Mutagenetix > Incidental Mutation

Incidental Mutation 'R7699:Fry'

593846

Institutional Source

Beutler Lab

Gene Symbol

Fry

Ensembl Gene

ENSMUSG00000056602

Gene Name

FRY microtubule binding protein

Synonyms

9330186A19Rik, cg003

MMRRC Submission

045760-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.585) question?

Stock #

R7699 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

150118645-150497753 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 150405327 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 1308 (H1308Q)

Ref Sequence

ENSEMBL: ENSMUSP00000084454 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000087204
AA Change: H1308Q

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000084454
Gene: ENSMUSG00000056602
AA Change: H1308Q

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

Meta Mutation Damage Score

0.6329

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810009A15Rik	T	C	19: 8,890,053 (GRCm38)	L72P	probably benign	Het
4930407I10Rik	C	A	15: 82,064,105 (GRCm38)	H734Q	probably benign	Het
4932438A13Rik	C	T	3: 37,026,154 (GRCm38)	S267L	probably benign	Het
4932438A13Rik	T	A	3: 36,974,172 (GRCm38)	N2329K	possibly damaging	Het
Acadl	A	G	1: 66,838,363 (GRCm38)	V343A	possibly damaging	Het
Acot4	A	T	12: 84,043,237 (GRCm38)	D236V	probably damaging	Het
App	T	A	16: 85,040,309 (GRCm38)		probably null	Het
Arfgef1	G	A	1: 10,194,411 (GRCm38)	T470I	possibly damaging	Het
Arhgef5	T	C	6: 43,274,757 (GRCm38)	I814T	probably benign	Het
Atr	A	T	9: 95,875,690 (GRCm38)	R968*	probably null	Het
C130060K24Rik	T	A	6: 65,452,956 (GRCm38)	I212N	probably benign	Het
Capn7	C	T	14: 31,352,444 (GRCm38)	T268I	probably benign	Het
Cbwd1	A	G	19: 24,942,681 (GRCm38)		probably null	Het
Cubn	A	G	2: 13,489,917 (GRCm38)	V107A	possibly damaging	Het
Cubn	A	T	2: 13,348,178 (GRCm38)	F1916L	probably benign	Het
Cyp11b1	T	A	15: 74,835,842 (GRCm38)	T473S	probably damaging	Het
Cyr61	C	T	3: 145,648,692 (GRCm38)	G155R	probably damaging	Het
Dip2c	T	G	13: 9,659,311 (GRCm38)	S1396A	probably benign	Het
Dyrk1b	T	C	7: 28,184,312 (GRCm38)	Y198H	probably damaging	Het
Echdc2	G	T	4: 108,174,077 (GRCm38)	R206L	probably benign	Het
Ep400	C	T	5: 110,696,032 (GRCm38)	R1594Q	unknown	Het
Fmnl2	G	A	2: 53,036,508 (GRCm38)	R69Q		Het
Fyb2	T	A	4: 105,010,454 (GRCm38)	D667E	probably benign	Het
Gimap7	T	A	6: 48,723,857 (GRCm38)	Y126N	possibly damaging	Het
Gm1979	A	T	5: 26,000,180 (GRCm38)	W266R	probably damaging	Het
Gm28042	T	A	2: 120,039,716 (GRCm38)	M712K	possibly damaging	Het
Gm3238	A	G	10: 77,770,635 (GRCm38)	*231R	probably null	Het
Gm5592	C	A	7: 41,286,407 (GRCm38)	A111E	probably damaging	Het
Gm7694	A	G	1: 170,301,148 (GRCm38)	*271Q	probably null	Het
Ift81	T	C	5: 122,594,560 (GRCm38)	M304V	possibly damaging	Het
Igfals	T	C	17: 24,880,574 (GRCm38)	L213P	probably damaging	Het
Ints3	G	A	3: 90,421,804 (GRCm38)	P83S	probably benign	Het
Kcna10	T	G	3: 107,195,540 (GRCm38)	S496A	probably damaging	Het
Kmt2d	G	A	15: 98,843,719 (GRCm38)	A4520V	unknown	Het
Lemd3	A	T	10: 120,978,090 (GRCm38)	Y413N	probably damaging	Het
