Mutagenetix > Incidental Mutation

Incidental Mutation 'R7395:Fry'

573728

Institutional Source

Beutler Lab

Gene Symbol

Fry

Ensembl Gene

ENSMUSG00000056602

Gene Name

FRY microtubule binding protein

Synonyms

9330186A19Rik, cg003

MMRRC Submission

045477-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.469) question?

Stock #

R7395 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

150118645-150497753 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 150380883 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 579 (M579I)

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: M579I

PolyPhen 2 Score 0.817 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000084454
Gene: ENSMUSG00000056602
AA Change: M579I

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

99% (92/93)

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3830403N18Rik	G	T	X: 56,138,780 (GRCm38)		probably null	Het
4930433I11Rik	A	T	7: 40,989,678 (GRCm38)	T13S	probably damaging	Het
Abca13	A	G	11: 9,291,658 (GRCm38)	I1174V	probably benign	Het
Acoxl	G	A	2: 127,884,416 (GRCm38)	V237M	probably damaging	Het
Adam33	A	C	2: 131,061,169 (GRCm38)	W52G	probably benign	Het
Adgrv1	T	C	13: 81,559,348 (GRCm38)	H1313R	probably damaging	Het
Ap3d1	T	C	10: 80,730,882 (GRCm38)	T89A	probably benign	Het
Armc8	T	C	9: 99,533,132 (GRCm38)	E165G	probably damaging	Het
Atp6v1c1	T	C	15: 38,691,705 (GRCm38)	*383Q	probably null	Het
Atp8b4	A	T	2: 126,375,694 (GRCm38)	L634Q	possibly damaging	Het
B3glct	A	G	5: 149,725,604 (GRCm38)		probably null	Het
Bhlhe40	TG	TGG	6: 108,664,857 (GRCm38)	254	probably null	Het
Bicd2	A	G	13: 49,378,230 (GRCm38)	D316G	possibly damaging	Het
Bop1	A	T	15: 76,453,841 (GRCm38)	S610T	probably damaging	Het
Car11	T	A	7: 45,701,321 (GRCm38)	Y80*	probably null	Het
Ccdc121rt2	A	T	5: 112,450,169 (GRCm38)	E194V	possibly damaging	Het
Ccdc96	T	C	5: 36,485,265 (GRCm38)	I205T	probably benign	Het
Ces2a	A	G	8: 104,739,641 (GRCm38)	E390G	probably benign	Het
Cfap54	C	A	10: 92,884,703 (GRCm38)	V2630L	unknown	Het
Chek2	G	T	5: 110,872,108 (GRCm38)		probably null	Het
Cntn3	C	T	6: 102,337,394 (GRCm38)		probably null	Het
Cpne3	A	T	4: 19,528,239 (GRCm38)	D339E	probably damaging	Het
Crocc2	C	T	1: 93,216,107 (GRCm38)	Q1403*	probably null	Het
Crppa	A	T	12: 36,501,995 (GRCm38)	I283F	possibly damaging	Het
Csnka2ip	G	A	16: 64,479,440 (GRCm38)	T187I		Het
Ctu1	A	G	7: 43,676,595 (GRCm38)	H226R	possibly damaging	Het
Cubn	G	T	2: 13,287,064 (GRCm38)	Q3317K	probably damaging	Het
Cyp17a1	A	G	19: 46,670,695 (GRCm38)	L169P	probably benign	Het
Dcc	T	A	18: 71,374,569 (GRCm38)	K911*	probably null	Het
Dcun1d2	G	A	8: 13,278,675 (GRCm38)	R75*	probably null	Het
Defb19	A	T	2: 152,580,023 (GRCm38)		probably null	Het
Dffb	A	T	4: 153,969,113 (GRCm38)	S257R	probably damaging	Het
Dip2c	A	C	13: 9,614,377 (GRCm38)	N942T	probably damaging	Het
Dnah3	T	A	7: 119,966,251 (GRCm38)	I169F		Het
Dnah3	T	C	7: 120,060,960 (GRCm38)	M830V	probably benign	Het
Dnajc5g	G	A	5: 31,111,665 (GRCm38)	S130N	possibly damaging	Het
Dscaml1	C	A	9: 45,702,405 (GRCm38)	Q939K	possibly damaging	Het
Evpl	G	C	11: 116,227,079 (GRCm38)	N761K	possibly damaging	Het
Fbxw8	A	T	5: 118,068,215 (GRCm38)	I556N	probably damaging	Het
Ggt7	A	T	2: 155,495,880 (GRCm38)	M488K	probably benign	Het
Gnpnat1	T	A	14: 45,381,581 (GRCm38)	H107L	probably benign	Het
Golga2	C	A	2: 32,305,587 (GRCm38)	P798Q	possibly damaging	Het
Gpr35	G	A	1: 92,983,207 (GRCm38)	A214T	probably damaging	Het
