Mutagenetix > Incidental Mutation

Incidental Mutation 'R4858:Fry'

372216

Institutional Source

Beutler Lab

Gene Symbol

Fry

Ensembl Gene

ENSMUSG00000056602

Gene Name

FRY microtubule binding protein

Synonyms

9330186A19Rik, cg003

MMRRC Submission

042469-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.585) question?

Stock #

R4858 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

150118645-150497753 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 150401643 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 1175 (V1175A)

Ref Sequence

ENSEMBL: ENSMUSP00000084454 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000087204
AA Change: V1175A

PolyPhen 2 Score 0.783 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000084454
Gene: ENSMUSG00000056602
AA Change: V1175A

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

0.0873

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 96.0%
20x: 91.5%

Validation Efficiency

94% (103/109)

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgb	T	C	10: 10,349,577 (GRCm38)	Y1415C	probably damaging	Het
Adgrf1	T	C	17: 43,303,672 (GRCm38)	S216P	probably damaging	Het
Ankrd12	T	C	17: 66,031,433 (GRCm38)	D197G	probably damaging	Het
Aoc3	C	A	11: 101,331,662 (GRCm38)	H198Q	probably damaging	Het
Aox1	C	A	1: 58,104,481 (GRCm38)	H1253N	probably benign	Het
Arg1	T	A	10: 24,922,638 (GRCm38)	E38V	possibly damaging	Het
Baz2b	T	A	2: 59,907,743 (GRCm38)	M1741L	probably benign	Het
Bend4	T	C	5: 67,417,572 (GRCm38)	E322G	probably damaging	Het
Brpf1	T	C	6: 113,317,678 (GRCm38)	V661A	possibly damaging	Het
C2cd3	A	T	7: 100,454,953 (GRCm38)	T2058S	probably damaging	Het
Camk4	T	C	18: 33,176,213 (GRCm38)	V223A	probably damaging	Het
Casp1	C	T	9: 5,306,742 (GRCm38)	R395C	probably damaging	Het
Ccdc180	T	G	4: 45,923,244 (GRCm38)	I1066S	probably damaging	Het
Ccne1	A	G	7: 38,099,319 (GRCm38)	F292L	probably damaging	Het
Ccz1	A	T	5: 144,012,810 (GRCm38)	M100K	probably damaging	Het
Cep128	T	C	12: 91,260,162 (GRCm38)	T678A	probably benign	Het
Cep290	G	A	10: 100,494,911 (GRCm38)	R151Q	probably benign	Het
Crip3	A	G	17: 46,430,747 (GRCm38)		probably benign	Het
Ddx60	A	G	8: 62,021,314 (GRCm38)	M1479V	possibly damaging	Het
Defb40	T	A	8: 18,975,077 (GRCm38)	I38F	probably benign	Het
Diexf	A	G	1: 193,113,764 (GRCm38)	Y686H	probably damaging	Het
Dnajb2	C	T	1: 75,243,554 (GRCm38)	T221I	possibly damaging	Het
Dpcr1	G	A	17: 35,637,576 (GRCm38)	T377I	possibly damaging	Het
Dpysl3	T	C	18: 43,334,014 (GRCm38)	I279V	probably damaging	Het
Echs1	G	A	7: 140,112,586 (GRCm38)		probably benign	Het
Efl1	T	A	7: 82,671,627 (GRCm38)	N89K	probably damaging	Het
Extl3	T	C	14: 65,075,994 (GRCm38)	T580A	probably benign	Het
Fam171a2	C	T	11: 102,440,156 (GRCm38)	G193E	probably damaging	Het
Fam234a	A	T	17: 26,216,617 (GRCm38)	D264E	probably benign	Het
Fbxw20	A	T	9: 109,234,695 (GRCm38)	V3D	possibly damaging	Het
Fig4	G	A	10: 41,233,590 (GRCm38)	P637L	probably benign	Het
Fnbp1l	G	A	3: 122,546,315 (GRCm38)	T496I	probably benign	Het
Gm5617	C	T	9: 48,495,668 (GRCm38)	A34V	possibly damaging	Het
Gnai1	A	T	5: 18,291,598 (GRCm38)	V109E	probably benign	Het
H2-K1	A	T	17: 33,997,324 (GRCm38)	Y283N	probably benign	Het
