Mutagenetix > Incidental Mutation

Incidental Mutation 'R5718:Fbxw18'

451293

Institutional Source

Beutler Lab

Gene Symbol

Fbxw18

Ensembl Gene

ENSMUSG00000074059

Gene Name

F-box and WD-40 domain protein 18

Synonyms

MMRRC Submission

043338-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R5718 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

109676734-109702700 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 109691568 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 241 (E241G)

Ref Sequence

ENSEMBL: ENSMUSP00000095962 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098359]

AlphaFold

Q3TSA9

Predicted Effect

probably benign
Transcript: ENSMUST00000098359
AA Change: E241G

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000095962
Gene: ENSMUSG00000074059
AA Change: E241G

Domain	Start	End	E-Value	Type
FBOX	8	48	4.13e-6	SMART
Blast:WD40	140	179	2e-7	BLAST

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgra2	T	C	8: 27,113,486		probably null	Het
Ahctf1	G	T	1: 179,769,339	H81N	possibly damaging	Het
Alyref2	T	C	1: 171,504,110	S152P	possibly damaging	Het
Arhgef7	C	T	8: 11,785,774	T20I	probably damaging	Het
Armc3	T	G	2: 19,303,799	Y759*	probably null	Het
Atg5	A	G	10: 44,362,987	S255G	probably benign	Het
Atp11b	A	G	3: 35,837,516	I1026V	probably benign	Het
Atp1a2	C	A	1: 172,279,442	K770N	probably damaging	Het
Bptf	G	T	11: 107,111,434	A284E	probably damaging	Het
Celsr2	A	G	3: 108,393,358	S815P	probably benign	Het
Chrna5	A	G	9: 54,998,105	H67R	probably benign	Het
Cic	A	G	7: 25,272,778	I645V	probably benign	Het
Clpx	A	T	9: 65,299,964	Q48L	probably benign	Het
Crhr2	G	A	6: 55,092,100	Q397*	probably null	Het
Cyp11a1	G	A	9: 58,018,225	V48I	probably benign	Het
Dchs1	C	T	7: 105,755,748	R2529H	probably benign	Het
Dnah7c	A	T	1: 46,748,666	H3293L	possibly damaging	Het
Dock6	G	T	9: 21,824,493	D986E	probably benign	Het
Efcab6	T	A	15: 83,904,238	N952Y	probably damaging	Het
Eml2	G	A	7: 19,201,163	V432I	probably damaging	Het
Epg5	G	A	18: 77,986,403	C1327Y	probably damaging	Het
Fsd1	T	G	17: 55,990,542		probably benign	Het
Gcnt3	A	G	9: 70,034,270	S339P	probably benign	Het
Gldc	T	A	19: 30,110,772	K829*	probably null	Het
Gli3	G	A	13: 15,478,165		probably null	Het
Gm11595	G	A	11: 99,772,555	R100C	unknown	Het
Greb1l	G	A	18: 10,542,427	E1341K	probably damaging	Het
Hmcn1	A	T	1: 150,609,666	I4395N	probably damaging	Het
Hmcn1	A	T	1: 150,690,600	C2217*	probably null	Het
Hmgxb3	A	G	18: 61,140,837	M861T	probably benign	Het
Ift172	A	G	5: 31,255,277	S1545P	possibly damaging	Het
Jak3	C	A	8: 71,684,354	L725M	probably damaging	Het
Lrig2	A	T	3: 104,468,615	C90*	probably null	Het
Mcm7	C	T	5: 138,164,819	R357H	possibly damaging	Het
Mcoln2	T	C	3: 146,181,826	S333P	probably damaging	Het
Mrpl22	A	T	11: 58,177,283	I136L	probably benign	Het
Ncam2	A	T	16: 81,589,814		probably null	Het
Ncdn	G	A	4: 126,749,950	Q360*	probably null	Het
Nsun2	A	G	13: 69,623,284	K338E	probably benign	Het
Obscn	T	C	11: 59,036,808	T6105A	probably damaging	Het
Olfr171	G	A	16: 19,624,389	S237F	probably benign	Het
Olfr957	A	T	9: 39,511,042	L226H	probably damaging	Het
Pcnx4	T	A	12: 72,567,194	F638I	possibly damaging	Het
Pfn3	T	C	13: 55,415,040	I43V	probably benign	Het
Pigm	C	A	1: 172,377,445		probably null	Het
Pkhd1l1	T	A	15: 44,545,417	S2433R	probably damaging	Het
Pomt1	C	A	2: 32,248,692	A440D	possibly damaging	Het
Ptprj	T	C	2: 90,458,269	D691G	probably benign	Het
Qrich1	T	A	9: 108,528,823	S72T	probably damaging	Het
Ralgapa2	T	A	2: 146,453,406		probably null	Het
Rarg	A	C	15: 102,241,067	S156A	probably damaging	Het
Rasl11a	A	G	5: 146,847,144	K133R	probably benign	Het
Rcor1	A	G	12: 111,101,635	D158G	probably benign	Het
Rpn2	C	T	2: 157,321,827	T613M	probably damaging	Het
Sipa1l2	T	A	8: 125,491,248	H450L	probably damaging	Het
Slc25a21	T	C	12: 56,718,156	I263V	probably benign	Het
Slc25a32	A	T	15: 39,097,562	V242E	probably benign	Het
Slc5a5	T	A	8: 70,887,755	T484S	probably benign	Het
Tdrd3	T	C	14: 87,506,440	V608A	probably benign	Het
Thnsl1	C	A	2: 21,212,000	H188Q	possibly damaging	Het
Tshz1	A	T	18: 84,014,524	H586Q	probably damaging	Het
Vmn2r27	C	T	6: 124,192,144	A676T	possibly damaging	Het
Wasf1	G	A	10: 40,926,574	R75Q	probably damaging	Het
Xbp1	T	A	11: 5,521,903	F10I	probably benign	Het
Zbtb1	G	A	12: 76,386,924	M561I	probably benign	Het
Zfp708	T	C	13: 67,070,458	K446E	probably benign	Het