Greb1	A	T	12: 16,709,430 (GRCm38)		probably null	Het
Hdac10	G	A	15: 89,128,284 (GRCm38)	T32I	probably benign	Het
Hkdc1	G	A	10: 62,385,699 (GRCm38)	T860I	probably damaging	Het
Icam5	C	A	9: 21,035,442 (GRCm38)	P422Q	possibly damaging	Het
Ist1	A	C	8: 109,677,527 (GRCm38)	S238A	probably benign	Het
Lrig2	T	C	3: 104,497,520 (GRCm38)	N91D	probably benign	Het
Mapt	A	C	11: 104,328,123 (GRCm38)	D352A	probably damaging	Het
Micall2	G	A	5: 139,716,369 (GRCm38)	P373L	possibly damaging	Het
Mocs1	A	G	17: 49,454,557 (GRCm38)	S560G	possibly damaging	Het
Mpo	A	G	11: 87,801,124 (GRCm38)	D461G	probably damaging	Het
Myo1a	G	T	10: 127,710,440 (GRCm38)	V271L	probably damaging	Het
Ncoa1	G	A	12: 4,295,188 (GRCm38)	P720S	not run	Het
Ncr1	T	A	7: 4,338,151 (GRCm38)	I47N	probably damaging	Het
Ndufb6	G	A	4: 40,277,730 (GRCm38)	R66C	probably damaging	Het
Obox5	A	T	7: 15,758,743 (GRCm38)	S208C	probably damaging	Het
Or10q1	T	C	19: 13,749,138 (GRCm38)	S11P	probably damaging	Het
Or2n1d	A	T	17: 38,335,864 (GRCm38)	K236*	probably null	Het
Or5p75-ps1	T	A	7: 108,508,404 (GRCm38)	F116Y	unknown	Het
Or7d9	T	A	9: 20,286,530 (GRCm38)	M285K	probably damaging	Het
Padi4	A	C	4: 140,761,672 (GRCm38)	V152G	probably damaging	Het
Pdzd7	A	T	19: 45,037,011 (GRCm38)	D348E	probably damaging	Het
Pdzph1	T	A	17: 58,879,159 (GRCm38)	K1212N	possibly damaging	Het
Piezo2	C	T	18: 63,027,563 (GRCm38)	G2341R	probably damaging	Het
Plb1	A	G	5: 32,353,684 (GRCm38)	K1298E	probably benign	Het
Prr14l	A	G	5: 32,828,638 (GRCm38)	L1171P	probably benign	Het
Rab11fip5	T	C	6: 85,341,868 (GRCm38)	T680A	probably benign	Het
Rev1	A	T	1: 38,088,065 (GRCm38)	N371K	possibly damaging	Het
Rsf1	CGGCGGCGG	CGGCGGCGGGGGCGGCGG	7: 97,579,926 (GRCm38)		probably benign	Het
Ryr2	A	G	13: 11,785,111 (GRCm38)	C917R	probably damaging	Het
Sall1	A	T	8: 89,030,921 (GRCm38)	S852T	possibly damaging	Het
Serpine2	A	G	1: 79,801,555 (GRCm38)	F296L	probably damaging	Het
Slc12a6	A	T	2: 112,352,542 (GRCm38)	N754I	probably damaging	Het
Slc39a6	A	T	18: 24,585,275 (GRCm38)	L575Q	probably damaging	Het
Smarcc2	T	A	10: 128,485,606 (GRCm38)	L890Q	probably damaging	Het
Smg5	T	A	3: 88,361,071 (GRCm38)	V1006D	probably damaging	Het
Ssh2	T	C	11: 77,393,073 (GRCm38)	V51A	probably damaging	Het
St14	T	C	9: 31,096,899 (GRCm38)	K547E	probably benign	Het
Stag1	T	G	9: 100,796,728 (GRCm38)	V234G	probably damaging	Het
Stag3	A	T	5: 138,281,945 (GRCm38)	Q24L	probably benign	Het
Stra6	T	C	9: 58,141,097 (GRCm38)	Y158H	probably damaging	Het
Tcstv1	A	T	13: 119,894,130 (GRCm38)		probably null	Het
Tmem196	G	A	12: 120,011,267 (GRCm38)	C62Y	probably damaging	Het
Tmem265	T	A	7: 127,564,867 (GRCm38)	F84L		Het
Tph1	C	T	7: 46,657,203 (GRCm38)		probably null	Het
Ttn	A	G	2: 76,946,490 (GRCm38)	I1522T	unknown	Het
Ulk4	T	A	9: 121,255,112 (GRCm38)	Q129L	probably benign	Het
Usp17la	T	A	7: 104,861,585 (GRCm38)	S466T	probably benign	Het
Vmn2r31	A	T	7: 7,384,745 (GRCm38)	V609E	probably damaging	Het
Vmn2r52	C	T	7: 10,170,817 (GRCm38)	C365Y	probably benign	Het
Zbtb4	A	T	11: 69,776,111 (GRCm38)	T81S	possibly damaging	Het
Zfp605	A	T	5: 110,112,019 (GRCm38)		probably benign	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
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
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'- AGGAGAAATGCTGTAGACCCTG -3'
(R):5'- CTCAGAGTTTCACGAATGTCAATGG -3'

Sequencing Primer
(F):5'- TGCTGTAGACCCTGTGTAAACCAG -3'
(R):5'- TACAGAGGACCCAGGTTTGATTCC -3'

Posted On

2019-09-13