Hectd2	A	T	19: 36,605,282 (GRCm38)	I471F	probably damaging	Het
Hsdl2	T	C	4: 59,612,812 (GRCm38)		probably null	Het
Igkv3-1	T	C	6: 70,704,044 (GRCm38)	S76P	probably damaging	Het
Krt15	A	T	11: 100,132,071 (GRCm38)	S439R	probably benign	Het
Lama2	TTTGCGCATT	TTT	10: 27,043,643 (GRCm38)		probably null	Het
Lima1	G	A	15: 99,819,576 (GRCm38)	T23I	probably benign	Het
Map4k1	C	A	7: 28,988,770 (GRCm38)	H248Q	probably damaging	Het
Mcf2l	C	A	8: 13,013,972 (GRCm38)	T1004K	probably damaging	Het
Micall1	T	A	15: 79,122,946 (GRCm38)		probably benign	Het
Ms4a14	A	G	19: 11,301,612 (GRCm38)	I1194T	probably benign	Het
Mtor	T	C	4: 148,454,816 (GRCm38)	*257Q	probably null	Het
Ncan	T	A	8: 70,104,055 (GRCm38)	T961S	probably benign	Het
Olfr1100	T	G	2: 86,978,349 (GRCm38)	Y149S	probably damaging	Het
Olfr161	T	C	16: 3,592,842 (GRCm38)	S149P	probably damaging	Het
Olfr311	T	A	11: 58,841,207 (GRCm38)	L31H	possibly damaging	Het
Olfr331	T	A	11: 58,501,909 (GRCm38)	I216F	probably damaging	Het
Olfr389	T	A	11: 73,776,546 (GRCm38)	L260F	probably benign	Het
Olfr419	A	T	1: 174,250,696 (GRCm38)	I77N	probably damaging	Het
Pcdhgb2	A	G	18: 37,692,100 (GRCm38)	R715G	probably benign	Het
Pik3c3	T	C	18: 30,344,078 (GRCm38)		probably null	Het
Pkhd1l1	A	T	15: 44,491,101 (GRCm38)	D296V	probably damaging	Het
Plekhh2	A	G	17: 84,600,697 (GRCm38)	I1189V	probably damaging	Het
Psg18	A	T	7: 18,353,484 (GRCm38)	L83Q	possibly damaging	Het
Rps6kc1	A	G	1: 190,800,318 (GRCm38)	W496R	probably damaging	Het
Setd5	C	T	6: 113,149,566 (GRCm38)	T1188I	probably damaging	Het
Slc4a3	T	C	1: 75,555,085 (GRCm38)	F899L	probably damaging	Het
Slitrk6	T	C	14: 110,751,883 (GRCm38)	T131A	probably damaging	Het
Speg	G	T	1: 75,421,735 (GRCm38)	R1942L	probably damaging	Het
Sulf2	C	A	2: 166,081,604 (GRCm38)	R565L	probably benign	Het
Tcerg1	T	C	18: 42,523,981 (GRCm38)	M176T	unknown	Het
Tfcp2l1	T	C	1: 118,669,509 (GRCm38)	I440T	possibly damaging	Het
Tgm7	A	T	2: 121,098,964 (GRCm38)		probably null	Het
Tjp2	C	A	19: 24,122,120 (GRCm38)	G433V	probably damaging	Het
Tldc1	T	G	8: 119,772,523 (GRCm38)	T77P	probably benign	Het
Tmc7	C	T	7: 118,543,342 (GRCm38)	G608R	probably damaging	Het
Tmed4	A	G	11: 6,274,456 (GRCm38)	F68S	possibly damaging	Het
Tmem30b	G	A	12: 73,545,912 (GRCm38)	P143L	probably damaging	Het
Tnfrsf23	C	T	7: 143,681,480 (GRCm38)	C49Y	probably damaging	Het
Tnni3k	A	T	3: 154,786,808 (GRCm38)		probably null	Het
Trav12-2	G	T	14: 53,616,693 (GRCm38)	M41I	probably benign	Het
Trim6	T	A	7: 104,232,485 (GRCm38)	Y314*	probably null	Het
Ttc25	A	G	11: 100,550,321 (GRCm38)	N126S	probably damaging	Het
Vmn2r118	A	G	17: 55,592,894 (GRCm38)	V670A	probably damaging	Het
Zfp438	A	T	18: 5,213,154 (GRCm38)	D601E	probably benign	Het
Zfp606	T	A	7: 12,493,056 (GRCm38)	I310N	possibly 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
R1929:Fry	UTSW	5	150,400,924 (GRCm38)	missense	probably null	0.02
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
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'- ATCTGAAGCAGTGTGGGACTC -3'
(R):5'- TACACCCCACTGCAATGTTC -3'

Sequencing Primer
(F):5'- TCCATTACCGGGATGAAGTACCATG -3'
(R):5'- CCACTGCAATGTTCCTAAGTAC -3'

Posted On

2016-03-01