Het
Mfsd11	T	C	11: 116,873,914 (GRCm38)	V388A	probably benign	Het
Mki67	C	T	7: 135,698,065 (GRCm38)	V1747I	possibly damaging	Het
Mms22l	T	C	4: 24,535,936 (GRCm38)		probably benign	Het
Msh5	A	G	17: 35,044,390 (GRCm38)	I154T	probably benign	Het
Myo5b	G	T	18: 74,733,925 (GRCm38)	L1382F	probably damaging	Het
Ncbp2	T	C	16: 31,956,951 (GRCm38)	Y138H	probably damaging	Het
Ndufv1	C	A	19: 4,008,347 (GRCm38)	R359L	probably benign	Het
Ntrk3	A	C	7: 78,516,723 (GRCm38)		probably null	Het
Or1e1c	T	A	11: 73,375,601 (GRCm38)	V287E	probably damaging	Het
Or4a15	A	G	2: 89,363,009 (GRCm38)	V140A	probably benign	Het
Or8b12i	T	A	9: 20,171,409 (GRCm38)	H54L	possibly damaging	Het
P4ha1	A	G	10: 59,371,037 (GRCm38)	E523G	probably damaging	Het
Per3	T	A	4: 151,018,885 (GRCm38)	Y530F	probably damaging	Het
Pes1	C	A	11: 3,969,524 (GRCm38)	L66I	probably damaging	Het
Pigr	G	A	1: 130,846,662 (GRCm38)		probably benign	Het
Pkd1l1	A	T	11: 8,836,197 (GRCm38)		probably benign	Het
Plch1	T	A	3: 63,744,535 (GRCm38)	K378N	probably damaging	Het
Plxnb1	T	C	9: 109,102,708 (GRCm38)		probably null	Het
Pramel22	G	A	4: 143,654,142 (GRCm38)	T437I	probably damaging	Het
Prkdc	A	G	16: 15,654,817 (GRCm38)		probably null	Het
Prrc1	G	T	18: 57,381,646 (GRCm38)	D312Y	probably damaging	Het
Psma5-ps	A	G	10: 85,313,731 (GRCm38)		noncoding transcript	Het
Rab3gap2	T	A	1: 185,283,542 (GRCm38)		probably null	Het
Rgs3	A	G	4: 62,702,147 (GRCm38)	I537V	probably damaging	Het
Rhobtb2	T	G	14: 69,796,444 (GRCm38)	D444A	probably damaging	Het
Rnf40	T	C	7: 127,591,784 (GRCm38)	S314P	probably damaging	Het
Rngtt	T	A	4: 33,500,302 (GRCm38)	C565*	probably null	Het
Samd3	A	G	10: 26,263,986 (GRCm38)		probably benign	Het
Sec61a2	A	G	2: 5,873,736 (GRCm38)		probably benign	Het
Serpina3m	G	A	12: 104,389,322 (GRCm38)	A83T	probably damaging	Het
Serpinb13	A	T	1: 106,999,026 (GRCm38)	I251L	possibly damaging	Het
Sez6	C	T	11: 77,972,932 (GRCm38)	T439I	probably damaging	Het
Shc1	G	A	3: 89,423,542 (GRCm38)	G91S	probably damaging	Het
Slc26a2	A	G	18: 61,198,578 (GRCm38)	C594R	possibly damaging	Het
Specc1l	C	T	10: 75,245,604 (GRCm38)	S278F	probably damaging	Het
Spg11	C	T	2: 122,060,207 (GRCm38)	V2044M	probably damaging	Het
Stx18	T	A	5: 38,128,039 (GRCm38)		probably null	Het
Suclg2	T	C	6: 95,589,094 (GRCm38)		probably benign	Het
Tlr4	A	T	4: 66,839,444 (GRCm38)	H158L	probably damaging	Het
Tmem131	A	G	1: 36,812,271 (GRCm38)	V966A	possibly damaging	Het
Tram1l1	T	A	3: 124,321,986 (GRCm38)	I265N	probably damaging	Het
Trim58	T	A	11: 58,640,667 (GRCm38)	F67Y	possibly damaging	Het
Ttc19	A	G	11: 62,281,824 (GRCm38)	Q74R	probably benign	Het
Usp7	T	C	16: 8,698,469 (GRCm38)	S649G	probably benign	Het
Vmn2r16	A	G	5: 109,339,258 (GRCm38)	Y115C	possibly damaging	Het
Zfp444	T	C	7: 6,189,555 (GRCm38)	C191R	probably damaging	Het
Zfp451	G	A	1: 33,783,856 (GRCm38)	P99S	probably benign	Het
Zfp451	A	G	1: 33,782,193 (GRCm38)	F151L	probably damaging	Het
Zfp729b	A	T	13: 67,592,233 (GRCm38)	C648S	probably damaging	Het
Zfp799	A	G	17: 32,821,803 (GRCm38)	Y58H	probably damaging	Het