Lgr6	T	C	1: 134,996,032 (GRCm38)	N453S	probably damaging	Het
Lmtk3	A	C	7: 45,792,574 (GRCm38)	D352A	probably damaging	Het
Lrrc4c	T	C	2: 97,630,679 (GRCm38)	M550T	possibly damaging	Het
Maml2	A	T	9: 13,621,089 (GRCm38)	Q533L		Het
Mdn1	T	A	4: 32,741,344 (GRCm38)	D3815E	probably damaging	Het
Megf8	C	T	7: 25,329,928 (GRCm38)	A299V	possibly damaging	Het
Meis3	G	T	7: 16,177,556 (GRCm38)	E59D	probably benign	Het
Mppe1	A	G	18: 67,225,704 (GRCm38)	*398R	probably null	Het
Mtmr7	G	A	8: 40,606,884 (GRCm38)	A62V	possibly damaging	Het
Mtus1	T	A	8: 41,083,969 (GRCm38)	T237S	possibly damaging	Het
Ndfip2	T	A	14: 105,287,759 (GRCm38)	V158E	possibly damaging	Het
Nrbp2	T	G	15: 76,090,897 (GRCm38)	T53P	probably damaging	Het
Nrde2	G	A	12: 100,130,835 (GRCm38)	P902L	probably benign	Het
Olfr1383	A	G	11: 49,524,554 (GRCm38)	Y277C	probably damaging	Het
Olfr509	T	A	7: 108,645,672 (GRCm38)	K301N	probably damaging	Het
Olfr642	T	A	7: 104,050,593 (GRCm38)		probably benign	Het
Olfr739	T	A	14: 50,425,335 (GRCm38)	M272K	probably benign	Het
Olfr771	T	C	10: 129,160,055 (GRCm38)	M310V	probably benign	Het
Pcdha1	A	G	18: 36,931,062 (GRCm38)	T260A	probably damaging	Het
Pdlim1	T	G	19: 40,249,658 (GRCm38)	K98N	probably damaging	Het
Phrf1	G	A	7: 141,254,929 (GRCm38)	G207R	unknown	Het
Pik3r6	A	G	11: 68,528,563 (GRCm38)	K124R	probably damaging	Het
Polr2b	T	A	5: 77,340,421 (GRCm38)	F823I	probably benign	Het
Prss58	T	C	6: 40,895,388 (GRCm38)	I234V	probably damaging	Het
Ptpn14	A	T	1: 189,865,411 (GRCm38)	N766I	probably benign	Het
Repin1	T	A	6: 48,597,822 (GRCm38)	S562T	probably damaging	Het
Rgr	C	T	14: 37,044,595 (GRCm38)	D165N	probably damaging	Het
Rho	T	C	6: 115,935,239 (GRCm38)	F221L	probably damaging	Het
Rictor	C	T	15: 6,772,154 (GRCm38)	S441L	probably benign	Het
Rnase2a	A	G	14: 51,255,791 (GRCm38)	I39T	probably damaging	Het
Rpl13a	T	G	7: 45,127,236 (GRCm38)	I43L	probably benign	Het
Rpp30	T	C	19: 36,089,158 (GRCm38)	V97A	probably benign	Het
Scube3	T	C	17: 28,167,049 (GRCm38)	Y755H	probably damaging	Het
Sec24a	A	T	11: 51,712,257 (GRCm38)	V788E	probably damaging	Het
Spns2	A	T	11: 72,489,617 (GRCm38)	L60*	probably null	Het
Strc	T	C	2: 121,371,748 (GRCm38)	N1213S	possibly damaging	Het
Tec	A	T	5: 72,786,024 (GRCm38)	I116N	possibly damaging	Het
Tll1	A	T	8: 64,093,954 (GRCm38)	D319E	probably benign	Het
Tmem121b	T	C	6: 120,493,427 (GRCm38)	T110A	unknown	Het
Tmem232	T	A	17: 65,265,218 (GRCm38)	I593F	probably damaging	Het
Tpp2	A	G	1: 43,970,466 (GRCm38)	I487V	probably benign	Het
Ubr4	C	A	4: 139,408,867 (GRCm38)	C934*	probably null	Het
Vmn1r68	A	G	7: 10,527,632 (GRCm38)	Y180H	probably benign	Het
Vmn2r25	T	C	6: 123,839,923 (GRCm38)	D233G	possibly damaging	Het
Wdr6	A	G	9: 108,576,361 (GRCm38)	W108R	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
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
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'- CTGCGAGGAAACATGCACAG -3'
(R):5'- CACTAAGACTGCAACGGACTTAGG -3'

Sequencing Primer
(F):5'- ATGCACAGAGTGTTCTCCAG -3'
(R):5'- CTGCAACGGACTTAGGAAAGCTC -3'

Posted On

2019-11-12