Other mutations in Fbxw18

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00226:Fbxw18	APN	9	109693343	missense	probably benign	0.00
IGL00820:Fbxw18	APN	9	109693369	missense	probably damaging	1.00
IGL01447:Fbxw18	APN	9	109701607	missense	probably damaging	1.00
IGL01511:Fbxw18	APN	9	109688821	missense	possibly damaging	0.83
IGL01956:Fbxw18	APN	9	109693357	missense	probably damaging	0.98
IGL02089:Fbxw18	APN	9	109701322	missense	probably benign	0.00
PIT4810001:Fbxw18	UTSW	9	109676890	nonsense	probably null
R0004:Fbxw18	UTSW	9	109701313	missense	probably damaging	0.96
R0124:Fbxw18	UTSW	9	109691515	missense	probably benign	0.00
R0375:Fbxw18	UTSW	9	109688839	missense	possibly damaging	0.63
R1652:Fbxw18	UTSW	9	109690627	missense	probably benign	0.35
R2153:Fbxw18	UTSW	9	109693370	missense	probably damaging	1.00
R2294:Fbxw18	UTSW	9	109676797	missense	probably damaging	1.00
R3738:Fbxw18	UTSW	9	109688913	missense	possibly damaging	0.57
R4706:Fbxw18	UTSW	9	109690517	missense	probably benign	0.00
R4982:Fbxw18	UTSW	9	109702651	start gained	probably benign
R4990:Fbxw18	UTSW	9	109688393	missense	probably damaging	0.99
R5314:Fbxw18	UTSW	9	109693178	missense	possibly damaging	0.90
R5520:Fbxw18	UTSW	9	109691521	missense	probably benign	0.00
R5634:Fbxw18	UTSW	9	109676803	missense	possibly damaging	0.49
R5894:Fbxw18	UTSW	9	109700167	missense	possibly damaging	0.83
R5928:Fbxw18	UTSW	9	109700081	missense	probably damaging	0.99
R6175:Fbxw18	UTSW	9	109676879	missense	probably damaging	1.00
R6696:Fbxw18	UTSW	9	109688764	missense	probably benign	0.09
R6944:Fbxw18	UTSW	9	109702587	missense	probably damaging	1.00
R7396:Fbxw18	UTSW	9	109688886	missense	probably benign	0.19
R7737:Fbxw18	UTSW	9	109701263	nonsense	probably null
R7883:Fbxw18	UTSW	9	109688406	missense	probably damaging	1.00
R9002:Fbxw18	UTSW	9	109690592	missense	probably damaging	1.00
R9053:Fbxw18	UTSW	9	109688423	missense	probably benign	0.02
R9782:Fbxw18	UTSW	9	109693308	missense	probably benign	0.07

Predicted Primers

PCR Primer
(F):5'- TTCGTATGATAGGGCTTAGGAGAAG -3'
(R):5'- TGTGAGGCAGGCTGTTAACAG -3'

Sequencing Primer
(F):5'- CTTAGGAGAAGGGGAGTGGTCTG -3'
(R):5'- GGTCTCATTACTGGACTTGAAGACAC -3'

Posted On

2017-01-03