Zfp804b	A	G	5: 6,769,748 (GRCm38)	V1069A	probably benign	Het
Zfp938	C	T	10: 82,225,547 (GRCm38)	G413D	probably damaging	Het

Other mutations in Fry

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00327:Fry	APN	5	150,340,404 (GRCm38)	nonsense	probably null
IGL00328:Fry	APN	5	150,340,404 (GRCm38)	nonsense	probably null
IGL00841:Fry	APN	5	150,422,724 (GRCm38)	missense	probably benign
IGL00938:Fry	APN	5	150,370,180 (GRCm38)	missense	probably damaging	1.00
IGL01015:Fry	APN	5	150,422,787 (GRCm38)	missense	probably benign	0.18
IGL01401:Fry	APN	5	150,438,788 (GRCm38)	missense	probably benign
IGL01616:Fry	APN	5	150,399,599 (GRCm38)	missense	probably damaging	1.00
IGL01616:Fry	APN	5	150,438,811 (GRCm38)	splice site	probably null
IGL01748:Fry	APN	5	150,345,651 (GRCm38)	splice site	probably benign
IGL01965:Fry	APN	5	150,381,621 (GRCm38)	missense	probably damaging	1.00
IGL02030:Fry	APN	5	150,471,618 (GRCm38)	splice site	probably benign
IGL02079:Fry	APN	5	150,399,624 (GRCm38)	missense	probably damaging	0.97
IGL02087:Fry	APN	5	150,403,594 (GRCm38)	missense	probably benign	0.23
IGL02113:Fry	APN	5	150,399,605 (GRCm38)	missense	probably benign
IGL02209:Fry	APN	5	150,437,026 (GRCm38)	missense	probably benign	0.00
IGL02250:Fry	APN	5	150,403,434 (GRCm38)	splice site	probably benign
IGL02265:Fry	APN	5	150,437,153 (GRCm38)	missense	probably damaging	1.00
IGL02486:Fry	APN	5	150,491,177 (GRCm38)	missense	probably damaging	0.99
IGL02552:Fry	APN	5	150,380,910 (GRCm38)	missense	probably damaging	1.00
IGL02881:Fry	APN	5	150,359,051 (GRCm38)	missense	probably damaging	0.99
IGL03008:Fry	APN	5	150,345,556 (GRCm38)	missense	possibly damaging	0.82
IGL03140:Fry	APN	5	150,495,701 (GRCm38)	missense	probably damaging	0.98
IGL03171:Fry	APN	5	150,380,809 (GRCm38)	missense	probably damaging	1.00
IGL03389:Fry	APN	5	150,394,231 (GRCm38)	missense	probably damaging	1.00
IGL03404:Fry	APN	5	150,326,168 (GRCm38)	missense	probably damaging	1.00
Brook	UTSW	5	150,326,132 (GRCm38)	missense	probably damaging	1.00
haydn	UTSW	5	150,418,464 (GRCm38)	missense	possibly damaging	0.94
miracle	UTSW	5	150,437,159 (GRCm38)	missense	probably damaging	0.99
quickening	UTSW	5	150,434,776 (GRCm38)	missense	probably damaging	1.00
seasons	UTSW	5	150,466,437 (GRCm38)	missense	probably benign	0.06
Vivaldi	UTSW	5	150,394,138 (GRCm38)	missense	possibly damaging	0.80
R0023:Fry	UTSW	5	150,451,098 (GRCm38)	missense	possibly damaging	0.78
R0024:Fry	UTSW	5	150,380,803 (GRCm38)	missense	probably benign	0.03
R0030:Fry	UTSW	5	150,372,569 (GRCm38)	nonsense	probably null
R0053:Fry	UTSW	5	150,461,377 (GRCm38)	splice site	probably benign
R0089:Fry	UTSW	5	150,340,427 (GRCm38)	missense	possibly damaging	0.91
R0212:Fry	UTSW	5	150,496,397 (GRCm38)	missense	probably damaging	0.99
R0241:Fry	UTSW	5	150,260,346 (GRCm38)	intron	probably benign
R0265:Fry	UTSW	5	150,434,776 (GRCm38)	missense	probably damaging	1.00
R0317:Fry	UTSW	5	150,471,468 (GRCm38)	missense	probably damaging	1.00
R0532:Fry	UTSW	5	150,478,761 (GRCm38)	splice site	probably benign
R0532:Fry	UTSW	5	150,433,707 (GRCm38)	unclassified	probably benign
R0599:Fry	UTSW	5	150,437,159 (GRCm38)	missense	probably damaging	0.99
R0631:Fry	UTSW	5	150,496,352 (GRCm38)	missense	possibly damaging	0.82
R0723:Fry	UTSW	5	150,496,360 (GRCm38)	missense	probably damaging	1.00
R0766:Fry	UTSW	5	150,403,432 (GRCm38)	splice site	probably benign
R0790:Fry	UTSW	5	150,466,437 (GRCm38)	missense	probably benign	0.06
R0928:Fry	UTSW	5	150,437,084 (GRCm38)	missense	probably damaging	1.00
R1104:Fry	UTSW	5	150,496,289 (GRCm38)	missense	probably damaging	1.00
R1144:Fry	UTSW	5	150,418,464 (GRCm38)	missense	possibly damaging	0.94
R1172:Fry	UTSW	5	150,481,494 (GRCm38)	nonsense	probably null
R1312:Fry	UTSW	5	150,403,432 (GRCm38)	splice site	probably benign
R1347:Fry	UTSW	5	150,495,818 (GRCm38)	missense	probably damaging	1.00
R1347:Fry	UTSW	5	150,495,818 (GRCm38)	missense	probably damaging	1.00
R1437:Fry	UTSW	5	150,310,425 (GRCm38)	missense	possibly damaging	0.92
R1458:Fry	UTSW	5	150,380,859 (GRCm38)	missense	probably damaging	1.00
R1542:Fry	UTSW	5	150,404,966 (GRCm38)	missense	probably benign	0.13
R1692:Fry	UTSW	5	150,370,227 (GRCm38)	missense	probably damaging	1.00
R1826:Fry	UTSW	5	150,436,709 (GRCm38)	missense	possibly damaging	0.82
R1874:Fry	UTSW	5	150,345,921 (GRCm38)	missense	probably damaging	1.00
R1875:Fry	UTSW	5	150,326,132 (GRCm38)	missense	probably damaging	1.00
R1881:Fry	UTSW	5	150,478,046 (GRCm38)	missense	probably damaging	0.97
R1884:Fry	UTSW	5	150,403,520 (GRCm38)	missense	probably benign	0.00
R2066:Fry	UTSW	5	150,370,119 (GRCm38)	splice site	probably benign
R2270:Fry	UTSW	5	150,400,924 (GRCm38)	missense	probably null	0.02
R2356:Fry	UTSW	5	150,471,432 (GRCm38)	missense	probably benign
R3720:Fry	UTSW	5	150,454,572 (GRCm38)	missense	probably damaging	1.00
R3773:Fry	UTSW	5	150,398,198 (GRCm38)	missense	probably damaging	0.96
R3824:Fry	UTSW	5	150,496,419 (GRCm38)	missense	possibly damaging	0.94
R3902:Fry	UTSW	5	150,345,927 (GRCm38)	missense	probably damaging	1.00
R3923:Fry	UTSW	5	150,413,349 (GRCm38)	missense	probably benign
R4250:Fry	UTSW	5	150,310,360 (GRCm38)	missense	probably damaging	0.99
R4332:Fry	UTSW	5	150,381,663 (GRCm38)	missense	probably damaging	1.00
R4495:Fry	UTSW	5	150,310,463 (GRCm38)	missense	probably damaging	1.00
R4610:Fry	UTSW	5	150,386,104 (GRCm38)	missense	probably damaging	1.00
R4682:Fry	UTSW	5	150,422,754 (GRCm38)	missense	probably damaging	1.00
R4732:Fry	UTSW	5	150,386,007 (GRCm38)	missense
R4733:Fry	UTSW	5	150,386,007 (GRCm38)	missense
R4755:Fry	UTSW	5	150,398,254 (GRCm38)	missense	probably damaging	0.99
R4788:Fry	UTSW	5	150,399,636 (GRCm38)	missense	probably benign	0.00
R4803:Fry	UTSW	5	150,399,533 (GRCm38)	missense	probably benign	0.31
R4858:Fry	UTSW	5	150,401,643 (GRCm38)	missense	possibly damaging	0.78
R4872:Fry	UTSW	5	150,394,239 (GRCm38)	critical splice donor site	probably null
R4902:Fry	UTSW	5	150,495,703 (GRCm38)	missense	probably benign	0.43
R4915:Fry	UTSW	5	150,478,863 (GRCm38)	missense	probably benign	0.30
R4938:Fry	UTSW	5	150,477,989 (GRCm38)	missense	probably damaging	1.00
R4983:Fry	UTSW	5	150,398,254 (GRCm38)	missense	probably damaging	1.00
R5004:Fry	UTSW	5	150,433,604 (GRCm38)	missense	probably benign	0.16
R5040:Fry	UTSW	5	150,388,854 (GRCm38)	missense	probably damaging	0.99
R5145:Fry	UTSW	5	150,370,224 (GRCm38)	missense	probably damaging	0.98
R5170:Fry	UTSW	5	150,429,854 (GRCm38)	missense	probably benign	0.03
R5233:Fry	UTSW	5	150,469,720 (GRCm38)	missense	possibly damaging	0.71
R5428:Fry	UTSW	5	150,405,359 (GRCm38)	missense	possibly damaging	0.89
R5468:Fry	UTSW	5	150,399,588 (GRCm38)	missense	probably benign	0.44
R5481:Fry	UTSW	5	150,260,319 (GRCm38)	missense	probably benign	0.01
R5494:Fry	UTSW	5	150,390,667 (GRCm38)	missense	probably damaging	1.00
R5538:Fry	UTSW	5	150,495,848 (GRCm38)	missense	probably damaging	1.00
R5638:Fry	UTSW	5	150,359,081 (GRCm38)	missense	possibly damaging	0.46
R5645:Fry	UTSW	5	150,380,867 (GRCm38)	missense	probably damaging	1.00
R5716:Fry	UTSW	5	150,370,221 (GRCm38)	nonsense	probably null
R5812:Fry	UTSW	5	150,399,671 (GRCm38)	missense	probably damaging	0.99
R5813:Fry	UTSW	5	150,399,671 (GRCm38)	missense	probably damaging	0.99
R5873:Fry	UTSW	5	150,378,885 (GRCm38)	missense	probably damaging	1.00
R5933:Fry	UTSW	5	150,390,800 (GRCm38)	intron	probably benign
R6037:Fry	UTSW	5	150,428,179 (GRCm38)	missense	probably benign	0.03
R6037:Fry	UTSW	5	150,428,179 (GRCm38)	missense	probably benign	0.03
R6158:Fry	UTSW	5	150,454,572 (GRCm38)	missense	probably damaging	1.00
R6178:Fry	UTSW	5	150,454,522 (GRCm38)	missense	probably damaging	1.00
R6481:Fry	UTSW	5	150,386,014 (GRCm38)	missense	probably damaging	1.00
R6562:Fry	UTSW	5	150,326,149 (GRCm38)	missense	probably damaging	1.00
R6676:Fry	UTSW	5	150,380,922 (GRCm38)	missense	probably benign	0.22
R6717:Fry	UTSW	5	150,496,312 (GRCm38)	missense	probably benign	0.00
R6828:Fry	UTSW	5	150,466,446 (GRCm38)	splice site	probably null
R6874:Fry	UTSW	5	150,437,303 (GRCm38)	missense	probably benign	0.00
R6930:Fry	UTSW	5	150,428,230 (GRCm38)	missense	probably benign	0.00
R6963:Fry	UTSW	5	150,457,844 (GRCm38)	missense	probably benign	0.17
R6965:Fry	UTSW	5	150,416,220 (GRCm38)	missense	possibly damaging	0.79
R7051:Fry	UTSW	5	150,395,169 (GRCm38)	missense	possibly damaging	0.93
R7085:Fry	UTSW	5	150,438,749 (GRCm38)	missense	probably benign	0.02
R7108:Fry	UTSW	5	150,491,090 (GRCm38)	missense
R7108:Fry	UTSW	5	150,395,786 (GRCm38)	missense	probably damaging	1.00
R7115:Fry	UTSW	5	150,386,067 (GRCm38)	missense	probably damaging	1.00
R7116:Fry	UTSW	5	150,395,869 (GRCm38)	critical splice donor site	probably null
R7197:Fry	UTSW	5	150,469,767 (GRCm38)	missense
R7256:Fry	UTSW	5	150,466,786 (GRCm38)	missense
R7318:Fry	UTSW	5	150,436,993 (GRCm38)	missense	probably damaging	0.98
R7323:Fry	UTSW	5	150,496,349 (GRCm38)	missense
R7358:Fry	UTSW	5	150,416,323 (GRCm38)	missense	probably benign
R7361:Fry	UTSW	5	150,436,847 (GRCm38)	missense	possibly damaging	0.92
R7395:Fry	UTSW	5	150,380,883 (GRCm38)	missense	possibly damaging	0.82
R7487:Fry	UTSW	5	150,414,574 (GRCm38)	missense	possibly damaging	0.79
R7491:Fry	UTSW	5	150,466,326 (GRCm38)	missense
R7574:Fry	UTSW	5	150,380,894 (GRCm38)	missense	probably benign	0.00
R7582:Fry	UTSW	5	150,496,382 (GRCm38)	missense
R7586:Fry	UTSW	5	150,426,218 (GRCm38)	missense	probably damaging	1.00
R7650:Fry	UTSW	5	150,413,418 (GRCm38)	missense	probably damaging	1.00
R7699:Fry	UTSW	5	150,405,327 (GRCm38)	missense	probably damaging	0.98
R7700:Fry	UTSW	5	150,405,327 (GRCm38)	missense	probably damaging	0.98
R7972:Fry	UTSW	5	150,310,396 (GRCm38)	missense	probably benign	0.05
R8058:Fry	UTSW	5	150,495,767 (GRCm38)	missense
R8070:Fry	UTSW	5	150,478,007 (GRCm38)	missense
R8159:Fry	UTSW	5	150,399,533 (GRCm38)	missense	probably benign	0.31
R8202:Fry	UTSW	5	150,431,737 (GRCm38)	missense	probably damaging	1.00
R8261:Fry	UTSW	5	150,445,907 (GRCm38)	missense	probably damaging	1.00
R8279:Fry	UTSW	5	150,496,261 (GRCm38)	missense
R8338:Fry	UTSW	5	150,359,051 (GRCm38)	missense	probably damaging	0.99
R8370:Fry	UTSW	5	150,395,819 (GRCm38)	missense	probably damaging	1.00
R8673:Fry	UTSW	5	150,395,111 (GRCm38)	missense	possibly damaging	0.91
R8786:Fry	UTSW	5	150,394,036 (GRCm38)	missense	probably benign	0.00
R8815:Fry	UTSW	5	150,394,138 (GRCm38)	missense	possibly damaging	0.80
R8847:Fry	UTSW	5	150,386,007 (GRCm38)	missense
R9023:Fry	UTSW	5	150,437,303 (GRCm38)	missense	probably benign	0.00
R9025:Fry	UTSW	5	150,295,808 (GRCm38)	intron	probably benign
R9125:Fry	UTSW	5	150,346,060 (GRCm38)	missense	probably damaging	0.97
R9172:Fry	UTSW	5	150,413,328 (GRCm38)	missense	probably benign
R9262:Fry	UTSW	5	150,381,644 (GRCm38)	missense	probably damaging	1.00
R9263:Fry	UTSW	5	150,399,263 (GRCm38)	missense	probably damaging	1.00
R9293:Fry	UTSW	5	150,495,832 (GRCm38)	missense
R9368:Fry	UTSW	5	150,477,938 (GRCm38)	missense
R9401:Fry	UTSW	5	150,378,938 (GRCm38)	missense	probably damaging	1.00
R9402:Fry	UTSW	5	150,436,853 (GRCm38)	missense	probably damaging	1.00
R9402:Fry	UTSW	5	150,433,696 (GRCm38)	missense	possibly damaging	0.91
R9420:Fry	UTSW	5	150,433,529 (GRCm38)	missense	possibly damaging	0.72
R9557:Fry	UTSW	5	150,466,316 (GRCm38)	missense
R9647:Fry	UTSW	5	150,369,519 (GRCm38)	missense	probably damaging	1.00
R9650:Fry	UTSW	5	150,445,910 (GRCm38)	missense	probably damaging	1.00
R9655:Fry	UTSW	5	150,438,786 (GRCm38)	missense	possibly damaging	0.90
R9664:Fry	UTSW	5	150,359,023 (GRCm38)	missense	probably damaging	0.98
R9668:Fry	UTSW	5	150,358,853 (GRCm38)	missense	probably damaging	1.00
R9732:Fry	UTSW	5	150,405,293 (GRCm38)	missense	probably benign	0.00
R9773:Fry	UTSW	5	150,399,263 (GRCm38)	missense	probably damaging	1.00
Z1177:Fry	UTSW	5	150,310,437 (GRCm38)	missense	possibly damaging	0.80

Predicted Primers

PCR Primer
(F):5'- TGAGGGTAATATTCAGTAGTGCTAC -3'
(R):5'- CCAGATGGTGTGCTTATGTATTTACCC -3'

Sequencing Primer
(F):5'- CAGCCTAATATAGACTAACAACAGTC -3'
(R):5'- GGTGTGCTTATGTATTTACCCACATC -3'

Posted On

2014-07-14